Metrikler
Yayın
293
Açık Erişim
59
BM Sürdürülebilir Kalkınma Amaçları
Eğitim Bilgileri
2004 - 2005
2004 - 2005Post Doktora
The University of Michigan, Medical School, Pediatric Nephrology, Amerika Birleşik Devletleri
2000 - 2002
2000 - 2002Doktora
Hacettepe Üniversitesi, Tıp Fakültesi, Çocuk Nefrolojisi , Türkiye
1994 - 2000
1994 - 2000Tıpta Uzmanlık
Hacettepe Üniversitesi, Tıp Fakültesi, Çocuk Sağlığı Ve Hastalıkları, Türkiye
1988 - 1994
1988 - 1994Lisans
Ege Üniversitesi, Tıp Fakültesi, Türkiye
Yabancı Diller
B2 Orta Üstü
B2 Orta Üstüİngilizce
Araştırma Alanları
Tıp
Sağlık Bilimleri
Dahili Tıp Bilimleri
Çocuk Sağlığı ve Hastalıkları
Pediatrik Nefroloji
Akademik Faaliyetlere Dayalı Araştırma Alanları
Avesis Araştırma Alanları
WoS Araştırma Alanları
Scopus Araştırma Alanları
Akademik Ünvanlar / Görevler
2018 - Devam Ediyor
2018 - Devam EdiyorProf. Dr.
Hacettepe Üniversitesi, Tıp Fakültesi (İngilizce), Dahili Tıp Bilimleri Bölümü
2006 - 2018
2006 - 2018Doç. Dr.
Hacettepe Üniversitesi, Tıp Fakültesi (İngilizce), Dahili Tıp Bilimleri Bölümü
2005 - 2006
2005 - 2006Yrd. Doç. Dr.
Hacettepe Üniversitesi, Tıp Fakültesi (İngilizce), Dahili Tıp Bilimleri Bölümü
Yönetimsel Görevler
2023 - Devam Ediyor
2023 - Devam EdiyorMerkez Müdürü
Hacettepe Üniversitesi, Tıp Fakültesi (Türkçe), Dahili Tıp Bilimleri Bölümü
1998 - 1999
1998 - 1999Başasistanlık
Hacettepe Üniversitesi, Tıp Fakültesi (Türkçe), Dahili Tıp Bilimleri Bölümü
Akademi Dışı Deneyim
1994 - Devam Ediyor
1994 - Devam EdiyorTıp Doktoru
Hacettepe Üniversitesi Tıp Fakültesi, Tıp Doktoru
Verdiği Dersler
Ön Lisans
Ön Lisans
SODYUM VE SU DENGESİ VE BOZUKLUKLARI (DÖNEM III, TÜRKÇE TIP)
AKUT BÖBREK YETMEZLİĞİ (DÖNEM III, TÜRKÇE TIP)
SIVI-ELEKTROLİT (DÖNEM IV, PDÖ),
DEHİDRATASYON VE TEDAVİSİ (DÖNEM IV, TÜRKÇE TIP),
SODYUM VE SU DENGESİ BOZUKLUKLARI (DÖNEM III, İNGİLİZCE TIP)
AKUT VE KRONİK BÖBREK YETMEZLİĞİNE YAKLAŞIM (DÖNEM IV)
POTASYUM DENGESİ VE BOZUKLUKLARI (DÖNEM III, TÜRKÇE TIP)
EKSTREMİTE MUAYENESİ VE KAN BASINCI ÖLÇÜMÜ (DÖNEM IV)
DEHİDRATASYON VE TEDAVİSİ (DÖNEM IV, İNGİLİZCE TIP),
POTASYUM DENGESİ VE BOZUKLUKLARI (DÖNEM III, İNGİLİZCE TIP)
İDRAR KAÇIRAN ÇOCUĞA YAKLAŞIM
Yönetilen Tezler
2023
2023Doktora
Kimyasal ve Genetik Podosit Hasar Modellerinde İndüklenmiş Mezenkimal Kök Hücrelerin Etkisi
Özaltın F. (Danışman)
Ö.Burcu(Öğrenci)
2022
2022Tıpta Uzmanlık
Üriner Sistem Taş Hastalığı Olan Çocukların Retrospektif Analizi
Özaltın F. (Danışman)
U.Kavgacı(Öğrenci)
2021
2021Tıpta Uzmanlık
Çocukluk çağı otozomal dominant ve otozomal resesif polikistik böbrek hastalıklarının klinik ve genetik özelliklerinin araştırılması
Özaltın F. (Danışman)
Ö.TUTAL(Öğrenci)
2017
2017Tıpta Uzmanlık
ADCK4 mutasyonu saptanan hastaların uzun dönem izlem sonuçları
Özaltın F. (Danışman)
M.ATMACA(Öğrenci)
2013
2013Tıpta Uzmanlık
Üriner sistemin konjenital anomalisi (USKA) olan çocukların klinik seyirleri ve bu hastalarda son durum hakkında fikir verebilecek ilk değişkenlerin saptanması
Özaltın F. (Danışman)
P.GÜR(Öğrenci)
Makaleler
Tümü (232)
SCI-E, SSCI, AHCI (228)
SCI-E, SSCI, AHCI, ESCI (231)
ESCI (3)
Scopus (230)
TRDizin (14)
2025
20251. Renal Artery Involvement in Pediatric-Onset Takayasu Arteritis: Renal Characteristics and Mid-Term Follow-up Outcomes
Ozturk T. T., Baltu D., Kurt-Sukur E. D., GÜLHAN B., BİLGİNER Y., ÖZEN S., et al.
KLINISCHE PADIATRIE
, 2025 (SCI-Expanded, Scopus)
2025
20252. The clinical characteristics of patients with congenital nephrotic syndrome secondary to NPHS1 mutation: Is nephrectomy still a therapeutic option for selected cases?
Ugurlu Y., GÜLHAN B., DURSUN İ., Nalcacioglu H., Kaya Aksoy G., CANPOLAT N., et al.
PEDIATRIC NEPHROLOGY
, 2025 (SCI-Expanded, Scopus)
2025
20253. A Novel NUP85 Variant Expanding the Phenotypic Spectrum of NUP85-Associated Steroid-Resistant Nephrotic Syndrome
KURT ŞÜKÜR E. D., TİMUÇİN E., BAŞTUĞ T., ÖZALTIN F.
CLINICAL GENETICS
, 2025 (SCI-Expanded, Scopus)
2024
20244. Short Bowel Syndrome Is Not a Contraindication for Kidney Transplantation
TAŞTEMEL ÖZTÜRK T., GÜLHAN B., GÜMÜŞ E., HIZARCIOĞLU GÜLŞEN H., KURT ŞÜKÜR E. D., BOZACI A. C., et al.
PEDIATRIC TRANSPLANTATION
, cilt.28, sa.8, 2024 (SCI-Expanded, Scopus)
2024
20245. Adolescence-onset atypical hemolytic uremic syndrome: is it different from infant-onset?
Celegen K., Gulhan B., Fidan K., Yuksel S., Yilmaz N., Yılmaz A. C., et al.
Clinical and experimental nephrology
, cilt.28, ss.1027-1037, 2024 (SCI-Expanded, Scopus)
2024
20246. Long Term Follow-up Of Children With Nephrocalcinosis: A Tertiary Center Experience
Yavuz G., OĞUZ B., Ozcan N., Ozdemir G., KURT ŞÜKÜR E. D., ÖZALTIN F., et al.
PEDIATRIC NEPHROLOGY
, sa.1, 2024 (SCI-Expanded, Scopus)
2024
20247. A Rare Kidney Involvement in Juvenile Dermatomyositis: Focal Segmental Glomerulosclerosis
KAHYA H. H., ORUÇ Ç., BAYINDIR Y., KURT ŞÜKÜR E. D., GÜLHAN B., ÖZALTIN F., et al.
PEDIATRIC NEPHROLOGY
, sa.1, 2024 (SCI-Expanded, Scopus)
2024
20248. Variable phenotype and genotype of pediatric patients with HNF1B nephropathy
GÜLHAN B., Ekici O., DURSUN İ., GÖKNAR N., YÜKSEL S., Alaygut D., et al.
PEDIATRIC NEPHROLOGY
, sa.1, 2024 (SCI-Expanded, Scopus)
2024
20249. NUP85 NM_024844:c.1379G> A (p.Arg460Gln), a novel variant in nephrotic syndrome
KURT ŞÜKÜR E. D., TİMUÇİN E., BAŞTUĞ T., ÖZALTIN F.
PEDIATRIC NEPHROLOGY
, sa.1, 2024 (SCI-Expanded, Scopus)
2024
202410. Does nephrectomy affect patient survival in patients with congenital nephrotic syndrome secondary to nephrin mutations?
Turkel Y., GÜLHAN B., Ozdemir G., KURT ŞÜKÜR E. D., DÜZOVA A., ÖZALTIN F.
PEDIATRIC NEPHROLOGY
, sa.1, 2024 (SCI-Expanded, Scopus)
2024
202411. Brown Tumor in Pediatric Patients with Chronic Kidney Disease: Two Cases of a Rare Condition
ORUÇ Ç., KURT ŞÜKÜR E. D., GÜLHAN B., VARAN A., ÖZALTIN F., DÜZOVA A.
PEDIATRIC NEPHROLOGY
, sa.1, 2024 (SCI-Expanded, Scopus)
2024
202412. Variable phenotype and genotype of pediatric patients with HNF1B nephropathy.
Gülhan B., Ekici O., Dursun İ., Göknar N., Yüksel S., Alaygut D., et al.
Clinical nephrology
, cilt.102, ss.79-88, 2024 (SCI-Expanded, Scopus)
2024
202413. Calcineurin inhibitor-related hyperkalemia is caused by hyporeninemic hypoaldosteronism and fludrocortisone is an effective treatment: Report of a case series and review of the literature
ÜNSAL Y., BALTU D., GÜLHAN B., OKUR F. V., ÖZALTIN F., DÜZOVA A., et al.
PEDIATRIC TRANSPLANTATION
, cilt.28, sa.4, 2024 (SCI-Expanded, Scopus)
2024
202414. COVID-19 vaccination among adolescents and young adults with chronic kidney conditions: a single-center experience.
Baltu D., Kurt-Sukur E. D., Tastemel Ozturk T., Gulhan B., Ozaltin F., Duzova A., et al.
Klinische Padiatrie
, 2024 (SCI-Expanded, Scopus)
2024
202415. Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)
Riedhammer K. M., Nguyen T. T., KOŞUKCU C., Calzada-Wack J., Li Y., Assia Batzir N., et al.
Kidney International
, cilt.105, sa.4, ss.844-864, 2024 (SCI-Expanded, Scopus)
2024
202416. Steroid-Resistant Nephrotic Syndrome due to NPHS2 Variants Is Not Associated With Posttransplant Recurrence
Kachmar J., Boyer O., Lipska-Ziętkiewicz B., Morinière V., Gribouval O., Heidet L., et al.
Kidney International Reports
, cilt.9, sa.4, ss.973-981, 2024 (SCI-Expanded, Scopus)
2024
202417. Acute kidney injury in children with moderate-severe COVID-19 and multisystem inflammatory syndrome in children: a referral center experience
TAŞTEMEL ÖZTÜRK T., DÜZOVA A., OYGAR P. D., BALTU D., ÖZÇİLİNGİR P., LAÇİNEL GÜRLEVİK S., et al.
Pediatric Nephrology
, cilt.39, sa.3, ss.867-877, 2024 (SCI-Expanded, Scopus)
2024
202418. Genotype/phenotype relationship in mild congenital nephrotic syndrome
Mulic B., Peco-Antic A., ÖZALTIN F.
SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO
, cilt.2024-January-February, sa.1-2, ss.81-84, 2024 (SCI-Expanded, Scopus)
2024
202419. Omic Studies on In Vitro Cystinosis Model: siRNA-Mediated CTNS Gene Silencing in HK-2 Cells
Baysal İ., YABANOĞLU ÇİFTÇİ S., NEMUTLU E., EYLEM C. C., Gök-Topak E. D., ULUBAYRAM K., et al.
Laboratory investigation; a journal of technical methods and pathology
, cilt.104, sa.1, ss.100287, 2024 (SCI-Expanded, Scopus)
2024
202420. Management of pediatric hemolytic uremic syndrome
GÜLHAN B., ÖZALTIN F., Fidan K., ÖZÇAKAR Z. B., Söylemezoğlu O.
Turkish Journal of Pediatrics
, cilt.66, sa.1, ss.1-16, 2024 (SCI-Expanded, Scopus, TRDizin)
2023
202321. A novel homozygous missense variant in TBC1D31 in a consanguineous family with congenital anomalies of the kidney and urinary tract (CAKUT)
SAYGILI S. K., KOŞUKCU C., BAŞTUĞ T., DOĞAN EKİCİ A. I., YILMAZ E. M., Kalyoncu A. U., et al.
Clinical Genetics
, cilt.104, sa.6, ss.679-685, 2023 (SCI-Expanded, Scopus)
2023
202322. An unusual cause of diarrhea in a child with nephrotic syndrome: Questions.
Baltu D., Kurt Sukur E. D., Gumus E., Tastemel Ozturk T., Ergen Y. M., Demirtas D., et al.
Pediatric nephrology (Berlin, Germany)
, cilt.38, sa.12, ss.3975-3976, 2023 (SCI-Expanded, Scopus)
2023
202323. An unusual cause of diarrhea in a child with nephrotic syndrome: Answers.
Baltu D., Kurt Sukur E. D., Gumus E., Tastemel Ozturk T., Ergen Y. M., Demirtas D., et al.
Pediatric nephrology (Berlin, Germany)
, cilt.38, sa.12, ss.3977-3981, 2023 (SCI-Expanded, Scopus)
2023
202324. Long-term kidney follow-up after pediatric acute kidney support therapy for children less than 15 kg
GÜLÇEK Ö. N., GÜLHAN B., KESİCİ S., KURT ŞÜKÜR E. D., HAYRAN K. M., ÖZALTIN F., et al.
Pediatric Nephrology
, cilt.38, sa.11, ss.3811-3821, 2023 (SCI-Expanded, Scopus)
2023
202325. COVID-19 associated thrombotic microangiopathy
YILMAZ E. M., Cebi M. N., Karahan I., SAYGILI S. K., Gulmez R., Demirgan E. B., et al.
