Yayınlar & Eserler

Yayın Ağı
Makaleler 231
Tümü (231)
SCI-E, SSCI, AHCI (226)
SCI-E, SSCI, AHCI, ESCI (230)
ESCI (3)
Scopus (229)
TRDizin (14)

1. The clinical characteristics of patients with congenital nephrotic syndrome secondary to NPHS1 mutation: Is nephrectomy still a therapeutic option for selected cases?

Ugurlu Y., GÜLHAN B., DURSUN İ., Nalcacioglu H., Kaya Aksoy G., CANPOLAT N., et al.
PEDIATRIC NEPHROLOGY , 2025 (SCI-Expanded, Scopus) identifier identifier

2. A Novel NUP85 Variant Expanding the Phenotypic Spectrum of NUP85-Associated Steroid-Resistant Nephrotic Syndrome

KURT ŞÜKÜR E. D., TİMUÇİN E., BAŞTUĞ T., ÖZALTIN F.
CLINICAL GENETICS , 2025 (SCI-Expanded, Scopus) identifier identifier

3. Short Bowel Syndrome Is Not a Contraindication for Kidney Transplantation

TAŞTEMEL ÖZTÜRK T., GÜLHAN B., GÜMÜŞ E., HIZARCIOĞLU GÜLŞEN H., KURT ŞÜKÜR E. D., BOZACI A. C., et al.
PEDIATRIC TRANSPLANTATION , cilt.28, sa.8, 2024 (SCI-Expanded, Scopus) identifier identifier identifier

4. Adolescence-onset atypical hemolytic uremic syndrome: is it different from infant-onset?

Celegen K., Gulhan B., Fidan K., Yuksel S., Yilmaz N., Yılmaz A. C., et al.
Clinical and experimental nephrology , cilt.28, ss.1027-1037, 2024 (SCI-Expanded, Scopus) identifier identifier identifier

5. A Rare Kidney Involvement in Juvenile Dermatomyositis: Focal Segmental Glomerulosclerosis

KAHYA H. H., ORUÇ Ç., BAYINDIR Y., KURT ŞÜKÜR E. D., GÜLHAN B., ÖZALTIN F., et al.
PEDIATRIC NEPHROLOGY , sa.1, 2024 (SCI-Expanded, Scopus) identifier

6. NUP85 NM_024844:c.1379G> A (p.Arg460Gln), a novel variant in nephrotic syndrome

KURT ŞÜKÜR E. D., TİMUÇİN E., BAŞTUĞ T., ÖZALTIN F.
PEDIATRIC NEPHROLOGY , sa.1, 2024 (SCI-Expanded, Scopus) identifier

7. Variable phenotype and genotype of pediatric patients with HNF1B nephropathy

GÜLHAN B., Ekici O., DURSUN İ., GÖKNAR N., YÜKSEL S., Alaygut D., et al.
PEDIATRIC NEPHROLOGY , sa.1, 2024 (SCI-Expanded, Scopus) identifier

8. Does nephrectomy affect patient survival in patients with congenital nephrotic syndrome secondary to nephrin mutations?

Turkel Y., GÜLHAN B., Ozdemir G., KURT ŞÜKÜR E. D., DÜZOVA A., ÖZALTIN F.
PEDIATRIC NEPHROLOGY , sa.1, 2024 (SCI-Expanded, Scopus) identifier

9. Brown Tumor in Pediatric Patients with Chronic Kidney Disease: Two Cases of a Rare Condition

ORUÇ Ç., KURT ŞÜKÜR E. D., GÜLHAN B., VARAN A., ÖZALTIN F., DÜZOVA A.
PEDIATRIC NEPHROLOGY , sa.1, 2024 (SCI-Expanded, Scopus) identifier

10. Long Term Follow-up Of Children With Nephrocalcinosis: A Tertiary Center Experience

Yavuz G., OĞUZ B., Ozcan N., Ozdemir G., KURT ŞÜKÜR E. D., ÖZALTIN F., et al.
PEDIATRIC NEPHROLOGY , sa.1, 2024 (SCI-Expanded, Scopus) identifier

11. Variable phenotype and genotype of pediatric patients with HNF1B nephropathy.

Gülhan B., Ekici O., Dursun İ., Göknar N., Yüksel S., Alaygut D., et al.
Clinical nephrology , cilt.102, ss.79-88, 2024 (SCI-Expanded, Scopus) identifier identifier identifier

12. Calcineurin inhibitor-related hyperkalemia is caused by hyporeninemic hypoaldosteronism and fludrocortisone is an effective treatment: Report of a case series and review of the literature

ÜNSAL Y., BALTU D., GÜLHAN B., OKUR F. V., ÖZALTIN F., DÜZOVA A., et al.
PEDIATRIC TRANSPLANTATION , cilt.28, sa.4, 2024 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

13. COVID-19 vaccination among adolescents and young adults with chronic kidney conditions: a single-center experience.

Baltu D., Kurt-Sukur E. D., Tastemel Ozturk T., Gulhan B., Ozaltin F., Duzova A., et al.
Klinische Padiatrie , 2024 (SCI-Expanded, Scopus) identifier identifier identifier

14. Steroid-Resistant Nephrotic Syndrome due to NPHS2 Variants Is Not Associated With Posttransplant Recurrence

Kachmar J., Boyer O., Lipska-Ziętkiewicz B., Morinière V., Gribouval O., Heidet L., et al.
Kidney International Reports , cilt.9, sa.4, ss.973-981, 2024 (SCI-Expanded, Scopus) identifier identifier identifier

15. Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)

Riedhammer K. M., Nguyen T. T., KOŞUKCU C., Calzada-Wack J., Li Y., Assia Batzir N., et al.
Kidney International , cilt.105, sa.4, ss.844-864, 2024 (SCI-Expanded, Scopus) identifier identifier identifier

16. Acute kidney injury in children with moderate-severe COVID-19 and multisystem inflammatory syndrome in children: a referral center experience

TAŞTEMEL ÖZTÜRK T., DÜZOVA A., OYGAR P. D., BALTU D., ÖZÇİLİNGİR P., LAÇİNEL GÜRLEVİK S., et al.
Pediatric Nephrology , cilt.39, sa.3, ss.867-877, 2024 (SCI-Expanded, Scopus) identifier identifier identifier

17. Omic Studies on In Vitro Cystinosis Model: siRNA-Mediated CTNS Gene Silencing in HK-2 Cells

Baysal İ., YABANOĞLU ÇİFTÇİ S., NEMUTLU E., EYLEM C. C., Gök-Topak E. D., ULUBAYRAM K., et al.
Laboratory investigation; a journal of technical methods and pathology , cilt.104, sa.1, ss.100287, 2024 (SCI-Expanded, Scopus) identifier identifier identifier

18. Genotype/phenotype relationship in mild congenital nephrotic syndrome

Mulic B., Peco-Antic A., ÖZALTIN F.
SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO , cilt.2024-January-February, sa.1-2, ss.81-84, 2024 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier

19. Management of pediatric hemolytic uremic syndrome

GÜLHAN B., ÖZALTIN F., Fidan K., ÖZÇAKAR Z. B., Söylemezoğlu O.
Turkish Journal of Pediatrics , cilt.66, sa.1, ss.1-16, 2024 (SCI-Expanded, Scopus, TRDizin) identifier identifier identifier identifier

20. An unusual cause of diarrhea in a child with nephrotic syndrome: Answers.

Baltu D., Kurt Sukur E. D., Gumus E., Tastemel Ozturk T., Ergen Y. M., Demirtas D., et al.
Pediatric nephrology (Berlin, Germany) , cilt.38, sa.12, ss.3977-3981, 2023 (SCI-Expanded, Scopus) identifier identifier

21. A novel homozygous missense variant in TBC1D31 in a consanguineous family with congenital anomalies of the kidney and urinary tract (CAKUT)

SAYGILI S. K., KOŞUKCU C., BAŞTUĞ T., DOĞAN EKİCİ A. I., YILMAZ E. M., Kalyoncu A. U., et al.
Clinical Genetics , cilt.104, sa.6, ss.679-685, 2023 (SCI-Expanded, Scopus) identifier identifier identifier

22. An unusual cause of diarrhea in a child with nephrotic syndrome: Questions.

Baltu D., Kurt Sukur E. D., Gumus E., Tastemel Ozturk T., Ergen Y. M., Demirtas D., et al.
Pediatric nephrology (Berlin, Germany) , cilt.38, sa.12, ss.3975-3976, 2023 (SCI-Expanded, Scopus) identifier identifier

23. Long-term kidney follow-up after pediatric acute kidney support therapy for children less than 15 kg

GÜLÇEK Ö. N., GÜLHAN B., KESİCİ S., KURT ŞÜKÜR E. D., HAYRAN K. M., ÖZALTIN F., et al.
Pediatric Nephrology , cilt.38, sa.11, ss.3811-3821, 2023 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

24. BK Virus Infections in Pediatric Kidney Transplant Recipients: A Single-Center Experience

KURT ŞÜKÜR E. D., GÜLHAN B., Özdemir G., Öztürk T. T., BALTU D., ÖZALTIN F., et al.
Turkish Journal of Nephrology , cilt.32, sa.4, ss.353-360, 2023 (ESCI, Scopus, TRDizin) identifier identifier identifier

25. COVID-19 associated thrombotic microangiopathy

YILMAZ E. M., Cebi M. N., Karahan I., SAYGILI S. K., Gulmez R., Demirgan E. B., et al.
Nephrology , cilt.28, sa.10, ss.557-560, 2023 (SCI-Expanded, Scopus) identifier identifier identifier

26. Nefrotik Düzey Proteinüri ile Başvurunun Çocukluk Çağı Iga Vasküliti Nefriti Seyrine Etkileri

Kurt Şükür E. D., METE O., Yılmaz T., Gülhan B., Orhan D., Ozaltin F., et al.
Osmangazi Tıp Dergisi , cilt.45, sa.4, ss.581-589, 2023 (TRDizin) Creative Commons License identifier

27. The outcomes of renin-angiotensin-aldosterone system inhibition and immunosuppressive therapy in children with X-linked Alport syndrome

OZDEMIR E. G., GÜLHAN B., ŞÜKÜR E. D. K., Atayar E., ATAN R., DURSUN İ., et al.
Turkish Journal of Pediatrics , cilt.65, sa.3, ss.456-468, 2023 (SCI-Expanded, Scopus, TRDizin) Creative Commons License identifier identifier identifier identifier

28. Outcomes of steroid-resistant nephrotic syndrome in children not treated with intensified immunosuppression

Trautmann A., Seide S., Lipska-Zietkiewicz B. S., ÖZALTIN F., Szczepanska M., Azocar M., et al.
PEDIATRIC NEPHROLOGY , cilt.38, sa.5, ss.1499-1511, 2023 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

29. A rare cause of nephrotic syndrome-sphingosine-1-phosphate lyase (SGPL1) deficiency: 6 cases and a review of the literature

TAŞTEMEL ÖZTÜRK T., CANPOLAT N., SAYGILI S. K., BAYRAKCİ U. S., Soylemezoglu O., ÖZALTIN F., et al.
PEDIATRIC NEPHROLOGY , cilt.38, sa.3, ss.711-719, 2023 (SCI-Expanded, Scopus) identifier identifier identifier

30. HOXA11 is another monogenic cause of congenital anomalies of the kidney and urinary tract

SAYGILI S. K., ÇALIŞKAN S., ÖZALTIN F.
PEDIATRIC NEPHROLOGY , cilt.38, sa.3, ss.933-934, 2023 (SCI-Expanded, Scopus) identifier identifier identifier

31. Metabolomic Analyses to Identify Candidate Biomarkers of Cystinosis

NEMUTLU E., ÖZALTIN F., YABANOĞLU ÇİFTÇİ S., GÜLHAN B., Eylem C. C., BAYSAL İ., et al.
International Journal of Molecular Sciences , cilt.24, sa.3, 2023 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

32. Predictors of kidney complications and analysis of hypertension in children with allogeneic hematopoietic stem cell transplantation

Gurbanov A., GÜLHAN B., KUŞKONMAZ B. B., OKUR F. V., ÖZALTIN F., DÜZOVA A., et al.
PEDIATRIC NEPHROLOGY , cilt.38, sa.2, ss.461-469, 2023 (SCI-Expanded, Scopus) identifier identifier identifier

33. Hearing Loss Related to Gene Mutations in Distal Renal Tubular Acidosis

Ay E., GÜRSES E., ASLAN F., GÜLHAN B., Alniacik A., DÜZOVA A., et al.
Audiology & neuro-otology , cilt.28, sa.5, ss.350-359, 2023 (SCI-Expanded, Scopus) identifier identifier identifier

34. Response to Dr. Spizzirri et al

TAŞTEMEL ÖZTÜRK T., ÖZALTIN F., TOPALOĞLU R.
Pediatric Nephrology , cilt.38, sa.1, ss.309-310, 2023 (SCI-Expanded, Scopus) identifier identifier identifier

35. Hemoglobin cast nephropathy: a rare but serious complication of hemolysis in a pediatric patient

BALTU D., Oral N. A., KESİCİ S., TOPALOĞLU R., ÖZCEBE O. İ., AKSU T., et al.
Turkish Journal of Pediatrics , cilt.65, sa.5, ss.874-880, 2023 (SCI-Expanded, Scopus, TRDizin) Creative Commons License identifier identifier identifier identifier

36. Albuminuria is associated with 24-hour and night-time diastolic blood pressure in urinary tract infection with renal scarring

BALTU D., Salancı B. V., GÜLHAN B., ÖZALTIN F., DÜZOVA A., TOPALOĞLU R.
The Turkish journal of pediatrics , cilt.65, sa.4, ss.620-629, 2023 (Scopus, TRDizin) Creative Commons License identifier identifier identifier identifier

