Prof. FATİH ÖZALTIN | AVESİS

Research Information System

Publications & Works

Publication Network

Journal articles indexed in SCI, SSCI, and AHCI

The clinical characteristics of patients with congenital nephrotic syndrome secondary to <i>NPHS1</i> 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)

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)

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 , vol.28, no.8, 2024 (SCI-Expanded)

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 , vol.28, pp.1027-1037, 2024 (SCI-Expanded)

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 , no.1, 2024 (SCI-Expanded)

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 , no.1, 2024 (SCI-Expanded)

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 , no.1, 2024 (SCI-Expanded)

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 , no.1, 2024 (SCI-Expanded)

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 , no.1, 2024 (SCI-Expanded)

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 , no.1, 2024 (SCI-Expanded)

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 , vol.102, pp.79-88, 2024 (SCI-Expanded)

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 , vol.28, no.4, 2024 (SCI-Expanded) Sustainable Development

Sustainable Development

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)

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 , vol.105, no.4, pp.844-864, 2024 (SCI-Expanded)

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 , vol.9, no.4, pp.973-981, 2024 (SCI-Expanded)

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 , vol.39, no.3, pp.867-877, 2024 (SCI-Expanded)

Management of pediatric hemolytic uremic syndrome

GÜLHAN B., ÖZALTIN F., Fidan K., ÖZÇAKAR Z. B., Söylemezoğlu O.

Turkish Journal of Pediatrics , vol.66, no.1, pp.1-16, 2024 (SCI-Expanded)

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 , vol.104, no.1, pp.100287, 2024 (SCI-Expanded)

Genotype/phenotype relationship in mild congenital nephrotic syndrome

Mulic B., Peco-Antic A., ÖZALTIN F.

SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO , vol.2024-January-February, no.1-2, pp.81-84, 2024 (SCI-Expanded) Sustainable Development

Sustainable Development

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) , vol.38, no.12, pp.3975-3976, 2023 (SCI-Expanded)

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 , vol.104, no.6, pp.679-685, 2023 (SCI-Expanded)

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) , vol.38, no.12, pp.3977-3981, 2023 (SCI-Expanded)

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 , vol.38, no.11, pp.3811-3821, 2023 (SCI-Expanded)

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COVID-19 associated thrombotic microangiopathy

YILMAZ E. M., Cebi M. N., Karahan I., SAYGILI S. K., Gulmez R., Demirgan E. B., et al.

Nephrology , vol.28, no.10, pp.557-560, 2023 (SCI-Expanded)

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 , vol.65, no.3, pp.456-468, 2023 (SCI-Expanded)

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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 , vol.38, no.5, pp.1499-1511, 2023 (SCI-Expanded)

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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 , vol.38, no.3, pp.711-719, 2023 (SCI-Expanded)

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

SAYGILI S. K., ÇALIŞKAN S., ÖZALTIN F.

PEDIATRIC NEPHROLOGY , vol.38, no.3, pp.933-934, 2023 (SCI-Expanded)

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 , vol.38, no.2, pp.461-469, 2023 (SCI-Expanded)

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 , vol.24, no.3, 2023 (SCI-Expanded)

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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)

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 , vol.28, no.5, pp.350-359, 2023 (SCI-Expanded)

Response to Dr. Spizzirri et al

TAŞTEMEL ÖZTÜRK T., ÖZALTIN F., TOPALOĞLU R.

Pediatric Nephrology , vol.38, no.1, pp.309-310, 2023 (SCI-Expanded)

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 , vol.65, no.5, pp.874-880, 2023 (SCI-Expanded)

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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 , vol.41, no.9, pp.2883-2892, 2022 (SCI-Expanded) Sustainable Development

Sustainable Development

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 , vol.102, no.3, pp.604-612, 2022 (SCI-Expanded)

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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 , vol.102, no.3, pp.592-603, 2022 (SCI-Expanded)

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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 , vol.37, no.8, pp.1855-1866, 2022 (SCI-Expanded)

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 , vol.37, no.6, pp.1069-1077, 2022 (SCI-Expanded)

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 , vol.20, no.5, pp.45-48, 2022 (SCI-Expanded)

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 , vol.35, no.4, pp.1213-1222, 2022 (SCI-Expanded)

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 , vol.173, pp.22-33, 2022 (SCI-Expanded) Sustainable Development