Nephrology
, cilt.28, sa.10, ss.557-560, 2023 (SCI-Expanded, Scopus)
2023
202326. BK Virus Infections in Pediatric Kidney Transplant Recipients: A Single-Center Experience
KURT ŞÜKÜR E. D., GÜLHAN B., Özdemir G., Öztürk T. T., BALTU D., ÖZALTIN F., et al.
Turkish Journal of Nephrology
, cilt.32, sa.4, ss.353-360, 2023 (ESCI, Scopus, TRDizin)
2023
202327. Nefrotik Düzey Proteinüri ile Başvurunun Çocukluk Çağı Iga Vasküliti Nefriti Seyrine Etkileri
Kurt Şükür E. D., METE O., Yılmaz T., Gülhan B., Orhan D., Ozaltin F., et al.
Osmangazi Tıp Dergisi
, cilt.45, sa.4, ss.581-589, 2023 (TRDizin)
2023
202328. The outcomes of renin-angiotensin-aldosterone system inhibition and immunosuppressive therapy in children with X-linked Alport syndrome
OZDEMIR E. G., GÜLHAN B., ŞÜKÜR E. D. K., Atayar E., ATAN R., DURSUN İ., et al.
Turkish Journal of Pediatrics
, cilt.65, sa.3, ss.456-468, 2023 (SCI-Expanded, Scopus, TRDizin)
2023
202329. Albuminuria is associated with 24-hour and night-time diastolic blood pressure in urinary tract infection with renal scarring
BALTU D., Salancı B., GÜLHAN B., ÖZALTIN F., DÜZOVA A., TOPALOĞLU R.
TURKISH JOURNAL OF PEDIATRICS
, cilt.65, sa.4, ss.620-629, 2023 (SCI-Expanded, Scopus, TRDizin)
2023
202330. Outcomes of steroid-resistant nephrotic syndrome in children not treated with intensified immunosuppression
Trautmann A., Seide S., Lipska-Zietkiewicz B. S., ÖZALTIN F., Szczepanska M., Azocar M., et al.
PEDIATRIC NEPHROLOGY
, cilt.38, sa.5, ss.1499-1511, 2023 (SCI-Expanded, Scopus)
2023
202331. A rare cause of nephrotic syndrome-sphingosine-1-phosphate lyase (SGPL1) deficiency: 6 cases and a review of the literature
TAŞTEMEL ÖZTÜRK T., CANPOLAT N., SAYGILI S. K., BAYRAKCİ U. S., Soylemezoglu O., ÖZALTIN F., et al.
PEDIATRIC NEPHROLOGY
, cilt.38, sa.3, ss.711-719, 2023 (SCI-Expanded, Scopus)
2023
202332. HOXA11 is another monogenic cause of congenital anomalies of the kidney and urinary tract
SAYGILI S. K., ÇALIŞKAN S., ÖZALTIN F.
PEDIATRIC NEPHROLOGY
, cilt.38, sa.3, ss.933-934, 2023 (SCI-Expanded, Scopus)
2023
202333. Metabolomic Analyses to Identify Candidate Biomarkers of Cystinosis
NEMUTLU E., ÖZALTIN F., YABANOĞLU ÇİFTÇİ S., GÜLHAN B., Eylem C. C., BAYSAL İ., et al.
International Journal of Molecular Sciences
, cilt.24, sa.3, 2023 (SCI-Expanded, Scopus)
2023
202334. Predictors of kidney complications and analysis of hypertension in children with allogeneic hematopoietic stem cell transplantation
Gurbanov A., GÜLHAN B., KUŞKONMAZ B. B., OKUR F. V., ÖZALTIN F., DÜZOVA A., et al.
PEDIATRIC NEPHROLOGY
, cilt.38, sa.2, ss.461-469, 2023 (SCI-Expanded, Scopus)
2023
202335. Response to Dr. Spizzirri et al
TAŞTEMEL ÖZTÜRK T., ÖZALTIN F., TOPALOĞLU R.
Pediatric Nephrology
, cilt.38, sa.1, ss.309-310, 2023 (SCI-Expanded, Scopus)
2023
202336. Hearing Loss Related to Gene Mutations in Distal Renal Tubular Acidosis
Ay E., GÜRSES E., ASLAN F., GÜLHAN B., Alniacik A., DÜZOVA A., et al.
Audiology & neuro-otology
, cilt.28, sa.5, ss.350-359, 2023 (SCI-Expanded, Scopus)
2023
202337. The Clinical and Mutational Spectrum of 69 Turkish Children with Autosomal Recessive or Autosomal Dominant Polycystic Kidney Disease: A Multicenter Retrospective Cohort Study
Tutal O., GÜLHAN B., Atayar E., Yuksel S., ÖZÇAKAR Z. B., Soylemezoglu O., et al.
Nephron
, 2023 (SCI-Expanded, Scopus)
2023
202338. Hemoglobin cast nephropathy: a rare but serious complication of hemolysis in a pediatric patient
BALTU D., Oral N. A., KESİCİ S., TOPALOĞLU R., ÖZCEBE O. İ., AKSU T., et al.
Turkish Journal of Pediatrics
, cilt.65, sa.5, ss.874-880, 2023 (SCI-Expanded, Scopus, TRDizin)
2022
202239. Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy
Drovandi S., Lipska-Zietkiewicz B. S., ÖZALTIN F., Emma F., GÜLHAN B., Boyer O., et al.
KIDNEY INTERNATIONAL
, cilt.102, sa.3, ss.592-603, 2022 (SCI-Expanded, Scopus)
2022
202240. Oral Coenzyme Q10 supplementation leads to better preservation of kidney function in steroid-resistant nephrotic syndrome due to primary Coenzyme Q10 deficiency
Drovandi S., Lipska-Zietkiewicz B. S., ÖZALTIN F., Emma F., GÜLHAN B., Boyer O., et al.
KIDNEY INTERNATIONAL
, cilt.102, sa.3, ss.604-612, 2022 (SCI-Expanded, Scopus)
2022
202241. Childhood-onset Takayasu arteritis and immunodeficiency: case-based review.
Sener S., Basaran O., Batu E. D., Atalay E., Esenboga S., Cagdas D. N., et al.
Clinical rheumatology
, cilt.41, sa.9, ss.2883-2892, 2022 (SCI-Expanded, Scopus)
2022
202242. A broad clinical spectrum of PLC epsilon 1-related kidney disease and intrafamilial variability
Yilmaz E. K., Saygili S., GÜLHAN B., Canpolat N., KARABAY BAYAZIT A., KILIÇ B. D., et al.
PEDIATRIC NEPHROLOGY
, cilt.37, sa.8, ss.1855-1866, 2022 (SCI-Expanded, Scopus)
2022
202243. Long-term renal survival of paediatric patients with lupus nephritis
Demir S., GÜLHAN B., ÖZEN S., Çelĕgen K., BATU AKAL E. D., Taş N., et al.
Nephrology Dialysis Transplantation
, cilt.37, sa.6, ss.1069-1077, 2022 (SCI-Expanded, Scopus)
2022
202244. Eculizumab treatment and discontinuation in pediatric patients with atypical hemolytic uremic syndrome: a multicentric retrospective study
Baskin E., Fidan K., GÜLHAN B., Gulleroglu K., CANPOLAT N., Yilmaz A., et al.
JOURNAL OF NEPHROLOGY
, cilt.35, sa.4, ss.1213-1222, 2022 (SCI-Expanded, Scopus)
2022
202245. Clinically Different Presentations of Family Members With thSame Homozygote Diacylglycerol Kinase Epsilon Mutation: Case Report
Çelikkaya E., Güngör T., Karakaya D., Çakıcı E. K., Yazılıtaş F., ÖZALTIN F., et al.
Experimental and Clinical Transplantation
, cilt.20, sa.5, ss.45-48, 2022 (SCI-Expanded, Scopus)
2022
202246. Mitochondria-targeted CoQ(10) loaded PLGA-b-PEG-TPP nanoparticles: Their effects on mitochondrial functions of COQ8B(-/-) HK-2 cells
Sena Ozbay H., Yabanoglu-Ciftci S., Baysal I., Gultekinoglu M., Can Eylem C. C., Ulubayram K., et al.
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS
, cilt.173, ss.22-33, 2022 (SCI-Expanded, Scopus)
2022
202247. A splice site mutation in the TSEN2 causes a new syndrome with craniofacial and central nervous system malformations, and atypical hemolytic uremic syndrome
CANPOLAT N., Liu D., Atayar E., SAYGILI S. K., Kara N. S., Westfall T. A., et al.
CLINICAL GENETICS
, cilt.101, ss.346-358, 2022 (SCI-Expanded, Scopus)
2022
202248. Mitigation of portal fibrosis and cholestatic liver disease in ANKS6-deficient livers by macrophage depletion
Airik M., McCourt B., TAŞTEMEL ÖZTÜRK T., Huynh A. B., Zhang X., Tometich J. T., et al.
FASEB JOURNAL
, cilt.36, sa.2, 2022 (SCI-Expanded, Scopus)
2022
202249. Glomerulonephritis with crescents in childhood; etiologies and significance of M2 macrophages
KAYKI G., ORHAN D., GÜLHAN B., TOPALOĞLU R., AKÇÖREN Z., DÜZOVA A., et al.
TURKISH JOURNAL OF PEDIATRICS
, cilt.64, sa.1, ss.59-68, 2022 (SCI-Expanded, Scopus, TRDizin)
2021
202150. Could plasma based therapies still be considered in selected cases with atypical hemolytic uremic syndrome?
ÖZLÜ S. G., GÜLHAN B., Aydog O., Atayar E., Delibas A., Parmaksiz G., et al.
TURKISH JOURNAL OF PEDIATRICS
, cilt.63, sa.6, ss.986-993, 2021 (SCI-Expanded, Scopus, TRDizin)
2021
202151. An international cohort study spanning five decades assessed outcomes of nephropathic cystinosis
Emma F., van't Hoff W., Hohenfellner K., TOPALOĞLU R., Greco M., Ariceta G., et al.
KIDNEY INTERNATIONAL
, cilt.100, sa.5, ss.1112-1123, 2021 (SCI-Expanded, Scopus)
2021
202152. TAKAYASU ARTERITIS WITH RENAL ARTERY INVOLVEMENT IN CHILDREN: 12 YEARS EXPERIENCE OF A TERTIARY CENTER
TAŞTEMEL ÖZTÜRK T., BALTU D., KURT ŞÜKÜR E. D., GÜLHAN B., ÖZEN S., DÜZOVA A., et al.
PEDIATRIC NEPHROLOGY
, cilt.36, sa.10, ss.3441, 2021 (SCI-Expanded, Scopus)
2021
202153. CHARACTERISTICS AND OUTCOME OF BK VIRUS INFECTION IN PEDIATRIC RENAL TRANSPLANT RECIPIENT
KURT ŞÜKÜR E. D., Ozdemir G., TAŞTEMEL ÖZTÜRK T., BALTU D., GÜLHAN B., ÖZALTIN F., et al.
PEDIATRIC NEPHROLOGY
, cilt.36, sa.10, ss.3460, 2021 (SCI-Expanded, Scopus)
2021
202154. NEPHROTIC SYNDROME WITH MUTATION IN SPHINGOSINE-1-PHOSPHATE LYASE: 6 CASES
TAŞTEMEL ÖZTÜRK T., CANPOLAT N., Saygili S., BAYRAKCİ U. S., Soylemezoglu O., ÖZALTIN F., et al.
PEDIATRIC NEPHROLOGY
, cilt.36, sa.10, ss.3476, 2021 (SCI-Expanded, Scopus)
2021
202155. PRIMARY COQ10 DEFICIENCY: CLINICAL SPECTRUM AND GENOTYPE-PHENOTYPE CORRELATIONS
Drovandi S., Lipska-zietkiewicz B. S., ÖZALTIN F., Emma F., GÜLHAN B., Boyer O., et al.
PEDIATRIC NEPHROLOGY
, cilt.36, sa.10, ss.3445-3446, 2021 (SCI-Expanded, Scopus)
2021
202156. DGKE MUTATION IN A CHILD TREATED WITH ECULIZUMAB
Tekcan D., Nalcacioglu H., Karadag S. I. K., Onal H. G., ÖZALTIN F., AYDOĞ Ö.
PEDIATRIC NEPHROLOGY
, cilt.36, sa.10, ss.3403, 2021 (SCI-Expanded, Scopus)
2021
202157. AGTR1-RELATED RENAL TUBULAR DYSGENESES MAY NOT BE FATAL
Demirgan E. B., Saygili S., CANPOLAT N., Sever L., Kilicaslan I., Taylan D., et al.
PEDIATRIC NEPHROLOGY
, cilt.36, sa.10, ss.3455, 2021 (SCI-Expanded, Scopus)
2021
202158. EFFECTS OF RAAS INHIBITION AND IMMUNOSUPPRESSIVE THERAPY IN PEDIATRIC PATIENTS WITH X-LINKED ALPORT SYNDROME
Ozdemir G., GÜLHAN B., KURT ŞÜKÜR E. D., Atayar E., DURSUN İ., ÖZÇAKAR Z. B., et al.
PEDIATRIC NEPHROLOGY
, cilt.36, sa.10, ss.3366, 2021 (SCI-Expanded, Scopus)
2021
202159. A HOMOZYGOUS HOXA11 VARIATION AS A POTENTIAL NOVEL CAUSE OF AUTOSOMAL RECESSIVE CONGENITAL ANOMALIES OF THE KIDNEY AND URINARY TRACT
Saygili S., Atayar E., CANPOLAT N., ELİÇEVİK M., KURUĞOĞLU S., Sever L., et al.
PEDIATRIC NEPHROLOGY
, cilt.36, sa.10, ss.3404-3405, 2021 (SCI-Expanded, Scopus)
2021
202160. INFANTILE NEPHROTIC SYNDROME WITH PLCE1 MUTATION; TREATMENT OF CYCLOSPORINE-3-YEAR FOLLOW-UP
Tekcan D., Nalcacioglu H., Onal H. G., ÖZALTIN F., AYDOĞ Ö.
PEDIATRIC NEPHROLOGY
, cilt.36, sa.10, ss.3475-3476, 2021 (SCI-Expanded, Scopus)
2021
202161. AUDIOLOGICAL FINDINGS IN DISTAL RENAL TUBULAR ACIDOSIS
Ay E., GÜRSES E., Arslan F., GÜLHAN B., Alniacik A., DÜZOVA A., et al.