37. The Clinical and Mutational Spectrum of 69 Turkish Children with Autosomal Recessive or Autosomal Dominant Polycystic Kidney Disease: A Multicenter Retrospective Cohort Study

Tutal O., GÜLHAN B., Atayar E., Yuksel S., ÖZÇAKAR Z. B., Soylemezoglu O., et al.
Nephron , 2023 (SCI-Expanded, Scopus) identifier identifier identifier

38. Oral Coenzyme Q10 supplementation leads to better preservation of kidney function in steroid-resistant nephrotic syndrome due to primary Coenzyme Q10 deficiency

Drovandi S., Lipska-Zietkiewicz B. S., ÖZALTIN F., Emma F., GÜLHAN B., Boyer O., et al.
KIDNEY INTERNATIONAL , cilt.102, sa.3, ss.604-612, 2022 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

39. Childhood-onset Takayasu arteritis and immunodeficiency: case-based review.

Sener S., Basaran O., Batu E. D., Atalay E., Esenboga S., Cagdas D. N., et al.
Clinical rheumatology , cilt.41, sa.9, ss.2883-2892, 2022 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

40. Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy

Drovandi S., Lipska-Zietkiewicz B. S., ÖZALTIN F., Emma F., GÜLHAN B., Boyer O., et al.
KIDNEY INTERNATIONAL , cilt.102, sa.3, ss.592-603, 2022 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

41. A broad clinical spectrum of PLC epsilon 1-related kidney disease and intrafamilial variability

Yilmaz E. K., Saygili S., GÜLHAN B., Canpolat N., KARABAY BAYAZIT A., KILIÇ B. D., et al.
PEDIATRIC NEPHROLOGY , cilt.37, sa.8, ss.1855-1866, 2022 (SCI-Expanded, Scopus) identifier identifier identifier

42. Long-term renal survival of paediatric patients with lupus nephritis

Demir S., GÜLHAN B., ÖZEN S., Çelĕgen K., BATU AKAL E. D., Taş N., et al.
Nephrology Dialysis Transplantation , cilt.37, sa.6, ss.1069-1077, 2022 (SCI-Expanded, Scopus) identifier identifier identifier

43. Eculizumab treatment and discontinuation in pediatric patients with atypical hemolytic uremic syndrome: a multicentric retrospective study

Baskin E., Fidan K., GÜLHAN B., Gulleroglu K., CANPOLAT N., Yilmaz A., et al.
JOURNAL OF NEPHROLOGY , cilt.35, sa.4, ss.1213-1222, 2022 (SCI-Expanded, Scopus) identifier identifier identifier

44. Clinically Different Presentations of Family Members With thSame Homozygote Diacylglycerol Kinase Epsilon Mutation: Case Report

Çelikkaya E., Güngör T., Karakaya D., Çakıcı E. K., Yazılıtaş F., ÖZALTIN F., et al.
Experimental and Clinical Transplantation , cilt.20, sa.5, ss.45-48, 2022 (SCI-Expanded, Scopus) identifier identifier identifier

45. Mitochondria-targeted CoQ(10) loaded PLGA-b-PEG-TPP nanoparticles: Their effects on mitochondrial functions of COQ8B(-/-) HK-2 cells

Sena Ozbay H., Yabanoglu-Ciftci S., Baysal I., Gultekinoglu M., Can Eylem C. C., Ulubayram K., et al.
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS , cilt.173, ss.22-33, 2022 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

46. A splice site mutation in the TSEN2 causes a new syndrome with craniofacial and central nervous system malformations, and atypical hemolytic uremic syndrome

CANPOLAT N., Liu D., Atayar E., SAYGILI S. K., Kara N. S., Westfall T. A., et al.
CLINICAL GENETICS , cilt.101, ss.346-358, 2022 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

47. Mitigation of portal fibrosis and cholestatic liver disease in ANKS6-deficient livers by macrophage depletion

Airik M., McCourt B., TAŞTEMEL ÖZTÜRK T., Huynh A. B., Zhang X., Tometich J. T., et al.
FASEB JOURNAL , cilt.36, sa.2, 2022 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

48. Glomerulonephritis with crescents in childhood; etiologies and significance of M2 macrophages

KAYKI G., ORHAN D., GÜLHAN B., TOPALOĞLU R., AKÇÖREN Z., DÜZOVA A., et al.
TURKISH JOURNAL OF PEDIATRICS , cilt.64, sa.1, ss.59-68, 2022 (SCI-Expanded, Scopus, TRDizin) Creative Commons License identifier identifier identifier identifier

49. An international cohort study spanning five decades assessed outcomes of nephropathic cystinosis

Emma F., van't Hoff W., Hohenfellner K., TOPALOĞLU R., Greco M., Ariceta G., et al.
KIDNEY INTERNATIONAL , cilt.100, sa.5, ss.1112-1123, 2021 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

50. Could plasma based therapies still be considered in selected cases with atypical hemolytic uremic syndrome?

ÖZLÜ S. G., GÜLHAN B., Aydog O., Atayar E., Delibas A., Parmaksiz G., et al.
TURKISH JOURNAL OF PEDIATRICS , cilt.63, sa.6, ss.986-993, 2021 (SCI-Expanded, Scopus, TRDizin) Creative Commons License identifier identifier identifier identifier

51. EFFECTS OF RAAS INHIBITION AND IMMUNOSUPPRESSIVE THERAPY IN PEDIATRIC PATIENTS WITH X-LINKED ALPORT SYNDROME

Ozdemir G., GÜLHAN B., KURT ŞÜKÜR E. D., Atayar E., DURSUN İ., ÖZÇAKAR Z. B., et al.
PEDIATRIC NEPHROLOGY , cilt.36, sa.10, ss.3366, 2021 (SCI-Expanded, Scopus) identifier

52. TAKAYASU ARTERITIS WITH RENAL ARTERY INVOLVEMENT IN CHILDREN: 12 YEARS EXPERIENCE OF A TERTIARY CENTER

TAŞTEMEL ÖZTÜRK T., BALTU D., KURT ŞÜKÜR E. D., GÜLHAN B., ÖZEN S., DÜZOVA A., et al.
PEDIATRIC NEPHROLOGY , cilt.36, sa.10, ss.3441, 2021 (SCI-Expanded, Scopus) identifier

53. PRIMARY COQ10 DEFICIENCY: CLINICAL SPECTRUM AND GENOTYPE-PHENOTYPE CORRELATIONS

Drovandi S., Lipska-zietkiewicz B. S., ÖZALTIN F., Emma F., GÜLHAN B., Boyer O., et al.
PEDIATRIC NEPHROLOGY , cilt.36, sa.10, ss.3445-3446, 2021 (SCI-Expanded, Scopus) identifier

54. DGKE MUTATION IN A CHILD TREATED WITH ECULIZUMAB

Tekcan D., Nalcacioglu H., Karadag S. I. K., Onal H. G., ÖZALTIN F., AYDOĞ Ö.
PEDIATRIC NEPHROLOGY , cilt.36, sa.10, ss.3403, 2021 (SCI-Expanded, Scopus) identifier

55. AGTR1-RELATED RENAL TUBULAR DYSGENESES MAY NOT BE FATAL

Demirgan E. B., Saygili S., CANPOLAT N., Sever L., Kilicaslan I., Taylan D., et al.
PEDIATRIC NEPHROLOGY , cilt.36, sa.10, ss.3455, 2021 (SCI-Expanded, Scopus) identifier

56. NEPHROTIC SYNDROME WITH MUTATION IN SPHINGOSINE-1-PHOSPHATE LYASE: 6 CASES

TAŞTEMEL ÖZTÜRK T., CANPOLAT N., Saygili S., BAYRAKCİ U. S., Soylemezoglu O., ÖZALTIN F., et al.
PEDIATRIC NEPHROLOGY , cilt.36, sa.10, ss.3476, 2021 (SCI-Expanded, Scopus) identifier

57. INFANTILE NEPHROTIC SYNDROME WITH PLCE1 MUTATION; TREATMENT OF CYCLOSPORINE-3-YEAR FOLLOW-UP

Tekcan D., Nalcacioglu H., Onal H. G., ÖZALTIN F., AYDOĞ Ö.
PEDIATRIC NEPHROLOGY , cilt.36, sa.10, ss.3475-3476, 2021 (SCI-Expanded, Scopus) identifier

58. A HOMOZYGOUS HOXA11 VARIATION AS A POTENTIAL NOVEL CAUSE OF AUTOSOMAL RECESSIVE CONGENITAL ANOMALIES OF THE KIDNEY AND URINARY TRACT

Saygili S., Atayar E., CANPOLAT N., ELİÇEVİK M., KURUĞOĞLU S., Sever L., et al.
PEDIATRIC NEPHROLOGY , cilt.36, sa.10, ss.3404-3405, 2021 (SCI-Expanded, Scopus) identifier

59. AUDIOLOGICAL FINDINGS IN DISTAL RENAL TUBULAR ACIDOSIS

Ay E., GÜRSES E., Arslan F., GÜLHAN B., Alniacik A., DÜZOVA A., et al.
PEDIATRIC NEPHROLOGY , cilt.36, sa.10, ss.3428, 2021 (SCI-Expanded, Scopus) identifier

60. LONG TERM FOLLOW UP IN RENAL SCARRING OF URINARY TRACT INFECTION: ALBUMINURIA, DIASTOLIC BLOOD PRESSURE

BALTU D., VOLKAN SALANCI B., GÜLHAN B., TAŞTEMEL ÖZTÜRK T., KURT ŞÜKÜR E. D., ÖZALTIN F., et al.
PEDIATRIC NEPHROLOGY , cilt.36, sa.10, ss.3434, 2021 (SCI-Expanded, Scopus) identifier

61. CHARACTERISTICS AND OUTCOME OF BK VIRUS INFECTION IN PEDIATRIC RENAL TRANSPLANT RECIPIENT

KURT ŞÜKÜR E. D., Ozdemir G., TAŞTEMEL ÖZTÜRK T., BALTU D., GÜLHAN B., ÖZALTIN F., et al.
PEDIATRIC NEPHROLOGY , cilt.36, sa.10, ss.3460, 2021 (SCI-Expanded, Scopus) identifier

62. CLINICAL AND MUTATIONAL SPECTRUM OF CHILDREN WITH AUTOSOMAL RECESSIVE AND AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE

Tutal O., GÜLHAN B., Atayar E., YÜKSEL S., Ozcakar B., Soylemezoglu O., et al.
PEDIATRIC NEPHROLOGY , cilt.36, sa.10, ss.3421-3422, 2021 (SCI-Expanded, Scopus) identifier

63. Hemolytic Uremic Syndrome in Children

GÜLHAN B., ÖZALTIN F.
TURKISH ARCHIVES OF PEDIATRICS , cilt.56, sa.5, ss.415-422, 2021 (ESCI, TRDizin) identifier identifier identifier

64. Single dose application IGF-1 and HGF induced bone marrow mesenchymal stem cells reduced proteinuria in focal segmental gomerulosclerosis model

Şahan Ö. B., Onbaşılar İ., Güçer K. Ş., Kaymaz F. F., Atayar E., Özaltın F., et al.
FEBS OPEN BIO , cilt.11, ss.35, 2021 (SCI-Expanded, Scopus) identifier

65. Outcome of diacylglycerol kinase epsilon-mediated hemolytic uremic syndrome in an infant

KOYUN M., KAYA AKSOY G., ÇOMAK E., ÖZALTIN F., AKMAN S.
KIDNEY INTERNATIONAL , cilt.99, sa.6, ss.1500-1501, 2021 (SCI-Expanded, Scopus) identifier identifier identifier

66. CLINICAL AND MUTATIONAL SPECTRUM OF CHILDREN WITH AUTOSOMAL RECESSIVE AND AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE

Tutal O., GÜLHAN B., Atayar E., YÜKSEL S., ÖZÇAKAR Z. B., Soylemezoglu O., et al.
NEPHROLOGY DIALYSIS TRANSPLANTATION , cilt.36, 2021 (SCI-Expanded, Scopus) identifier

67. EARLY URINARY SYSTEM COMPLICATIONS IN CHILDREN WITH HEMATOPOETIC STEM CELL TRANSPLANTATION

Gurbanov A., GÜLHAN B., KUŞKONMAZ B. B., OKUR F. V., ÇETİNKAYA F. D., Ozdemir G., et al.
NEPHROLOGY DIALYSIS TRANSPLANTATION , cilt.36, 2021 (SCI-Expanded, Scopus) identifier

68. Transplantation in pediatric aHUS within the era of eculizumab therapy

ÖZÇAKAR Z. B., ÖZALTIN F., GÜLHAN B., ÇOMAK E., Parmaksiz G., Baskin E., et al.
PEDIATRIC TRANSPLANTATION , cilt.25, sa.3, 2021 (SCI-Expanded, Scopus) identifier identifier identifier

69. Management of congenital nephrotic syndrome: consensus recommendations of the ERKNet-ESPN Working Group

Boyer O., Schaefer F., Haffner D., Bockenhauer D., Holtta T., Berody S., et al.
NATURE REVIEWS NEPHROLOGY , cilt.17, sa.4, ss.277-289, 2021 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

70. Gastric duplication cyst in an infant with Finnish-type congenital nephrotic syndrome: concurrence or coincidence?

Güngör T., Eroğlu F. K., Kargın Çakıcı E., Yazılıtaş F., Can G., Çelikkaya E., et al.
Acta clinica Belgica , cilt.76, sa.2, ss.155-157, 2021 (SCI-Expanded, Scopus) identifier

71. AGTR1-related Renal Tubular Dysgeneses May Not Be Fatal

Demirgan E. B., SAYGILI S. K., CANPOLAT N., Sever L., Kilicaslan I., Taylan D., et al.
KIDNEY INTERNATIONAL REPORTS , cilt.6, sa.3, ss.846-852, 2021 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