Sustainable Development

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 , vol.101, pp.346-358, 2022 (SCI-Expanded) Sustainable Development

Sustainable Development

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 , vol.36, no.2, 2022 (SCI-Expanded) Sustainable Development

Sustainable Development

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 , vol.64, no.1, pp.59-68, 2022 (SCI-Expanded)

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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 , vol.100, no.5, pp.1112-1123, 2021 (SCI-Expanded)

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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 , vol.63, no.6, pp.986-993, 2021 (SCI-Expanded)

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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 , vol.36, no.10, pp.3434, 2021 (SCI-Expanded)

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 , vol.36, no.10, pp.3366, 2021 (SCI-Expanded)

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 , vol.36, no.10, pp.3475-3476, 2021 (SCI-Expanded)

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 , vol.36, no.10, pp.3404-3405, 2021 (SCI-Expanded)

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 , vol.36, no.10, pp.3455, 2021 (SCI-Expanded)

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 , vol.36, no.10, pp.3403, 2021 (SCI-Expanded)

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 , vol.36, no.10, pp.3445-3446, 2021 (SCI-Expanded)

AUDIOLOGICAL FINDINGS IN DISTAL RENAL TUBULAR ACIDOSIS

Ay E., GÜRSES E., Arslan F., GÜLHAN B., Alniacik A., DÜZOVA A., et al.

PEDIATRIC NEPHROLOGY , vol.36, no.10, pp.3428, 2021 (SCI-Expanded)

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 , vol.36, no.10, pp.3441, 2021 (SCI-Expanded)

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 , vol.36, no.10, pp.3421-3422, 2021 (SCI-Expanded)

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 , vol.36, no.10, pp.3460, 2021 (SCI-Expanded)

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 , vol.36, no.10, pp.3476, 2021 (SCI-Expanded)

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 , vol.11, pp.35, 2021 (SCI-Expanded)

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 , vol.99, no.6, pp.1500-1501, 2021 (SCI-Expanded)

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 , vol.36, 2021 (SCI-Expanded)

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 , vol.36, 2021 (SCI-Expanded)

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 , vol.25, no.3, 2021 (SCI-Expanded)

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 , vol.17, no.4, pp.277-289, 2021 (SCI-Expanded)

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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 , vol.76, no.2, pp.155-157, 2021 (SCI-Expanded)

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 , vol.6, no.3, pp.846-852, 2021 (SCI-Expanded)

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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 , vol.180, no.1, pp.253-262, 2021 (SCI-Expanded) Sustainable Development

Sustainable Development

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 , vol.36, no.12, pp.4109-4110, 2020 (SCI-Expanded)

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Sustainable Development

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 , vol.36, no.12, pp.4111-4113, 2020 (SCI-Expanded)

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Sustainable Development

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 , vol.62, no.6, pp.940-948, 2020 (SCI-Expanded)

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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 , vol.98, no.4, pp.390-395, 2020 (SCI-Expanded)

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 , vol.35, no.10, pp.1941-1952, 2020 (SCI-Expanded) Sustainable Development

Sustainable Development

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 , vol.23, no.5, pp.362-371, 2020 (SCI-Expanded)

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 , vol.28, no.10, pp.1368-1378, 2020 (SCI-Expanded)

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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 , vol.62, no.5, pp.746-755, 2020 (SCI-Expanded)

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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 , vol.20, no.1, 2020 (SCI-Expanded)

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 , vol.22, no.5, 2020 (SCI-Expanded)

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 , vol.61, no.12, pp.1250-1256, 2019 (SCI-Expanded)

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 , vol.29, no.5, pp.746-752, 2019 (SCI-Expanded)

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 , vol.61, no.5, pp.657-663, 2019 (SCI-Expanded)

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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 , vol.7, 2019 (SCI-Expanded)

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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 , vol.96, no.1, pp.214-221, 2019 (SCI-Expanded)

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 , vol.34, no.1, pp.75-79, 2019 (SCI-Expanded)

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 , vol.61, no.1, pp.111-116, 2019 (SCI-Expanded)

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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 , vol.99, no.1, pp.128-137, 2019 (SCI-Expanded)

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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 , vol.88, pp.71-74, 2018 (SCI-Expanded)

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 , vol.33, no.10, pp.1826-1827, 2018 (SCI-Expanded)

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 , vol.33, no.10, pp.1832, 2018 (SCI-Expanded)