PEDIATRIC NEPHROLOGY
, cilt.36, sa.10, ss.3428, 2021 (SCI-Expanded, Scopus)
2021
202162. CLINICAL AND MUTATIONAL SPECTRUM OF CHILDREN WITH AUTOSOMAL RECESSIVE AND AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE
Tutal O., GÜLHAN B., Atayar E., YÜKSEL S., Ozcakar B., Soylemezoglu O., et al.
PEDIATRIC NEPHROLOGY
, cilt.36, sa.10, ss.3421-3422, 2021 (SCI-Expanded, Scopus)
2021
202163. LONG TERM FOLLOW UP IN RENAL SCARRING OF URINARY TRACT INFECTION: ALBUMINURIA, DIASTOLIC BLOOD PRESSURE
BALTU D., VOLKAN SALANCI B., GÜLHAN B., TAŞTEMEL ÖZTÜRK T., KURT ŞÜKÜR E. D., ÖZALTIN F., et al.
PEDIATRIC NEPHROLOGY
, cilt.36, sa.10, ss.3434, 2021 (SCI-Expanded, Scopus)
2021
202164. Hemolytic Uremic Syndrome in Children
GÜLHAN B., ÖZALTIN F.
TURKISH ARCHIVES OF PEDIATRICS
, cilt.56, sa.5, ss.415-422, 2021 (ESCI, TRDizin)
2021
202165. Single dose application IGF-1 and HGF induced bone marrow mesenchymal stem cells reduced proteinuria in focal segmental gomerulosclerosis model
Şahan Ö. B., Onbaşılar İ., Güçer K. Ş., Kaymaz F. F., Atayar E., Özaltın F., et al.
FEBS OPEN BIO
, cilt.11, ss.35, 2021 (SCI-Expanded, Scopus)
2021
202166. Outcome of diacylglycerol kinase epsilon-mediated hemolytic uremic syndrome in an infant
KOYUN M., KAYA AKSOY G., ÇOMAK E., ÖZALTIN F., AKMAN S.
KIDNEY INTERNATIONAL
, cilt.99, sa.6, ss.1500-1501, 2021 (SCI-Expanded, Scopus)
2021
202167. Transplantation in pediatric aHUS within the era of eculizumab therapy
ÖZÇAKAR Z. B., ÖZALTIN F., GÜLHAN B., ÇOMAK E., Parmaksiz G., Baskin E., et al.
PEDIATRIC TRANSPLANTATION
, cilt.25, sa.3, 2021 (SCI-Expanded, Scopus)
2021
202168. CLINICAL AND MUTATIONAL SPECTRUM OF CHILDREN WITH AUTOSOMAL RECESSIVE AND AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE
Tutal O., GÜLHAN B., Atayar E., YÜKSEL S., ÖZÇAKAR Z. B., Soylemezoglu O., et al.
NEPHROLOGY DIALYSIS TRANSPLANTATION
, cilt.36, 2021 (SCI-Expanded, Scopus)
2021
202169. EARLY URINARY SYSTEM COMPLICATIONS IN CHILDREN WITH HEMATOPOETIC STEM CELL TRANSPLANTATION
Gurbanov A., GÜLHAN B., KUŞKONMAZ B. B., OKUR F. V., ÇETİNKAYA F. D., Ozdemir G., et al.
NEPHROLOGY DIALYSIS TRANSPLANTATION
, cilt.36, 2021 (SCI-Expanded, Scopus)
2021
202170. Gastric duplication cyst in an infant with Finnish-type congenital nephrotic syndrome: concurrence or coincidence?
Güngör T., Eroğlu F. K., Kargın Çakıcı E., Yazılıtaş F., Can G., Çelikkaya E., et al.
Acta clinica Belgica
, cilt.76, sa.2, ss.155-157, 2021 (SCI-Expanded, Scopus)
2021
202171. Management of congenital nephrotic syndrome: consensus recommendations of the ERKNet-ESPN Working Group
Boyer O., Schaefer F., Haffner D., Bockenhauer D., Holtta T., Berody S., et al.
NATURE REVIEWS NEPHROLOGY
, cilt.17, sa.4, ss.277-289, 2021 (SCI-Expanded, Scopus)
2021
202172. AGTR1-related Renal Tubular Dysgeneses May Not Be Fatal
Demirgan E. B., SAYGILI S. K., CANPOLAT N., Sever L., Kilicaslan I., Taylan D., et al.
KIDNEY INTERNATIONAL REPORTS
, cilt.6, sa.3, ss.846-852, 2021 (SCI-Expanded, Scopus)
2021
202173. Predictors for the use of herbal and dietary supplements in children and adolescents with kidney and urinary tract diseases
Ozturk T. T., KANBUR N., ÖZMERT E. N., GÜLHAN B., ÖZALTIN F., TOPALOĞLU R., et al.
EUROPEAN JOURNAL OF PEDIATRICS
, cilt.180, sa.1, ss.253-262, 2021 (SCI-Expanded, Scopus)
2020
202074. Acute kidney injury in a patient with COVID-19: Answers
TAŞTEMEL ÖZTÜRK T., BALTU D., KURT ŞÜKÜR E. D., ÖZSÜREKCİ Y., Gucer S., BAŞARAN H. Ö., et al.
PEDIATRIC NEPHROLOGY
, cilt.36, sa.12, ss.4111-4113, 2020 (SCI-Expanded, Scopus)
2020
202075. Acute kidney injury in a patient with COVID-19: Questions
Tastemel Ozturk T., Baltu D., Kurt Sukur E. D., Ozsurekci Y., Gucer S., Basaran O., et al.
PEDIATRIC NEPHROLOGY
, cilt.36, sa.12, ss.4109-4110, 2020 (SCI-Expanded, Scopus)
2020
202076. Determinants of outcomes in chronic pediatric peritoneal dialysis: a single center experience
Asi T., DÜZOVA A., DOĞAN H. S., Karakurt G., BAHADIR Ö. F., Bozaci A. C., et al.
TURKISH JOURNAL OF PEDIATRICS
, cilt.62, sa.6, ss.940-948, 2020 (SCI-Expanded, Scopus, TRDizin)
2020
202077. Genetic aspects of congenital nephrotic syndrome: a consensus statement from the ERKNet-ESPN inherited glomerulopathy working group
Lipska-Zietkiewicz B. S., ÖZALTIN F., Holtta T., Bockenhauer D., Berody S., Levtchenko E., et al.
EUROPEAN JOURNAL OF HUMAN GENETICS
, cilt.28, sa.10, ss.1368-1378, 2020 (SCI-Expanded, Scopus)
2020
202078. COL4A3 mutation is an independent risk factor for poor prognosis in children with Alport syndrome
Ozdemir G., GÜLHAN B., Atayar E., Saygili S., Soylemezoglu O., Ozcakar Z. B., et al.
PEDIATRIC NEPHROLOGY
, cilt.35, sa.10, ss.1941-1952, 2020 (SCI-Expanded, Scopus)
2020
202079. Renal Biopsy Prognostic Findings in Children With Atypical Hemolytic Uremic Syndrome
YÜKSEL S., GÖNÜL İ. I., Canpolat N., GÖKCE İ., Ozlu S. G., ÖZÇAKAR Z. B., et al.
PEDIATRIC AND DEVELOPMENTAL PATHOLOGY
, cilt.23, sa.5, ss.362-371, 2020 (SCI-Expanded, Scopus)
2020
202080. A homozygousHOXA11variation as a potential novel cause of autosomal recessive congenital anomalies of the kidney and urinary tract
Saygili S., Atayar E., Canpolat N., ELİÇEVİK M., KURUĞOĞLU S., Sever L., et al.
CLINICAL GENETICS
, cilt.98, sa.4, ss.390-395, 2020 (SCI-Expanded, Scopus)
2020
202081. Clinical characteristics of children with congenital anomalies of the kidney and urinary tract and predictive factors of chronic kidney disease
Cetinkaya P. G., GÜLHAN B., DÜZOVA A., Besbas N., HAYRAN K. M., TOPALOĞLU R., et al.
TURKISH JOURNAL OF PEDIATRICS
, cilt.62, sa.5, ss.746-755, 2020 (SCI-Expanded, Scopus, TRDizin)
2020
202082. Cystinosis beyond kidneys: gastrointestinal system and muscle involvement
TOPALOĞLU R., GÜLTEKİNGİL KESER A., GÜLHAN B., ÖZALTIN F., DEMİR H., Ciftci T., et al.
BMC GASTROENTEROLOGY
, cilt.20, sa.1, 2020 (SCI-Expanded, Scopus)
2020
202083. IGF-1 and HGF Preconditioning of Bone Marrow Mesenchymal Stem Cells Reduced Proteinuria in Rat Focal Segmental Glomerulosclerosis Model
Sahan Ö. B., Onbaşılar İ., Güçer K. Ş., Kaymaz F. F., Atayar E., Özaltın F., et al.
CYTOTHERAPY
, cilt.22, sa.5, 2020 (SCI-Expanded, Scopus)
2019
201984. CD80 expression and infiltrating regulatory T cells in idiopathic nephrotic syndrome of childhood
Eroglu F. K., ORHAN D., Inozu M., DÜZOVA A., GÜLHAN B., ÖZALTIN F., et al.
PEDIATRICS INTERNATIONAL
, cilt.61, sa.12, ss.1250-1256, 2019 (SCI-Expanded, Scopus)
2019
201985. Surgical management of renovascular hypertension in children and young adults: a 13-year experience
Peker O., AKI F. T., Kumbasar U., GÜVENER M., YILMAZ M., DOĞAN R., et al.
INTERACTIVE CARDIOVASCULAR AND THORACIC SURGERY
, cilt.29, sa.5, ss.746-752, 2019 (SCI-Expanded, Scopus)
2019
201986. Long-term follow-up results of patients with ADCK4 mutations who have been diagnosed in the asymptomatic period: effects of early initiation of CoQ10 supplementation
ATMACA M., GÜLHAN B., Atayar E., KARABAY BAYAZIT A., CANDAN C., ARICI M., et al.
TURKISH JOURNAL OF PEDIATRICS
, cilt.61, sa.5, ss.657-663, 2019 (SCI-Expanded, Scopus, TRDizin)
2019
201987. Rituximab for Children With Difficult-to-Treat Nephrotic Syndrome: Its Effects on Disease Progression and Growth
TOPALOĞLU R., GÜLHAN B., Celegen K., Inozu M., Hayran M., Duzoya A., et al.
FRONTIERS IN PEDIATRICS
, cilt.7, 2019 (SCI-Expanded, Scopus)
2019
201988. Low levels of urinary epidermal growth factor predict chronic kidney disease progression in children
Azukaitis K., Ju W., Kirchner M., Nair V., Smith M., Fang Z., et al.
KIDNEY INTERNATIONAL
, cilt.96, sa.1, ss.214-221, 2019 (SCI-Expanded, Scopus)
2019
201989. An immunohistochemical approach to detect oncogenic CTNNB1 mutations in primary neoplastic tissues
AKYOL A., GUNER G., OZSEKER H. S., IŞIK A., Atci O., UZUN S., et al.
LABORATORY INVESTIGATION
, cilt.99, sa.1, ss.128-137, 2019 (SCI-Expanded, Scopus)
2019
201990. Persistent hypoglycemic attacks during hemodialysis sessions in an infant with congenital nephrotic syndrome: Questions and Answers
Saygili S., CANPOLAT N., Sever L., ÇALIŞKAN S., Atayar E., ÖZALTIN F.
PEDIATRIC NEPHROLOGY
, cilt.34, sa.1, ss.75-79, 2019 (SCI-Expanded, Scopus)
2019
201991. BK virus associated nephropathy and severe pneumonia in a kidney transplanted adolescent with Schimke immune-osseous-dysplasia
DÜZOVA A., GÜLHAN B., TOPALOĞLU R., ÖZALTIN F., CENGİZ A. B., Yetimakman A. F., et al.
TURKISH JOURNAL OF PEDIATRICS
, cilt.61, sa.1, ss.111-116, 2019 (SCI-Expanded, Scopus, TRDizin)
2018
201892. Response to Early Coenzyme Q10 Supplementation Is not Sustained in CoQ10 Deficiency Caused by CoQ2 Mutation
Eroglu F. K., ÖZALTIN F., Gonc N., Nalcacioglu H., Ozcakar Z. B., YALNIZOĞLU D., et al.
PEDIATRIC NEUROLOGY
, cilt.88, ss.71-74, 2018 (SCI-Expanded, Scopus)
2018
201893. TURKISH ATYPICAL HEMOLYTIC UREMIC SYNDROME REGISTRY: ECULIZUMAB TREATMENT IN AHUS PATIENTS
Baskin E., Canpolat N., Gulleroglu K., Yilmaz A., MELEK E., Yuksel S., et al.
PEDIATRIC NEPHROLOGY
, cilt.33, sa.10, ss.1832, 2018 (SCI-Expanded, Scopus)
2018
201894. LONG-TERM FOLLOW-UP RESULTS OF PATIENTS WITH ADCK4 MUTATIONS WHO HAVE BEEN DIAGNOSED IN ASYMPTOMATIC PERIOD: EFFECTS OF EARLY INITIATION OF COQ10 SUPPLEMENTATION
ATMACA M., GÜLHAN B., KARABAY BAYAZIT A., CANDAN C., ARICI M., TOPALOĞLU R., et al.
PEDIATRIC NEPHROLOGY
, cilt.33, sa.10, ss.1821-1822, 2018 (SCI-Expanded, Scopus)
2018
201895. CLINICAL AND MUTATIONAL SPECTRUM OF CHILDREN WITH AUTOSOMAL RECESSIVE AND AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE
TÜRKOĞLU Ö., GÜLHAN B., YÜKSEL S., Caliskan S., DÜZOVA A., ÇAKAR N., et al.
PEDIATRIC NEPHROLOGY
, cilt.33, sa.10, ss.1814, 2018 (SCI-Expanded, Scopus)
2018
201896. ADRENAL INSUFFICIENCY IN AN INFANT WITH CONGENITAL NEPHROTIC SYNDROME: NEPHROTIC SYNDROME-14
Saygili S., Canpolat N., Caliskan S., Atayar E., Sever L., ÖZALTIN F.
PEDIATRIC NEPHROLOGY
, cilt.33, sa.10, ss.1929, 2018 (SCI-Expanded, Scopus)
2018
201897. CLINICAL AND PATHOLOGIC CHARACTERISTICS OF GENETICALLY CONFIRMED ALPORT SYNDROME PATIENTS
TOPALOĞLU R., Ozdemir G., GÜLHAN B., Atayar E., DÜZOVA A., SOYLU A., et al.