72. Predictors for the use of herbal and dietary supplements in children and adolescents with kidney and urinary tract diseases

Ozturk T. T., KANBUR N., ÖZMERT E. N., GÜLHAN B., ÖZALTIN F., TOPALOĞLU R., et al.
EUROPEAN JOURNAL OF PEDIATRICS , cilt.180, sa.1, ss.253-262, 2021 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

73. Acute kidney injury in a patient with COVID-19: Answers

TAŞTEMEL ÖZTÜRK T., BALTU D., KURT ŞÜKÜR E. D., ÖZSÜREKCİ Y., Gucer S., BAŞARAN H. Ö., et al.
PEDIATRIC NEPHROLOGY , cilt.36, sa.12, ss.4111-4113, 2020 (SCI-Expanded, Scopus) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

74. Acute kidney injury in a patient with COVID-19: Questions

Tastemel Ozturk T., Baltu D., Kurt Sukur E. D., Ozsurekci Y., Gucer S., Basaran O., et al.
PEDIATRIC NEPHROLOGY , cilt.36, sa.12, ss.4109-4110, 2020 (SCI-Expanded, Scopus) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

75. Determinants of outcomes in chronic pediatric peritoneal dialysis: a single center experience

Asi T., DÜZOVA A., DOĞAN H. S., Karakurt G., BAHADIR Ö. F., Bozaci A. C., et al.
TURKISH JOURNAL OF PEDIATRICS , cilt.62, sa.6, ss.940-948, 2020 (SCI-Expanded, Scopus, TRDizin) Creative Commons License identifier identifier identifier

76. Genetic aspects of congenital nephrotic syndrome: a consensus statement from the ERKNet-ESPN inherited glomerulopathy working group

Lipska-Zietkiewicz B. S., ÖZALTIN F., Holtta T., Bockenhauer D., Berody S., Levtchenko E., et al.
EUROPEAN JOURNAL OF HUMAN GENETICS , cilt.28, sa.10, ss.1368-1378, 2020 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

77. COL4A3 mutation is an independent risk factor for poor prognosis in children with Alport syndrome

Ozdemir G., GÜLHAN B., Atayar E., Saygili S., Soylemezoglu O., Ozcakar Z. B., et al.
PEDIATRIC NEPHROLOGY , cilt.35, sa.10, ss.1941-1952, 2020 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

78. Renal Biopsy Prognostic Findings in Children With Atypical Hemolytic Uremic Syndrome

YÜKSEL S., GÖNÜL İ. I., Canpolat N., GÖKCE İ., Ozlu S. G., ÖZÇAKAR Z. B., et al.
PEDIATRIC AND DEVELOPMENTAL PATHOLOGY , cilt.23, sa.5, ss.362-371, 2020 (SCI-Expanded, Scopus) identifier identifier identifier

79. A homozygousHOXA11variation as a potential novel cause of autosomal recessive congenital anomalies of the kidney and urinary tract

Saygili S., Atayar E., Canpolat N., ELİÇEVİK M., KURUĞOĞLU S., Sever L., et al.
CLINICAL GENETICS , cilt.98, sa.4, ss.390-395, 2020 (SCI-Expanded, Scopus) identifier identifier identifier

80. Clinical characteristics of children with congenital anomalies of the kidney and urinary tract and predictive factors of chronic kidney disease

Cetinkaya P. G., GÜLHAN B., DÜZOVA A., Besbas N., HAYRAN K. M., TOPALOĞLU R., et al.
TURKISH JOURNAL OF PEDIATRICS , cilt.62, sa.5, ss.746-755, 2020 (SCI-Expanded, Scopus, TRDizin) Creative Commons License identifier identifier identifier

81. Cystinosis beyond kidneys: gastrointestinal system and muscle involvement

TOPALOĞLU R., GÜLTEKİNGİL KESER A., GÜLHAN B., ÖZALTIN F., DEMİR H., Ciftci T., et al.
BMC GASTROENTEROLOGY , cilt.20, sa.1, 2020 (SCI-Expanded, Scopus) identifier identifier identifier

82. IGF-1 and HGF Preconditioning of Bone Marrow Mesenchymal Stem Cells Reduced Proteinuria in Rat Focal Segmental Glomerulosclerosis Model

Sahan Ö. B., Onbaşılar İ., Güçer K. Ş., Kaymaz F. F., Atayar E., Özaltın F., et al.
CYTOTHERAPY , cilt.22, sa.5, 2020 (SCI-Expanded, Scopus) identifier

83. CD80 expression and infiltrating regulatory T cells in idiopathic nephrotic syndrome of childhood

Eroglu F. K., ORHAN D., Inozu M., DÜZOVA A., GÜLHAN B., ÖZALTIN F., et al.
PEDIATRICS INTERNATIONAL , cilt.61, sa.12, ss.1250-1256, 2019 (SCI-Expanded, Scopus) identifier identifier identifier

84. Surgical management of renovascular hypertension in children and young adults: a 13-year experience

Peker O., AKI F. T., Kumbasar U., GÜVENER M., YILMAZ M., DOĞAN R., et al.
INTERACTIVE CARDIOVASCULAR AND THORACIC SURGERY , cilt.29, sa.5, ss.746-752, 2019 (SCI-Expanded, Scopus) identifier identifier identifier

85. Long-term follow-up results of patients with ADCK4 mutations who have been diagnosed in the asymptomatic period: effects of early initiation of CoQ10 supplementation

ATMACA M., GÜLHAN B., Atayar E., KARABAY BAYAZIT A., CANDAN C., ARICI M., et al.
TURKISH JOURNAL OF PEDIATRICS , cilt.61, sa.5, ss.657-663, 2019 (SCI-Expanded, Scopus, TRDizin) Creative Commons License identifier identifier identifier

86. Low levels of urinary epidermal growth factor predict chronic kidney disease progression in children

Azukaitis K., Ju W., Kirchner M., Nair V., Smith M., Fang Z., et al.
KIDNEY INTERNATIONAL , cilt.96, sa.1, ss.214-221, 2019 (SCI-Expanded, Scopus) identifier identifier identifier

87. Rituximab for Children With Difficult-to-Treat Nephrotic Syndrome: Its Effects on Disease Progression and Growth

TOPALOĞLU R., GÜLHAN B., Celegen K., Inozu M., Hayran M., Duzoya A., et al.
FRONTIERS IN PEDIATRICS , cilt.7, 2019 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

88. Persistent hypoglycemic attacks during hemodialysis sessions in an infant with congenital nephrotic syndrome: Questions and Answers

Saygili S., CANPOLAT N., Sever L., ÇALIŞKAN S., Atayar E., ÖZALTIN F.
PEDIATRIC NEPHROLOGY , cilt.34, sa.1, ss.75-79, 2019 (SCI-Expanded, Scopus) identifier identifier identifier

89. BK virus associated nephropathy and severe pneumonia in a kidney transplanted adolescent with Schimke immune-osseous-dysplasia

DÜZOVA A., GÜLHAN B., TOPALOĞLU R., ÖZALTIN F., CENGİZ A. B., Yetimakman A. F., et al.
TURKISH JOURNAL OF PEDIATRICS , cilt.61, sa.1, ss.111-116, 2019 (SCI-Expanded, Scopus, TRDizin) Creative Commons License identifier identifier identifier

90. An immunohistochemical approach to detect oncogenic CTNNB1 mutations in primary neoplastic tissues

AKYOL A., GUNER G., OZSEKER H. S., IŞIK A., Atci O., UZUN S., et al.
LABORATORY INVESTIGATION , cilt.99, sa.1, ss.128-137, 2019 (SCI-Expanded, Scopus) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

91. Response to Early Coenzyme Q10 Supplementation Is not Sustained in CoQ10 Deficiency Caused by CoQ2 Mutation

Eroglu F. K., ÖZALTIN F., Gonc N., Nalcacioglu H., Ozcakar Z. B., YALNIZOĞLU D., et al.
PEDIATRIC NEUROLOGY , cilt.88, ss.71-74, 2018 (SCI-Expanded, Scopus) identifier identifier identifier

92. CLINICAL AND PATHOLOGIC CHARACTERISTICS OF GENETICALLY CONFIRMED ALPORT SYNDROME PATIENTS

TOPALOĞLU R., Ozdemir G., GÜLHAN B., Atayar E., DÜZOVA A., SOYLU A., et al.
PEDIATRIC NEPHROLOGY , cilt.33, sa.10, ss.1826-1827, 2018 (SCI-Expanded, Scopus) identifier

93. TURKISH ATYPICAL HEMOLYTIC UREMIC SYNDROME REGISTRY: ECULIZUMAB TREATMENT IN AHUS PATIENTS

Baskin E., Canpolat N., Gulleroglu K., Yilmaz A., MELEK E., Yuksel S., et al.
PEDIATRIC NEPHROLOGY , cilt.33, sa.10, ss.1832, 2018 (SCI-Expanded, Scopus) identifier

94. GASTROINTESTINAL SYSTEM INVOLVEMENT IN ATYPICAL HEMOLYTIC UREMIC SYNDROME

Fidan K., Yildirim Z. Y., Goknar N., GÜLHAN B., Gulleroglu K., Ozcakar Z. B., et al.
PEDIATRIC NEPHROLOGY , cilt.33, sa.10, ss.1843, 2018 (SCI-Expanded, Scopus) identifier

95. EARLY USE OF ECULIZUMAB IN A CASE OF STEC-HUS BEFORE THE DEVELOPMENT OF CLINICAL SYMPTOMS

BAYRAM M. T., DEMİR B. K., SOYLU A., KAVUKÇU S., ÖZALTIN F.
PEDIATRIC NEPHROLOGY , cilt.33, sa.10, ss.1845, 2018 (SCI-Expanded, Scopus) identifier

96. Familial Mediterranean fever patients homozygous for E148Q variant may have milder disease

TOPALOĞLU R., BATU AKAL E. D., Yildiz C., Korkmaz E., ÖZEN S., BEŞBAŞ N., et al.
INTERNATIONAL JOURNAL OF RHEUMATIC DISEASES , cilt.21, sa.10, ss.1857-1862, 2018 (SCI-Expanded, Scopus) identifier identifier identifier

97. LUPUS NEPHRITIS: LONG TERM FOLLOW-UP AND EFFECT OF TREATMENT ON GROWTH

TOPALOĞLU R., TAŞ N., Celegen K., Ozdemir G., GÜLHAN B., DÜZOVA A., et al.
PEDIATRIC NEPHROLOGY , cilt.33, sa.10, ss.1947, 2018 (SCI-Expanded, Scopus) identifier

98. LONG-TERM FOLLOW-UP RESULTS OF PATIENTS WITH ADCK4 MUTATIONS WHO HAVE BEEN DIAGNOSED IN ASYMPTOMATIC PERIOD: EFFECTS OF EARLY INITIATION OF COQ10 SUPPLEMENTATION

ATMACA M., GÜLHAN B., KARABAY BAYAZIT A., CANDAN C., ARICI M., TOPALOĞLU R., et al.
PEDIATRIC NEPHROLOGY , cilt.33, sa.10, ss.1821-1822, 2018 (SCI-Expanded, Scopus) identifier

99. CLINICAL AND MUTATIONAL SPECTRUM OF CHILDREN WITH AUTOSOMAL RECESSIVE AND AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE

TÜRKOĞLU Ö., GÜLHAN B., YÜKSEL S., Caliskan S., DÜZOVA A., ÇAKAR N., et al.
PEDIATRIC NEPHROLOGY , cilt.33, sa.10, ss.1814, 2018 (SCI-Expanded, Scopus) identifier

100. GASTRIC DUPLICATION CYST IN AN INFANT WITH FINNISH-TYPE CONGENITAL NEPHROTIC SYNDROME: CONCURRENCE OR COINCIDENCE?

Eroglu T. G. F. K., Can G. G., Cakici E. K., Yazilitas F., Celikkaya E., ÖZALTIN F., et al.
PEDIATRIC NEPHROLOGY , cilt.33, sa.10, ss.1931-1932, 2018 (SCI-Expanded, Scopus) identifier

101. MYCETOMA OF THE URINARY TRACT IN AN INFANT WITH HORSESHOE KIDNEY: USEFULNESS OF MECHANICAL REMOVAL AND AMPHOTERICIN-B IRRIGATION

OĞUZ B., Celegen K., ÇİFTÇİ A. Ö., ÜNAL E., ŞENOCAK M. E., ÖZKALE YAVUZ Ö., et al.
PEDIATRIC NEPHROLOGY , cilt.33, sa.10, ss.1984, 2018 (SCI-Expanded, Scopus) identifier

102. ADRENAL INSUFFICIENCY IN AN INFANT WITH CONGENITAL NEPHROTIC SYNDROME: NEPHROTIC SYNDROME-14

Saygili S., Canpolat N., Caliskan S., Atayar E., Sever L., ÖZALTIN F.
PEDIATRIC NEPHROLOGY , cilt.33, sa.10, ss.1929, 2018 (SCI-Expanded, Scopus) identifier

103. ACUTE HEMODIALYSIS EXPERIENCE IN CHILDREN WEIGHING LESS THAN 15 KG

TAŞ N., GÜLHAN B., Celegen K., Ozdemir G., DÜZOVA A., ÖZALTIN F., et al.
PEDIATRIC NEPHROLOGY , cilt.33, sa.10, ss.1893, 2018 (SCI-Expanded, Scopus) identifier

104. Extra-Renal manifestations of atypical hemolytic uremic syndrome in children

Fidan K., Goknar N., GÜLHAN B., MELEK E., Yildirim Z. Y., Baskin E., et al.
PEDIATRIC NEPHROLOGY , cilt.33, sa.8, ss.1395-1403, 2018 (SCI-Expanded, Scopus) identifier identifier identifier

