Prof. FATİH ÖZALTIN

Publication Network

Published journal articles indexed by SCI, SSCI, and AHCI

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

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)

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)

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)

Genotype/phenotype relationship in mild congenital nephrotic syndrome

Mulic B., Peco-Antic A., ÖZALTIN F.

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

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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., Ulubayram K., et al.

EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS , vol.173, pp.22-33, 2022 (SCI-Expanded) 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

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

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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

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)

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)

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)

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)

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)

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

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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

ÖZALTIN F.

PEDIATRIC NEPHROLOGY , vol.29, no.6, pp.961-969, 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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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

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)

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)

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)

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)

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)

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)

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)

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)

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)

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

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

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)

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)

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)

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)

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)

Refereed Congress / Symposium Publications in Proceedings

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

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

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

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

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

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

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

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