PEDIATRIC NEPHROLOGY
, cilt.33, sa.10, ss.1826-1827, 2018 (SCI-Expanded, Scopus)
2018
201898. LUPUS NEPHRITIS: LONG TERM FOLLOW-UP AND EFFECT OF TREATMENT ON GROWTH
TOPALOĞLU R., TAŞ N., Celegen K., Ozdemir G., GÜLHAN B., DÜZOVA A., et al.
PEDIATRIC NEPHROLOGY
, cilt.33, sa.10, ss.1947, 2018 (SCI-Expanded, Scopus)
2018
201899. MYCETOMA OF THE URINARY TRACT IN AN INFANT WITH HORSESHOE KIDNEY: USEFULNESS OF MECHANICAL REMOVAL AND AMPHOTERICIN-B IRRIGATION
OĞUZ B., Celegen K., ÇİFTÇİ A. Ö., ÜNAL E., ŞENOCAK M. E., ÖZKALE YAVUZ Ö., et al.
PEDIATRIC NEPHROLOGY
, cilt.33, sa.10, ss.1984, 2018 (SCI-Expanded, Scopus)
2018
2018100. ACUTE HEMODIALYSIS EXPERIENCE IN CHILDREN WEIGHING LESS THAN 15 KG
TAŞ N., GÜLHAN B., Celegen K., Ozdemir G., DÜZOVA A., ÖZALTIN F., et al.
PEDIATRIC NEPHROLOGY
, cilt.33, sa.10, ss.1893, 2018 (SCI-Expanded, Scopus)
2018
2018101. GASTROINTESTINAL SYSTEM INVOLVEMENT IN ATYPICAL HEMOLYTIC UREMIC SYNDROME
Fidan K., Yildirim Z. Y., Goknar N., GÜLHAN B., Gulleroglu K., Ozcakar Z. B., et al.
PEDIATRIC NEPHROLOGY
, cilt.33, sa.10, ss.1843, 2018 (SCI-Expanded, Scopus)
2018
2018102. EARLY USE OF ECULIZUMAB IN A CASE OF STEC-HUS BEFORE THE DEVELOPMENT OF CLINICAL SYMPTOMS
BAYRAM M. T., DEMİR B. K., SOYLU A., KAVUKÇU S., ÖZALTIN F.
PEDIATRIC NEPHROLOGY
, cilt.33, sa.10, ss.1845, 2018 (SCI-Expanded, Scopus)
2018
2018103. GASTRIC DUPLICATION CYST IN AN INFANT WITH FINNISH-TYPE CONGENITAL NEPHROTIC SYNDROME: CONCURRENCE OR COINCIDENCE?
Eroglu T. G. F. K., Can G. G., Cakici E. K., Yazilitas F., Celikkaya E., ÖZALTIN F., et al.
PEDIATRIC NEPHROLOGY
, cilt.33, sa.10, ss.1931-1932, 2018 (SCI-Expanded, Scopus)
2018
2018104. Familial Mediterranean fever patients homozygous for E148Q variant may have milder disease
TOPALOĞLU R., BATU AKAL E. D., Yildiz C., Korkmaz E., ÖZEN S., BEŞBAŞ N., et al.
INTERNATIONAL JOURNAL OF RHEUMATIC DISEASES
, cilt.21, sa.10, ss.1857-1862, 2018 (SCI-Expanded, Scopus)
2018
2018105. Extra-Renal manifestations of atypical hemolytic uremic syndrome in children
Fidan K., Goknar N., GÜLHAN B., MELEK E., Yildirim Z. Y., Baskin E., et al.
PEDIATRIC NEPHROLOGY
, cilt.33, sa.8, ss.1395-1403, 2018 (SCI-Expanded, Scopus)
2018
2018106. Effect of IGF-1 and HGF induced bone marrow mesenchymal stem cells on focal segmental glomerulosclerosis in Sprague-Dawley rats: a pilot study
ŞAHAN Ö., KORKMAZ E., ONBAŞILAR İ., Gucer S., KAYMAZ F. F., ÖZALTIN F., et al.
FEBS OPEN BIO
, cilt.8, ss.152, 2018 (SCI-Expanded, Scopus)
2018
2018107. Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome
Warejko J. K., Tan W., Daga A., Schapiro D., Lawson J. A., Shril S., et al.
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
, cilt.13, sa.1, ss.53-62, 2018 (SCI-Expanded, Scopus)
2018
2018108. Hemolytic uremic syndrome and IgA nephropathy in a child: Coincidence or not?
Surmeli-Doven S., Delibas A., Gurses I., Kayacan U. R., Coskun-Yilmaz B., Esen K., et al.
TURKISH JOURNAL OF PEDIATRICS
, cilt.60, sa.1, ss.81-85, 2018 (SCI-Expanded, Scopus, TRDizin)
2018
2018109. Nephropathic Cystinosis Mimicking Bartter Syndrome A Novel Mutation
Bastug F., Nalcacioglu H., ÖZALTIN F., Korkmaz E., Yel S.
IRANIAN JOURNAL OF KIDNEY DISEASES
, cilt.12, sa.1, ss.61-63, 2018 (SCI-Expanded, Scopus)
2018
2018110. Atypical Hemolytic Uremic Syndrome in Children Aged < 2 Years
ÇAKAR N., ÖZÇAKAR Z. B., ÖZALTIN F., KOYUN M., ACAR B. Ç., BAHAT ÖZDOĞAN E., et al.
NEPHRON
, cilt.139, sa.3, ss.211-218, 2018 (SCI-Expanded, Scopus)
2017
2017111. Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly
Braun D. A., Rao J., Mollet G., Schapiro D., Daugeron M., Tan W., et al.
NATURE GENETICS
, cilt.49, sa.10, ss.1529-1541, 2017 (SCI-Expanded, Scopus)
2017
2017112. Long-Term Outcome of Steroid-Resistant Nephrotic Syndrome in Children
Trautmann A., Schnaidt S., Lipska-Zietkiewicz B. S., Bodria M., ÖZALTIN F., Emma F., et al.
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
, cilt.28, sa.10, ss.3055-3065, 2017 (SCI-Expanded, Scopus)
2017
2017113. The Clinical and Mutational Spectrum of Turkish Patients with Cystinosis
TOPALOĞLU R., Gulhan B., Inozu M., Canpolat N., Yilmaz A., Noyan A., et al.
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
, cilt.12, sa.10, ss.1634-1641, 2017 (SCI-Expanded, Scopus)
2017
2017114. IS RAAS BLOCKADE EFFECTIVE IN NPHS2 GLOMERULOPATHY?
Trautmann A., ÖZALTIN F., Zurowksa A., Helena H., Saeed B., Azocar M., et al.
PEDIATRIC NEPHROLOGY
, cilt.32, sa.9, ss.1661, 2017 (SCI-Expanded, Scopus)
2017
2017115. GENETIC AND CLINICAL CHARACTERISTICS OF PATIENTS WITH C3 GLOMERULOPATHY
TOPALOĞLU R., GÜLHAN B., Korkmaz E., DÜZOVA A., ÖZALTIN F.
PEDIATRIC NEPHROLOGY
, cilt.32, sa.9, ss.1669, 2017 (SCI-Expanded, Scopus)
2017
2017116. USE OF HERBAL AND DIETARY SUPPLEMENTS IN CHILDREN WITH KIDNEY AND URINARY TRACT DISEASE
TAŞTEMEL ÖZTÜRK T., Ozmert E., KANBUR N., GÜLHAN B., ÖZALTIN F., TOPALOĞLU R., et al.
PEDIATRIC NEPHROLOGY
, cilt.32, sa.9, ss.1675, 2017 (SCI-Expanded, Scopus)
2017
2017117. LONG TERM RESULTS OF RITUXIMAB IN A TERTIARY REFERRAL CENTER FOR DIFFICULT-TO-TREAT NEPHROTIC SYNDROME
Celegen K., GÜLHAN B., Inozu M., TAŞ N., ÖZALTIN F., DÜZOVA A., et al.
PEDIATRIC NEPHROLOGY
, cilt.32, sa.9, ss.1769-1770, 2017 (SCI-Expanded, Scopus)
2017
2017118. RISK FACTORS FOR CARDIOVASCULAR COMORBIDITIES IN CHILDREN WITH STEROID-SENSITIVE AND STEROID-RESISTANT NEPHROTIC SYNDROME
Eroglu F. K., TOPALOĞLU R., KARAGÖZ T., OĞUZ B., ÖZALTIN F., GÜLHAN B., et al.
PEDIATRIC NEPHROLOGY
, cilt.32, sa.9, ss.1661, 2017 (SCI-Expanded, Scopus)
2017
2017119. CLINICAL CHARACTERISTICS OF PATIENTS WITH MTORI CONVERSION AND EFFECTS ON RENAL OUTCOME
TAŞ N., GÜLHAN B., Inozu M., Celegen K., DÜZOVA A., ÖZALTIN F., et al.
PEDIATRIC NEPHROLOGY
, cilt.32, sa.9, ss.1803, 2017 (SCI-Expanded, Scopus)
2017
2017120. DOES C.3979 G > A/P.VAL1327MET VARIANT OF COL4A4 HAS ANY PATHOGENIC EFFECT IN TURKISH PATIENTS WITH ALPORT SYNDROME?
YILDIZ N., ATA P., ALPAY H., GÖKCE İ., ÖZALTIN F.
PEDIATRIC NEPHROLOGY
, cilt.32, sa.9, ss.1773, 2017 (SCI-Expanded, Scopus)
2017
2017121. Low renal but high extrarenal phenotype variability in Schimke immuno-osseous dysplasia
Lipska-Zietkiewicz B. S., Gellermann J., Boyer O., Gribouval O., Zietkiewicz S., Kari J. A., et al.
PLOS ONE
, cilt.12, sa.8, 2017 (SCI-Expanded, Scopus)
2017
2017122. Follow-up results of patients with ADCK4 mutations and the efficacy of CoQ10 treatment
Atmaca M., GÜLHAN B., KORKMAZ E., INOZU M., Soylemezoglu O., CANDAN C., et al.
PEDIATRIC NEPHROLOGY
, cilt.32, sa.8, ss.1369-1375, 2017 (SCI-Expanded, Scopus)
2017
2017123. Tocilizumab treatment in childhood Takayasu arteritis: Case series of four patients and systematic review of the literature
Batu E. D., Sonmez H. E., HAZIROLAN T., ÖZALTIN F., BİLGİNER Y., ÖZEN S.
SEMINARS IN ARTHRITIS AND RHEUMATISM
, cilt.46, sa.4, ss.529-535, 2017 (SCI-Expanded, Scopus)
2017
2017124. Epidermolysis Bullosa with Pyloric Atresia and Aplasia Cutis in a Newborn Due to Homozygous Mutation in ITGB
KAYKI G., Bozkaya D., Fatih O., ORHAN D., Kaymaz F., KORKMAZ E., et al.
FETAL AND PEDIATRIC PATHOLOGY
, cilt.36, sa.4, ss.332-339, 2017 (SCI-Expanded, Scopus)
2017
2017125. Turkish pediatric atypical hemolytic uremic syndrome registry: initial analysis of 146 patients
BESBAS N., GULHAN B., SOYLEMEZOGLU O., OZCAKAR Z. B., KORKMAZ E., HAYRAN M., et al.
BMC NEPHROLOGY
, cilt.18, 2017 (SCI-Expanded, Scopus)
2016
2016126. Timing of renal replacement therapy does not influence survival and growth in children with congenital nephrotic syndrome caused by mutations in NPHS1: data from the ESPN/ERA-EDTA Registry
Holtta T., Bonthuis M., Van Stralen K. J., Bjerre A., TOPALOĞLU R., ÖZALTIN F., et al.
PEDIATRIC NEPHROLOGY
, cilt.31, sa.12, ss.2317-2325, 2016 (SCI-Expanded, Scopus)
2016
2016127. First-Line, Early and Long-Term Eculizumab Therapy in Atypical Hemolytic Uremic Syndrome: A Case Series in Pediatric Patients
YÜKSEL S., Evrengul H., ÖZÇAKAR Z. B., Becerir T., Yalcin N., Korkmaz E., et al.
PEDIATRIC DRUGS
, cilt.18, sa.6, ss.413-420, 2016 (SCI-Expanded, Scopus)
2016
2016128. Genetic and clinical features of cryopyrin-associated periodic syndromes in Turkish children
EROGLU F. K., Kasapcopur O., BESBAS N., ÖZALTIN F., BİLGİNER Y., Barut K., et al.
CLINICAL AND EXPERIMENTAL RHEUMATOLOGY
, cilt.34, sa.6, 2016 (SCI-Expanded, Scopus)
2016
2016129. Turkish Atypical Hemolytic Uremic Syndrome Registry: Evaluation of 146 Patients
Besbas N., Soylemezoglu O., GÜLHAN B., Ozcakar Z. B., KORKMAZ E., HAYRAN K. M., et al.
PEDIATRIC NEPHROLOGY
, cilt.31, sa.10, ss.1884, 2016 (SCI-Expanded, Scopus)
2016
2016130. Loss of diacylglycerol kinase epsilon in mice causes endothelial distress and impairs glomerular Cox-2 and PGE(2) production
Zhu J., Chaki M., Lu D., Ren C., Wang S., Rauhauser A., et al.
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY
, cilt.310, sa.9, 2016 (SCI-Expanded, Scopus)
2016
2016131. Mutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndrome
Braun D. A., Sadowski C. E., Kohl S., Lovric S., Astrinidis S. A., Pabst W. L., et al.
NATURE GENETICS
, cilt.48, sa.4, ss.457-467, 2016 (SCI-Expanded, Scopus)
2016
2016132. Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicity
Braun D. A., Schueler M., Halbritter J., Gee H. Y., Porath J. D., Lawson J. A., et al.
KIDNEY INTERNATIONAL
, cilt.89, sa.2, ss.468-475, 2016 (SCI-Expanded, Scopus)
2016
2016133. Normal 25-Hydroxyvitamin D Levels Are Associated with Less Proteinuria and Attenuate Renal Failure Progression in Children with CKD
Shroff R., Aitkenhead H., Costa N., Trivelli A., Litwin M., Picca S., et al.
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
, cilt.27, sa.1, ss.314-322, 2016 (SCI-Expanded, Scopus)
2016
2016134. ADCK4-Associated Glomerulopathy Causes Adolescence-Onset FSGS
Korkmaz E., Lipska-Zietkiewicz B. S., Boyer O., Gribouval O., Fourrage C., Tabatabaei M., et al.