105. Effect of IGF-1 and HGF induced bone marrow mesenchymal stem cells on focal segmental glomerulosclerosis in Sprague-Dawley rats: a pilot study

ŞAHAN Ö., KORKMAZ E., ONBAŞILAR İ., Gucer S., KAYMAZ F. F., ÖZALTIN F., et al.
FEBS OPEN BIO , cilt.8, ss.152, 2018 (SCI-Expanded, Scopus) identifier

106. Atypical Hemolytic Uremic Syndrome in Children Aged < 2 Years

ÇAKAR N., ÖZÇAKAR Z. B., ÖZALTIN F., KOYUN M., ACAR B. Ç., BAHAT ÖZDOĞAN E., et al.
NEPHRON , cilt.139, sa.3, ss.211-218, 2018 (SCI-Expanded, Scopus) identifier identifier identifier

107. Nephropathic Cystinosis Mimicking Bartter Syndrome A Novel Mutation

Bastug F., Nalcacioglu H., ÖZALTIN F., Korkmaz E., Yel S.
IRANIAN JOURNAL OF KIDNEY DISEASES , cilt.12, sa.1, ss.61-63, 2018 (SCI-Expanded, Scopus) identifier identifier identifier

108. Hemolytic uremic syndrome and IgA nephropathy in a child: Coincidence or not?

Surmeli-Doven S., Delibas A., Gurses I., Kayacan U. R., Coskun-Yilmaz B., Esen K., et al.
TURKISH JOURNAL OF PEDIATRICS , cilt.60, sa.1, ss.81-85, 2018 (SCI-Expanded, Scopus, TRDizin) Creative Commons License identifier identifier identifier

109. Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome

Warejko J. K., Tan W., Daga A., Schapiro D., Lawson J. A., Shril S., et al.
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY , cilt.13, sa.1, ss.53-62, 2018 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

110. Long-Term Outcome of Steroid-Resistant Nephrotic Syndrome in Children

Trautmann A., Schnaidt S., Lipska-Zietkiewicz B. S., Bodria M., ÖZALTIN F., Emma F., et al.
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY , cilt.28, sa.10, ss.3055-3065, 2017 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

111. Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly

Braun D. A., Rao J., Mollet G., Schapiro D., Daugeron M., Tan W., et al.
NATURE GENETICS , cilt.49, sa.10, ss.1529-1541, 2017 (SCI-Expanded, Scopus) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

112. The Clinical and Mutational Spectrum of Turkish Patients with Cystinosis

TOPALOĞLU R., Gulhan B., Inozu M., Canpolat N., Yilmaz A., Noyan A., et al.
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY , cilt.12, sa.10, ss.1634-1641, 2017 (SCI-Expanded, Scopus) Creative Commons License identifier identifier

113. RISK FACTORS FOR CARDIOVASCULAR COMORBIDITIES IN CHILDREN WITH STEROID-SENSITIVE AND STEROID-RESISTANT NEPHROTIC SYNDROME

Eroglu F. K., TOPALOĞLU R., KARAGÖZ T., OĞUZ B., ÖZALTIN F., GÜLHAN B., et al.
PEDIATRIC NEPHROLOGY , cilt.32, sa.9, ss.1661, 2017 (SCI-Expanded, Scopus) identifier

114. GENETIC AND CLINICAL CHARACTERISTICS OF PATIENTS WITH C3 GLOMERULOPATHY

TOPALOĞLU R., GÜLHAN B., Korkmaz E., DÜZOVA A., ÖZALTIN F.
PEDIATRIC NEPHROLOGY , cilt.32, sa.9, ss.1669, 2017 (SCI-Expanded, Scopus) identifier

115. DOES C.3979 G > A/P.VAL1327MET VARIANT OF COL4A4 HAS ANY PATHOGENIC EFFECT IN TURKISH PATIENTS WITH ALPORT SYNDROME?

YILDIZ N., ATA P., ALPAY H., GÖKCE İ., ÖZALTIN F.
PEDIATRIC NEPHROLOGY , cilt.32, sa.9, ss.1773, 2017 (SCI-Expanded, Scopus) identifier

116. CLINICAL CHARACTERISTICS OF PATIENTS WITH MTORI CONVERSION AND EFFECTS ON RENAL OUTCOME

TAŞ N., GÜLHAN B., Inozu M., Celegen K., DÜZOVA A., ÖZALTIN F., et al.
PEDIATRIC NEPHROLOGY , cilt.32, sa.9, ss.1803, 2017 (SCI-Expanded, Scopus) identifier

117. USE OF HERBAL AND DIETARY SUPPLEMENTS IN CHILDREN WITH KIDNEY AND URINARY TRACT DISEASE

TAŞTEMEL ÖZTÜRK T., Ozmert E., KANBUR N., GÜLHAN B., ÖZALTIN F., TOPALOĞLU R., et al.
PEDIATRIC NEPHROLOGY , cilt.32, sa.9, ss.1675, 2017 (SCI-Expanded, Scopus) identifier

118. IS RAAS BLOCKADE EFFECTIVE IN NPHS2 GLOMERULOPATHY?

Trautmann A., ÖZALTIN F., Zurowksa A., Helena H., Saeed B., Azocar M., et al.
PEDIATRIC NEPHROLOGY , cilt.32, sa.9, ss.1661, 2017 (SCI-Expanded, Scopus) identifier

119. LONG TERM RESULTS OF RITUXIMAB IN A TERTIARY REFERRAL CENTER FOR DIFFICULT-TO-TREAT NEPHROTIC SYNDROME

Celegen K., GÜLHAN B., Inozu M., TAŞ N., ÖZALTIN F., DÜZOVA A., et al.
PEDIATRIC NEPHROLOGY , cilt.32, sa.9, ss.1769-1770, 2017 (SCI-Expanded, Scopus) identifier

120. Low renal but high extrarenal phenotype variability in Schimke immuno-osseous dysplasia

Lipska-Zietkiewicz B. S., Gellermann J., Boyer O., Gribouval O., Zietkiewicz S., Kari J. A., et al.
PLOS ONE , cilt.12, sa.8, 2017 (SCI-Expanded, Scopus) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

121. Follow-up results of patients with ADCK4 mutations and the efficacy of CoQ10 treatment

Atmaca M., GÜLHAN B., KORKMAZ E., INOZU M., Soylemezoglu O., CANDAN C., et al.
PEDIATRIC NEPHROLOGY , cilt.32, sa.8, ss.1369-1375, 2017 (SCI-Expanded, Scopus) identifier identifier identifier

122. Tocilizumab treatment in childhood Takayasu arteritis: Case series of four patients and systematic review of the literature

Batu E. D., Sonmez H. E., HAZIROLAN T., ÖZALTIN F., BİLGİNER Y., ÖZEN S.
SEMINARS IN ARTHRITIS AND RHEUMATISM , cilt.46, sa.4, ss.529-535, 2017 (SCI-Expanded, Scopus) identifier identifier identifier

123. Turkish pediatric atypical hemolytic uremic syndrome registry: initial analysis of 146 patients

BESBAS N., GULHAN B., SOYLEMEZOGLU O., OZCAKAR Z. B., KORKMAZ E., HAYRAN M., et al.
BMC NEPHROLOGY , cilt.18, 2017 (SCI-Expanded, Scopus) identifier identifier identifier

124. Epidermolysis Bullosa with Pyloric Atresia and Aplasia Cutis in a Newborn Due to Homozygous Mutation in ITGB

KAYKI G., Bozkaya D., Fatih O., ORHAN D., Kaymaz F., KORKMAZ E., et al.
FETAL AND PEDIATRIC PATHOLOGY , cilt.36, sa.4, ss.332-339, 2017 (SCI-Expanded, Scopus) identifier identifier identifier

125. Timing of renal replacement therapy does not influence survival and growth in children with congenital nephrotic syndrome caused by mutations in NPHS1: data from the ESPN/ERA-EDTA Registry

Holtta T., Bonthuis M., Van Stralen K. J., Bjerre A., TOPALOĞLU R., ÖZALTIN F., et al.
PEDIATRIC NEPHROLOGY , cilt.31, sa.12, ss.2317-2325, 2016 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

126. First-Line, Early and Long-Term Eculizumab Therapy in Atypical Hemolytic Uremic Syndrome: A Case Series in Pediatric Patients

YÜKSEL S., Evrengul H., ÖZÇAKAR Z. B., Becerir T., Yalcin N., Korkmaz E., et al.
PEDIATRIC DRUGS , cilt.18, sa.6, ss.413-420, 2016 (SCI-Expanded, Scopus) identifier identifier identifier

127. Genetic and clinical features of cryopyrin-associated periodic syndromes in Turkish children

EROGLU F. K., Kasapcopur O., BESBAS N., ÖZALTIN F., BİLGİNER Y., Barut K., et al.
CLINICAL AND EXPERIMENTAL RHEUMATOLOGY , cilt.34, sa.6, 2016 (SCI-Expanded, Scopus) identifier identifier identifier

128. Turkish Atypical Hemolytic Uremic Syndrome Registry: Evaluation of 146 Patients

Besbas N., Soylemezoglu O., GÜLHAN B., Ozcakar Z. B., KORKMAZ E., HAYRAN K. M., et al.
PEDIATRIC NEPHROLOGY , cilt.31, sa.10, ss.1884, 2016 (SCI-Expanded, Scopus) identifier

129. Loss of diacylglycerol kinase epsilon in mice causes endothelial distress and impairs glomerular Cox-2 and PGE(2) production

Zhu J., Chaki M., Lu D., Ren C., Wang S., Rauhauser A., et al.
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY , cilt.310, sa.9, 2016 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

130. Mutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndrome

Braun D. A., Sadowski C. E., Kohl S., Lovric S., Astrinidis S. A., Pabst W. L., et al.
NATURE GENETICS , cilt.48, sa.4, ss.457-467, 2016 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

131. Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicity

Braun D. A., Schueler M., Halbritter J., Gee H. Y., Porath J. D., Lawson J. A., et al.
KIDNEY INTERNATIONAL , cilt.89, sa.2, ss.468-475, 2016 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

132. ADCK4-Associated Glomerulopathy Causes Adolescence-Onset FSGS

Korkmaz E., Lipska-Zietkiewicz B. S., Boyer O., Gribouval O., Fourrage C., Tabatabaei M., et al.
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY , cilt.27, sa.1, ss.63-68, 2016 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

133. Normal 25-Hydroxyvitamin D Levels Are Associated with Less Proteinuria and Attenuate Renal Failure Progression in Children with CKD

Shroff R., Aitkenhead H., Costa N., Trivelli A., Litwin M., Picca S., et al.
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY , cilt.27, sa.1, ss.314-322, 2016 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

134. Lupus in a patient with cystinosis: is it drug induced?

Eroglu F. K., BESBAS N., ÖZALTIN F., TOPALOĞLU R., ÖZEN S.
LUPUS , cilt.24, sa.13, ss.1452-1454, 2015 (SCI-Expanded, Scopus) identifier identifier identifier

135. MCP1 2518 A/G polymorphism affects progression of childhood focal segmental glomerulosclerosis

Besbas N., KALYONCU M., Cil O., ÖZGÜL R. K., Bakkaloglu A., ÖZALTIN F.
RENAL FAILURE , cilt.37, sa.9, ss.1435-1439, 2015 (SCI-Expanded, Scopus) identifier identifier identifier

136. RESPONSE TO INTENSIFIED IMMUNOSUPPRESSIVE THERAPYAND IDENTIFICATION OF GENETIC DISEASE ARE HIGHLY PREDICTIVE OF LONG-TERM RENAL OUTCOME IN CHILDREN WITH STEROID RESISTANT NEPHROTIC SYNDROME (SRNS)

Trautmann A., Schnaidt S., Ghiggeri G. M., ÖZALTIN F., Saeed B., Drozdz D., et al.
PEDIATRIC NEPHROLOGY , cilt.30, sa.9, ss.1556-1557, 2015 (SCI-Expanded, Scopus) identifier

137. RESULTS OF TURKISH MULTICENTRIC NATIONAL CYSTINOSIS REGISTRY

TOPALOĞLU R., GÜLHAN B., ÖZALTIN F., BODUR İ., BEŞBAŞ N., Dursun H., et al.
PEDIATRIC NEPHROLOGY , cilt.30, sa.9, ss.1668-1669, 2015 (SCI-Expanded, Scopus) identifier

138. NEPHROPATHIC CYSTINOSIS MIMICKING BARTTER SYNDROME: NOVEL MUTATION

BaStuG F., Yel S., ÖZALTIN F., Korkmaz E., Uytun S., DÜŞÜNSEL R.
PEDIATRIC NEPHROLOGY , cilt.30, sa.9, ss.1681, 2015 (SCI-Expanded, Scopus) identifier

139. SEVERE PNEUMONIA ASSOCIATED WITH BK VIRUS NEPHROPATHY IN A KIDNEY TRANSPLANTED ADOLESCENT WITH SCHIMKE IMMUNO-OSSEOUS-DYSPLASIA

DÜZOVA A., GÜLHAN B., ÖZALTIN F., TOPALOĞLU R., BİLGİNER Y., BEŞBAŞ N.
PEDIATRIC NEPHROLOGY , cilt.30, sa.9, ss.1619-1620, 2015 (SCI-Expanded, Scopus) identifier

140. ATYPICAL HEMOLYTIC UREMIC SYNDROME UNRESPONSIVE TO ECULIZUMAB THERAPY

Inozu M., BODUR İ., DÜZOVA A., BİLGİNER Y., ÖZALTIN F., BEŞBAŞ N.
PEDIATRIC NEPHROLOGY , cilt.30, sa.9, ss.1648, 2015 (SCI-Expanded, Scopus) identifier