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 , vol.33, no.10, pp.1843, 2018 (SCI-Expanded)

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 , vol.33, no.10, pp.1845, 2018 (SCI-Expanded)

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 , vol.21, no.10, pp.1857-1862, 2018 (SCI-Expanded)

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 , vol.33, no.10, pp.1947, 2018 (SCI-Expanded)

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 , vol.33, no.10, pp.1821-1822, 2018 (SCI-Expanded)

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 , vol.33, no.10, pp.1814, 2018 (SCI-Expanded)

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 , vol.33, no.10, pp.1931-1932, 2018 (SCI-Expanded)

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 , vol.33, no.10, pp.1984, 2018 (SCI-Expanded)

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 , vol.33, no.10, pp.1929, 2018 (SCI-Expanded)

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 , vol.33, no.10, pp.1893, 2018 (SCI-Expanded)

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 , vol.33, no.8, pp.1395-1403, 2018 (SCI-Expanded)

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 , vol.8, pp.152, 2018 (SCI-Expanded)

Nephropathic Cystinosis Mimicking Bartter Syndrome A Novel Mutation

Bastug F., Nalcacioglu H., ÖZALTIN F., Korkmaz E., Yel S.

IRANIAN JOURNAL OF KIDNEY DISEASES , vol.12, no.1, pp.61-63, 2018 (SCI-Expanded)

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 , vol.139, no.3, pp.211-218, 2018 (SCI-Expanded)

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 , vol.60, no.1, pp.81-85, 2018 (SCI-Expanded)

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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 , vol.13, no.1, pp.53-62, 2018 (SCI-Expanded)

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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 , vol.49, no.10, pp.1529-1541, 2017 (SCI-Expanded)

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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 , vol.28, no.10, pp.3055-3065, 2017 (SCI-Expanded)

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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 , vol.12, no.10, pp.1634-1641, 2017 (SCI-Expanded)

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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 , vol.32, no.9, pp.1675, 2017 (SCI-Expanded)

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 , vol.32, no.9, pp.1661, 2017 (SCI-Expanded)

GENETIC AND CLINICAL CHARACTERISTICS OF PATIENTS WITH C3 GLOMERULOPATHY

TOPALOĞLU R., GÜLHAN B., Korkmaz E., DÜZOVA A., ÖZALTIN F.

PEDIATRIC NEPHROLOGY , vol.32, no.9, pp.1669, 2017 (SCI-Expanded)

IS RAAS BLOCKADE EFFECTIVE IN NPHS2 GLOMERULOPATHY?

Trautmann A., ÖZALTIN F., Zurowksa A., Helena H., Saeed B., Azocar M., et al.

PEDIATRIC NEPHROLOGY , vol.32, no.9, pp.1661, 2017 (SCI-Expanded)

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 , vol.32, no.9, pp.1773, 2017 (SCI-Expanded)

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 , vol.32, no.9, pp.1803, 2017 (SCI-Expanded)

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 , vol.32, no.9, pp.1769-1770, 2017 (SCI-Expanded)

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 , vol.12, no.8, 2017 (SCI-Expanded)

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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 , vol.32, no.8, pp.1369-1375, 2017 (SCI-Expanded)

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 , vol.46, no.4, pp.529-535, 2017 (SCI-Expanded)

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 , vol.18, 2017 (SCI-Expanded)

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 , vol.36, no.4, pp.332-339, 2017 (SCI-Expanded)

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 , vol.18, no.6, pp.413-420, 2016 (SCI-Expanded)

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 , vol.31, no.12, pp.2317-2325, 2016 (SCI-Expanded)

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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 , vol.34, no.6, 2016 (SCI-Expanded)

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 , vol.31, no.10, pp.1884, 2016 (SCI-Expanded)

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 , vol.310, no.9, 2016 (SCI-Expanded)

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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 , vol.48, no.4, pp.457-467, 2016 (SCI-Expanded)

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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 , vol.89, no.2, pp.468-475, 2016 (SCI-Expanded)

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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 , vol.27, no.1, pp.63-68, 2016 (SCI-Expanded)

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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 , vol.27, no.1, pp.314-322, 2016 (SCI-Expanded)

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

Eroglu F. K., BESBAS N., ÖZALTIN F., TOPALOĞLU R., ÖZEN S.