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
, cilt.27, sa.1, ss.63-68, 2016 (SCI-Expanded, Scopus)
2015
2015135. Lupus in a patient with cystinosis: is it drug induced?
Eroglu F. K., BESBAS N., ÖZALTIN F., TOPALOĞLU R., ÖZEN S.
LUPUS
, cilt.24, sa.13, ss.1452-1454, 2015 (SCI-Expanded, Scopus)
2015
2015136. MCP1 2518 A/G polymorphism affects progression of childhood focal segmental glomerulosclerosis
Besbas N., KALYONCU M., Cil O., ÖZGÜL R. K., Bakkaloglu A., ÖZALTIN F.
RENAL FAILURE
, cilt.37, sa.9, ss.1435-1439, 2015 (SCI-Expanded, Scopus)
2015
2015137. RESPONSE TO INTENSIFIED IMMUNOSUPPRESSIVE THERAPYAND IDENTIFICATION OF GENETIC DISEASE ARE HIGHLY PREDICTIVE OF LONG-TERM RENAL OUTCOME IN CHILDREN WITH STEROID RESISTANT NEPHROTIC SYNDROME (SRNS)
Trautmann A., Schnaidt S., Ghiggeri G. M., ÖZALTIN F., Saeed B., Drozdz D., et al.
PEDIATRIC NEPHROLOGY
, cilt.30, sa.9, ss.1556-1557, 2015 (SCI-Expanded, Scopus)
2015
2015138. ATYPICAL HEMOLYTIC UREMIC SYNDROME UNRESPONSIVE TO ECULIZUMAB THERAPY
Inozu M., BODUR İ., DÜZOVA A., BİLGİNER Y., ÖZALTIN F., BEŞBAŞ N.
PEDIATRIC NEPHROLOGY
, cilt.30, sa.9, ss.1648, 2015 (SCI-Expanded, Scopus)
2015
2015139. SEVERE PNEUMONIA ASSOCIATED WITH BK VIRUS NEPHROPATHY IN A KIDNEY TRANSPLANTED ADOLESCENT WITH SCHIMKE IMMUNO-OSSEOUS-DYSPLASIA
DÜZOVA A., GÜLHAN B., ÖZALTIN F., TOPALOĞLU R., BİLGİNER Y., BEŞBAŞ N.
PEDIATRIC NEPHROLOGY
, cilt.30, sa.9, ss.1619-1620, 2015 (SCI-Expanded, Scopus)
2015
2015140. CHARACTERISTICS OF RENAL TRANSPLANT CHILDREN WITH CHRONIC ALLOGRAFT NEPHROPATHY: EXPERIENCE OF A TERTIARY REFERRAL CENTER
GÜLHAN B., INOZU M., BİLGİNER Y., ÖZALTIN F., DÜZOVA A., ÖZEN S., et al.
PEDIATRIC NEPHROLOGY
, cilt.30, sa.9, ss.1721, 2015 (SCI-Expanded, Scopus)
2015
2015141. NEPHROPATHIC CYSTINOSIS MIMICKING BARTTER SYNDROME: NOVEL MUTATION
BaStuG F., Yel S., ÖZALTIN F., Korkmaz E., Uytun S., DÜŞÜNSEL R.
PEDIATRIC NEPHROLOGY
, cilt.30, sa.9, ss.1681, 2015 (SCI-Expanded, Scopus)
2015
2015142. RISK FACTORS FOR POST-TRANSPLANT RECURRENCE OF STEROID RESISTANT NEPHROTIC SYNDROME (SRNS): RESULTS FROM THE PODONET REGISTRY
Trautmann A., Ghiggeri G. M., Azocar M., Remuzzi G., ÖZALTIN F., Melk A., et al.
PEDIATRIC NEPHROLOGY
, cilt.30, sa.9, ss.1557-1558, 2015 (SCI-Expanded, Scopus)
2015
2015143. RESULTS OF TURKISH MULTICENTRIC NATIONAL CYSTINOSIS REGISTRY
TOPALOĞLU R., GÜLHAN B., ÖZALTIN F., BODUR İ., BEŞBAŞ N., Dursun H., et al.
PEDIATRIC NEPHROLOGY
, cilt.30, sa.9, ss.1668-1669, 2015 (SCI-Expanded, Scopus)
2015
2015144. RITUXIMAB EXPERIENCE OF A TERTIARY REFERRAL CENTER FOR DIFFICULT-TO-TREAT NEPHROTIC SYNDROME
GÜLHAN B., TOPALOĞLU R., ÖZALTIN F., DÜZOVA A., EROGLU F. K., Bodur I., et al.
PEDIATRIC NEPHROLOGY
, cilt.30, sa.9, ss.1692, 2015 (SCI-Expanded, Scopus)
2015
2015145. Genetic abnormalities and prognosis in patients with congenital and infantile nephrotic syndrome
Cil O., Besbas N., DÜZOVA A., TOPALOĞLU R., PECO-ANTIC A., KORKMAZ E., et al.
PEDIATRIC NEPHROLOGY
, cilt.30, sa.8, ss.1279-1287, 2015 (SCI-Expanded, Scopus)
2014
2014146. Mutations In Anks6 Cause A Nephronophthisis-like Phenotype With End Stage Renal Disease
Taskiran E., Korkmaz E., Gucer S., KOŞUKCU C., Kaymaz F., Koyunlar C., et al.
PEDIATRIC NEPHROLOGY
, cilt.29, sa.9, ss.1820, 2014 (SCI-Expanded, Scopus)
2014
2014147. Thrombophilic Risk Factors And The Efficiency Of Prophylactic Anticoagulation Therapy In Children Who Underwent Renal Transplantation
GÜLHAN B., Tavil B., DÜZOVA A., ÖZALTIN F., ÖZEN S., TOPALOĞLU R., et al.
PEDIATRIC NEPHROLOGY
, cilt.29, sa.9, ss.1694, 2014 (SCI-Expanded, Scopus)
2014
2014148. A novel CFHR5 mutation associated with C3 glomerulonephritis in a Turkish girl
BEŞBAŞ N., GÜLHAN B., GÜÇER K. Ş., Korkmaz E., ÖZALTIN F.
JOURNAL OF NEPHROLOGY
, cilt.27, sa.4, ss.457-460, 2014 (SCI-Expanded, Scopus)
2014
2014149. Mutations in ANKS6 Cause a Nephronophthisis-Like Phenotype with ESRD
Taskiran E. Z., Korkmaz E., Gucer S., KOŞUKCU C., Kaymaz F., Koyunlar C., et al.
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
, cilt.25, sa.8, ss.1653-1661, 2014 (SCI-Expanded, Scopus)
2014
2014150. Diagnostic validity of colchicine in patients with Familial Mediterranean fever
ÖZALTIN F., BİLGİNER Y., GÜLHAN B., Bajin I., Erdogan O., HAYRAN K. M., et al.
CLINICAL RHEUMATOLOGY
, cilt.33, sa.7, ss.969-974, 2014 (SCI-Expanded, Scopus)
2014
2014151. Primary coenzyme Q(10) (CoQ(10)) deficiencies and related nephropathies
ÖZALTIN F.
PEDIATRIC NEPHROLOGY
, cilt.29, sa.6, ss.961-969, 2014 (SCI-Expanded, Scopus)
2014
2014152. Mutations in EMP2 Cause Childhood-Onset Nephrotic Syndrome
Gee H. Y., Ashraf S., Wan X., Vega-Warner V., Esteve-Rudd J., Lovric S., et al.
AMERICAN JOURNAL OF HUMAN GENETICS
, cilt.94, sa.6, ss.884-890, 2014 (SCI-Expanded, Scopus)
2014
2014153. Post-transplant hypertension in pediatric kidney transplant recipients
GÜLHAN B., TOPALOĞLU R., KARABULUT E., ÖZALTIN F., AKI F. T., BİLGİNER Y., et al.
PEDIATRIC NEPHROLOGY
, cilt.29, sa.6, ss.1075-1080, 2014 (SCI-Expanded, Scopus)
2014
2014154. Genotype-phenotype associations in WT1 glomerulopathy
Lipska-Zietkiewicz B. S., Ranchin B., Iatropoulos P., Gellermann J., Melk A., ÖZALTIN F., et al.
KIDNEY INTERNATIONAL
, cilt.85, sa.5, ss.1169-1178, 2014 (SCI-Expanded, Scopus)
2014
2014155. NPHS2 Mutations in Steroid-Resistant Nephrotic Syndrome: A Mutation Update and the Associated Phenotypic Spectrum
Bouchireb K., Boyer O., Gribouval O., Nevo F., Huynh-Cong E., Moriniere V., et al.
HUMAN MUTATION
, cilt.35, sa.2, ss.178-186, 2014 (SCI-Expanded, Scopus)
2013
2013156. Proteinuria in Frasier Syndrome
Peco-Antic A., ÖZALTIN F., Parezanovic V., Milosevski-Lomic G., Zdravkovic V.
SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO
, cilt.141, ss.685-688, 2013 (SCI-Expanded, Scopus)
2013
2013157. The Effect Of Fibroblast Growth Factor 23 On Left Ventricular Function In Peritoneal Dialysis Children
Hacihamdioglu D. O., BEŞBAŞ N., ALEHAN D., OĞUZ B., ÖZALTIN F., DÜZOVA A., et al.
PEDIATRIC NEPHROLOGY
, cilt.28, sa.8, ss.1643, 2013 (SCI-Expanded, Scopus)
2013
2013158. CONTRIBUTORY RISK FACTORS FOR DEVELOPMENT OF THROMBOSIS IN CHILDRENWITH NEPHROTIC SYNDROME
KaraEroglu F., Tavil B., ÖZALTIN F., BEŞBAŞ N., ÖZEN S., ÇETİN M., et al.
PEDIATRIC NEPHROLOGY
, cilt.28, sa.8, ss.1584, 2013 (SCI-Expanded, Scopus)
2013
2013159. Genetic screening in adolescents with steroid-resistant nephrotic syndrome
Lipska-Zietkiewicz B. S., Iatropoulos P., Maranta R., Caridi G., ÖZALTIN F., Anarat A., et al.
KIDNEY INTERNATIONAL
, cilt.84, sa.1, ss.206-213, 2013 (SCI-Expanded, Scopus)
2013
2013160. Clinicopathological and immunohistological features in childhood IgA nephropathy: a single-centre experience
TOPALOĞLU R., Orhan D., BİLGİNER Y., KARABULUT E., ÖZALTIN F., DÜZOVA A., et al.
CLINICAL KIDNEY JOURNAL
, cilt.6, sa.2, ss.169-175, 2013 (ESCI, Scopus)
2013
2013161. DGKE Variants Cause a Glomerular Microangiopathy That Mimics Membranoproliferative GN
ÖZALTIN F., Li B., Rauhauser A., An S., Soylemezoglu O., Gonul I. I., et al.
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
, cilt.24, sa.3, ss.377-384, 2013 (SCI-Expanded, Scopus)
2013
2013162. Neonatal onset atypical hemolytic uremic syndrome successfully treated with eculizumab
Besbas N., Gulhan B., Karpman D., Topaloglu R., Duzova A., Korkmaz E., et al.
PEDIATRIC NEPHROLOGY
, cilt.28, sa.1, ss.155-158, 2013 (SCI-Expanded, Scopus)
2013
2013163. Role of CXCR1 (CKR-1) in inflammation of experimental mesangioproliferative glomerulonephritis.
Ozaltin F., Besbas N., Iskit A. B., Cil O., Akcoren Z., Kale G., et al.
Renal failure
, cilt.35, ss.380-5, 2013 (SCI-Expanded, Scopus)
2012
2012164. Circulating suPAR in Two Cohorts of Primary FSGS
Wei C., Trachtman H., Li J., Dong C., Friedman A. L., Gassman J. J., et al.
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
, cilt.23, sa.12, ss.2051-2059, 2012 (SCI-Expanded, Scopus)
2012
2012165. PERITONEAL DIALYSIS IN CHILDREN UNDER TWO YEARS OF AGE
GÜLHAN B., DÜZOVA A., ÖZALTIN F., TOPALOĞLU R., ÖZEN S., BİLGİNER Y., et al.
PEDIATRIC NEPHROLOGY
, cilt.27, sa.9, ss.1799-1800, 2012 (SCI-Expanded, Scopus)
2012
2012166. Takayasu arteritis in a 4-year-old girl: case report and brief overview of the pediatric literature
Aypar E., Celebi-Tayfur A., Keser M., Odabas D., ÖZALTIN F., PAKSOY Y., et al.
TURKISH JOURNAL OF PEDIATRICS
, cilt.54, sa.5, ss.536-539, 2012 (SCI-Expanded, Scopus)
2012
2012167. WT1 screening in nephrotic syndrome - lessons from PodoNet
Lipska-Zietkiewicz B. S., Iatropoulos P., Ranchin B., Dusek J., ÖZALTIN F., Melk A., et al.
PEDIATRIC NEPHROLOGY
, cilt.27, sa.9, ss.1617-1618, 2012 (SCI-Expanded, Scopus)
2012
2012168. Response to Intensified Immunosuppressive Therapy Predicts Long-Term Prognosis in Steroid Resistant Nephrotic Syndrome (SRNS)
Trautmann A., ÖZALTIN F., Bodria M., Anarat A., Saeed B., Azocar M., et al.
PEDIATRIC NEPHROLOGY
, cilt.27, sa.9, ss.1639-1640, 2012 (SCI-Expanded, Scopus)
2012
2012169. Rituximab in steroid-dependent and resistant nephrotic syndrome patients
TOPALOĞLU R., GÜLHAN B., ÖZALTIN F., DÜZOVA A., BEŞBAŞ N.
PEDIATRIC NEPHROLOGY
, cilt.27, sa.9, ss.1710-1711, 2012 (SCI-Expanded, Scopus)
2012
2012170. THE BENEFITS OF CYCLOSPORINE TREATMENT OF THE PATIENT WITH NPHS2 MUTATION
Hacihamdioglu D. O., ÖZALTIN F., Zeybek C., Kalman S., Demirkaya E., Gok F.
PEDIATRIC NEPHROLOGY
, cilt.27, sa.9, ss.1703-1704, 2012 (SCI-Expanded, Scopus)
2012
2012171. ATYPICAL HUS AND ECULIZUMAB TREATMENT: EXPERIENCE OF A TERTIARY CENTER
BEŞBAŞ N., GÜLHAN B., ÖZEN S., TOPALOĞLU R., DÜZOVA A., Yildiz C., et al.