141. RITUXIMAB EXPERIENCE OF A TERTIARY REFERRAL CENTER FOR DIFFICULT-TO-TREAT NEPHROTIC SYNDROME

GÜLHAN B., TOPALOĞLU R., ÖZALTIN F., DÜZOVA A., EROGLU F. K., Bodur I., et al.
PEDIATRIC NEPHROLOGY , cilt.30, sa.9, ss.1692, 2015 (SCI-Expanded, Scopus) identifier

142. CHARACTERISTICS OF RENAL TRANSPLANT CHILDREN WITH CHRONIC ALLOGRAFT NEPHROPATHY: EXPERIENCE OF A TERTIARY REFERRAL CENTER

GÜLHAN B., INOZU M., BİLGİNER Y., ÖZALTIN F., DÜZOVA A., ÖZEN S., et al.
PEDIATRIC NEPHROLOGY , cilt.30, sa.9, ss.1721, 2015 (SCI-Expanded, Scopus) identifier

143. RISK FACTORS FOR POST-TRANSPLANT RECURRENCE OF STEROID RESISTANT NEPHROTIC SYNDROME (SRNS): RESULTS FROM THE PODONET REGISTRY

Trautmann A., Ghiggeri G. M., Azocar M., Remuzzi G., ÖZALTIN F., Melk A., et al.
PEDIATRIC NEPHROLOGY , cilt.30, sa.9, ss.1557-1558, 2015 (SCI-Expanded, Scopus) identifier

144. Genetic abnormalities and prognosis in patients with congenital and infantile nephrotic syndrome

Cil O., Besbas N., DÜZOVA A., TOPALOĞLU R., PECO-ANTIC A., KORKMAZ E., et al.
PEDIATRIC NEPHROLOGY , cilt.30, sa.8, ss.1279-1287, 2015 (SCI-Expanded, Scopus) identifier identifier identifier

145. Mutations In Anks6 Cause A Nephronophthisis-like Phenotype With End Stage Renal Disease

Taskiran E., Korkmaz E., Gucer S., KOŞUKCU C., Kaymaz F., Koyunlar C., et al.
PEDIATRIC NEPHROLOGY , cilt.29, sa.9, ss.1820, 2014 (SCI-Expanded, Scopus) identifier

146. Thrombophilic Risk Factors And The Efficiency Of Prophylactic Anticoagulation Therapy In Children Who Underwent Renal Transplantation

GÜLHAN B., Tavil B., DÜZOVA A., ÖZALTIN F., ÖZEN S., TOPALOĞLU R., et al.
PEDIATRIC NEPHROLOGY , cilt.29, sa.9, ss.1694, 2014 (SCI-Expanded, Scopus) identifier

147. A novel CFHR5 mutation associated with C3 glomerulonephritis in a Turkish girl

BEŞBAŞ N., GÜLHAN B., GÜÇER K. Ş., Korkmaz E., ÖZALTIN F.
JOURNAL OF NEPHROLOGY , cilt.27, sa.4, ss.457-460, 2014 (SCI-Expanded, Scopus) identifier identifier identifier

148. Mutations in ANKS6 Cause a Nephronophthisis-Like Phenotype with ESRD

Taskiran E. Z., Korkmaz E., Gucer S., KOŞUKCU C., Kaymaz F., Koyunlar C., et al.
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY , cilt.25, sa.8, ss.1653-1661, 2014 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

149. Diagnostic validity of colchicine in patients with Familial Mediterranean fever

ÖZALTIN F., BİLGİNER Y., GÜLHAN B., Bajin I., Erdogan O., HAYRAN K. M., et al.
CLINICAL RHEUMATOLOGY , cilt.33, sa.7, ss.969-974, 2014 (SCI-Expanded, Scopus) identifier identifier identifier

150. Primary coenzyme Q(10) (CoQ(10)) deficiencies and related nephropathies

ÖZALTIN F.
PEDIATRIC NEPHROLOGY , cilt.29, sa.6, ss.961-969, 2014 (SCI-Expanded, Scopus) identifier identifier identifier

151. Post-transplant hypertension in pediatric kidney transplant recipients

GÜLHAN B., TOPALOĞLU R., KARABULUT E., ÖZALTIN F., AKI F. T., BİLGİNER Y., et al.
PEDIATRIC NEPHROLOGY , cilt.29, sa.6, ss.1075-1080, 2014 (SCI-Expanded, Scopus) identifier identifier identifier

152. Mutations in EMP2 Cause Childhood-Onset Nephrotic Syndrome

Gee H. Y., Ashraf S., Wan X., Vega-Warner V., Esteve-Rudd J., Lovric S., et al.
AMERICAN JOURNAL OF HUMAN GENETICS , cilt.94, sa.6, ss.884-890, 2014 (SCI-Expanded, Scopus) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

153. Genotype-phenotype associations in WT1 glomerulopathy

Lipska-Zietkiewicz B. S., Ranchin B., Iatropoulos P., Gellermann J., Melk A., ÖZALTIN F., et al.
KIDNEY INTERNATIONAL , cilt.85, sa.5, ss.1169-1178, 2014 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

154. NPHS2 Mutations in Steroid-Resistant Nephrotic Syndrome: A Mutation Update and the Associated Phenotypic Spectrum

Bouchireb K., Boyer O., Gribouval O., Nevo F., Huynh-Cong E., Moriniere V., et al.
HUMAN MUTATION , cilt.35, sa.2, ss.178-186, 2014 (SCI-Expanded, Scopus) identifier identifier identifier

155. Proteinuria in Frasier Syndrome

Peco-Antic A., ÖZALTIN F., Parezanovic V., Milosevski-Lomic G., Zdravkovic V.
SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO , cilt.141, ss.685-688, 2013 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

156. The Effect Of Fibroblast Growth Factor 23 On Left Ventricular Function In Peritoneal Dialysis Children

Hacihamdioglu D. O., BEŞBAŞ N., ALEHAN D., OĞUZ B., ÖZALTIN F., DÜZOVA A., et al.
PEDIATRIC NEPHROLOGY , cilt.28, sa.8, ss.1643, 2013 (SCI-Expanded, Scopus) identifier

157. CONTRIBUTORY RISK FACTORS FOR DEVELOPMENT OF THROMBOSIS IN CHILDRENWITH NEPHROTIC SYNDROME

KaraEroglu F., Tavil B., ÖZALTIN F., BEŞBAŞ N., ÖZEN S., ÇETİN M., et al.
PEDIATRIC NEPHROLOGY , cilt.28, sa.8, ss.1584, 2013 (SCI-Expanded, Scopus) identifier

158. Genetic screening in adolescents with steroid-resistant nephrotic syndrome

Lipska-Zietkiewicz B. S., Iatropoulos P., Maranta R., Caridi G., ÖZALTIN F., Anarat A., et al.
KIDNEY INTERNATIONAL , cilt.84, sa.1, ss.206-213, 2013 (SCI-Expanded, Scopus) Creative Commons License identifier identifier

159. Clinicopathological and immunohistological features in childhood IgA nephropathy: a single-centre experience

TOPALOĞLU R., Orhan D., BİLGİNER Y., KARABULUT E., ÖZALTIN F., DÜZOVA A., et al.
CLINICAL KIDNEY JOURNAL , cilt.6, sa.2, ss.169-175, 2013 (ESCI, Scopus) Creative Commons License identifier identifier

160. DGKE Variants Cause a Glomerular Microangiopathy That Mimics Membranoproliferative GN

ÖZALTIN F., Li B., Rauhauser A., An S., Soylemezoglu O., Gonul I. I., et al.
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY , cilt.24, sa.3, ss.377-384, 2013 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

161. Neonatal onset atypical hemolytic uremic syndrome successfully treated with eculizumab

Besbas N., Gulhan B., Karpman D., Topaloglu R., Duzova A., Korkmaz E., et al.
PEDIATRIC NEPHROLOGY , cilt.28, sa.1, ss.155-158, 2013 (SCI-Expanded, Scopus) identifier identifier identifier

162. Role of CXCR1 (CKR-1) in inflammation of experimental mesangioproliferative glomerulonephritis.

Ozaltin F., Besbas N., Iskit A. B., Cil O., Akcoren Z., Kale G., et al.
Renal failure , cilt.35, ss.380-5, 2013 (SCI-Expanded, Scopus) identifier identifier identifier

163. Circulating suPAR in Two Cohorts of Primary FSGS

Wei C., Trachtman H., Li J., Dong C., Friedman A. L., Gassman J. J., et al.
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY , cilt.23, sa.12, ss.2051-2059, 2012 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

164. WT1 screening in nephrotic syndrome - lessons from PodoNet

Lipska-Zietkiewicz B. S., Iatropoulos P., Ranchin B., Dusek J., ÖZALTIN F., Melk A., et al.
PEDIATRIC NEPHROLOGY , cilt.27, sa.9, ss.1617-1618, 2012 (SCI-Expanded, Scopus) identifier

165. Rituximab in steroid-dependent and resistant nephrotic syndrome patients

TOPALOĞLU R., GÜLHAN B., ÖZALTIN F., DÜZOVA A., BEŞBAŞ N.
PEDIATRIC NEPHROLOGY , cilt.27, sa.9, ss.1710-1711, 2012 (SCI-Expanded, Scopus) identifier

166. ATYPICAL HUS AND ECULIZUMAB TREATMENT: EXPERIENCE OF A TERTIARY CENTER

BEŞBAŞ N., GÜLHAN B., ÖZEN S., TOPALOĞLU R., DÜZOVA A., Yildiz C., et al.
PEDIATRIC NEPHROLOGY , cilt.27, sa.9, ss.1630, 2012 (SCI-Expanded, Scopus) identifier

167. PERITONEAL DIALYSIS IN CHILDREN UNDER TWO YEARS OF AGE

GÜLHAN B., DÜZOVA A., ÖZALTIN F., TOPALOĞLU R., ÖZEN S., BİLGİNER Y., et al.
PEDIATRIC NEPHROLOGY , cilt.27, sa.9, ss.1799-1800, 2012 (SCI-Expanded, Scopus) identifier

168. THE BENEFITS OF CYCLOSPORINE TREATMENT OF THE PATIENT WITH NPHS2 MUTATION

Hacihamdioglu D. O., ÖZALTIN F., Zeybek C., Kalman S., Demirkaya E., Gok F.
PEDIATRIC NEPHROLOGY , cilt.27, sa.9, ss.1703-1704, 2012 (SCI-Expanded, Scopus) identifier

169. Response to Intensified Immunosuppressive Therapy Predicts Long-Term Prognosis in Steroid Resistant Nephrotic Syndrome (SRNS)

Trautmann A., ÖZALTIN F., Bodria M., Anarat A., Saeed B., Azocar M., et al.
PEDIATRIC NEPHROLOGY , cilt.27, sa.9, ss.1639-1640, 2012 (SCI-Expanded, Scopus) identifier

170. Takayasu arteritis in a 4-year-old girl: case report and brief overview of the pediatric literature

Aypar E., Celebi-Tayfur A., Keser M., Odabas D., ÖZALTIN F., PAKSOY Y., et al.
TURKISH JOURNAL OF PEDIATRICS , cilt.54, sa.5, ss.536-539, 2012 (SCI-Expanded, Scopus) identifier identifier identifier

171. C1q deficiency: identification of a novel missense mutation and treatment with fresh frozen plasma

TOPALOĞLU R., TASKIRAN E. Z., TAN Ç., Erman B., ÖZALTIN F., SANAL O.
CLINICAL RHEUMATOLOGY , cilt.31, sa.7, ss.1123-1126, 2012 (SCI-Expanded, Scopus) identifier identifier identifier

172. Genetic basis of cystinosis in Turkish patients: a single-center experience

TOPALOĞLU R., Vilboux T., COŞKUN T., ÖZALTIN F., Tinloy B., Gunay-Aygun M., et al.
PEDIATRIC NEPHROLOGY , cilt.27, sa.1, ss.115-121, 2012 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

173. Endothelial Dysfunction and Increased Responses to Renal Nerve Stimulation in Rat Kidneys during Rhabdomyolysis-Induced Acute Renal Failure: Role of Hydroxyl Radical

Cil O., Ertunc M., Gucer K. Ş., Ozaltin F., Iskit A. B., Onur R.
RENAL FAILURE , cilt.34, sa.2, ss.211-220, 2012 (SCI-Expanded, Scopus) identifier identifier identifier

174. NPHS2 gene mutation in an Iranian family with familial steroid-resistant nephrotic syndrome

Ameli S., Mazaheri M., Zare-Shahabadi A., ÖZALTIN F., Asgarian F., Monajemzadeh M., et al.
NEFROLOGIA , cilt.32, sa.5, ss.674-676, 2012 (SCI-Expanded, Scopus) identifier identifier identifier

175. OUTCOME OF NEPHROPATHIC CYSTINOSIS IN PEDIATRIC RENAL TRANSPLANTATION: A SINGLE CENTRE EXPERIENCE

TOPALOĞLU R., BİLGİNER Y., ÖZALTIN F., DÜZOVA A., Aki T., ÖZEN S., et al.
PEDIATRIC TRANSPLANTATION , cilt.15, ss.82, 2011 (SCI-Expanded, Scopus) identifier

176. Disruption of PTPRO Causes Childhood-Onset Nephrotic Syndrome

ÖZALTIN F., Ibsirlioglu T., Taskiran E. Z., Baydar D. E., Kaymaz F., Buyukcelik M., et al.
AMERICAN JOURNAL OF HUMAN GENETICS , cilt.89, sa.1, ss.139-147, 2011 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

177. Respiratory-chain deficiency presenting as diffuse mesangial sclerosis with NPHS3 mutation

Baskin E., Bayrakci U. S., Alehan F., Ozdemir H., Oner A., Horvath R., et al.
PEDIATRIC NEPHROLOGY , cilt.26, sa.7, ss.1157-1161, 2011 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