LUPUS , vol.24, no.13, pp.1452-1454, 2015 (SCI-Expanded)

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 , vol.37, no.9, pp.1435-1439, 2015 (SCI-Expanded)

NEPHROPATHIC CYSTINOSIS MIMICKING BARTTER SYNDROME: NOVEL MUTATION

BaStuG F., Yel S., ÖZALTIN F., Korkmaz E., Uytun S., DÜŞÜNSEL R.

PEDIATRIC NEPHROLOGY , vol.30, no.9, pp.1681, 2015 (SCI-Expanded)

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 , vol.30, no.9, pp.1692, 2015 (SCI-Expanded)

RESULTS OF TURKISH MULTICENTRIC NATIONAL CYSTINOSIS REGISTRY

TOPALOĞLU R., GÜLHAN B., ÖZALTIN F., BODUR İ., BEŞBAŞ N., Dursun H., et al.

PEDIATRIC NEPHROLOGY , vol.30, no.9, pp.1668-1669, 2015 (SCI-Expanded)

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 , vol.30, no.9, pp.1721, 2015 (SCI-Expanded)

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 , vol.30, no.9, pp.1556-1557, 2015 (SCI-Expanded)

ATYPICAL HEMOLYTIC UREMIC SYNDROME UNRESPONSIVE TO ECULIZUMAB THERAPY

Inozu M., BODUR İ., DÜZOVA A., BİLGİNER Y., ÖZALTIN F., BEŞBAŞ N.

PEDIATRIC NEPHROLOGY , vol.30, no.9, pp.1648, 2015 (SCI-Expanded)

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 , vol.30, no.9, pp.1557-1558, 2015 (SCI-Expanded)

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 , vol.30, no.9, pp.1619-1620, 2015 (SCI-Expanded)

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 , vol.30, no.8, pp.1279-1287, 2015 (SCI-Expanded)

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 , vol.29, no.9, pp.1820, 2014 (SCI-Expanded)

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 , vol.29, no.9, pp.1694, 2014 (SCI-Expanded)

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 , vol.27, no.4, pp.457-460, 2014 (SCI-Expanded)

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 , vol.25, no.8, pp.1653-1661, 2014 (SCI-Expanded)

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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 , vol.33, no.7, pp.969-974, 2014 (SCI-Expanded)

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 , vol.94, no.6, pp.884-890, 2014 (SCI-Expanded)

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

PEDIATRIC NEPHROLOGY , vol.29, no.6, pp.961-969, 2014 (SCI-Expanded)

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 , vol.29, no.6, pp.1075-1080, 2014 (SCI-Expanded)

Genotype-phenotype associations in WT1 glomerulopathy

Lipska-Zietkiewicz B. S., Ranchin B., Iatropoulos P., Gellermann J., Melk A., ÖZALTIN F., et al.

KIDNEY INTERNATIONAL , vol.85, no.5, pp.1169-1178, 2014 (SCI-Expanded)

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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 , vol.35, no.2, pp.178-186, 2014 (SCI-Expanded)

Proteinuria in Frasier Syndrome

Peco-Antic A., ÖZALTIN F., Parezanovic V., Milosevski-Lomic G., Zdravkovic V.

SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO , vol.141, pp.685-688, 2013 (SCI-Expanded)

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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 , vol.28, no.8, pp.1643, 2013 (SCI-Expanded)

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 , vol.28, no.8, pp.1584, 2013 (SCI-Expanded)

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 , vol.84, no.1, pp.206-213, 2013 (SCI-Expanded)

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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 , vol.24, no.3, pp.377-384, 2013 (SCI-Expanded)

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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 , vol.28, no.1, pp.155-158, 2013 (SCI-Expanded)

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 , vol.35, pp.380-5, 2013 (SCI-Expanded)

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 , vol.23, no.12, pp.2051-2059, 2012 (SCI-Expanded)

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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 , vol.27, no.9, pp.1799-1800, 2012 (SCI-Expanded)

Rituximab in steroid-dependent and resistant nephrotic syndrome patients

TOPALOĞLU R., GÜLHAN B., ÖZALTIN F., DÜZOVA A., BEŞBAŞ N.

PEDIATRIC NEPHROLOGY , vol.27, no.9, pp.1710-1711, 2012 (SCI-Expanded)

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 , vol.27, no.9, pp.1639-1640, 2012 (SCI-Expanded)

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 , vol.27, no.9, pp.1630, 2012 (SCI-Expanded)

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 , vol.27, no.9, pp.1703-1704, 2012 (SCI-Expanded)

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 , vol.27, no.9, pp.1617-1618, 2012 (SCI-Expanded)

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 , vol.54, no.5, pp.536-539, 2012 (SCI-Expanded)

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 , vol.31, no.7, pp.1123-1126, 2012 (SCI-Expanded)

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 , vol.32, no.5, pp.674-676, 2012 (SCI-Expanded)

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 , vol.34, no.2, pp.211-220, 2012 (SCI-Expanded)

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 , vol.27, no.1, pp.115-121, 2012 (SCI-Expanded)

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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 , vol.15, pp.82, 2011 (SCI-Expanded)

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 , vol.89, no.1, pp.139-147, 2011 (SCI-Expanded)

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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 , vol.26, no.7, pp.1157-1161, 2011 (SCI-Expanded)

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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 , vol.365, no.4, pp.295-306, 2011 (SCI-Expanded)

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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 , vol.121, no.5, pp.2013-2024, 2011 (SCI-Expanded)

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Sustainable Development

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 , vol.43, no.3, pp.847-849, 2011 (SCI-Expanded)

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 , vol.29, no.2, pp.430, 2011 (SCI-Expanded)

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 , vol.53, no.2, pp.194-198, 2011 (SCI-Expanded) Sustainable Development

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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 , vol.29, no.2, pp.463, 2011 (SCI-Expanded)

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 , vol.78, no.12, pp.1295-1304, 2010 (SCI-Expanded)

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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 , vol.52, no.6, pp.588-593, 2010 (SCI-Expanded)

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 , vol.5, no.9, pp.1655-1662, 2010 (SCI-Expanded)

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

Balci S., ÖZALTIN F., Bostanoglu S.

CLINICAL DYSMORPHOLOGY , vol.19, no.3, pp.173-174, 2010 (SCI-Expanded)

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 , vol.52, no.3, pp.255-261, 2010 (SCI-Expanded)

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 , vol.25, no.5, pp.919-925, 2010 (SCI-Expanded)

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 , vol.14, no.2, pp.226-229, 2010 (SCI-Expanded)

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 , vol.52, pp.22-7, 2010 (SCI-Expanded)

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 , vol.168, no.12, pp.1449-1454, 2009 (SCI-Expanded)

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 , vol.51, no.6, pp.551-555, 2009 (SCI-Expanded)

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 , vol.23, no.11, pp.3527-3533, 2008 (SCI-Expanded)

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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 , vol.28, no.12, pp.1211-1216, 2008 (SCI-Expanded)

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 , vol.23, no.4, pp.1291-1297, 2008 (SCI-Expanded)

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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 , vol.12, no.2, pp.251-255, 2008 (SCI-Expanded)

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 , vol.23, no.3, pp.421-427, 2008 (SCI-Expanded)

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 , vol.19, no.2, pp.365-371, 2008 (SCI-Expanded)

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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 , vol.40, no.1, pp.132-134, 2008 (SCI-Expanded)

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 , vol.11, no.8, pp.888-894, 2007 (SCI-Expanded) Sustainable Development

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Cerebral sinovenous thrombosis in a child with steroid sensitive nephrotic syndrome

Isik Balci Y., Tavil B., Fidan G., Ozaltin F.

EUROPEAN JOURNAL OF PEDIATRICS , vol.166, no.7, pp.757-758, 2007 (SCI-Expanded)

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 , vol.119, no.4, 2007 (SCI-Expanded)

Childhood vasculitides in Turkey: a nationwide survey

Ozen S., Bakkaloglu A., Dusunsel R., Soylemezoglu O., Ozaltin F., Poyrazoglu H., et al.

CLINICAL RHEUMATOLOGY , vol.26, no.2, pp.196-200, 2007 (SCI-Expanded) Sustainable Development

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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 , vol.48, no.6, pp.942-954, 2006 (SCI-Expanded)

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 , vol.38, no.12, pp.1397-1405, 2006 (SCI-Expanded) Sustainable Development

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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 , vol.10, no.2, pp.168-171, 2006 (SCI-Expanded)

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 , vol.59, no.2, pp.325-331, 2006 (SCI-Expanded)

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Apoptosis and proliferation in childhood acute proliferative glomerulonephritis

Ozaltin F., Besbas N., Bakkaloglu A., Gucer S., Topaloglu R., Ozen S., et al.

PEDIATRIC NEPHROLOGY , vol.20, no.11, pp.1572-1577, 2005 (SCI-Expanded) Sustainable Development

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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 , vol.20, no.7, pp.1476-1479, 2005 (SCI-Expanded)

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 , vol.64, no.5, pp.750-752, 2005 (SCI-Expanded)

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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 , vol.84, no.1, pp.1-11, 2005 (SCI-Expanded)

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 , vol.23, no.5, pp.426-429, 2004 (SCI-Expanded)

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 , vol.19, no.8, pp.912-914, 2004 (SCI-Expanded)

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 , vol.19, no.8, pp.864-868, 2004 (SCI-Expanded)

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 , vol.66, no.2, pp.564-570, 2004 (SCI-Expanded)

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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 , vol.31, no.6, pp.1139-42, 2004 (SCI-Expanded)

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 , vol.23, no.3, pp.230-234, 2004 (SCI-Expanded)

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 , vol.23, no.2, pp.186-187, 2004 (SCI-Expanded)

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 , vol.63, pp.187-90, 2004 (SCI-Expanded)

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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 , vol.18, no.12, pp.1255-1259, 2003 (SCI-Expanded)

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 , vol.22, pp.265-267, 2003 (SCI-Expanded)

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 , vol.18, no.7, pp.696-699, 2003 (SCI-Expanded)

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 , vol.21, no.4, pp.509-514, 2003 (SCI-Expanded)

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 , vol.21, no.2, pp.176-179, 2002 (SCI-Expanded)

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 , no.5, 2001 (SCI-Expanded) Sustainable Development

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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 , vol.20, no.4, pp.293-296, 2001 (SCI-Expanded)

Acute parvovirus B19 infection mimicking juvenile myelomonocytic leukemia

Yetgin S., Cetin M., Yenicesu I., Ozaltin F., Uckan D.

EUROPEAN JOURNAL OF HAEMATOLOGY , vol.65, no.4, pp.276-278, 2000 (SCI-Expanded) Sustainable Development

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Acute parvovirus infection mimicking juvenile myelomonocytic leukemia

Yetgin S., Cetin M., Yenicesu Y., Ozaltin F., Uckan D.

LEUKEMIA , vol.14, no.5, pp.966, 2000 (SCI-Expanded)

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 , vol.90, no.3, pp.185-187, 2000 (SCI-Expanded)

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 , vol.116, no.3, pp.246, 1998 (SCI-Expanded)

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Articles Published in Other Journals

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 , vol.32, no.4, pp.353-360, 2023 (ESCI)

Effects of Presentation with Nephrotic Range Proteinuria on Childhood Iga Vasculitis Nephritis

Kurt Şükür E. D., METE O., Yılmaz T., Gülhan B., Orhan D., Ozaltin F., et al.

Osmangazi Tıp Dergisi , vol.45, no.4, pp.581-589, 2023 (Peer-Reviewed Journal)

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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 , vol.65, no.4, pp.620-629, 2023 (Scopus)

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Hemolytic Uremic Syndrome in Children

GÜLHAN B., ÖZALTIN F.

TURKISH ARCHIVES OF PEDIATRICS , vol.56, no.5, pp.415-422, 2021 (ESCI)

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 , vol.6, no.2, pp.169-175, 2013 (ESCI)

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Papers Presented at Peer-Reviewed Scientific Conferences

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 November 2022, vol.37, pp.2813, (Full Text)

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 June 2022, vol.37, pp.2804, (Full Text)

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, Netherlands, 16 - 19 September 2021, vol.36, pp.3366, (Summary Text)

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, Netherlands, 16 September 2021 - 16 September 2022, (Summary Text)

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, Turkey, 4 - 05 December 2020, pp.34, (Full Text)

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 June 2020, vol.35, pp.2140, (Summary Text)

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 June 2020, vol.35, pp.2123, (Summary Text)

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 June 2020, vol.35, pp.359, (Summary Text)

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, Turkey, 1 - 04 May 2019, (Summary Text)

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, Turkey, 1 - 04 May 2019, (Summary Text)

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, Turkey, 1 - 04 May 2019, (Summary Text)

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 October 2018, (Summary Text)

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 October 2018, (Full Text)

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 October 2018, (Full Text)

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 October 2018, (Full Text)

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 October 2018, (Full Text)

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 October 2018, (Summary Text)

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 October 2018, (Summary Text)

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 October 2018, (Full Text)

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, Czech Republic, 7 - 12 July 2018, (Summary Text)

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, Denmark, 24 - 27 May 2018, vol.33, (Summary Text)

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, Turkey, 11 - 14 April 2018, (Summary Text)

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, Cyprus (Kktc), 9 - 12 December 2017, (Summary Text)

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, Turkey, 9 - 12 November 2017

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, Turkey, 9 - 12 November 2017

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 September 2017, vol.32, pp.1675, (Summary Text)

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 September 2017, vol.32, pp.1675, (Summary Text)

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 September 2017, vol.32, pp.1661, (Summary Text)

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 September 2017, (Summary Text)

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 September 2017, (Summary Text)

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 September 2017, (Summary Text)

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 June 2017, (Full Text)

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 September - 01 October 2016, (Summary Text)

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, Austria, 21 - 24 May 2016, vol.31, pp.353, (Summary Text)

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, Austria, 21 - 24 May 2016, vol.31, pp.353-354, (Summary Text)

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, Canada, 28 - 31 May 2015, vol.30, (Summary Text)

Creative Commons License

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, Turkey, 19 - 22 April 2015, (Summary Text)

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, Turkey, 18 - 21 May 2013, vol.28, pp.294, (Summary Text)

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, Spain, 22 - 24 June 2007, vol.22, pp.292, (Summary Text)

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, United Kingdom, 15 - 18 July 2006, vol.21, pp.328, (Summary Text)

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, Austria, 8 - 11 June 2005, vol.64, pp.509, (Summary Text)

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, Northern Mariana Islands, 16 - 21 October 2004, vol.50, pp.4093, (Summary Text)

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, Germany, 9 - 12 June 2004, vol.63, pp.382, (Summary Text)

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, Northern Mariana Islands, 2 - 06 October 2004, vol.65, (Summary Text)

Books

Primer Podositopatiler

KURT ŞÜKÜR E. D., ÖZALTIN F.

in: Genetik böbrek hastalıkları, , Editor, Güneş Tıp Kitabevleri, İstanbul, pp.59-71, 2022

Çocukluk Çağında Mitokondriyal Hastalıklar

KURT ŞÜKÜR E. D., ÖZALTIN F.

in: Çocukluk Çağında Mitokondriyal Hastalıklar, Ünal Uzun Özlem, Editor, Türkiye Klinikleri, Ankara, pp.46-52, 2022

Nefrotik Sendrom ve Genetik

GÜLHAN B., ÖZALTIN F.

in: Çocuklarda Nefrotik Sendrom, Prof. Dr. Lale Sever, Editor, Türkiye Klinikleri (Ortadoğu Reklam Tanıtım Yayıncılık Turizm Eğitim İnşaat Sanayi ve Ticaret A.Ş.), pp.28-38, 2021

The Kidney in Mitochondrial Diseases

ÖZALTIN F., Salviati L., Rahman S.

in: Pediatric Nephrology, Emma Francesco, Goldstein Stuart, Bagga Arvind, Bates Carlton M., Shroff Rukshana, Editor, Springer, Heidelberg, pp.1-13, 2021

Nefrotik Sendrom ve Genetik

GÜLHAN B., ÖZALTIN F.

in: Çocuklarda Nefrotik Sendrom - 2021, Lale Sever, Editor, Türkiye Klinikleri (Ortadoğu Reklam Tanıtım Yayıncılık Turizm Eğitim İnşaat Sanayi ve Ticaret A.Ş.), Ankara, pp.28-38, 2021

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

TAŞTEMEL ÖZTÜRK T., ÖZALTIN F.

in: Türkiye Klinikleri, Rezan Topaloğlu, Editor, Türkiye Klinikleri (Ortadoğu Reklam Tanıtım Yayıncılık Turizm Eğitim İnşaat Sanayi ve Ticaret A.Ş.), pp.29-37, 2021

Metrics

Publication

292

Citation (WoS)

6522

H-Index (WoS)

39

Citation (Scopus)

8632

H-Index (Scopus)

45

Citation (Scholar)

11162

H-Index (Scholar)

52

Citiation (TrDizin)

1

H-Index (TrDizin)

1

Citation (Sobiad)

158

H-Index (Sobiad)

7

Citiation (Sum Other)

1

Total Citation Count

7721

Project

8

Thesis Advisory

7

Open Access

59

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