PEDIATRIC NEPHROLOGY
, cilt.27, sa.9, ss.1630, 2012 (SCI-Expanded, Scopus)
2012
2012172. C1q deficiency: identification of a novel missense mutation and treatment with fresh frozen plasma
TOPALOĞLU R., TASKIRAN E. Z., TAN Ç., Erman B., ÖZALTIN F., SANAL O.
CLINICAL RHEUMATOLOGY
, cilt.31, sa.7, ss.1123-1126, 2012 (SCI-Expanded, Scopus)
2012
2012173. Endothelial Dysfunction and Increased Responses to Renal Nerve Stimulation in Rat Kidneys during Rhabdomyolysis-Induced Acute Renal Failure: Role of Hydroxyl Radical
Cil O., Ertunc M., Gucer K. Ş., Ozaltin F., Iskit A. B., Onur R.
RENAL FAILURE
, cilt.34, sa.2, ss.211-220, 2012 (SCI-Expanded, Scopus)
2012
2012174. Genetic basis of cystinosis in Turkish patients: a single-center experience
TOPALOĞLU R., Vilboux T., COŞKUN T., ÖZALTIN F., Tinloy B., Gunay-Aygun M., et al.
PEDIATRIC NEPHROLOGY
, cilt.27, sa.1, ss.115-121, 2012 (SCI-Expanded, Scopus)
2012
2012175. NPHS2 gene mutation in an Iranian family with familial steroid-resistant nephrotic syndrome
Ameli S., Mazaheri M., Zare-Shahabadi A., ÖZALTIN F., Asgarian F., Monajemzadeh M., et al.
NEFROLOGIA
, cilt.32, sa.5, ss.674-676, 2012 (SCI-Expanded, Scopus)
2011
2011176. OUTCOME OF NEPHROPATHIC CYSTINOSIS IN PEDIATRIC RENAL TRANSPLANTATION: A SINGLE CENTRE EXPERIENCE
TOPALOĞLU R., BİLGİNER Y., ÖZALTIN F., DÜZOVA A., Aki T., ÖZEN S., et al.
PEDIATRIC TRANSPLANTATION
, cilt.15, ss.82, 2011 (SCI-Expanded, Scopus)
2011
2011177. Disruption of PTPRO Causes Childhood-Onset Nephrotic Syndrome
ÖZALTIN F., Ibsirlioglu T., Taskiran E. Z., Baydar D. E., Kaymaz F., Buyukcelik M., et al.
AMERICAN JOURNAL OF HUMAN GENETICS
, cilt.89, sa.1, ss.139-147, 2011 (SCI-Expanded, Scopus)
2011
2011178. MYO1E Mutations and Childhood Familial Focal Segmental Glomerulosclerosis
Mele C., Iatropoulos P., Donadelli R., Calabria A., Maranta R., Cassis P., et al.
NEW ENGLAND JOURNAL OF MEDICINE
, cilt.365, sa.4, ss.295-306, 2011 (SCI-Expanded, Scopus)
2011
2011179. Respiratory-chain deficiency presenting as diffuse mesangial sclerosis with NPHS3 mutation
Baskin E., Bayrakci U. S., Alehan F., Ozdemir H., Oner A., Horvath R., et al.
PEDIATRIC NEPHROLOGY
, cilt.26, sa.7, ss.1157-1161, 2011 (SCI-Expanded, Scopus)
2011
2011180. COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness
Heeringa S. F., Chernin G., Chaki M., Zhou W., Sloan A. J., Ji Z., et al.
JOURNAL OF CLINICAL INVESTIGATION
, cilt.121, sa.5, ss.2013-2024, 2011 (SCI-Expanded, Scopus)
2011
2011181. Follow-Up of Patients With Juvenile Nephronophthisis After Renal Transplantation: A Single Center Experience
Tayfur A. C., Besbas N., BİLGİNER Y., ÖZALTIN F., DÜZOVA A., Bakkaloglu M., et al.
TRANSPLANTATION PROCEEDINGS
, cilt.43, sa.3, ss.847-849, 2011 (SCI-Expanded, Scopus)
2011
2011182. Macrophage Activating Syndrome complicating Wegener Granulomatosis: treatment with plasma exchange
Eroglu F. K., GÜLHAN B., ÜNAL S., ÖZALTIN F., ORHAN D., ÖZEN S.
CLINICAL AND EXPERIMENTAL RHEUMATOLOGY
, cilt.29, sa.2, ss.463, 2011 (SCI-Expanded, Scopus)
2011
2011183. Three cases of a rare disease, congenital chloride diarrhea, summons up the variation in the clinical course and significance of early diagnosis and adequate treatment in the prevention of intellectual disability
Gurakan F., Baysoy G., Wedenoja S., Uslu N., ÖZEN H., ÖZALTIN F., et al.
TURKISH JOURNAL OF PEDIATRICS
, cilt.53, sa.2, ss.194-198, 2011 (SCI-Expanded, Scopus)
2011
2011184. Spondyloenchondrodysplasia with Systemic Lupus Erythematosus: a report of three cases
BİLGİNER Y., ALANAY Y., DÜZOVA A., TOPALOĞLU R., Superti-Furga A., ÖZEN S., et al.
CLINICAL AND EXPERIMENTAL RHEUMATOLOGY
, cilt.29, sa.2, ss.430, 2011 (SCI-Expanded, Scopus)
2010
2010185. The bone and mineral disorder of children undergoing chronic peritoneal dialysis
Borzych D., Rees L., Ha I. S., Chua A., Valles P. G., Lipka M., et al.
KIDNEY INTERNATIONAL
, cilt.78, sa.12, ss.1295-1304, 2010 (SCI-Expanded, Scopus)
2010
2010186. Neuroendocrine immune system in familial Mediterranean fever
TOPALOĞLU R., BİLGİNER Y., ALİKAŞİFOĞLU A., ÖZALTIN F., BEŞBAŞ N., ÖZEN S., et al.
TURKISH JOURNAL OF PEDIATRICS
, cilt.52, sa.6, ss.588-593, 2010 (SCI-Expanded, Scopus)
2010
2010187. Genotype/Phenotype Correlation in Nephrotic Syndrome Caused by WT1 Mutations
Chernin G., Vega-Warner V., Schoeb D. S., Heeringa S. F., Ovunc B., Saisawat P., et al.
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
, cilt.5, sa.9, ss.1655-1662, 2010 (SCI-Expanded, Scopus)
2010
2010188. New syndrome - Situs inversus totalis with cystic dysplasia of kidneys, pancreas and bowing
Balci S., ÖZALTIN F., Bostanoglu S.
CLINICAL DYSMORPHOLOGY
, cilt.19, sa.3, ss.173-174, 2010 (SCI-Expanded, Scopus)
2010
2010189. Risk factors in community-acquired urinary tract infections caused by ESBL-producing bacteria in children
TOPALOĞLU R., Er I., Dogan B. G., BİLGİNER Y., ÖZALTIN F., Besbas N., et al.
PEDIATRIC NEPHROLOGY
, cilt.25, sa.5, ss.919-925, 2010 (SCI-Expanded, Scopus)
2010
2010190. Clinical course of primary focal segmental glomerulosclerosis (FSGS) in Turkish children: a report from the Turkish Pediatric Nephrology FSGS Study Group
BEŞBAŞ N., ÖZALTIN F., Emre S., Anarat A., ALPAY H., BAKKALOĞLU A., et al.
TURKISH JOURNAL OF PEDIATRICS
, cilt.52, sa.3, ss.255-261, 2010 (SCI-Expanded, Scopus)
2010
2010191. A Case Report of Thrombocytopenia-associated Multiple Organ Failure Secondary to Salmonella enterica Serotype Typhi Infection in a Pediatric Patient: Successful Treatment With Plasma Exchange
Yildirim I., CEYHAN M., BAYRAKCİ B., Uysal M., Kuskonmaz B. B., ÖZALTIN F.
THERAPEUTIC APHERESIS AND DIALYSIS
, cilt.14, sa.2, ss.226-229, 2010 (SCI-Expanded, Scopus)
2010
2010192. Toll-like receptors 2 and 4 cell surface expression reflects endotoxin tolerance in Henoch-Schönlein purpura.
CANPINAR H., ÖZALTıN F., BILGINER Y., BAKKALOĞLU A., Ozen S.
The Turkish journal of pediatrics
, cilt.52, ss.22-7, 2010 (SCI-Expanded, Scopus)
2009
2009193. A novel CLCN7 mutation resulting in a most severe form of autosomal recessive osteopetrosis
BEŞBAŞ N., Draaken M., Ludwig M., DEREN Ö., ORHAN D., BİLGİNER Y., et al.
EUROPEAN JOURNAL OF PEDIATRICS
, cilt.168, sa.12, ss.1449-1454, 2009 (SCI-Expanded, Scopus)
2009
2009194. Treatment of severe Henoch-Schonlein nephritis: justifying more immunosuppression
Altugan F. S., ÖZEN S., Aktay-Ayaz N., Gucer S., TOPALOĞLU R., DÜZOVA A., et al.
TURKISH JOURNAL OF PEDIATRICS
, cilt.51, sa.6, ss.551-555, 2009 (SCI-Expanded, Scopus)
2008
2008195. Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome
Heeringa S. F., Vlangos C. N., Chernin G., Hinkes B., Gbadegesin R., Liu J., et al.
NEPHROLOGY DIALYSIS TRANSPLANTATION
, cilt.23, sa.11, ss.3527-3533, 2008 (SCI-Expanded, Scopus)
2008
2008196. Evaluation of intima media thickness of the common and internal carotid arteries with inflammatory markers in familial Mediterranean fever as possible predictors for atherosclerosis
BİLGİNER Y., ÖZALTIN F., Basaran C., DÜZOVA A., Besbas N., TOPALOĞLU R., et al.
RHEUMATOLOGY INTERNATIONAL
, cilt.28, sa.12, ss.1211-1216, 2008 (SCI-Expanded, Scopus)
2008
2008197. Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS)
Gbadegesin R., Hinkes B. G., Hoskins B. E., Vlangos C. N., Heeringa S. F., Liu J., et al.
NEPHROLOGY DIALYSIS TRANSPLANTATION
, cilt.23, sa.4, ss.1291-1297, 2008 (SCI-Expanded, Scopus)
2008
2008198. Right atrial thrombosis complicating renal transplantation in a child
BİLGİNER Y., ÖZALTIN F., DÜZOVA A., Erdogan I., AKI F. T., DEMİRCİN M., et al.
PEDIATRIC TRANSPLANTATION
, cilt.12, sa.2, ss.251-255, 2008 (SCI-Expanded, Scopus)
2008
2008199. Eye involvement in children with primary focal segmental glomerulosclerosis
ÖZALTIN F., Heeringa S., Poyraz C. E., BİLGİNER Y., KADAYIFÇILAR S., BEŞBAŞ N., et al.
PEDIATRIC NEPHROLOGY
, cilt.23, sa.3, ss.421-427, 2008 (SCI-Expanded, Scopus)
2008
2008200. Specific podocin mutations correlate with age of onset in steroid-resistant nephrotic syndrome
Hinkes B., Vlangos C., Heeringa S., Mucha B., Gbadegesin R., Liu J., et al.
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
, cilt.19, sa.2, ss.365-371, 2008 (SCI-Expanded, Scopus)
2008
2008201. Triple immunosuppression with tacrolimus in pediatric renal transplantation: Single-center experience
DÜZOVA A., AKI F. T., Bakkaloglu A., Besbas N., TOPALOĞLU R., ÖZEN S., et al.
TRANSPLANTATION PROCEEDINGS
, cilt.40, sa.1, ss.132-134, 2008 (SCI-Expanded, Scopus)
2007
2007202. Carotid intima-media thickness in children and young adults with renal transplant: Internal carotid artery vs. common carotid artery
Bilginer Y., Ozaltin F., Basaran C., Aki T. F., Karabulut E., Duzova A., et al.
PEDIATRIC TRANSPLANTATION
, cilt.11, sa.8, ss.888-894, 2007 (SCI-Expanded, Scopus)
2007
2007203. Cerebral sinovenous thrombosis in a child with steroid sensitive nephrotic syndrome
Isik Balci Y., Tavil B., Fidan G., Ozaltin F.
EUROPEAN JOURNAL OF PEDIATRICS
, cilt.166, sa.7, ss.757-758, 2007 (SCI-Expanded, Scopus)
2007
2007204. Nephrotic syndrome in the first year of life: Two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2)
Hinkes B. G., Mucha B., Vlangos C. N., Gbadegesin R., Liu J., Hasselbachera K., et al.
PEDIATRICS
, cilt.119, sa.4, 2007 (SCI-Expanded, Scopus)
2007
2007205. Childhood vasculitides in Turkey: a nationwide survey
Ozen S., Bakkaloglu A., Dusunsel R., Soylemezoglu O., Ozaltin F., Poyrazoglu H., et al.
CLINICAL RHEUMATOLOGY
, cilt.26, sa.2, ss.196-200, 2007 (SCI-Expanded, Scopus)
2006
2006206. Novel OCRL1 mutations in patients with the phenotype of dent disease
Utsch B., Boekenkamp A., Benz M. R., Besbas N., Doetsch J., Franke I., et al.
AMERICAN JOURNAL OF KIDNEY DISEASES
, cilt.48, sa.6, ss.942-954, 2006 (SCI-Expanded, Scopus)
2006
2006207. Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible
Hinkes B., Wiggins R. C., Gbadegesin R., Vlangos C. N., Seelow D., Nuernberg G., et al.
NATURE GENETICS
, cilt.38, sa.12, ss.1397-1405, 2006 (SCI-Expanded, Scopus)
2006
2006208. Cyclosporine drug monitoring with C0 and C2 concentrations in children with stable renal allograft function
Kalyoncu M., Topaloglu R., Bayrakci U., Bakkaloglu A., Besbas N., Ozaltin F., et al.
PEDIATRIC TRANSPLANTATION
, cilt.10, sa.2, ss.168-171, 2006 (SCI-Expanded, Scopus)
2006
2006209. Mutations in the Wilms' tumor 1 gene cause isolated steroid resistant nephrotic syndrome and occur in exons 8 and 9
Mucha B., Ozaltin F., Hinkes B., Hasselbacher K., Ruf R., Schultheiss M., et al.