178. MYO1E Mutations and Childhood Familial Focal Segmental Glomerulosclerosis

Mele C., Iatropoulos P., Donadelli R., Calabria A., Maranta R., Cassis P., et al.
NEW ENGLAND JOURNAL OF MEDICINE , cilt.365, sa.4, ss.295-306, 2011 (SCI-Expanded, Scopus) Creative Commons License identifier identifier

179. COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness

Heeringa S. F., Chernin G., Chaki M., Zhou W., Sloan A. J., Ji Z., et al.
JOURNAL OF CLINICAL INVESTIGATION , cilt.121, sa.5, ss.2013-2024, 2011 (SCI-Expanded, Scopus) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

180. Follow-Up of Patients With Juvenile Nephronophthisis After Renal Transplantation: A Single Center Experience

Tayfur A. C., Besbas N., BİLGİNER Y., ÖZALTIN F., DÜZOVA A., Bakkaloglu M., et al.
TRANSPLANTATION PROCEEDINGS , cilt.43, sa.3, ss.847-849, 2011 (SCI-Expanded, Scopus) identifier identifier identifier

181. Macrophage Activating Syndrome complicating Wegener Granulomatosis: treatment with plasma exchange

Eroglu F. K., GÜLHAN B., ÜNAL S., ÖZALTIN F., ORHAN D., ÖZEN S.
CLINICAL AND EXPERIMENTAL RHEUMATOLOGY , cilt.29, sa.2, ss.463, 2011 (SCI-Expanded, Scopus) identifier

182. Spondyloenchondrodysplasia with Systemic Lupus Erythematosus: a report of three cases

BİLGİNER Y., ALANAY Y., DÜZOVA A., TOPALOĞLU R., Superti-Furga A., ÖZEN S., et al.
CLINICAL AND EXPERIMENTAL RHEUMATOLOGY , cilt.29, sa.2, ss.430, 2011 (SCI-Expanded, Scopus) identifier

183. Three cases of a rare disease, congenital chloride diarrhea, summons up the variation in the clinical course and significance of early diagnosis and adequate treatment in the prevention of intellectual disability

Gurakan F., Baysoy G., Wedenoja S., Uslu N., ÖZEN H., ÖZALTIN F., et al.
TURKISH JOURNAL OF PEDIATRICS , cilt.53, sa.2, ss.194-198, 2011 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

184. The bone and mineral disorder of children undergoing chronic peritoneal dialysis

Borzych D., Rees L., Ha I. S., Chua A., Valles P. G., Lipka M., et al.
KIDNEY INTERNATIONAL , cilt.78, sa.12, ss.1295-1304, 2010 (SCI-Expanded, Scopus) Creative Commons License identifier identifier

185. Neuroendocrine immune system in familial Mediterranean fever

TOPALOĞLU R., BİLGİNER Y., ALİKAŞİFOĞLU A., ÖZALTIN F., BEŞBAŞ N., ÖZEN S., et al.
TURKISH JOURNAL OF PEDIATRICS , cilt.52, sa.6, ss.588-593, 2010 (SCI-Expanded, Scopus) identifier identifier identifier

186. Genotype/Phenotype Correlation in Nephrotic Syndrome Caused by WT1 Mutations

Chernin G., Vega-Warner V., Schoeb D. S., Heeringa S. F., Ovunc B., Saisawat P., et al.
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY , cilt.5, sa.9, ss.1655-1662, 2010 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

187. New syndrome - Situs inversus totalis with cystic dysplasia of kidneys, pancreas and bowing

Balci S., ÖZALTIN F., Bostanoglu S.
CLINICAL DYSMORPHOLOGY , cilt.19, sa.3, ss.173-174, 2010 (SCI-Expanded, Scopus) identifier identifier identifier

188. Clinical course of primary focal segmental glomerulosclerosis (FSGS) in Turkish children: a report from the Turkish Pediatric Nephrology FSGS Study Group

BEŞBAŞ N., ÖZALTIN F., Emre S., Anarat A., ALPAY H., BAKKALOĞLU A., et al.
TURKISH JOURNAL OF PEDIATRICS , cilt.52, sa.3, ss.255-261, 2010 (SCI-Expanded, Scopus) identifier identifier identifier

189. Risk factors in community-acquired urinary tract infections caused by ESBL-producing bacteria in children

TOPALOĞLU R., Er I., Dogan B. G., BİLGİNER Y., ÖZALTIN F., Besbas N., et al.
PEDIATRIC NEPHROLOGY , cilt.25, sa.5, ss.919-925, 2010 (SCI-Expanded, Scopus) identifier identifier identifier

190. A Case Report of Thrombocytopenia-associated Multiple Organ Failure Secondary to Salmonella enterica Serotype Typhi Infection in a Pediatric Patient: Successful Treatment With Plasma Exchange

Yildirim I., CEYHAN M., BAYRAKCİ B., Uysal M., Kuskonmaz B. B., ÖZALTIN F.
THERAPEUTIC APHERESIS AND DIALYSIS , cilt.14, sa.2, ss.226-229, 2010 (SCI-Expanded, Scopus) identifier identifier identifier

191. Toll-like receptors 2 and 4 cell surface expression reflects endotoxin tolerance in Henoch-Schönlein purpura.

CANPINAR H., ÖZALTıN F., BILGINER Y., BAKKALOĞLU A., Ozen S.
The Turkish journal of pediatrics , cilt.52, ss.22-7, 2010 (SCI-Expanded, Scopus) identifier identifier identifier

192. A novel CLCN7 mutation resulting in a most severe form of autosomal recessive osteopetrosis

BEŞBAŞ N., Draaken M., Ludwig M., DEREN Ö., ORHAN D., BİLGİNER Y., et al.
EUROPEAN JOURNAL OF PEDIATRICS , cilt.168, sa.12, ss.1449-1454, 2009 (SCI-Expanded, Scopus) identifier identifier identifier

193. Treatment of severe Henoch-Schonlein nephritis: justifying more immunosuppression

Altugan F. S., ÖZEN S., Aktay-Ayaz N., Gucer S., TOPALOĞLU R., DÜZOVA A., et al.
TURKISH JOURNAL OF PEDIATRICS , cilt.51, sa.6, ss.551-555, 2009 (SCI-Expanded, Scopus) identifier identifier identifier

194. Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome

Heeringa S. F., Vlangos C. N., Chernin G., Hinkes B., Gbadegesin R., Liu J., et al.
NEPHROLOGY DIALYSIS TRANSPLANTATION , cilt.23, sa.11, ss.3527-3533, 2008 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

195. Evaluation of intima media thickness of the common and internal carotid arteries with inflammatory markers in familial Mediterranean fever as possible predictors for atherosclerosis

BİLGİNER Y., ÖZALTIN F., Basaran C., DÜZOVA A., Besbas N., TOPALOĞLU R., et al.
RHEUMATOLOGY INTERNATIONAL , cilt.28, sa.12, ss.1211-1216, 2008 (SCI-Expanded, Scopus) identifier identifier identifier

196. Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS)

Gbadegesin R., Hinkes B. G., Hoskins B. E., Vlangos C. N., Heeringa S. F., Liu J., et al.
NEPHROLOGY DIALYSIS TRANSPLANTATION , cilt.23, sa.4, ss.1291-1297, 2008 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

197. Right atrial thrombosis complicating renal transplantation in a child

BİLGİNER Y., ÖZALTIN F., DÜZOVA A., Erdogan I., AKI F. T., DEMİRCİN M., et al.
PEDIATRIC TRANSPLANTATION , cilt.12, sa.2, ss.251-255, 2008 (SCI-Expanded, Scopus) identifier identifier identifier

198. Eye involvement in children with primary focal segmental glomerulosclerosis

ÖZALTIN F., Heeringa S., Poyraz C. E., BİLGİNER Y., KADAYIFÇILAR S., BEŞBAŞ N., et al.
PEDIATRIC NEPHROLOGY , cilt.23, sa.3, ss.421-427, 2008 (SCI-Expanded, Scopus) identifier identifier identifier

199. Specific podocin mutations correlate with age of onset in steroid-resistant nephrotic syndrome

Hinkes B., Vlangos C., Heeringa S., Mucha B., Gbadegesin R., Liu J., et al.
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY , cilt.19, sa.2, ss.365-371, 2008 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

200. Triple immunosuppression with tacrolimus in pediatric renal transplantation: Single-center experience

DÜZOVA A., AKI F. T., Bakkaloglu A., Besbas N., TOPALOĞLU R., ÖZEN S., et al.
TRANSPLANTATION PROCEEDINGS , cilt.40, sa.1, ss.132-134, 2008 (SCI-Expanded, Scopus) identifier identifier identifier

201. Carotid intima-media thickness in children and young adults with renal transplant: Internal carotid artery vs. common carotid artery

Bilginer Y., Ozaltin F., Basaran C., Aki T. F., Karabulut E., Duzova A., et al.
PEDIATRIC TRANSPLANTATION , cilt.11, sa.8, ss.888-894, 2007 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

202. Cerebral sinovenous thrombosis in a child with steroid sensitive nephrotic syndrome

Isik Balci Y., Tavil B., Fidan G., Ozaltin F.
EUROPEAN JOURNAL OF PEDIATRICS , cilt.166, sa.7, ss.757-758, 2007 (SCI-Expanded, Scopus) identifier identifier identifier

203. Nephrotic syndrome in the first year of life: Two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2)

Hinkes B. G., Mucha B., Vlangos C. N., Gbadegesin R., Liu J., Hasselbachera K., et al.
PEDIATRICS , cilt.119, sa.4, 2007 (SCI-Expanded, Scopus) identifier identifier identifier

204. Childhood vasculitides in Turkey: a nationwide survey

Ozen S., Bakkaloglu A., Dusunsel R., Soylemezoglu O., Ozaltin F., Poyrazoglu H., et al.
CLINICAL RHEUMATOLOGY , cilt.26, sa.2, ss.196-200, 2007 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

205. Novel OCRL1 mutations in patients with the phenotype of dent disease

Utsch B., Boekenkamp A., Benz M. R., Besbas N., Doetsch J., Franke I., et al.
AMERICAN JOURNAL OF KIDNEY DISEASES , cilt.48, sa.6, ss.942-954, 2006 (SCI-Expanded, Scopus) identifier identifier identifier

206. Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible

Hinkes B., Wiggins R. C., Gbadegesin R., Vlangos C. N., Seelow D., Nuernberg G., et al.
NATURE GENETICS , cilt.38, sa.12, ss.1397-1405, 2006 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

207. Cyclosporine drug monitoring with C0 and C2 concentrations in children with stable renal allograft function

Kalyoncu M., Topaloglu R., Bayrakci U., Bakkaloglu A., Besbas N., Ozaltin F., et al.
PEDIATRIC TRANSPLANTATION , cilt.10, sa.2, ss.168-171, 2006 (SCI-Expanded, Scopus) identifier identifier identifier

208. Mutations in the Wilms' tumor 1 gene cause isolated steroid resistant nephrotic syndrome and occur in exons 8 and 9

Mucha B., Ozaltin F., Hinkes B., Hasselbacher K., Ruf R., Schultheiss M., et al.
PEDIATRIC RESEARCH , cilt.59, sa.2, ss.325-331, 2006 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

209. Apoptosis and proliferation in childhood acute proliferative glomerulonephritis

Ozaltin F., Besbas N., Bakkaloglu A., Gucer S., Topaloglu R., Ozen S., et al.
PEDIATRIC NEPHROLOGY , cilt.20, sa.11, ss.1572-1577, 2005 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

210. CLCN5 mutation (R347X) associated with hypokalaemic metabolic alkalosis in a Turkish child: an unusual presentation of Dent's disease

Besbas N., Ozaltin F., Jeck N., Seyberth H., Ludwig M.
NEPHROLOGY DIALYSIS TRANSPLANTATION , cilt.20, sa.7, ss.1476-1479, 2005 (SCI-Expanded, Scopus) identifier identifier identifier

211. E148Q is a disease-causing MEFV mutation: a phenotypic evaluation in patients with familial Mediterranean fever

Topaloglu R., Ozaltin F., Yilmaz E., Ozen S., Balci B., Besbas N., et al.
ANNALS OF THE RHEUMATIC DISEASES , cilt.64, sa.5, ss.750-752, 2005 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

212. Familial Mediterranean fever (FMF) in Turkey - Results of a nationwide multicenter study

Tunca M., Akar S., Onen F., Ozdogan H., KASAPÇOPUR Ö., Yalcinkaya F., et al.
MEDICINE , cilt.84, sa.1, ss.1-11, 2005 (SCI-Expanded, Scopus) identifier identifier identifier

213. The significance of IgA class of antineutrophil cytoplasmic antibodies (ANCA) in childhood Henoch-Schonlein purpura

Ozaltin F., Bakkaloglu A., Ozen S., Topaloglu R., Kavak U., Kalyoncu M., et al.
CLINICAL RHEUMATOLOGY , cilt.23, sa.5, ss.426-429, 2004 (SCI-Expanded, Scopus) identifier identifier identifier

214. Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome

Ruf R., Schultheiss M., Lichtenberger A., Karle S., Zalewski I., Mucha B., et al.
KIDNEY INTERNATIONAL , cilt.66, sa.2, ss.564-570, 2004 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

215. Monocyte chemoattractant protein-1 and interleukin-8 levels in children with acute poststreptococcal glomerulonephritis

Besbas N., Ozaltin F., Catal F., Ozen S., Topaloglu R., Bakkaloglu A.
PEDIATRIC NEPHROLOGY , cilt.19, sa.8, ss.864-868, 2004 (SCI-Expanded, Scopus) identifier identifier identifier

216. An unusual cause of acute renal failure: renal lymphoma

Ozaltin F., Yalcin B., Orhan D., Sari N., Caglar M., Besbas N., et al.
PEDIATRIC NEPHROLOGY , cilt.19, sa.8, ss.912-914, 2004 (SCI-Expanded, Scopus) identifier identifier identifier

217. Bone mineral density in children with familial Mediterranean fever

Duzova A., Ozaltin F., Ozon A., Besbas N., Topaloglu R., Ozen S., et al.
CLINICAL RHEUMATOLOGY , cilt.23, sa.3, ss.230-234, 2004 (SCI-Expanded, Scopus) identifier identifier identifier

218. Influence of Serum Amyloid A (SAA1) and SAA2 gene polymorphisms on renal amyloidosis, and on SAA/C-reactive protein values in patients with familial mediterranean fever in the Turkish population.

