Fatih Ozaltin
Fatih Ozaltin
Hacettepe University Faculty of Medicine
Verified email at - Homepage
Cited by
Cited by
Familial Mediterranean fever (FMF) in Turkey: results of a nationwide multicenter study
M Tunca, H Ozdogan, O Kasapcopur, F Yalcinkaya, E Tutar, R Topaloglu, ...
Medicine (Baltimore) 84 (1), 1-11, 2005
Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible
B Hinkes, RC Wiggins, R Gbadegesin, CN Vlangos, D Seelow, ...
Nature genetics 38 (12), 1397-1405, 2006
Nephrotic Syndrome in the First Year of Life: Two Thirds of Cases Are Caused by Mutations in 4 Genes (NPHS1, NPHS2, WT1, and LAMB2)
BG Hinkes, B Mucha, CN Vlangos, R Gbadegesin, J Liu, K Hasselbacher, ...
Pediatrics 119 (4), e907-e919, 2007
COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness
SF Heeringa, G Chernin, M Chaki, W Zhou, AJ Sloan, Z Ji, LX Xie, ...
The Journal of clinical investigation 121 (5), 2013-2024, 2011
Spectrum of steroid-resistant and congenital nephrotic syndrome in children: the PodoNet registry cohort
A Trautmann, M Bodria, F Ozaltin, A Gheisari, A Melk, M Azocar, A Anarat, ...
Clinical Journal of the American Society of Nephrology 10 (4), 592-600, 2015
MYO1E mutations and childhood familial focal segmental glomerulosclerosis
C Mele, P Iatropoulos, R Donadelli, A Calabria, R Maranta, P Cassis, ...
New England Journal of Medicine 365 (4), 295-306, 2011
Circulating suPAR in two cohorts of primary FSGS
C Wei, H Trachtman, J Li, C Dong, AL Friedman, JJ Gassman, ...
Journal of the American Society of Nephrology 23 (12), 2051-2059, 2012
Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders
K Hasselbacher, RC Wiggins, V Matejas, BG Hinkes, B Mucha, ...
Kidney international 70 (6), 1008-1012, 2006
Whole exome sequencing of patients with steroid-resistant nephrotic syndrome
JK Warejko, W Tan, A Daga, D Schapiro, JA Lawson, S Shril, S Lovric, ...
Clinical Journal of the American Society of Nephrology 13 (1), 53-62, 2018
Long-term outcome of steroid-resistant nephrotic syndrome in children
A Trautmann, S Schnaidt, BS Lipska-Ziętkiewicz, M Bodria, F Ozaltin, ...
Journal of the American Society of Nephrology 28 (10), 3055-3065, 2017
Role of A-SAA in monitoring subclinical inflammation and in colchicine dosage in familial Mediterranean fever
A Duzova, A Bakkaloglu, N Besbas, R Topaloglu, S Ozen, F Ozaltin, ...
Clinical and experimental rheumatology 21 (4), 509-514, 2003
Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly
DA Braun, J Rao, G Mollet, D Schapiro, MC Daugeron, W Tan, ...
Nature genetics 49 (10), 1529-1538, 2017
E148Q is a disease-causing MEFV mutation: a phenotypic evaluation in patients with familial Mediterranean fever
R Topaloglu, F Ozaltin, E Yilmaz, S Ozen, B Balci, N Besbas, ...
Annals of the rheumatic diseases 64 (5), 750-752, 2005
Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome
RG Ruf, M Schultheiss, A Lichtenberger, SM Karle, I Zalewski, B Mucha, ...
Kidney international 66 (2), 564-570, 2004
Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS)
R Gbadegesin, BG Hinkes, BE Hoskins, CN Vlangos, SF Heeringa, J Liu, ...
Nephrology dialysis transplantation 23 (4), 1291-1297, 2008
Specific podocin mutations correlate with age of onset in steroid-resistant nephrotic syndrome
B Hinkes, C Vlangos, S Heeringa, B Mucha, R Gbadegesin, J Liu, ...
Journal of the American Society of Nephrology 19 (2), 365-371, 2008
Mutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndrome
DA Braun, CE Sadowski, S Kohl, S Lovric, SA Astrinidis, WL Pabst, ...
Nature genetics 48 (4), 457-465, 2016
DGKE variants cause a glomerular microangiopathy that mimics membranoproliferative GN
F Ozaltin, B Li, A Rauhauser, SW An, O Soylemezoglu, II Gonul, ...
Journal of the American Society of Nephrology 24 (3), 377-384, 2013
Childhood vasculitides in Turkey: a nationwide survey
Turkish Pediatric Vasculitis Study Group, S Ozen, A Bakkaloglu, ...
Clinical rheumatology 26, 196-200, 2007
Mutations in the Wilms' tumor 1 gene cause isolated steroid resistant nephrotic syndrome and occur in exons 8 and 9
B Mucha, F Ozaltin, BG Hinkes, K Hasselbacher, RG Ruf, M Schultheiss, ...
Pediatric research 59 (2), 325-331, 2006
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