PEDIATRIC RESEARCH
, cilt.59, sa.2, ss.325-331, 2006 (SCI-Expanded, Scopus)
2005
2005210. Apoptosis and proliferation in childhood acute proliferative glomerulonephritis
Ozaltin F., Besbas N., Bakkaloglu A., Gucer S., Topaloglu R., Ozen S., et al.
PEDIATRIC NEPHROLOGY
, cilt.20, sa.11, ss.1572-1577, 2005 (SCI-Expanded, Scopus)
2005
2005211. CLCN5 mutation (R347X) associated with hypokalaemic metabolic alkalosis in a Turkish child: an unusual presentation of Dent's disease
Besbas N., Ozaltin F., Jeck N., Seyberth H., Ludwig M.
NEPHROLOGY DIALYSIS TRANSPLANTATION
, cilt.20, sa.7, ss.1476-1479, 2005 (SCI-Expanded, Scopus)
2005
2005212. E148Q is a disease-causing MEFV mutation: a phenotypic evaluation in patients with familial Mediterranean fever
Topaloglu R., Ozaltin F., Yilmaz E., Ozen S., Balci B., Besbas N., et al.
ANNALS OF THE RHEUMATIC DISEASES
, cilt.64, sa.5, ss.750-752, 2005 (SCI-Expanded, Scopus)
2005
2005213. Familial Mediterranean fever (FMF) in Turkey - Results of a nationwide multicenter study
Tunca M., Akar S., Onen F., Ozdogan H., KASAPÇOPUR Ö., Yalcinkaya F., et al.
MEDICINE
, cilt.84, sa.1, ss.1-11, 2005 (SCI-Expanded, Scopus)
2004
2004214. The significance of IgA class of antineutrophil cytoplasmic antibodies (ANCA) in childhood Henoch-Schonlein purpura
Ozaltin F., Bakkaloglu A., Ozen S., Topaloglu R., Kavak U., Kalyoncu M., et al.
CLINICAL RHEUMATOLOGY
, cilt.23, sa.5, ss.426-429, 2004 (SCI-Expanded, Scopus)
2004
2004215. Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome
Ruf R., Schultheiss M., Lichtenberger A., Karle S., Zalewski I., Mucha B., et al.
KIDNEY INTERNATIONAL
, cilt.66, sa.2, ss.564-570, 2004 (SCI-Expanded, Scopus)
2004
2004216. An unusual cause of acute renal failure: renal lymphoma
Ozaltin F., Yalcin B., Orhan D., Sari N., Caglar M., Besbas N., et al.
PEDIATRIC NEPHROLOGY
, cilt.19, sa.8, ss.912-914, 2004 (SCI-Expanded, Scopus)
2004
2004217. Monocyte chemoattractant protein-1 and interleukin-8 levels in children with acute poststreptococcal glomerulonephritis
Besbas N., Ozaltin F., Catal F., Ozen S., Topaloglu R., Bakkaloglu A.
PEDIATRIC NEPHROLOGY
, cilt.19, sa.8, ss.864-868, 2004 (SCI-Expanded, Scopus)
2004
2004218. Bone mineral density in children with familial Mediterranean fever
Duzova A., Ozaltin F., Ozon A., Besbas N., Topaloglu R., Ozen S., et al.
CLINICAL RHEUMATOLOGY
, cilt.23, sa.3, ss.230-234, 2004 (SCI-Expanded, Scopus)
2004
2004219. Influence of Serum Amyloid A (SAA1) and SAA2 gene polymorphisms on renal amyloidosis, and on SAA/C-reactive protein values in patients with familial mediterranean fever in the Turkish population.
Bakkaloglu A., Duzova A., Ozen S., Balci B., Besbas N., Topaloglu R., et al.
The Journal of rheumatology
, cilt.31, sa.6, ss.1139-42, 2004 (SCI-Expanded, Scopus)
2004
2004220. Helicobacter pylori infection in Turkish children with familial Mediterranean fever: is it a cause of persistent inflammation?
Ozaltin F., Bakkaloglu A., Saltik İ. N., Demir H., Duzova A., Bulun A., et al.
CLINICAL RHEUMATOLOGY
, cilt.23, sa.2, ss.186-187, 2004 (SCI-Expanded, Scopus)
2004
2004221. Decreased prevalence of atopy in paediatric patients with familial Mediterranean fever.
Sackesen C., Bakkaloglu A., Sekerel B. E., Ozaltin F., Besbas N., Yilmaz E., et al.
Annals of the rheumatic diseases
, cilt.63, ss.187-90, 2004 (SCI-Expanded, Scopus)
2003
2003222. Relationship of leptin and insulin-like growth factor I to nutritional status in hemodialyzed children
Besbas N., Ozaltin F., Coskun T., Ozalp S., Saatci U., Bakkaloglu A., et al.
PEDIATRIC NEPHROLOGY
, cilt.18, sa.12, ss.1255-1259, 2003 (SCI-Expanded, Scopus)
2003
2003223. The role of apoptosis in childhood Henoch-Schonlein purpura
Ozaltin F., Besbas N., Uckan D., Tuncer M., Topaloglu R., Ozen S., et al.
CLINICAL RHEUMATOLOGY
, cilt.22, ss.265-267, 2003 (SCI-Expanded, Scopus)
2003
2003224. Role of A-SAA in monitoring subclinical inflammation and in colchicine dosage in familial Mediterranean fever
Duzova A., Bakkaloglu A., Besbas N., Topaloglu R., Ozen S., Ozaltin F., et al.
CLINICAL AND EXPERIMENTAL RHEUMATOLOGY
, cilt.21, sa.4, ss.509-514, 2003 (SCI-Expanded, Scopus)
2003
2003225. Successful renal transplantation in a child with ANCA-associated microscopic polyangiitis
Besbas N., Ozaltin F., Tinaztepe K., Gucer S., Ozen S., Bakkaloglu M., et al.
PEDIATRIC NEPHROLOGY
, cilt.18, sa.7, ss.696-699, 2003 (SCI-Expanded, Scopus)
2002
2002226. Behcet's disease with severe arterial involvement in a child
Besbas N., Ozyurek E., Balkanci F., Ozen S., Saatci I., Ozaltin F., et al.
CLINICAL RHEUMATOLOGY
, cilt.21, sa.2, ss.176-179, 2002 (SCI-Expanded, Scopus)
2001
2001227. Bilateral uveitis in a 7-year-old patient with familial Mediterranean fever. An extremely rare complication
ÖZALTIN F., Bakkaloglu A., Orhon M., DÜZOVA A., Irkec M.
CLINICAL AND EXPERIMENTAL RHEUMATOLOGY
, sa.5, 2001 (SCI-Expanded, Scopus)
2001
2001228. Pulmonary haemorrhage in a 6-year-old boy with Henoch-Schonlein purpura
Besbas N., Duzova A., Topaloglu R., Gok F., Ozaltin F., Ozen S., et al.
CLINICAL RHEUMATOLOGY
, cilt.20, sa.4, ss.293-296, 2001 (SCI-Expanded, Scopus)
2000
2000229. Acute parvovirus B19 infection mimicking juvenile myelomonocytic leukemia
Yetgin S., Cetin M., Yenicesu I., Ozaltin F., Uckan D.
EUROPEAN JOURNAL OF HAEMATOLOGY
, cilt.65, sa.4, ss.276-278, 2000 (SCI-Expanded, Scopus)
2000
2000230. Acute parvovirus infection mimicking juvenile myelomonocytic leukemia
Yetgin S., Cetin M., Yenicesu Y., Ozaltin F., Uckan D.
LEUKEMIA
, cilt.14, sa.5, ss.966, 2000 (SCI-Expanded, Scopus)
2000
2000231. Three sibs diagnosed prenatally with situs inversus totalis, renal and pancreatic dysplasia, and cysts
Balci S., Bostanoglu S., Altinok G., Ozaltin F.
AMERICAN JOURNAL OF MEDICAL GENETICS
, cilt.90, sa.3, ss.185-187, 2000 (SCI-Expanded)
1998
1998232. Serum IgD concentrations in patients with ataxia telangiectasia and with selective IgA deficiency
SANAL O., Ozaltin F., TEZCAN İ., ERSOY F.
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY
, cilt.116, sa.3, ss.246, 1998 (SCI-Expanded, Scopus)
Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler
2022
20221. CLINICAL COURSE OF ADOLESCENT ONSET ATYPICAL HEMOLYTIC UREMIC SYNDROME: A STUDY OF TURKISH AHUS REGISTRY
ÇELEĞEN K., GÜLHAN B., FİDAN H. K., YÜKSEL S., YILMAZ N., ÇALTIK YILMAZ A., et al.
54th Congress of European Society of Pediatric Nephrology, 22 Kasım 2022, cilt.37, ss.2813, (Tam Metin Bildiri)
2022
20222. ACUTE KIDNEY INJURY ASSOCIATED WITH COVID-19 AND MULTISYSTEM INFLAMMATORY SYNDROME IN CHILDREN (MIS-C)
TAŞTEMEL ÖZTÜRK T., DÜZOVA A., oygar p., BALTU D., ÖZÇİLİNGİR P., LAÇİNEL GÜRLEVİK S., et al.
54th Congress of European Society of Pediatric Nephrology, 22 Haziran 2022, cilt.37, ss.2804, (Tam Metin Bildiri)
2021
20213. EFFECTS OF RAAS INHIBITION AND IMMUNOSUPPRESSIVE THERAPY IN PEDIATRIC PATIENTS WITH X-LINKED ALPORT SYNDROME
ÖZDEMİR E. G., GÜLHAN B., KURT ŞÜKÜR E. D., ATAYAR E., DURSUN İ., ÖZÇAKAR Z. B., et al.
53rd European society of pediatric nephrology congress 2021, Amsterdam, Hollanda, 16 - 19 Eylül 2021, cilt.36, ss.3366, (Özet Bildiri)
2021
20214. CLINICAL CHARACTERISTICS AND OUTCOME OF BK VIRUS INFECTION IN PEDIATRIC RENAL TRANSPLANT RECIPIENTS
KURT ŞÜKÜR E. D., ÖZDEMİR E. G., TAŞTEMEL ÖZTÜRK T., BALTU D., GÜLHAN B., ÖZALTIN F., et al.
53rd European society of pediatric nephrology congress 2021, Amsterdam, Hollanda, 16 Eylül 2021 - 16 Eylül 2022, (Özet Bildiri)
2020
20205. Lizinürik Protein İntoleransının Nadir Renal Tutulumu: Membranoproliferatif Glomerülonefrit
BALTU D., ÖZDEMİR E. G., GÜLHAN B., TAŞTEMEL ÖZTÜRK T., KURT ŞÜKÜR E. D., SİVRİ H. S., et al.
5. ÇOCUK NEFROLOJİ E-OLGU PANAYIRI, Online, Türkiye, 4 - 05 Aralık 2020, ss.34, (Tam Metin Bildiri)
2020
20206. ANALYSIS OF LATE RENAL COMPLICATIONS AND RISK FACTORS IN CHILDREN WITH HEMATOPOIETIC STEM CELL TRANSPLANTATION
Gurbanov A., GÜLHAN B., KUŞKONMAZ B. B., OKUR F. V., Cetinkaya D. U., Ozdemir G., et al.
57th ERA-EDTA Congress, ELECTR NETWORK, 6 - 09 Haziran 2020, cilt.35, ss.2140, (Özet Bildiri)
2020
20207. EARLY URINARY SYSTEM COMPLICATIONS IN CHILDREN WITH HEMATOPOIETIC STEM CELL TRANSPLANTATION
Gurbanov A., GÜLHAN B., KUŞKONMAZ B. B., OKUR F. V., Cetinkaya D. U., Ozdemir G., et al.
57th ERA-EDTA Congress, ELECTR NETWORK, 6 - 09 Haziran 2020, cilt.35, ss.2123, (Özet Bildiri)
2020
20208. CLINICAL CHARACTERISTICS OF PATIENTS WITH GENETICALLY CONFIRMED ALPORT SYNDROME
Ozdemir G., GÜLHAN B., Atayar E., Canpolat N., SÖYLEMEZOĞLU O., ÖZÇAKAR Z. B., et al.
57th ERA-EDTA Congress, ELECTR NETWORK, 6 - 09 Haziran 2020, cilt.35, ss.359, (Özet Bildiri)
2019
20199. Hematopoetik Kök Hücre Nakli Yapılan Çocuk Hastalarda Erken Dönem Üriner Sistem Komplikasyonları
Gurbanov A., GÜLHAN B., KUŞKONMAZ B. B., OKUR F. V., Uçkan Çetinkaya D., Özdemir G., et al.
10. Çocuk Nefrolojisi Kongresi, Türkiye, 1 - 04 Mayıs 2019, (Özet Bildiri)
2019
201910. Hematopoetik Kök Hücre Nakli Yapılan Çocuk Hastalarda Geç Dönem Renal Komplikasyonların Ve RiskFaktörlerinin Analizi
Gurbanov A., GÜLHAN B., KUŞKONMAZ B. B., OKUR F. V., Uçkan Çetinkaya D., Özdemir G., et al.
10. Çocuk Nefrolojisi Kongresi, Türkiye, 1 - 04 Mayıs 2019, (Özet Bildiri)
2019
201911. Çocukluk Çağı Preemptif Ve Preemptif Olmayan Böbrek Nakli Hastalarında Nakil Sonrası İlk Bir Yıldaki GreftFonksiyonlarının Değerlendirilmesi
TAŞ N., AKI F. T., GÜLHAN B., ÖZALTIN F., DÜZOVA A., TEKGÜL S., et al.
10. Çocuk Nefrolojisi Kongresi, Türkiye, 1 - 04 Mayıs 2019, (Özet Bildiri)
2018
201812. A REFRACTORY CLINICAL CASE OF LUPUS NEPHRITHIS WHO UNDERWENT BONE MARROW TRANSPLANTATION,
TAŞ N., DEMİR S., ÇAĞDAŞ AYVAZ D. N., ÖZALTIN F., KUŞKONMAZ B. B., TEZCAN F. İ., et al.
European Society for Paediatric Nephrology, 51th Annual Meeting, 3 - 06 Ekim 2018, (Özet Bildiri)
2018
201813. Clinical and Mutational Spectrum of Children with Autosomal Recessive and Autosomal Dominant Polycystic Kidney Disease
TÜRKOĞLU Ö., GÜLHAN B., YÜKSEL S., ÇALIŞKAN S., DÜZOVA A., ÇAKAR N., et al.