Bakkaloglu A., Duzova A., Ozen S., Balci B., Besbas N., Topaloglu R., et al.
The Journal of rheumatology , cilt.31, sa.6, ss.1139-42, 2004 (SCI-Expanded, Scopus) identifier identifier identifier

219. Helicobacter pylori infection in Turkish children with familial Mediterranean fever: is it a cause of persistent inflammation?

Ozaltin F., Bakkaloglu A., Saltik İ. N., Demir H., Duzova A., Bulun A., et al.
CLINICAL RHEUMATOLOGY , cilt.23, sa.2, ss.186-187, 2004 (SCI-Expanded, Scopus) identifier identifier identifier

220. Decreased prevalence of atopy in paediatric patients with familial Mediterranean fever.

Sackesen C., Bakkaloglu A., Sekerel B. E., Ozaltin F., Besbas N., Yilmaz E., et al.
Annals of the rheumatic diseases , cilt.63, ss.187-90, 2004 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

221. Relationship of leptin and insulin-like growth factor I to nutritional status in hemodialyzed children

Besbas N., Ozaltin F., Coskun T., Ozalp S., Saatci U., Bakkaloglu A., et al.
PEDIATRIC NEPHROLOGY , cilt.18, sa.12, ss.1255-1259, 2003 (SCI-Expanded, Scopus) identifier identifier identifier

222. The role of apoptosis in childhood Henoch-Schonlein purpura

Ozaltin F., Besbas N., Uckan D., Tuncer M., Topaloglu R., Ozen S., et al.
CLINICAL RHEUMATOLOGY , cilt.22, ss.265-267, 2003 (SCI-Expanded, Scopus) identifier identifier identifier

223. Successful renal transplantation in a child with ANCA-associated microscopic polyangiitis

Besbas N., Ozaltin F., Tinaztepe K., Gucer S., Ozen S., Bakkaloglu M., et al.
PEDIATRIC NEPHROLOGY , cilt.18, sa.7, ss.696-699, 2003 (SCI-Expanded, Scopus) identifier identifier identifier

224. Role of A-SAA in monitoring subclinical inflammation and in colchicine dosage in familial Mediterranean fever

Duzova A., Bakkaloglu A., Besbas N., Topaloglu R., Ozen S., Ozaltin F., et al.
CLINICAL AND EXPERIMENTAL RHEUMATOLOGY , cilt.21, sa.4, ss.509-514, 2003 (SCI-Expanded, Scopus) identifier identifier identifier

225. Behcet's disease with severe arterial involvement in a child

Besbas N., Ozyurek E., Balkanci F., Ozen S., Saatci I., Ozaltin F., et al.
CLINICAL RHEUMATOLOGY , cilt.21, sa.2, ss.176-179, 2002 (SCI-Expanded, Scopus) identifier identifier identifier

226. Bilateral uveitis in a 7-year-old patient with familial Mediterranean fever. An extremely rare complication

ÖZALTIN F., Bakkaloglu A., Orhon M., DÜZOVA A., Irkec M.
CLINICAL AND EXPERIMENTAL RHEUMATOLOGY , sa.5, 2001 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier

227. Pulmonary haemorrhage in a 6-year-old boy with Henoch-Schonlein purpura

Besbas N., Duzova A., Topaloglu R., Gok F., Ozaltin F., Ozen S., et al.
CLINICAL RHEUMATOLOGY , cilt.20, sa.4, ss.293-296, 2001 (SCI-Expanded, Scopus) identifier identifier identifier

228. Acute parvovirus B19 infection mimicking juvenile myelomonocytic leukemia

Yetgin S., Cetin M., Yenicesu I., Ozaltin F., Uckan D.
EUROPEAN JOURNAL OF HAEMATOLOGY , cilt.65, sa.4, ss.276-278, 2000 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

229. Acute parvovirus infection mimicking juvenile myelomonocytic leukemia

Yetgin S., Cetin M., Yenicesu Y., Ozaltin F., Uckan D.
LEUKEMIA , cilt.14, sa.5, ss.966, 2000 (SCI-Expanded, Scopus) identifier

230. Three sibs diagnosed prenatally with situs inversus totalis, renal and pancreatic dysplasia, and cysts

Balci S., Bostanoglu S., Altinok G., Ozaltin F.
AMERICAN JOURNAL OF MEDICAL GENETICS , cilt.90, sa.3, ss.185-187, 2000 (SCI-Expanded) identifier

231. Serum IgD concentrations in patients with ataxia telangiectasia and with selective IgA deficiency

SANAL O., Ozaltin F., TEZCAN İ., ERSOY F.
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY , cilt.116, sa.3, ss.246, 1998 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier
Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler 44

1. CLINICAL COURSE OF ADOLESCENT ONSET ATYPICAL HEMOLYTIC UREMIC SYNDROME: A STUDY OF TURKISH AHUS REGISTRY

ÇELEĞEN K., GÜLHAN B., FİDAN H. K., YÜKSEL S., YILMAZ N., ÇALTIK YILMAZ A., et al.
54th Congress of European Society of Pediatric Nephrology, 22 Kasım 2022, cilt.37, ss.2813, (Tam Metin Bildiri)

2. ACUTE KIDNEY INJURY ASSOCIATED WITH COVID-19 AND MULTISYSTEM INFLAMMATORY SYNDROME IN CHILDREN (MIS-C)

TAŞTEMEL ÖZTÜRK T., DÜZOVA A., oygar p., BALTU D., ÖZÇİLİNGİR P., LAÇİNEL GÜRLEVİK S., et al.
54th Congress of European Society of Pediatric Nephrology, 22 Haziran 2022, cilt.37, ss.2804, (Tam Metin Bildiri)

3. EFFECTS OF RAAS INHIBITION AND IMMUNOSUPPRESSIVE THERAPY IN PEDIATRIC PATIENTS WITH X-LINKED ALPORT SYNDROME

ÖZDEMİR E. G., GÜLHAN B., KURT ŞÜKÜR E. D., ATAYAR E., DURSUN İ., ÖZÇAKAR Z. B., et al.
53rd European society of pediatric nephrology congress 2021, Amsterdam, Hollanda, 16 - 19 Eylül 2021, cilt.36, ss.3366, (Özet Bildiri)

4. CLINICAL CHARACTERISTICS AND OUTCOME OF BK VIRUS INFECTION IN PEDIATRIC RENAL TRANSPLANT RECIPIENTS

KURT ŞÜKÜR E. D., ÖZDEMİR E. G., TAŞTEMEL ÖZTÜRK T., BALTU D., GÜLHAN B., ÖZALTIN F., et al.
53rd European society of pediatric nephrology congress 2021, Amsterdam, Hollanda, 16 Eylül 2021 - 16 Eylül 2022, (Özet Bildiri)

5. Lizinürik Protein İntoleransının Nadir Renal Tutulumu: Membranoproliferatif Glomerülonefrit

BALTU D., ÖZDEMİR E. G., GÜLHAN B., TAŞTEMEL ÖZTÜRK T., KURT ŞÜKÜR E. D., SİVRİ H. S., et al.
5. ÇOCUK NEFROLOJİ E-OLGU PANAYIRI, Online, Türkiye, 4 - 05 Aralık 2020, ss.34, (Tam Metin Bildiri)

6. ANALYSIS OF LATE RENAL COMPLICATIONS AND RISK FACTORS IN CHILDREN WITH HEMATOPOIETIC STEM CELL TRANSPLANTATION

Gurbanov A., GÜLHAN B., KUŞKONMAZ B. B., OKUR F. V., Cetinkaya D. U., Ozdemir G., et al.
57th ERA-EDTA Congress, ELECTR NETWORK, 6 - 09 Haziran 2020, cilt.35, ss.2140, (Özet Bildiri) identifier

7. EARLY URINARY SYSTEM COMPLICATIONS IN CHILDREN WITH HEMATOPOIETIC STEM CELL TRANSPLANTATION

Gurbanov A., GÜLHAN B., KUŞKONMAZ B. B., OKUR F. V., Cetinkaya D. U., Ozdemir G., et al.
57th ERA-EDTA Congress, ELECTR NETWORK, 6 - 09 Haziran 2020, cilt.35, ss.2123, (Özet Bildiri) identifier

8. CLINICAL CHARACTERISTICS OF PATIENTS WITH GENETICALLY CONFIRMED ALPORT SYNDROME

Ozdemir G., GÜLHAN B., Atayar E., Canpolat N., SÖYLEMEZOĞLU O., ÖZÇAKAR Z. B., et al.
57th ERA-EDTA Congress, ELECTR NETWORK, 6 - 09 Haziran 2020, cilt.35, ss.359, (Özet Bildiri) identifier

9. Hematopoetik Kök Hücre Nakli Yapılan Çocuk Hastalarda Erken Dönem Üriner Sistem Komplikasyonları

Gurbanov A., GÜLHAN B., KUŞKONMAZ B. B., OKUR F. V., Uçkan Çetinkaya D., Özdemir G., et al.
10. Çocuk Nefrolojisi Kongresi, Türkiye, 1 - 04 Mayıs 2019, (Özet Bildiri)

10. Hematopoetik Kök Hücre Nakli Yapılan Çocuk Hastalarda Geç Dönem Renal Komplikasyonların Ve RiskFaktörlerinin Analizi

Gurbanov A., GÜLHAN B., KUŞKONMAZ B. B., OKUR F. V., Uçkan Çetinkaya D., Özdemir G., et al.
10. Çocuk Nefrolojisi Kongresi, Türkiye, 1 - 04 Mayıs 2019, (Özet Bildiri)

11. Çocukluk Çağı Preemptif Ve Preemptif Olmayan Böbrek Nakli Hastalarında Nakil Sonrası İlk Bir Yıldaki GreftFonksiyonlarının Değerlendirilmesi

TAŞ N., AKI F. T., GÜLHAN B., ÖZALTIN F., DÜZOVA A., TEKGÜL S., et al.
10. Çocuk Nefrolojisi Kongresi, Türkiye, 1 - 04 Mayıs 2019, (Özet Bildiri)

12. A REFRACTORY CLINICAL CASE OF LUPUS NEPHRITHIS WHO UNDERWENT BONE MARROW TRANSPLANTATION,

TAŞ N., DEMİR S., ÇAĞDAŞ AYVAZ D. N., ÖZALTIN F., KUŞKONMAZ B. B., TEZCAN F. İ., et al.
European Society for Paediatric Nephrology, 51th Annual Meeting, 3 - 06 Ekim 2018, (Özet Bildiri) identifier

13. Clinical and Mutational Spectrum of Children with Autosomal Recessive and Autosomal Dominant Polycystic Kidney Disease

TÜRKOĞLU Ö., GÜLHAN B., YÜKSEL S., ÇALIŞKAN S., DÜZOVA A., ÇAKAR N., et al.
51st Annual Scientific Meeting of the European Society for the Paediatric Nephrology, 3 - 06 Ekim 2018, (Tam Metin Bildiri)

14. ACUTE HEMODIALYSIS EXPERIENCE IN CHILDRENWEIGHING LESS THAN 15 KG

TAŞ N., GÜLHAN B., çelegen k., ÖZDEMİR E. G., DÜZOVA A., ÖZALTIN F., et al.
51st Annual Scientific Meeting of the European Society for the Paediatric Nephrology, 3 - 06 Ekim 2018, (Tam Metin Bildiri)

15. CLINICAL AND PATHOLOGIC CHARACTERISTICS OF GENETICALLY CONFIRMED ALPORT SYNDROME PATIENTS

TOPALOĞLU R., ÖZDEMİR E. G., GÜLHAN B., ATAYAR E., DÜZOVA A., SOYLU A., et al.
51st Annual Scientific Meeting of the European Society for the Paediatric Nephrology, 3 - 06 Ekim 2018, (Tam Metin Bildiri)

16. TURKISH ATYPICAL HEMOLYTIC UREMIC SYNDROME REGISTRY: ECULIZUMAB TREATMENT IN AHUS PATIENTS

BASKIN S. E., CANPOLAT N., GÜLLEROĞLU K. S., YILMAZ A., MELEK E., YÜKSEL S., et al.
51st Annual Scientific Meeting of the European Society for the Paediatric Nephrology, 3 - 06 Ekim 2018, (Tam Metin Bildiri)

17. MYCETOMA OF THE URINARY TRACT IN AN INFANTWITH HORSESHOE KIDNEY: USEFULNESS OFMECHANICAL REMOVAL AND AMPHOTERICIN-BIRRIGATION

OĞUZ B., ÇELEGEN K., ÇİFTÇİ A. Ö., ÜNAL E., ŞENOCAK M. E., ÖZKALE YAVUZ Ö., et al.
51st Annual Scientific Meeting of the European Society for the Paediatric Nephrology, 3 - 06 Ekim 2018, (Özet Bildiri)

18. Lupus nephritis: Long term follow-up and effect of treatment on growth

TOPALOĞLU R., TAŞ N., çelegen k., ÖZDEMİR E. G., GÜLHAN B., DÜZOVA A., et al.
51st Annual Scientific Meeting of the European Society for the Paediatric Nephrology, 3 - 06 Ekim 2018, (Özet Bildiri)

19. Long-term follow-up results of patients with ADCK4 mutations who have been diagnosed in asymptomatic period: effects of early initiation of CoQ10 supplementation

ATMACA M., GÜLHAN B., KARABAY BAYAZIT A., CANDAN C., ARICI M., TOPALOĞLU R., et al.
51st Annual Scientific Meeting of the European Society for the Paediatric Nephrology, 3 - 06 Ekim 2018, (Tam Metin Bildiri)

20. Effect of IGF¬1 and HGF Induced Bone Marrow Mesenchymal Stem Cells on Focal Segmental Glomerulosclerosis in Sprague¬Dawley Rats: A pilot study

Sahan Ö. B., Korkmaz E., Onbaşılar İ., Güçer K. Ş., Kaymaz F. F., Özaltın F., et al.
43rd Febs Congress, Praha, Çek Cumhuriyeti, 7 - 12 Temmuz 2018, (Özet Bildiri)

21. PEPTIDE BIOMARKER SIGNATURES IN STEROID-RESISTANT NEPHROTIC SYNDROME

Zurbig P., ÖZALTIN F., Anarat A., Paripovic D., Yilmaz A., Caliskan S., et al.
55th Congress of the European-Renal-Association (ERA) and European-Dialysis-and-Transplantation-Association (EDTA), Copenhagen, Danimarka, 24 - 27 Mayıs 2018, cilt.33, (Özet Bildiri) identifier

22. Naif ve İnduklenmis Mezenkimal Kök Hücrelerin Fokal Segmental Glomeruloskleroz Üzerine Etkisinin Sprague-Dawley Modelinde İncelenmesi

Sahan Ö. B., Korkmaz E., ONBAŞILAR İ., GÜÇER K. Ş., KAYMAZ F. F., ÖZALTIN F., et al.
4. Klinik Immunoloji Kongresi, Antalya, Türkiye, 11 - 14 Nisan 2018, (Özet Bildiri)

23. Çocuk ve genç erişkinlerde renovasküler hipertansiyonda cerrahi tedaviler.

PEKER R. O., AKI F. T., KUMBASAR U., GÜVENER M., YILMAZ M., ÖZALTIN F., et al.
18. Ulusal Vasküler ve Endovasküler Cerrahi Kongresi 9. Ulusal Fleboloji Kongresi, Girne, Kıbrıs (Kktc), 9 - 12 Aralık 2017, (Özet Bildiri)

24. Çocuk ve genç erişkinlerde renovasküler hipertansiyonda cerrahi tedaviler

PEKER R. O., aki F. T., KUMBASAR U., GÜVENER M., YILMAZ M., DOĞAN R., et al.
18. Ulusal Vasküler ve Endovasküler Cerrahi Kongresi 9. Ulusal Fleboloji Kongresi, Türkiye, 9 - 12 Kasım 2017

25. Çocuk ve Genç Erişkinlerde Renovasküler Hipertansiyonda Cerrahi Tedavi

PEKER R. O., AKI F. T., KUMBASAR U., GÜVENER M., YILMAZ M., DOĞAN R., et al.
18. Ulusal Vasküler ve Endovasküler Cerrahi Kongresi, Türkiye, 9 - 12 Kasım 2017

26. USE OF HERBAL AND DIETARY SUPPLEMENTS IN CHILDREN WITH KIDNEY AND URINARY TRACT DISEASE

Öztürk T. T., ÖZMERT E. N., KANBUR N., GÜLHAN B., ÖZALTIN F., TOPALOĞLU R., et al.
PEDIATRIC NEPHROLOGY, 6 - 09 Eylül 2017, cilt.32, ss.1675, (Özet Bildiri)

27. Use of herbal and dietary supplements in children with kidney and urinary tract disease

Taştemel Öztürk T., KANBUR N., ÖZMERT E. N., GÜLHAN B., ÖZALTIN F., TOPALOĞLU R., et al.
50th Anniversary Meeting of the ESPN, 6 - 09 Eylül 2017, cilt.32, ss.1675, (Özet Bildiri)

28. Risk factors for cardiovascular comorbidities in children with steroid-sensitiveand steroid-resistant nephrotic syndrome.

Kara Eroğlu F., TOPALOĞLU R., KARAGÖZ T., OĞUZ B., ÖZALTIN F., GÜLHAN B., et al.
50th Anniversary Meeting of the ESPN, 6 - 09 Eylül 2017, cilt.32, ss.1661, (Özet Bildiri)

29. Genetic and clinical characteristics of patients with C3 glomerulopathy.

TOPALOĞLU R., GÜLHAN B., KORKMAZ E., DÜZOVA A., ÖZALTIN F.
50th Anniversary Meeting of the European Society for Paediatric Nephrology, 6 - 09 Eylül 2017, (Özet Bildiri)

30. GENETIC AND CLINICAL CHARACTERISTICS OFPATIENTS WITH C3 GLOMERULOPATHY

TOPALOĞLU R., GÜLHAN B., korkmaz e., DÜZOVA A., ÖZALTIN F., SOYLU A., et al.
The 50th Anniversary Meeting of the European Society for Pediatric Nephrology, 6 - 09 Eylül 2017, (Özet Bildiri)

31. Does C.3979 G A/P.VAL1327MET variant of COL4A4 has any pathogenic effect in Turkish patients with Alport Syndrome ?

YILDIZ N., ATA P., ALPAY H., GÖKCE İ., ÖZALTIN F.
48th Anniversary Meeting of the European Society for Paediatric Nephrology, 6 - 09 Eylül 2017, (Özet Bildiri)

32. OC-7 Cresentic glomerulonephritis (CGN) in childhood classification of aetiology and clinicopathological importance of cd163 positive (M2) macrophages

KAYKI G., ORHAN D., ÖZALTIN F., TALİM B., DÜZOVA A., AKÇAÖREN z., et al.
Oral Communications, 7 - 10 Haziran 2017, (Tam Metin Bildiri)

33. Tocilizumab Treatment in childhood takayasu arteritis case series of four patients and systematic review of the literature

BATU E. D., SÖNMEZ H. E., HAZIROLAN T., ÖZALTIN F., BİLGİNER Y., ÖZEN S.
PRES 2016 Genova, 28 Eylül - 01 Ekim 2016, (Özet Bildiri)

34. NEXT GENERATION GENE PANEL SCREENING IN STEROID-RESISTANT NEPHROTIC SYNDROME

Lipska-Zietkiewicz B. S., Boyer O., Gribouval O., Tabatabaei M., Fourrage C., Nischke P., et al.
53rd ERA-EDTA Congress, Vienna, Avusturya, 21 - 24 Mayıs 2016, cilt.31, ss.353, (Özet Bildiri) identifier

35. SMARCAL1 SCREENING IN NEPHROTIC SYNDROME - LESSONS FROM PODONET

Lipska-Zietkiewicz B. S., Gellermann J., Boyer O., Shalaby M. A., ÖZALTIN F., Dusek J., et al.
53rd ERA-EDTA Congress, Vienna, Avusturya, 21 - 24 Mayıs 2016, cilt.31, ss.353-354, (Özet Bildiri) identifier

36. NORMAL 25-HYDROXYVITAMIN D LEVELS ARE ASSOCIATED WITH LESS PROTEINURIA AND ATTENUATE RENAL FAILURE PROGRESSION IN CHILDREN WITH CHRONIC KIDNEY DISEASE

Shroff R., Trivelli A., Litwin M., Picca S., Anarat A., Sallay P., et al.
52nd Congress of the European-Renal-Association-European-Dialysis-and-Transplant-Assocation, London, Kanada, 28 - 31 Mayıs 2015, cilt.30, (Özet Bildiri) Creative Commons License identifier

37. YENİDOĞAN DÖNEMİNDE EPİDERMOLİZİS BÜLLOSA, PİLOR ATREZİSİ VE APLASİA KUTİS: BİR VAKA TAKDİMİ

KAYKI G., BOZKAYA D., ÖZALTIN F., ORHAN D., AYGÜN D., KAYMAZ F., et al.
23. ULUSAL NEONATOLOJİ KONGRESİ, Antalya, Türkiye, 19 - 22 Nisan 2015, (Özet Bildiri)

38. CONVERSION TO SIROLIMUS IN PEDIATRIC RENAL TRANSPLANT RECIPIENTS

TOPALOĞLU R., GÜLHAN B., BİLGİNER Y., Tayfur A. C., Yildiz C., ÖZALTIN F., et al.
50th European-Renal-Association - European-Dialysis-and-Transplant-Association Congress, İstanbul, Türkiye, 18 - 21 Mayıs 2013, cilt.28, ss.294, (Özet Bildiri) identifier

39. Eye involvement in children with primary FSGS

BİLGİNER Y., Poyraz C. E., ÖZALTIN F., KADAYIFÇILAR S., BEŞBAŞ N., Topaloglu R., et al.
44th ERA-EDTA Congress, Barcelona, İspanya, 22 - 24 Haziran 2007, cilt.22, ss.292, (Özet Bildiri) identifier

40. Influence of monocyte chemoattractant protein-1-2518A > G polymorphism on childhood focal segmental glomerulosclerosis

Kalyoncu M., Besbas N., Ozgul K., Ozaltin F., Duzova A., Topaloglu R., et al.
43rd ERA-EDTA Congress, Glasgow, Birleşik Krallık, 15 - 18 Temmuz 2006, cilt.21, ss.328, (Özet Bildiri) identifier

41. Familial Mediterranean Fever and sacroiliac joint involvement. A review of eight cases

Besbas N., Bilginer Y., Duzova A., Ozaltin F., Bayrakci U., Ozen S., et al.
Annual European Congress of Rheumatology, Vienna, Avusturya, 8 - 11 Haziran 2005, cilt.64, ss.509, (Özet Bildiri) identifier

42. T-Cell response against heat shock peptides and streptococci in pediatric Henoch Schonlein purpura and polyarteritis nodosa.

Bilginer Y., Guc D., Dogan L., Bakkaloglu A., Besbas N., Ozaltin F., et al.
68th Annual Scientific Meeting of the American-College-of-Rheumatology, San-Antonio, Kuzey Mariana Adaları, 16 - 21 Ekim 2004, cilt.50, ss.4093, (Özet Bildiri) identifier

43. Cellular response against streptococci in paediatric Henoch Schonlein purpura and polyarteritis nodosa

Guc D., Dogan A., Bakkaloglu A., Ozaltin F., Besbas N., Prakken B., et al.
Annual European Congress of Rheumatology (EULAR 2004), Berlin, Almanya, 9 - 12 Haziran 2004, cilt.63, ss.382, (Özet Bildiri) identifier

44. MICA exon 5 microsatellite alleles in Turkish patients with FMF

Yigitbas E., ÜNER A., Dorak M., Ding W., Tatayoglu G., Balci B., et al.
30th Annual Meeting of the American-Society-for-Histocompatibility-and-Immunogenetics, San-Antonio, Kuzey Mariana Adaları, 2 - 06 Ekim 2004, cilt.65, (Özet Bildiri) identifier
Kitaplar 6

1. Primer Podositopatiler

KURT ŞÜKÜR E. D., ÖZALTIN F.
Genetik böbrek hastalıkları, , Editör, Güneş Tıp Kitabevleri, İstanbul, ss.59-71, 2022

2. Çocukluk Çağında Mitokondriyal Hastalıklar

KURT ŞÜKÜR E. D., ÖZALTIN F.
Çocukluk Çağında Mitokondriyal Hastalıklar, Ünal Uzun Özlem, Editör, Türkiye Klinikleri, Ankara, ss.46-52, 2022

3. Nefrotik Sendrom ve Genetik

GÜLHAN B., ÖZALTIN F.
Çocuklarda Nefrotik Sendrom, Prof. Dr. Lale Sever, Editör, Türkiye Klinikleri (Ortadoğu Reklam Tanıtım Yayıncılık Turizm Eğitim İnşaat Sanayi ve Ticaret A.Ş.), ss.28-38, 2021

4. The Kidney in Mitochondrial Diseases

ÖZALTIN F., Salviati L., Rahman S.
Pediatric Nephrology, Emma Francesco, Goldstein Stuart, Bagga Arvind, Bates Carlton M., Shroff Rukshana, Editör, Springer, Heidelberg, ss.1-13, 2021

5. Nefrotik Sendrom ve Genetik

GÜLHAN B., ÖZALTIN F.
Çocuklarda Nefrotik Sendrom - 2021, Lale Sever, Editör, Türkiye Klinikleri (Ortadoğu Reklam Tanıtım Yayıncılık Turizm Eğitim İnşaat Sanayi ve Ticaret A.Ş.), Ankara, ss.28-38, 2021

6. İmmün Kompleks Aracılı Glomerülonefritler: Membranoproliferatif Glomerülonefrit, Yeni Sınıflandırma, C3 Glomerülopati

TAŞTEMEL ÖZTÜRK T., ÖZALTIN F.
Türkiye Klinikleri, Rezan Topaloğlu, Editör, Türkiye Klinikleri (Ortadoğu Reklam Tanıtım Yayıncılık Turizm Eğitim İnşaat Sanayi ve Ticaret A.Ş.), ss.29-37, 2021
Metrikler

Yayın

292

Yayın (WoS)

255

Yayın (Scopus)

239

Atıf (WoS)

6522

H-İndeks (WoS)

39

Atıf (Scopus)

8632

H-İndeks (Scopus)

45

Atıf (Scholar)

11162

H-İndeks (Scholar)

52

Atıf (TrDizin)

1

H-İndeks (TrDizin)

1

Atıf (Sobiad)

158

H-İndeks (Sobiad)

7

Atıf (Diğer Toplam)

1

Toplam Atıf Sayısı

5039

Proje

9

Tez Danışmanlığı

7

Açık Erişim

59
BM Sürdürülebilir Kalkınma Amaçları