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F. Ozaltin, N. Besbas, D. Uckan, M. Tuncer, R. Topaloglu, S. Ozen, U. Saatci, A.Bakkaloglu. The role of apoptosis in childhood Henoch Schonlein purpura. Clin Rheumatol 2003; 22: 265-267.
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A. Duzova , A. Bakkaloglu , N. Besbas, R. Topaloglu, S. Ozen, F. Ozaltin, Y. Bassoy, E. Yilmaz. Role of A-SAA in monitoring subclinical inflammation and in colchicine dosage in familial Mediterranean fever. Clin Exp Rheumatol 2003; 21: 509-514.
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Nesrin Besbas, Fatih Ozaltin, Turgay Coskun, Sila Ozalp, Umit Saatci, Aysin Bakkaloglu, A. Meguid El Nahas. Relationship of leptin and insulin-like growth factor I to nutritional status in hemodialyzed children. Pediatr Nephrol 2003;18(12):1255-1259.
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C Sackesen, A Bakkaloglu, B E Sekerel, F Ozaltin, N Besbas, E Yilmaz, G Adalioglu, S Ozen. Decreased frequency of atopy in pediatric patients with Familial Mediterranean Fever. Ann Rheum Dis 2004; 63: 187-190.
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Aysin Bakkaloglu, Ali Duzova, Seza Ozen, Banu Balci, Nesrin Besbas, Rezan Topaloglu, Fatih Ozaltin, Engin Yilmaz. The ınfluence of SAA1, SAA2 gene polymorphisms on renal amyloidosis, and on SAA/CRP value in patients with familial Mediterranean fever in the Turkish population. J Rheumatol 2004; 31(6): 1139-1142.
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Fatih Ozaltin, Aysin Bakkaloglu, Seza Ozen, Rezan Topaloglu, Umut Kavak, Mukaddes Kalyoncu, Nesrin Besbas. The significance of IgA class of antineutrophil cytoplasmic antibodies (ANCA) in childhood Henoch-Schonlein purpura. Clin Rheumatol. 2004;23(5): 426-429.
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Ali Duzova, Fatih Ozaltin, Alev Ozon, Nesrin Besbas, RezanTopaloglu, Seza Ozen, Aysin Bakkaloglu. Bone mineral density in children with familial Mediterranean fever. Clin Rheumatol 2004;23(3): 230-234.
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Nesrin Besbas, Fatih Ozaltin, Ferhat Catal, Seza Ozen, Rezan Topaloglu, Aysin Bakkaloglu. Macrophage chemoattractant protein-1 and interleukin-8 in acute poststreptococcal glomerulonephritis. Pediatr Nephrol 2004; 9(8): 864-868.
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Ruf RG, Schultheiss M, Lichtenberger A, Karle SM, Zalewski I, Mucha B, Everding AS, Neuhaus T, Patzer L, Plank C, Haas JP, Ozaltin F, Imm A, Fuchshuber A, Bakkaloglu A, Hildebrandt F; APN Study Group. Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome. Kidney Int 2004; 66(2): 564-570.
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Rezan Topaloglu, Fatih Ozaltin, Engin Yilmaz, Seza Ozen, Banu Balci, Nesrin Besbas, Aysin Bakkaloglu. E148Q is a disease causing MEFV mutation: a phenotypic evaluation in patients with familial Mediterranean fever. Ann Rheum Dis 2005; 64(5):750-752.
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Turkish FMF Study Group. Familial Mediterranean Fever (FMF) in Turkey: Results of a Nationwide Multicenter Study. Medicine (Baltimore), 2005; 84(1), 1-11
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Fatih Ozaltin, Nesrin Besbas, Aysin Bakkaloglu, Safak Gucer, Seza Ozen, Rezan Topaloglu, Gulsev Kale, Melda Caglar. Apoptosis and proliferation in childhood proliferative glomerulonephritis. Pediatr Nephrol 2005; 20, 1572-1577.
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Bettina Mucha, Fatih Ozaltin, Bernward G. Hinkes, Katrin Hasselbacher, Rainer G. Ruf, Michael Schultheiss, Daniela Hangan, Bethan Hoskins, Anne Schulze Everding, Radovan Bogdanovic, Thomas Seeman, Bernd Hoppe, Friedhelm Hildebrandt, and Members of the APN Study Group. Mutations in the Wilms’ Tumor 1 Gene Cause Isolated Steroid Resistant Nephrotic Syndrome and Occur in Exons 8 and 9. Pediatr Res 2006; 59(2): 325-331.
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Mukaddes Kalyoncu, Rezan Topaloglu, Umut Bayrakci, Aysin Bakkaloglu, Nesrin Besbas, Fatih Ozaltin, Mehmet Bakkaloglu. Cyclosporine drug monitoring with C0 and C2 concentrations in children with stable renal allograft function. Pediatr Transplant 2006, 10: 168-171.
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Hasselbacher K, Wiggins RC, Matejas V, Hinkes BG, Mucha B, Hoskins BE, Ozaltin F, Nurnberg G, Becker C, Hangan D, Pohl M, Kuwertz-Broking E, Griebel M, Schumacher V, Royer-Pokora B, Bakkaloglu A, Nurnberg P, Zenker M, Hildebrandt F. Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders. Kidney Int. 2006; 70(6): 1008-1012.
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Bernward Hinkes, Roger C Wiggins, Rasheed Gbadegesin, Christopher N Vlangos, Dominik Seelow, Gudrun Nürnberg, Puneet Garg, Rakesh Verma, Hassan Chaib, Bethan E Hoskins, Shazia Ashraf, Christian Becker, Hans Christian Hennies, Meera Goyal, Bryan L Wharram, Asher D Schachter, Sudha Mudumana, Iain Drummond, Dontscho Kerjaschki, Rüdiger Waldherr, Alexander Dietrich, Fatih Ozaltin, Aysin Bakkaloglu, Roxana Cleper, Lina Basel-Vanagaite, Martin Pohl, Martin Griebel, Alexey N Tsygin, Alper Soylu, Dominik Müller, Caroline S Sorli, Tom D Bunney, Matilda Katan, Jinhong Liu, Massimo Attanasio, John F O'Toole, Katrin Hasselbacher, Bettina Mucha, Edgar A Otto, Rannar Airik, Andreas Kispert, Grant G Kelley, Alan V Smrcka, Thomas Gudermann, Lawrence B Holzman, Peter Nürnberg & Friedhelm Hildebrandt. Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible. Nat Genet 2006; 38(12): 1397-1405.
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Utsch B, Bokenkamp A, Benz MR, Besbas N, Dotsch J, Franke I, Frund S, Gok F, Hoppe B, Karle S, Kuwertz-Broking E, Laube G, Neb M, Nuutinen M, Ozaltin F, Rascher W, Ring T, Tasic V, van Wijk JA, Ludwig M. Novel OCRL1 Mutations in Patients With the Phenotype of Dent Disease. Am J Kidney Dis 2006; 48(6): 942-954.
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Ozen S, Bakkaloglu A, Dusunsel R, Soylemezoglu O, Ozaltin F, Poyrazoglu H, Kasapcopur O, Ozkaya O, Yalcinkaya F, Balat A, Kural N, Donmez O, Alpay H, Anarat A, Mir S, Gur-Guven A, Sonmez F, Gok F; On behalf of Turkish Pediatric Vasculitis Study Group. Childhood vasculitides in Turkey: a nationwide survey. Clin Rheumatol 2007; 26(2): 196-200.
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Bernward G Hinkes, Bettina Mucha, Christopher N Vlangos, Rasheed Gbadegesin, Jinhong Liu, Katrin Hasselbacher, Daniela Hangan, Fatih Ozaltin, Martin Zenker, Friedhelm Hildebrandt and Members of the APN Study Group. Nephrotic syndrome in the first year of life: Two thirds of cases are caused by mutations in four genes (NPHS1, NPHS2, WT1, or LAMB2). Pediatrics 2007; 119(4): e907-919.
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Mehls, O .Wühl, E., Schaefer, F., Anarat, A., Bakkaloglu, A., Ozaltin, F., Peco-Antic, A., Querfeld, U., Gellermann, J., Sallay, P., Drozdz, D., Bonzel, K.-E., Wingen, A.-M., Zurowska, A., Balasz, I., Perfumo, F., Canepa, A., Müller-Wiefel, D.E., Zepf, K., Offner, G., Enke, B., Hadtstein, C., Berg, U., Celsi, G., Emre, S., Sirin, A., Bilge, I., Çaliskan, S, Mir, S., Serdaroglu, E., Greiner, C., Eichstädt, H., Wygoda, S., Hohbach-Hohenfeliner, K., Jeck, N., Klaus, G., Appiani, A., Ardissino, G., Testa, S., Montini, G., Niaudet, P., Charbit, M., Dusek, J., Caldas-Afonso, A., Teixeira, A., Picca, S., Matteucci, C., Wigger, M., Fischbach, M., Terzic, J., Fydryk, J., Urasinski, T., Coppo, R., Peruzzi, L., Jankauskiene, A., Litwin, M., Abuauba, M., Grenda, R., Arbeiter, K., Neuhaus, T.J. Pharmacological renoprotection in children with chronic kidney disease. Nieren- und Hochdruckkrankheiten 2007; 36 (1): 6-11.
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Bilginer Y, Ozaltin F, Basaran C, Aki TF, Karabulut E, Duzova A, Besbas N, Topaloglu R, Ozen S, Bakkaloglu M, Bakkaloglu A. Carotid intima-media thickness in children and young adults with renal transplant: internal carotid artery vs. common carotid artery. Pediatr Transplant 2007; 11(8): 888-894.
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Ozaltin F, Heeringa S, Poyraz CE, Bilginer Y, Kadayifcilar S, Besbas N, Topaloglu R, Ozen S, Hildebrandt F, Bakkaloglu A. Eye involvement in children with primary focal segmental glomerulosclerosis. Pediatr Nephrol 2008;23(3): 421-427.
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Gbadegesin R, Hinkes BG, Hoskins BE, Vlangos CN, Heeringa SF, Liu J, Loirat C, Ozaltin F, Hashmi S, Ulmer F, Cleper R, Ettenger R, Antignac C, Wiggins RC, Zenker M, Hildebrandt F. Mutations in PLCE1 are a Major Cause of Isolated Diffuse Mesangial Sclerosis (IDMS). Nephrol Dial Transplant. 2007; 23(4): 1291-1297.
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Hinkes B, Vlangos C, Heeringa S, Mucha B, Gbadegesin R, Liu J, Hasselbacher K, Ozaltin F, Hildebrandt F; and Members of the APN Study Group. Specific podocin mutations correlate with age of onset in steroid-resistant nephrotic syndrome. J Am Soc Nephrol 2008; 19(2):365-371.
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Duzova A, Aki T, Bakkaloglu A, Besbas N, Topaloglu R, Ozen S, Ozaltin F, Bilginer Y, Demirkaya E, Bakkaloglu M. Triple immunosuppression with tacrolimus in pediatric renal transplantation: single-center experience. Transplant Proc 2008;40(1):132-134.
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Bilginer Y, Topaloglu R, Aki FT, Demirkaya E, Ozaltin F, Besbas N, Ozen S, Bakkaloglu A, Erkan I, Bakkaloglu M. Outcome of primary glomerular disease in pediatric renal transplantation: a single-center experience. Transplant Proc. 2008;40(1):129-131.
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Bilginer Y, Ozaltin F, Basaran C, Duzova A, Besbas N, Topaloglu R, Ozen S, Bakkaloglu A. Evaluation of intima media thickness of the common and internal carotid arteries with inflammatory markers in familial Mediterranean fever as possible predictors for atherosclerosis. Rheumatol Int 2008; 28: 1211-1216.
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Heeringa SF, Vlangos CN, Chernin G, Hinkes B, Gbadegesin R, Liu J, Hoskins BE, Ozaltin F, Hildebrandt F; Members of the APN Study Group. Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome. Nephrol Dial Transplant 2008; 23(11): 3527-3533.
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Besbas N, Draaken M, Ludwig M, Deren O, Orhan D, Bilginer Y, Ozaltin F.A novel CLCN7 mutation resulting in a most severe form of autosomal recessive osteopetrosis. Eur J Pediatr 2009; 168: 1449-1454.
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Gimpel C, Wühl E, Arbeiter K, Drozdz D, Trivelli A, Charbit M, Gellermann J, Dusek J, Jankauskiene A, Emre S, Schaefer F; ESCAPE Trial Group. Superior consistency of ambulatory blood pressure monitoring in children: implications for clinical trials. J Hypertens 2009; 27: 1568-74.
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Tabatabaeifar M, Schlingmann KP, Litwin M, Emre S, Bakkaloglu A, Mehls O, Antignac C, Schaefer F, Weber S; ESCAPE Trial Group. Pediatr Nephrol 2009; 24: 2361236-8.
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ESCAPE Trial Group. Strict blood-pressure control and progression of renal failure in children. N Engl J Med 2009;361:1639-1650.
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Altugan FS, Ozen S, Aktay-Ayaz N, Güçer S, Topaloğlu R, Düzova A, Ozaltin F, Beşbaş N. Treatment of severe Henoch-Schönlein nephritis: justifying more immunosuppression. Turk J Pediatr 2009;51(6):551-555.
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Canpınar H, Özaltın F, Bilginer Y, Bakkaloğlu A, Özen S. Toll-like receptors 2 and 4 cell surface expression reflects endotoxin tolerance in Henoch-Schönlein purpura. Turk J Pediatr 2010; 52: 22-27.
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Topaloglu R, Er I, Dogan BG, Bilginer Y, Ozaltin F, Besbas N, Ozen S, Bakkaloglu A, Gur D. Risk factors in community-acquired urinary tract infections caused by ESBL-producing bacteria in children. Pediatr Nephrol 2010;25(5): 919-925.
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Beşbaş N, Ozaltin F, Emre S, Anarat A, Alpay H, Bakkaloğlu A, Baskin E, Buyan N, Dönmez O, Düşünsel R, Ekim M, Göko F, Gür-Güven A, Kavukçu S, Mir S, Sönmez F. Clinical course of primary focal segmental glomerulosclerosis (FSGS) in Turkish children: a report from the Turkish Pediatric Nephrology FSGS Study Group. Turk J Pediatr. 2010 May-Jun;52(3): 255-261.
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Chernin G, Vega-Warner V, Schoeb DS, Heeringa SF, Ovunc B, Saisawat P, Cleper R, Ozaltin F, Hildebrandt F; Group Members of the GPN Study. Genotype/Phenotype Correlation in Nephrotic Syndrome Caused by WT1 Mutations. Clin J Am Soc Nephrol 2010; 5(9): 1655-1662.
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Borzych D, Rees L, Ha IS, Chua A, Valles PG, Lipka M, Zambrano P, Ahlenstiel T, Bakkaloglu SA, Spizzirri AP, Lopez L, Ozaltin F, Printza N, Hari P, Klaus G, Bak M, Vogel A, Ariceta G, Yap HK, Warady BA, Schaefer F. The bone and mineral disorder of children undergoing chronic peritoneal dialysis. Kidney Int 2010;78(12): 1295-1304.
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Demirkaya E, Ozen S, Bilginer Y, Ayaz NA, Makay BB, Unsal E, Erguven M, Poyrazoglu H, Kasapcopur O, Gok F, Akman S, Balat A, Cavkaytar O, Kaya B, Duzova A, Ozaltin F, Topaloglu R, Besbas N, Bakkaloglu A, Arisoy N, Ozdogan H, Bakkaloglu S, Turker T. The distribution of juvenile idiopathic arthritis in the eastern Mediterranean: results from the registry of the Turkish Paediatric Rheumatology Association. Clin Exp Rheumatol 2011;29(1): 111-116.
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Topaloğlu R, Bilginer Y, Alikaşifoğlu A, Ozaltin F, Beşbaş N, Ozen S, Bakkaloğlu A. Neuroendocrine immune system in familial Mediterranean fever. Turk J Pediatr 2010;52(6): 588-593.
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Tayfur AC, Besbas N, Bilginer Y, Ozaltin F, Duzova A, Bakkaloglu M, Aki FT, Ozen S, Topaloglu R, Bakkaloglu A. Follow-up of patients with juvenile nephronophthisis after renal transplantation: a single center experience. Transplant Proc 2011;43(3):847-849.
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Heeringa SF, Chernin G, Chaki M, Zhou W, Sloan AJ, Ji Z, Xie LX, Salviati L, Hurd TW, Vega-Warner V, Killen PD, Raphael Y, Ashraf S, Ovunc B, Schoeb DS, McLaughlin HM, Airik R, Vlangos CN, Gbadegesin R, Hinkes B, Saisawat P, Trevisson E, Doimo M, Casarin A, Pertegato V, Giorgi G, Prokisch H, Rötig A, Nürnberg G, Becker C, Wang S, Ozaltin F, Topaloglu R, Bakkaloglu A, Bakkaloglu SA, Müller D, Beissert A, Mir S, Berdeli A, Varpizen S, Zenker M, Matejas V, Santos-Ocaña C, Navas P, Kusakabe T, Kispert A, Akman S, Soliman NA, Krick S, Mundel P, Reiser J, Nürnberg P, Clarke CF, Wiggins RC, Faul C, Hildebrandt F. COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness. J Clin Invest 2011;121(5): 2013-2024.
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Ozaltin F, Ibsirlioglu T, Taskiran EZ, Baydar DE, Kaymaz F, Buyukcelik M, Kilic BD, Balat A, Iatropoulos P, Asan E, Akarsu NA, Schaefer F, Yilmaz E, Bakkaloglu A; the PodoNet Consortium. Disruption of PTPRO Causes Childhood-Onset Nephrotic Syndrome. Am J Hum Genet 2011; 89: 139-147.
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Mele C,Iatropoulos P, Donadelli R, Calabria A,Maranta R, Cassis P,Buelli S,Tomasoni S,Piras R, Krendel M,Bettoni S,Morigi M, Delledonne M, Pecoraro C, Abbate I, Capobianchi MR, Hildebrandt F, Otto E, Schaefer F, Macciardi F, Ozaltin F, Emre S, Ibsirlioglu T, Benigni A, Remuzzi G, Noris M, PodoNet Consortium. MYO1E Mutations and Childhood Familial Focal Segmental Glomerulosclerosis. N Engl J Med 2011; 365: 295-306.
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Topaloglu R, Vilboux T, Coskun T, Ozaltin F, Tinloy B, Gunay-Aygun M, Bakkaloglu A, Besbas N, van den Heuvel L, Kleta R, Gahl WA. Genetic basis of cystinosis in Turkish patients: a single-center experience. 2012; 27(1):115-121.
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Gürakan F, Baysoy G, Wedenoja S, Uslu N, Ozen H, Ozaltin F, Höglund P. 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. Turk J Pediatr. 2011; 53(2): 194-198.
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Cil O, Ertunc M, Gucer KS, Ozaltin F, Iskit AB, Onur R. Endothelial Dysfunction and Increased Responses to Renal Nerve Stimulation in Rat Kidneys during Rhabdomyolysis-Induced Acute Renal Failure: Role of Hydroxyl Radical. Ren Fail 2012;34(2): 211-220.
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Gokce M, Bilginer Y, Besbas N, Ozaltin F, Cetin M, Gumruk F, Ozen S. Hematological features of pediatric systemic lupus erythematosus: suggesting management strategies in children. Lupus 2012; 21(8): 878-884.
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Wei C, Trachtman H, Li J, Dong C, Friedman AL, Gassman JJ, McMahan JL, Radeva M, Heil KM, Trautmann A, Anarat A, Emre S, Ghiggeri GM, Ozaltin F, Haffner D, Gipson DS, Kaskel F, Fischer DC, Schaefer F, Reiser J; for the PodoNet and FSGS CT Study Consortia. Circulating suPAR in Two Cohorts of Primary FSGS. J Am Soc Nephrol 2012; 23: 2051-2059.
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Ozaltin F, Li B, Rauhauser A, An SW, Soylemezoglu O, Gonul II, Taskiran EZ, Ibsirlioglu T, Korkmaz E, Bilginer Y, Duzova A, Ozen S, Topaloglu R, Besbas N, Ashraf S, Du Y, Liang C, Chen P, Lu D, Vadnagara K, Arbuckle S, Lewis D, Wakeland B, Quigg RJ, Ransom RF, Wakeland EK, Topham MK, Bazan NG, Mohan C, Hildebrandt F, Bakkaloglu A, Huang CL, Attanasio M. DGKE Variants Cause a Glomerular Microangiopathy That Mimics Membranoproliferative GN. J Am Soc Nephrol. 2013; 24: 377-384.
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Ozaltin F, Besbas N, Iskit AB, Cil O, Akcoren Z, Kale G, Bakkaloglu A. Role of CXCR1 (CKR-1) in Inflammation of Experimental Mesangioproliferative Glomerulonephritis. Ren Fail 2013;35(3): 380-385.
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Lipska BS, Iatropoulos P, Maranta R, Caridi G, Ozaltin F, Anarat A, Balat A, Gellermann J, Trautmann A, Erdogan O, Saeed B, Emre S, Bogdanovic R, Azocar M, Balasz-Chmielewska I, Benetti E, Caliskan S, Mir S, Melk A, Ertan P, Baskin E, Jardim H, Davitaia T, Wasilewska A, Drozdz D, Szczepanska M, Jankauskiene A, Higuita LM, Ardissino G, Ozkaya O, Kuzma-Mroczkowska E, Soylemezoglu O, Ranchin B, Medynska A, Tkaczyk M, Peco-Antic A, Akil I, Jarmolinski T, Firszt-Adamczyk A, Dusek J, Simonetti GD, Gok F, Gheissari A, Emma F, Krmar RT, Fischbach M, Printza N, Simkova E, Mele C, Ghiggeri GM, Schaefer F; PodoNet Consortium. Genetic screening in adolescents with steroid-resistant nephrotic syndrome. Kidney Int 2013;84(1): 206-213.
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Ozaltin F. Primary coenzyme Q10 (CoQ 10) deficiencies and related nephropathies. Pediatr Nephrol 2014; 29: 961-669.
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Topaloglu R, Orhan D, Bilginer Y, Karabulut E, Ozaltin F, Duzova A, Kale G, Besbas N. Clinicopathological and immunohistological features in childhood IgA nephropathy: a single-centre experience. Clin Kidney J 2013;6(2): 169-175.
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Bouchireb K, Boyer O, Gribouval O, Nevo F, Huynh-Cong E, Morinière V, Campait R, Ars E, Brackman D, Dantal J, Eckart P, Gigante M, Lipska BS, Liutkus A, Megarbane A, Mohsin N, Ozaltin F, Saleem MA, Schaefer F, Soulami K, Torra R, Garcelon N, Mollet G, Dahan K, Antignac C. NPHS2 Mutations in Steroid-Resistant Nephrotic Syndrome: A Mutation Update and the Associated Phenotypic Spectrum. Hum Mutat 2014; 35(2):178-186.
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Genotype–phenotype associations in WT1 glomerulopathy. Lipska BS, Ranchin B, Iatropoulos P, Gellermann J, Melk A, Ozaltin F, Caridi G, Seeman T, Tory K, Jankauskiene A, Zurowska A, Szczepanska M, Wasilewska A, Harambat J, Trautmann A, Peco-Antic A, Borzecka H, Moczulska A, Saeed B, Bogdanovic R, Kalyoncu M, Simkova E, Erdogan O, Vrljicak K, Teixeira A, Azocar M, Schaefer F and the PodoNet Consortium. Kidney Int 2014;85: 1169-1178.
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Gülhan B, Topaloğlu R, Karabulut E, Ozaltın F, Aki FT, Bilginer Y, Beşbaş N. Post-transplant hypertension in pediatric kidney transplant recipients. Pediatr Nephrol 2014; 29:1075-1080.
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Taskiran EZ, Korkmaz E, Gucer S, Kosukcu C, Kaymaz F, Koyunlar C, Bryda EC, Chaki M, Lu D, Vadnagara K, Candan C, Topaloglu R, Schaefer F, Attanasio M, Bergmann C, Ozaltin F. Mutations in ANKS6 cause a Nephronophthisis-Like Phenotype with End Stage Renal Disease. J Am Soc Nephrol 2014; 25: 1653-1661.
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Ozaltin F, Bilginer Y, Gülhan B, Bajin I, Erdogan O, Hayran M, Yılmaz E, Ozen S. Diagnostic validity of colchicine in patients with Familial Mediterranean fever. Clin Rheumatol. 2014; 33: 969-974.
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Gee HY, Ashraf S, Wan X, Vega-Warner V, Esteve-Rudd J, Lovric S, Fang H, Hurd TW, Sadowski CE, Allen SJ, Otto EA, Korkmaz E, Washburn J, Levy S, Williams DS, Bakkaloglu SA, Zolotnitskaya A, Ozaltin F, Zhou W, Hildebrandt F. Mutations in EMP2 cause childhood-onset nephrotic syndrome. Am J Hum Genet 2014; 94: 884-890.
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Trautmann A, Bodria M, Ozaltin F, Gheisari A, Melk A, Azocar M, Anarat A, Caliskan S, Emma F, Gellermann J, Oh J, Baskin E, Ksiazek J, Remuzzi G, Erdogan O, Akman S, Dusek J, Davitaia T, Özkaya O, Papachristou F, Firszt-Adamczyk A, Urasinski T, Testa S, Krmar RT, Hyla-Klekot L, Pasini A, Özcakar ZB, Sallay P, Cakar N, Galanti M, Terzic J, Aoun B, Caldas Afonso A, Szymanik-Grzelak H, Lipska BS, Schnaidt S, Schaefer F; PodoNet Consortium. Spectrum of steroid-resistant and congenital nephrotic syndrome in children: the PodoNet registry cohort. Clin J Am Soc Nephrol 2015;10: 592-600.
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Cil O, Besbas N, Duzova A, Topaloglu R, Peco-Antić A, Korkmaz E, Ozaltin F. Genetic abnormalities and prognosis in patients with congenital and infantile nephrotic syndrome. Pediatr Nephrol 2015; 30: 1279-1287.
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Korkmaz E, Lipska-Ziętkiewicz BS, Boyer O, Gribouval O, Fourrage C, Tabatabaei M, Schnaidt S, Gucer S, Kaymaz F, Arici M, Dinckan A, Mir S, Bayazit AK, Emre S, Balat A, Rees L, Shroff R, Bergmann C, Mourani C, Antignac C, Ozaltin F, Schaefer F; PodoNet Consortium. ADCK4-Associated Glomerulopathy Causes Adolescence-Onset FSGS. J Am Soc Nephrol 2016; 27: 63-68.
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Shroff R, Aitkenhead H, Costa N, Trivelli A, Litwin M, Picca S, Anarat A, Sallay P, Ozaltin F, Zurowska A, Jankauskiene A, Montini G, Charbit M, Schaefer F, Wühl E; ESCAPE Trial Group. Normal 25-Hydroxyvitamin D Levels Are Associated with Less Proteinuria and Attenuate Renal Failure Progression in Children with CKD. J Am Soc Nephrol 2016; 27: 314-322.
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Besbas N, Kalyoncu M, Cil O, Ozgul RK, Bakkaloglu A, Ozaltin F. MCP1 2518 A/G polymorphism affects progression of childhood focal segmental glomerulosclerosis. Ren Fail 2015; 37: 1435-1439.
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Braun DA, Schueler M, Halbritter J, Gee HY, Porath JD, Lawson JA, Airik R, Shril S, Allen SJ, Stein D, Al Kindy A, Beck BB, Cengiz N, Moorani KN, Ozaltin F, Hashmi S, Sayer JA, Bockenhauer D, Soliman NA, Otto EA, Lifton RP, Hildebrandt F. Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicity. Kidney Int 2016; 89:468-475.
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Braun DA, Sadowski CE, Kohl S, Lovric S, Astrinidis SA, Pabst WL, Gee HY, Ashraf S, Lawson JA, Shril S, Airik M, Tan W, Schapiro D, Rao J, Choi WI, Hermle T, Kemper MJ, Pohl M, Ozaltin F, Konrad M, Bogdanovic R, Büscher R, Helmchen U, Serdaroglu E, Lifton RP, Antonin W, Hildebrandt F. Mutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndrome. Nat Genet 2016;48: 457-465.
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Zhu J, Chaki M, Lu D, Ren C, Wang SS, Rauhauser AA, Li B, Zimmerman S, Jun B, Du Y, Vadnagara K, Wang H, Elhadi S, Quigg RJ, Topham MK, Mohan C, Ozaltin F, Zhou XJ, Marciano DK, Bazan NG, Attanasio M. Loss of diacylglycerol kinase epsilon in mice causes endothelial distress and impairs glomerular Cox-2 and PGE2 production. Am J Physiol Renal Physiol. 2016; 310(9): F895-908.
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Eroglu FK, Kasapçopur Ö, Beşbaş N, Ozaltin F, Bilginer Y, Barut K, Mensa-Vilaro A, Nakagawa K, Heike T, Nishikomori R, Arostegui J, Ozen S. Genetic and clinical features of cryopyrin-associated periodic syndromes in Turkish children. Clin Exp Rheumatol. 2016; 34(6 Suppl 102): S115-S120.
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Topaloglu R, Batu ED, Yıldız Ç, Korkmaz E, Özen S, Beşbaş N, Özaltın F. Familial Mediterranean fever patients homozygous for E148Q variant may have milder disease. Int J Rheum Dis 2018; 21(10): 1857-1862.
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Yüksel S, Evrengül H, Özçakar ZB, Becerir T, Yalçın N, Korkmaz E, Ozaltin F. First-Line, Early and Long-Term Eculizumab Therapy in Atypical Hemolytic Uremic Syndrome: A Case Series in Pediatric Patients. Paediatr Drugs 2016;18: 413-420.
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Batu ED, Sönmez HE, Hazırolan T, Özaltın F, Bilginer Y, Özen S. Tociluzumab treatment in childhood takayasu arteritis: Case series of four patients and systemic review of the literatüre. Semin Arthritis Rheum 2017; 46(4): 529-535.
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Hölttä T, Bonthuis M, Van Stralen KJ, Bjerre A , Topaloglu R, Ozaltin F, Holmberg C, Harambat J, Jager KJ, Schaefer F, Groothoff JW. 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. Pediatr Nephrol 2016; 31: 2317-2325.
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Besbas N, Gulhan B, Soylemezoglu O, Ozcakar ZB, Korkmaz E, Hayran M, Ozaltin F. Turkish pediatric atypical hemolytic uremic syndrome registry: initial analysis of 146 patients. BMC Nephrol 2017; 18:6, 2-10.
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Atmaca M, Gulhan B, Korkmaz E, Inozu M, Soylemezoglu O, Candan C, Bayazıt AK, Elmacı AM, Parmaksiz G, Duzova A, Besbas N, Topaloglu R, Ozaltin F. Follow-up results of patients with ADCK4 mutations and the efficacy of CoQ10 treatment. Pediatr Nephrol. 2017; 32: 1369-1375.
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Trautmann A, Schnaidt S, Lipska-Ziętkiewicz BS, Bodria M, Ozaltin F, Emma F, Anarat A, Melk A, Azocar M, Oh J, Saeed B, Gheisari A, Caliskan S, Gellermann J, Higuita LMS, Jankauskiene A, Drozdz D, Mir S, Balat A, Szczepanska M, Paripovic D, Zurowska A, Bogdanovic R, Yilmaz A, Ranchin B, Baskin E, Erdogan O, Remuzzi G, Firszt-Adamczyk A, Kuzma-Mroczkowska E, Litwin M, Murer L, Tkaczyk M, Jardim H, Wasilewska A, Printza N, Fidan K, Simkova E, Borzecka H, Staude H, Hees K, Schaefer F; PodoNet Consortium. Long-Term Outcome of Steroid-Resistant Nephrotic Syndrome in Children. J Am Soc Nephrol. 2017;28: 3055-3065.
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Topaloglu R, Gulhan B, İnözü M, Canpolat N, Yilmaz A, Noyan A, Dursun İ, Gökçe İ, Gürgöze MK, Akinci N, Baskin E, Serdaroğlu E, Demircioğlu Kiliç B, Yüksel S, Övünç Hacihamdioğlu D, Korkmaz E, Hayran M, Ozaltin F; contributors of The Turkish Cystinosis Study Group. The Clinical and Mutational Spectrum of Turkish Patients with Cystinosis. Clin J Am Soc Nephrol. 2017; 12: 1634-1641.
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Lipska-Ziętkiewicz BS, Gellermann J, Boyer O, Gribouval O, Ziętkiewicz S, Kari JA, Shalaby MA, Ozaltin F, Dusek J, Melk A, Bayazit AK, Massella L, Hyla-Klekot L, Habbig S, Godron A, Szczepańska M, Bieniaś B, Drożdż D, Odeh R, Jarmużek W, Zachwieja K, Trautmann A, Antignac C, Schaefer F; PodoNet Consortium. Low renal but high extrarenal phenotype variability in Schimke immuno-osseous dysplasia. PLoS One. 2017;12: e0180926.
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Braun DA, Rao J, Mollet G, Schapiro D, Daugeron MC, Tan W, Gribouval O, Boyer O, Revy P, Jobst-Schwan T, Schmidt JM, Lawson JA, Schanze D, Ashraf S, Ullmann JFP, Hoogstraten CA, Boddaert N, Collinet B, Martin G, Liger D, Lovric S, Furlano M, Guerrera IC, Sanchez-Ferras O, Hu JF, Boschat AC, Sanquer S, Menten B, Vergult S, De Rocker N, Airik M, Hermle T, Shril S, Widmeier E, Gee HY, Choi WI, Sadowski CE, Pabst WL, Warejko JK, Daga A, Basta T, Matejas V, Scharmann K, Kienast SD, Behnam B, Beeson B, Begtrup A, Bruce M, Ch'ng GS, Lin SP, Chang JH, Chen CH, Cho MT, Gaffney PM, Gipson PE, Hsu CH, Kari JA, Ke YY, Kiraly-Borri C, Lai WM, Lemyre E, Littlejohn RO, Masri A, Moghtaderi M, Nakamura K, Ozaltin F, Praet M, Prasad C, Prytula A, Roeder ER, Rump P, Schnur RE, Shiihara T, Sinha MD, Soliman NA, Soulami K, Sweetser DA, Tsai WH, Tsai JD, Topaloglu R, Vester U, Viskochil DH, Vatanavicharn N, Waxler JL, Wierenga KJ, Wolf MTF, Wong SN, Leidel SA, Truglio G, Dedon PC, Poduri A, Mane S, Lifton RP, Bouchard M, Kannu P, Chitayat D, Magen D, Callewaert B, van Tilbeurgh H, Zenker M, Antignac C, Hildebrandt F. Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly. Nat Genet. 2017;49: 1529-1538.
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Warejko JK, Tan W, Daga A, Schapiro D, Lawson JA, Shril S, Lovric S, Ashraf S, Rao J, Hermle T, Jobst-Schwan T, Widmeier E, Majmundar AJ, Schneider R, Gee HY, Schmidt JM, Vivante A, van der Ven AT, Ityel H, Chen J, Sadowski CE, Kohl S, Pabst WL, Nakayama M, Somers MJG, Rodig NM, Daouk G, Baum M, Stein DR, Ferguson MA, Traum AZ, Soliman NA, Kari JA, El Desoky S, Fathy H, Zenker M, Bakkaloglu SA, Müller D, Noyan A, Ozaltin F, Cadnapaphornchai MA, Hashmi S, Hopcian J, Kopp JB, Benador N, Bockenhauer D, Bogdanovic R, Stajić N, Chernin G, Ettenger R, Fehrenbach H, Kemper M, Munarriz RL, Podracka L, Büscher R, Serdaroglu E, Tasic V, Mane S, Lifton RP, Braun DA, Hildebrandt F. Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome. Clin J Am Soc Nephrol 2018;13: 53-62.
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Topaloglu R, Batu ED, Yıldız Ç, Korkmaz E, Özen S, Beşbaş N, Özaltın F. Familial Mediterranean fever patients homozygous for E148Q variant may have milder disease. Int J Rheum Dis. 2018;21:1857-1862.
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Çakar N, Ozcakar ZB, Ozaltin F, Koyun M, Celikel Acar B, Bahat E, Gulhan B, Korkmaz E, Yurt A, Yılmaz S, Soylemezoglu O, Yalcinkaya F. Atypical Hemolytic Uremic Syndrome in Children Aged <2 Years. Nephron. 2018;139: 211-218.
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Fidan K, Göknar N, Gülhan B, Melek E, Yıldırım ZY, Baskın E, Hayran M, Gülleroglu K, Özçakar ZB, Ozaltin F, Soylemezoglu O. Extra-Renal manifestations of atypical hemolytic uremic syndrome in children. Pediatr Nephrol 2018;33:1395-1403.
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Akyol A, Güner G, Özşeker HS, Işık A, Atcı Ö, Uzun S, Atayar E, Ozaltin F, Gedikoğlu G, Sökmensüer C, Fearon ER. An immunohistochemical approach to detect oncogenic CTNNB1 mutations in primary neoplastic tissues. Lab Invest 2019; 99: 128-137.
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Eroglu FK, Ozaltin F, Gönç N, Nalçacıoğlu H, Özçakar ZB, Yalnızoğlu D, Güçer Ş, Orhan D, Eminoğlu FT, Göçmen R, Alikaşifoğlu A, Topaloğlu R, Düzova A. Response to Early Coenzyme Q10 Supplementation Is not Sustained in CoQ10 Deficiency Caused by CoQ2 Mutation. Pediatr Neurol 2018; 88: 71-74.
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Topaloğlu R, Gülhan B, Çelegen K, İnözü M, Hayran M, Düzova A, Ozaltin F. Rituximab for Children With Difficult-to-Treat Nephrotic Syndrome: Its Effects on Disease Progression and Growth. Front Pediatr 2019; 7: 313.
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Eroglu FK, Orhan D, İnözü M, Duzova A, Gulhan B, Ozaltin F, Topaloglu R. CD80 expression and infiltrating regulatory T cells in idiopathic nephrotic syndrome of childhood. Pediatr Int. 2019; 61: 1250-1256.
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Peker O, Aki FT, Kumbasar U, Guvener M, Yılmaz M, Dogan R, Ozaltin F, Duzova A, Topaloglu R, Peynircioglu B, Demircin M. Surgical management of renovascular hypertension in children and young adults: a 13-year experience. Interact Cardiovasc Thorac Surg 2019; 29: 746-752.
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Atmaca M, Gülhan B, Atayar E, Bayazıt AK, Candan C, Arıcı M, Topaloğlu R, Özaltın F. 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. Turk J Pediatr 2019; 61: 657-663.
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Ozdemir G, Gulhan B, Atayar E, Saygılı S, Soylemezoglu O, Ozcakar ZB, Eroglu FK, Candan C, Demir BK, Soylu A, Yüksel S, Alpay H, Agbas A, Duzova A, Hayran M, Ozaltin F, Topaloglu R. COL4A3 mutation is an independent risk factor for poor prognosis in children with Alport syndrome. Pediatr Nephrol 2020; 35: 1941-1952.
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Yüksel S, Işık Gönül İ, Canpolat N, Gökçe İ, Gülfem Özlü S, Birsin Özçakar Z, Ozaltin F, Söylemezoğlu O. Renal Biopsy Prognostic Findings in Children With Atypical Hemolytic Uremic Syndrome. Pediatr Dev Pathol. 2020; 23: 362-371.
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Lipska-Ziętkiewicz BS, Ozaltin F, Hölttä T, Bockenhauer D, Bérody S, Levtchenko E, Vivarelli M, Webb H, Haffner D, Schaefer F, Boyer O. Genetic aspects of congenital nephrotic syndrome: a consensus statement from the ERKNet-ESPN inherited glomerulopathy working group. Eur J Hum Genet 2020; 28: 1368-1378.
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Saygili S, Atayar E, Canpolat N, Elicevik M, Kurugoglu S, Sever L, Caliskan S, Ozaltin F. A homozygous HOXA11 variation as a potential novel cause of autosomal recessive CAKUT. Clin Genet. 2020; 98: 390-395.
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Topaloglu R, Keser AG, Gülhan B, Ozaltin F, Demir H, Çiftci T, Demir N, Temucin ÇM, Yuce A, Akhan O. Cystinosis beyond kidneys: gastrointestinal system and muscle involvement. BMC Gastroenterol. 2020;20: 242.
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Tastemel Ozturk T, Kanbur N, Ozmert EN, Gulhan B, Ozaltin F, Topaloglu R, Duzova A. Predictors for the use of herbal and dietary supplements in children and adolescents with kidney and urinary tract diseases. Eur J Pediatr. 2020;180: 253-262.
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Çetinkaya PG, Gülhan B, Düzova A, Beşbaş N, Hayran M, Topaloğlu R, Özaltın F. Clinical characteristics of children with congenital anomalies of the kidney and urinary tract and predictive factors of chronic kidney disease. Turk J Pediatr. 2020;62(5):746-755.
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Özçakar ZB, Ozaltin F, Gülhan B, Çomak E, Parmaksız G, Baskın E, Topaloğlu R, Kasap Demir B, Canpolat N, Yuruk Yildirim Z, Demircioğlu Kılıç B, Yüksel S, Söylemezoğlu O. Transplantation in pediatric aHUS within the era of eculizumab therapy. Pediatr Transplant. 2020;25: e13914.
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Asi T, Düzova A, Doğan HS, Karakurt G, Bahadır ÖF, Bozacı AC, Gülhan B, Özaltın F, Aki FT, Tekgül S, Topaloğlu R. Determinants of outcomes in chronic pediatric peritoneal dialysis: a single center experience. Turk J Pediatr. 2020;62: 940-948.
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Boyer O, Schaefer F, Haffner D, Bockenhauer D, Hölttä T, Bérody S, Webb H, Heselden M, Lipska-Zie Tkiewicz BS, Ozaltin F, Levtchenko E, Vivarelli M. Management of congenital nephrotic syndrome: consensus recommendations of the ERKNet-ESPN Working Group. Nat Rev Nephrol. 2021;17: 277-289.
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Demir S, Gülhan B, Özen S, Çeleğen K, Batu ED, Taş N, Orhan D, Bilginer Y, Düzova A, Ozaltin F, Topaloğlu R. Long term renal survival of pediatric patients with lupus nephritis. Nephrol Dial Transplant. 2022; 37(6): 1069-1077.
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Emma F, Hoff WV, Hohenfellner K, Topaloglu R, Greco M, Ariceta G, Bettini C, Bockenhauer D, Veys K, Pape L, Hulton S, Collin S, Ozaltin F, Servais A, Deschênes G, Novo R, Bertholet-Thomas A, Oh J, Cornelissen E, Janssen M, Haffner D, Ravà L, Antignac C, Devuyst O, Niaudet P, Levtchenko E. An international cohort study spanning five decades assessed outcomes of nephropathic cystinosis. Kidney Int. 2021; 100: 1112-1123.
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Canpolat N, Liu D, Atayar E, Saygili S, Kara NS, Westfall TA, Ding Q, Brown BJ, Braun TA, Slusarski D, Karli Oguz K, Ozluk Y, Tuysuz B, Tastemel Ozturk T, Sever L, Sezerman OU, Topaloglu R, Caliskan S, Attanasio M, Ozaltin F. A splice site mutation in the TSEN2 causes a new syndrome with craniofacial and central nervous system malformations, and atypical hemolytic uremic syndrome. Clin Genet. 2022; 101: 346-358.
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Özlü SG, Gülhan B, Aydoğ Ö, Atayar E, Delibaş A, Parmaksız G, Özdoğan EB, Çomak E, Taşdemir M, Acar B, Özçakar ZB, Topaloğlu R, Söylemezoğlu O, Özaltın F. Could plasma based therapies still be considered in ed cases with atypical hemolytic uremic syndrome? Turk J Pediatr. 2021;63: 986-993.
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Airik M, McCourt B, Ozturk TT, Huynh AB, Zhang X, Tometich JT, Topaloglu R, Ozen H, Orhan D, Nejak-Bowen K, Monga SP, Hand TW, Ozaltin F, Airik R. Mitigation of portal fibrosis and cholestatic liver disease in ANKS6-deficient livers by macrophage depletion FASEB J. 2022 Feb;36(2): e22157.
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Yılmaz EK, Saygili S, Gulhan B, Canpolat N, Bayazıt AK, Kilic BD, Akıncı N, Benzer M, Goknar N, Tufan AK, Kalyoncu M, Nalcacioglu H, Tekcan D, Yıldız G, Agbas A, Nayır A, Topaloglu R, Caliskan S, Ozaltin F. A broad clinical spectrum of PLCε1-related kidney disease and intrafamilial variability. Pediatr Nephrol. 2022; 37(8): 1855-1866.
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Baskin E, Fidan K, Gulhan B, Gulleroglu K, Canpolat N, Yilmaz A, Parmakiz G, Özçakar ZB, Ozaltin F, Soylemezoglu O. Eculizumab treatment and discontinuation in pediatric patients with atypical hemolytic uremic syndrome: a multicentric retrospective study. J Nephrol 2022; 37(8): 1855-1866.
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Sena Ozbay H, Yabanoglu-Ciftci S, Baysal I, Gultekinoglu M, Can Eylem C, Ulubayram K, Nemutlu E, Topaloglu R, Ozaltin F. Mitochondria-Targeted CoQ 10 Loaded PLGA-b-PEG-TPP Nanoparticles: Their Effects on Mitochondrial Functions of COQ8B -/- HK-2 cells. Eur J Pharm Biopharm. 2022; 173: 22-33.
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Kaykı G, Orhan D, Gülhan B, Topaloğlu R, Akçören Z, Düzova A, Özaltın F, Özen S, Bilginer Y, Güçer Ş. Glomerulonephritis with crescents in childhood; etiologies and significance of M2 macrophages. Turk J Pediatr 2022;64: 59-68
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Drovandi S, Lipska-Ziętkiewicz BS, Ozaltin F, Emma F, Gulhan B, Boyer O, Trautmann A, Ziętkiewicz S, Xu H, Shen Q, Rao J, Riedhammer KM, Heemann U, Hoefele J, Stenton SL, Tsygin AN, Ng KH, Fomina S, Benetti E, Aurelle M, Prikhodina L, Schijvens AM, Tabatabaeifar M, Jankowski M, Baiko S, Mao J, Feng C, Deng F, Rousset-Rouviere C, Stańczyk M, Bałasz-Chmielewska I, Fila M, Durkan AM, Levart TK, Dursun I, Esfandiar N, Haas D, Bjerre A, Anarat A, Benz MR, Talebi S, Hooman N, Ariceta G; PodoNet Consortium; mitoNET Consortium; CCGKDD Consortium, Schaefer F. Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy. Kidney Int. 2022; 102 (3): 592-603.
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Gurbanov A, Gülhan B, Kuşkonmaz B, Okur FV, Ozaltin F, Düzova A, Çetinkaya DU, Topaloglu R. Predictors of kidney complications and analysis of hypertension in children with allogeneic hematopoietic stem cell transplantation. Pediatr Nephrol. 2023; 38: 461-469.
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Drovandi S, Lipska-Ziętkiewicz BS, Ozaltin F, Emma F, Gulhan B, Boyer O, Trautmann A, Xu H, Shen Q, Rao J, Riedhammer KM, Heemann U, Hoefele J, Stenton SL, Tsygin AN, Ng KH, Fomina S, Benetti E, Aurelle M, Prikhodina L, Schreuder MF, Tabatabaeifar M, Jankowski M, Baiko S, Mao J, Feng C, Liu C, Sun S, Deng F, Wang X, Clavé S, Stańczyk M, Bałasz-Chmielewska I, Fila M, Durkan AM, Levart TK, Dursun I, Esfandiar N, Haas D, Bjerre A, Anarat A, Benz MR, Talebi S, Hooman N, Ariceta G; PodoNet Consortium; MitoNet Consortium; CCGKDD Consortium, Schaefer F. Oral Coenzyme Q10 supplementation leads to better preservation of kidney function in steroid resistant nephrotic syndrome due to primary Coenzyme Q10 deficiency. Kidney Int. 2022; 102: 604-612.
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Tastemel Ozturk T, Canpolat N, Saygili S, Bayrakci US, Soylemezoglu O, Ozaltin F, Topaloglu R. A rare cause of nephrotic syndrome-sphingosine-1-phosphate lyase (SGPL1) deficiency: 6 cases and a review of the literature. Pediatr Nephrol. 2023; 38: 711-719.
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Sener S, Basaran O, Batu ED, Atalay E, Esenboga S, Cagdas D, Kuskonmaz BB, Bilginer Y, Ozaltin F, Oguz B, Duzova A, Tezcan I, Ozen S. Childhood-onset Takayasu arteritis and immunodeficiency: case-based review. Clin Rheumatol. 2022 Sep;41(9):2883-2892. doi: 10.1007/s10067-022-06295-9. Epub 2022 Jul 20.
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Trautmann A, Seide S, Lipska-Ziętkiewicz BS, Ozaltin F, Szczepanska M, Azocar M, Jankauskiene A, Zurowska A, Caliskan S, Saeed B, Morello W, Emma F, Litwin M, Tsygin A, Fomina S, Wasilewska A, Melk A, Benetti E, Gellermann J, Stajic N, Tkaczyk M, Baiko S, Prikhodina L, Csaicsich D, Medynska A, Krisam R, Breitschwerdt H, Schaefer F; PodoNet Consortium. Outcomes of steroid-resistant nephrotic syndrome in children not treated with intensified immunosuppression Pediatr Nephrol. 2022 Oct 31. doi: 10.1007/s00467-022-05762-4. Online ahead of print.
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Tutal O, Gulhan B, Atayar E, Yuksel S, Ozcakar ZB, Soylemezoglu O, Saygili S, Caliskan S, Inozu M, Baskin E, Duzova A, Hayran M, Topaloglu R, Ozaltin F. The Clinical and Mutational Spectrum of 69 Turkish Children with Autosomal Recessive or Autosomal Dominant Polycystic Kidney Disease: A Multicenter Retrospective Cohort Study. Nephron. 2023 Jan 19:1-14. doi: 10.1159/000528258
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Nemutlu E; Ozaltin F; Yabanoglu-Ciftci S; Gulhan B; Eylem CC; Baysal I; Gök-Topak ED; Ulubayram K; Sezerman OU; Ucar G; Kır S; Topaloglu R. Metabolomic Analyses to Identify Candidate Biomarkers of Cystinosis.Int. J. Mol. Sci. 2023, 24 (3): 2603
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Ay E, Gurses E, Aslan F, Gulhan B, Alniacik A, Duzova A, Bajin MD, Sennaroglu L, Genc GA, Ozaltin F, Topaloglu R. Hearing Loss Related to Gene Mutations in Distal Renal Tubular Acidosis. Audiol Neurootol. 2023; 28: 350-359.
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Gülçek ÖN, Gülhan B, Kesici S, Kurt Şükür ED, Hayran M, Ozaltin F, Duzova A, Bayrakçı B, Topaloglu R. Long-term kidney follow-up after pediatric acute kidney support therapy for children less than 15 kg. Pediatr Nephrol. 2023; 38: 3811-3821.
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Özdemir G, Gülhan B, Kurt-Şükür ED, Atayar E, Atan R, Dursun İ, Özçakar ZB, Saygılı S, Soylu A, Söylemezoğlu O, Yılmaz A, Bayazıt AK, Kara Eroğlu F, Kasap Demir B, Yüksel S, Tabel Y, Ağbaş A, Düzova A, Hayran M, Özaltın F, Topaloğlu R. The outcomes of renin-angiotensin-aldosterone system inhibition and immunosuppressive therapy in children with X-linked Alport syndrome. Turk J Pediatr. 2023;65(3): 456-468.
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Saygılı S, Koşukcu C, Baştuğ T, Doğan ÖA, Yılmaz EK, Kalyoncu AU, Ağbaş A, Canpolat N, Çalışkan S, Ozaltin F. A novel homozygous missense variant in TBC1D31 in a consanguineous family with congenital anomalies of the kidney and urinary tract (CAKUT). Clin Genet. 2023; 104: 679-685.
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Baltu D, Salancı BV, Gülhan B, Özaltın F, Düzova A, Topaloğlu R. Albuminuria is associated with 24-hour and night-time diastolic blood pressure in urinary tract infection with renal scarring. Turk J Pediatr. 2023;65(4): 620-629.
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Tastemel Ozturk T, Düzova A, Oygar PD, Baltu D, Ozcilingir Hakverdi P, Lacinel Gurlevik S, Kurt-Sukur ED, Aykan HH, Ozen S, Ertugrul I, Kesici S, Gulhan B, Ozaltin F, Ozsurekci Y, Cengiz AB, Topaloglu R. Acute kidney injury in children with moderate-severe COVID-19 and multisystem inflammatory syndrome in children: a referral center experience. Pediatr Nephrol. 2024;39(3): 867-877.
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Baysal İ, