Yayınlar & Eserler

Yayın Ağı

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

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) identifier identifier identifier

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) identifier

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) identifier

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) identifier

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) identifier

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) identifier

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) identifier

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 , sa.4, 2024 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier

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) identifier identifier

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) identifier identifier

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) identifier identifier

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) identifier identifier

Genotype/phenotype relationship in mild congenital nephrotic syndrome

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

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) identifier identifier

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) identifier identifier

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) Creative Commons License identifier identifier

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) identifier identifier

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) Creative Commons License identifier identifier identifier

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) identifier identifier identifier

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) identifier identifier identifier

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) Creative Commons License identifier identifier identifier

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) identifier identifier identifier

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) Creative Commons License identifier identifier identifier

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) identifier identifier identifier

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) identifier identifier

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) identifier identifier identifier

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) Creative Commons License identifier identifier identifier

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) Creative Commons License identifier identifier identifier

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) identifier identifier identifier

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) identifier identifier identifier

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) identifier identifier identifier

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) identifier identifier identifier

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) Sürdürülebilir Kalkınma identifier identifier identifier

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) Sürdürülebilir Kalkınma identifier identifier identifier

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) Sürdürülebilir Kalkınma identifier identifier identifier

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) Creative Commons License identifier identifier identifier identifier

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) Creative Commons License identifier identifier identifier identifier

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) Creative Commons License identifier identifier identifier

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) identifier

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) identifier

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) identifier

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) identifier

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) identifier

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) identifier

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) identifier

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) identifier

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) identifier

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) identifier

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) identifier

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) identifier

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) identifier identifier identifier

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) identifier identifier identifier

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) identifier

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) identifier

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) Creative Commons License identifier identifier identifier

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) Creative Commons License identifier identifier identifier

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) Sürdürülebilir Kalkınma identifier identifier identifier

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) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

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) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

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) Creative Commons License identifier identifier identifier

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) Creative Commons License identifier identifier identifier

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) identifier identifier identifier

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) identifier identifier identifier

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) Sürdürülebilir Kalkınma identifier identifier identifier

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) Creative Commons License identifier identifier identifier

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) identifier identifier identifier

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) identifier identifier identifier

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) identifier identifier identifier

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) Creative Commons License identifier identifier identifier

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) Creative Commons License identifier identifier identifier

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) Creative Commons License identifier identifier identifier

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) identifier identifier identifier

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) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

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) identifier identifier identifier

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) identifier

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) identifier

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) identifier

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) identifier

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) identifier

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) identifier

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) identifier

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) identifier identifier identifier

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) identifier

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) identifier

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) identifier

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) identifier

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) identifier identifier identifier

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) identifier

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) Creative Commons License identifier identifier identifier

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) identifier identifier identifier

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) Creative Commons License identifier identifier identifier

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) identifier identifier identifier

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) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

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) Creative Commons License identifier identifier identifier

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) identifier

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) identifier

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) identifier

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) identifier

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) identifier

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) identifier

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) identifier

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) identifier identifier identifier

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) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

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) identifier identifier identifier

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) identifier identifier identifier

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) Creative Commons License identifier identifier identifier

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) identifier identifier identifier

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) identifier identifier identifier

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) identifier

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) Creative Commons License identifier identifier identifier

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) Creative Commons License identifier identifier identifier

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) Creative Commons License identifier identifier identifier

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) Creative Commons License identifier identifier identifier

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) Creative Commons License identifier identifier identifier

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) identifier identifier identifier

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) identifier identifier identifier

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) identifier

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) identifier

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) identifier

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) identifier

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) identifier

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) identifier

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) identifier

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) identifier

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) identifier identifier identifier

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) identifier

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) identifier

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) identifier identifier identifier

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) identifier identifier identifier

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) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

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) identifier identifier identifier

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

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

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) Creative Commons License identifier identifier identifier

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) identifier identifier identifier

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) Creative Commons License identifier identifier identifier

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) identifier

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) identifier

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) Creative Commons License identifier identifier

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) Creative Commons License identifier identifier identifier

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) identifier identifier identifier

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) Creative Commons License identifier identifier identifier

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) identifier

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) identifier

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) identifier

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) identifier

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) identifier identifier identifier

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) identifier

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) identifier

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) identifier identifier identifier

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) identifier identifier identifier

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) Creative Commons License identifier identifier identifier

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) identifier

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) Creative Commons License identifier identifier identifier

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) Creative Commons License identifier identifier identifier

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) Creative Commons License identifier identifier

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) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

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) identifier identifier identifier

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) identifier

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) identifier

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) Sürdürülebilir Kalkınma identifier identifier identifier

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) Creative Commons License identifier identifier

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) identifier identifier identifier

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) Creative Commons License identifier identifier identifier

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) identifier identifier identifier

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) identifier identifier identifier

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) identifier identifier identifier

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) identifier identifier identifier

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) identifier identifier identifier

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) identifier identifier identifier

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) identifier identifier identifier

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) Creative Commons License identifier identifier identifier

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) identifier identifier identifier

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) Creative Commons License identifier identifier identifier

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) identifier identifier identifier

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) identifier identifier identifier

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) Creative Commons License identifier identifier identifier

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) identifier identifier identifier

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) identifier identifier identifier

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) identifier identifier identifier

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) Sürdürülebilir Kalkınma identifier identifier identifier

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) identifier identifier identifier

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) Sürdürülebilir Kalkınma identifier identifier identifier

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) Creative Commons License identifier identifier identifier

Diğer Dergilerde Yayınlanan Makaleler

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) identifier

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 (Hakemli Dergi) Creative Commons License identifier

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) Creative Commons License identifier identifier identifier

Hemolytic Uremic Syndrome in Children

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

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) Creative Commons License identifier identifier

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

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

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 identifier

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 identifier

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 identifier

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

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

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

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 identifier

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

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

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

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

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

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

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

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

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 identifier

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

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

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

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

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

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

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

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

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

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

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

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

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 identifier

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 identifier

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 Creative Commons License identifier

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

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 identifier

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 identifier

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 identifier

Kitap & Kitap Bölümleri

Primer Podositopatiler

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

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

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

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

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

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

241

Atıf (WoS)

3571

H-İndeks (WoS)

31

Atıf (Scopus)

4057

H-İndeks (Scopus)

31

Proje

7

Tez Danışmanlığı

5

Açık Erişim

52
BM Sürdürülebilir Kalkınma Amaçları