51st Annual Scientific Meeting of the European Society for the Paediatric Nephrology, 3 - 06 Ekim 2018, (Tam Metin Bildiri)
2018
201814. ACUTE HEMODIALYSIS EXPERIENCE IN CHILDRENWEIGHING LESS THAN 15 KG
TAŞ N., GÜLHAN B., çelegen k., ÖZDEMİR E. G., DÜZOVA A., ÖZALTIN F., et al.
51st Annual Scientific Meeting of the European Society for the Paediatric Nephrology, 3 - 06 Ekim 2018, (Tam Metin Bildiri)
2018
201815. CLINICAL AND PATHOLOGIC CHARACTERISTICS OF GENETICALLY CONFIRMED ALPORT SYNDROME PATIENTS
TOPALOĞLU R., ÖZDEMİR E. G., GÜLHAN B., ATAYAR E., DÜZOVA A., SOYLU A., et al.
51st Annual Scientific Meeting of the European Society for the Paediatric Nephrology, 3 - 06 Ekim 2018, (Tam Metin Bildiri)
2018
201816. TURKISH ATYPICAL HEMOLYTIC UREMIC SYNDROME REGISTRY: ECULIZUMAB TREATMENT IN AHUS PATIENTS
BASKIN S. E., CANPOLAT N., GÜLLEROĞLU K. S., YILMAZ A., MELEK E., YÜKSEL S., et al.
51st Annual Scientific Meeting of the European Society for the Paediatric Nephrology, 3 - 06 Ekim 2018, (Tam Metin Bildiri)
2018
201817. MYCETOMA OF THE URINARY TRACT IN AN INFANTWITH HORSESHOE KIDNEY: USEFULNESS OFMECHANICAL REMOVAL AND AMPHOTERICIN-BIRRIGATION
OĞUZ B., ÇELEGEN K., ÇİFTÇİ A. Ö., ÜNAL E., ŞENOCAK M. E., ÖZKALE YAVUZ Ö., et al.
51st Annual Scientific Meeting of the European Society for the Paediatric Nephrology, 3 - 06 Ekim 2018, (Özet Bildiri)
2018
201818. Lupus nephritis: Long term follow-up and effect of treatment on growth
TOPALOĞLU R., TAŞ N., çelegen k., ÖZDEMİR E. G., GÜLHAN B., DÜZOVA A., et al.
51st Annual Scientific Meeting of the European Society for the Paediatric Nephrology, 3 - 06 Ekim 2018, (Özet Bildiri)
2018
201819. Long-term follow-up results of patients with ADCK4 mutations who have been diagnosed in asymptomatic period: effects of early initiation of CoQ10 supplementation
ATMACA M., GÜLHAN B., KARABAY BAYAZIT A., CANDAN C., ARICI M., TOPALOĞLU R., et al.
51st Annual Scientific Meeting of the European Society for the Paediatric Nephrology, 3 - 06 Ekim 2018, (Tam Metin Bildiri)
2018
201820. Effect of IGF¬1 and HGF Induced Bone Marrow Mesenchymal Stem Cells on Focal Segmental Glomerulosclerosis in Sprague¬Dawley Rats: A pilot study
Sahan Ö. B., Korkmaz E., Onbaşılar İ., Güçer K. Ş., Kaymaz F. F., Özaltın F., et al.
43rd Febs Congress, Praha, Çek Cumhuriyeti, 7 - 12 Temmuz 2018, (Özet Bildiri)
2018
201821. PEPTIDE BIOMARKER SIGNATURES IN STEROID-RESISTANT NEPHROTIC SYNDROME
Zurbig P., ÖZALTIN F., Anarat A., Paripovic D., Yilmaz A., Caliskan S., et al.
55th Congress of the European-Renal-Association (ERA) and European-Dialysis-and-Transplantation-Association (EDTA), Copenhagen, Danimarka, 24 - 27 Mayıs 2018, cilt.33, (Özet Bildiri)
2018
201822. Naif ve İnduklenmis Mezenkimal Kök Hücrelerin Fokal Segmental Glomeruloskleroz Üzerine Etkisinin Sprague-Dawley Modelinde İncelenmesi
Sahan Ö. B., Korkmaz E., ONBAŞILAR İ., GÜÇER K. Ş., KAYMAZ F. F., ÖZALTIN F., et al.
4. Klinik Immunoloji Kongresi, Antalya, Türkiye, 11 - 14 Nisan 2018, (Özet Bildiri)
2017
201723. Çocuk ve genç erişkinlerde renovasküler hipertansiyonda cerrahi tedaviler.
PEKER R. O., AKI F. T., KUMBASAR U., GÜVENER M., YILMAZ M., ÖZALTIN F., et al.
18. Ulusal Vasküler ve Endovasküler Cerrahi Kongresi 9. Ulusal Fleboloji Kongresi, Girne, Kıbrıs (Kktc), 9 - 12 Aralık 2017, (Özet Bildiri)
2017
201724. 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
2017
201725. 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
2017
201726. USE OF HERBAL AND DIETARY SUPPLEMENTS IN CHILDREN WITH KIDNEY AND URINARY TRACT DISEASE
Öztürk T. T., ÖZMERT E. N., KANBUR N., GÜLHAN B., ÖZALTIN F., TOPALOĞLU R., et al.
PEDIATRIC NEPHROLOGY, 6 - 09 Eylül 2017, cilt.32, ss.1675, (Özet Bildiri)
2017
201727. Use of herbal and dietary supplements in children with kidney and urinary tract disease
Taştemel Öztürk T., KANBUR N., ÖZMERT E. N., GÜLHAN B., ÖZALTIN F., TOPALOĞLU R., et al.
50th Anniversary Meeting of the ESPN, 6 - 09 Eylül 2017, cilt.32, ss.1675, (Özet Bildiri)
2017
201728. Risk factors for cardiovascular comorbidities in children with steroid-sensitiveand steroid-resistant nephrotic syndrome.
Kara Eroğlu F., TOPALOĞLU R., KARAGÖZ T., OĞUZ B., ÖZALTIN F., GÜLHAN B., et al.
50th Anniversary Meeting of the ESPN, 6 - 09 Eylül 2017, cilt.32, ss.1661, (Özet Bildiri)
2017
201729. Genetic and clinical characteristics of patients with C3 glomerulopathy.
TOPALOĞLU R., GÜLHAN B., KORKMAZ E., DÜZOVA A., ÖZALTIN F.
50th Anniversary Meeting of the European Society for Paediatric Nephrology, 6 - 09 Eylül 2017, (Özet Bildiri)
2017
201730. GENETIC AND CLINICAL CHARACTERISTICS OFPATIENTS WITH C3 GLOMERULOPATHY
TOPALOĞLU R., GÜLHAN B., korkmaz e., DÜZOVA A., ÖZALTIN F., SOYLU A., et al.
The 50th Anniversary Meeting of the European Society for Pediatric Nephrology, 6 - 09 Eylül 2017, (Özet Bildiri)
2017
201731. Does C.3979 G A/P.VAL1327MET variant of COL4A4 has any pathogenic effect in Turkish patients with Alport Syndrome ?
YILDIZ N., ATA P., ALPAY H., GÖKCE İ., ÖZALTIN F.
48th Anniversary Meeting of the European Society for Paediatric Nephrology, 6 - 09 Eylül 2017, (Özet Bildiri)
2017
201732. OC-7 Cresentic glomerulonephritis (CGN) in childhood classification of aetiology and clinicopathological importance of cd163 positive (M2) macrophages
KAYKI G., ORHAN D., ÖZALTIN F., TALİM B., DÜZOVA A., AKÇAÖREN z., et al.
Oral Communications, 7 - 10 Haziran 2017, (Tam Metin Bildiri)
2016
201633. Tocilizumab Treatment in childhood takayasu arteritis case series of four patients and systematic review of the literature
BATU E. D., SÖNMEZ H. E., HAZIROLAN T., ÖZALTIN F., BİLGİNER Y., ÖZEN S.
PRES 2016 Genova, 28 Eylül - 01 Ekim 2016, (Özet Bildiri)
2016
201634. NEXT GENERATION GENE PANEL SCREENING IN STEROID-RESISTANT NEPHROTIC SYNDROME
Lipska-Zietkiewicz B. S., Boyer O., Gribouval O., Tabatabaei M., Fourrage C., Nischke P., et al.
53rd ERA-EDTA Congress, Vienna, Avusturya, 21 - 24 Mayıs 2016, cilt.31, ss.353, (Özet Bildiri)
2016
201635. SMARCAL1 SCREENING IN NEPHROTIC SYNDROME - LESSONS FROM PODONET
Lipska-Zietkiewicz B. S., Gellermann J., Boyer O., Shalaby M. A., ÖZALTIN F., Dusek J., et al.
53rd ERA-EDTA Congress, Vienna, Avusturya, 21 - 24 Mayıs 2016, cilt.31, ss.353-354, (Özet Bildiri)
2015
201536. NORMAL 25-HYDROXYVITAMIN D LEVELS ARE ASSOCIATED WITH LESS PROTEINURIA AND ATTENUATE RENAL FAILURE PROGRESSION IN CHILDREN WITH CHRONIC KIDNEY DISEASE
Shroff R., Trivelli A., Litwin M., Picca S., Anarat A., Sallay P., et al.
52nd Congress of the European-Renal-Association-European-Dialysis-and-Transplant-Assocation, London, Kanada, 28 - 31 Mayıs 2015, cilt.30, (Özet Bildiri)
2015
201537. YENİDOĞAN DÖNEMİNDE EPİDERMOLİZİS BÜLLOSA, PİLOR ATREZİSİ VE APLASİA KUTİS: BİR VAKA TAKDİMİ
KAYKI G., BOZKAYA D., ÖZALTIN F., ORHAN D., AYGÜN D., KAYMAZ F., et al.
23. ULUSAL NEONATOLOJİ KONGRESİ, Antalya, Türkiye, 19 - 22 Nisan 2015, (Özet Bildiri)
2013
201338. CONVERSION TO SIROLIMUS IN PEDIATRIC RENAL TRANSPLANT RECIPIENTS
TOPALOĞLU R., GÜLHAN B., BİLGİNER Y., Tayfur A. C., Yildiz C., ÖZALTIN F., et al.
50th European-Renal-Association - European-Dialysis-and-Transplant-Association Congress, İstanbul, Türkiye, 18 - 21 Mayıs 2013, cilt.28, ss.294, (Özet Bildiri)
2007
200739. Eye involvement in children with primary FSGS
BİLGİNER Y., Poyraz C. E., ÖZALTIN F., KADAYIFÇILAR S., BEŞBAŞ N., Topaloglu R., et al.
44th ERA-EDTA Congress, Barcelona, İspanya, 22 - 24 Haziran 2007, cilt.22, ss.292, (Özet Bildiri)
2006
200640. Influence of monocyte chemoattractant protein-1-2518A > G polymorphism on childhood focal segmental glomerulosclerosis
Kalyoncu M., Besbas N., Ozgul K., Ozaltin F., Duzova A., Topaloglu R., et al.
43rd ERA-EDTA Congress, Glasgow, Birleşik Krallık, 15 - 18 Temmuz 2006, cilt.21, ss.328, (Özet Bildiri)
2005
200541. Familial Mediterranean Fever and sacroiliac joint involvement. A review of eight cases
Besbas N., Bilginer Y., Duzova A., Ozaltin F., Bayrakci U., Ozen S., et al.
Annual European Congress of Rheumatology, Vienna, Avusturya, 8 - 11 Haziran 2005, cilt.64, ss.509, (Özet Bildiri)
2004
200442. T-Cell response against heat shock peptides and streptococci in pediatric Henoch Schonlein purpura and polyarteritis nodosa.
Bilginer Y., Guc D., Dogan L., Bakkaloglu A., Besbas N., Ozaltin F., et al.
68th Annual Scientific Meeting of the American-College-of-Rheumatology, San-Antonio, Kuzey Mariana Adaları, 16 - 21 Ekim 2004, cilt.50, ss.4093, (Özet Bildiri)
2004
200443. Cellular response against streptococci in paediatric Henoch Schonlein purpura and polyarteritis nodosa
Guc D., Dogan A., Bakkaloglu A., Ozaltin F., Besbas N., Prakken B., et al.
Annual European Congress of Rheumatology (EULAR 2004), Berlin, Almanya, 9 - 12 Haziran 2004, cilt.63, ss.382, (Özet Bildiri)
2004
200444. MICA exon 5 microsatellite alleles in Turkish patients with FMF
Yigitbas E., ÜNER A., Dorak M., Ding W., Tatayoglu G., Balci B., et al.
30th Annual Meeting of the American-Society-for-Histocompatibility-and-Immunogenetics, San-Antonio, Kuzey Mariana Adaları, 2 - 06 Ekim 2004, cilt.65, (Özet Bildiri)
Kitaplar
2022
20221. Primer Podositopatiler
KURT ŞÜKÜR E. D., ÖZALTIN F.
Genetik böbrek hastalıkları, , Editör, Güneş Tıp Kitabevleri, İstanbul, ss.59-71, 2022
2022
20222. 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
2021
20213. 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
2021
20214. 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
2021
20215. 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
2021
20216. 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
Desteklenen Projeler
2019 - 2021
2019 - 2021Çocukluk Çağı Otozomal Dominant ve Otozomal Resesif Polikistik Böbrek Hastalıklarının Genetik ve Klinik Özelliklerinin Araştırılması
Yükseköğretim Kurumları Destekli Proje , BAP Doktora
ÖZALTIN F. (Yürütücü), TOPALOĞLU R., TÜRKOĞLU Ö., ATAYAR E., GÜLHAN B.
2018 - 2021
2018 - 2021CoQ10 Nefropatisinde Koenzim Q10 İçerikli Nanoterapötiklerin Tedavi Etkiliğinin Araştırılması ve İn Vitro Modelde Mitokondriyal Fonksiyonlarının Karşılaştırılması
Yükseköğretim Kurumları Destekli Proje , BAP Araştırma Projesi
ÖZALTIN F. (Yürütücü), TOPALOĞLU R., EROĞLU İ., NEMUTLU E., ÖZBAY H. S., YABANOĞLU ÇİFTÇİ S.
2011 - 2016
2011 - 2016Atipik Hemolitik Üremik Sendromlu Hastalarda Kompleman Düzenleyici Genlerdeki Mutasyonların Saptanması
Yükseköğretim Kurumları Destekli Proje , BAP Alt Yapı
ÖZALTIN F. (Yürütücü), BEŞBAŞ N.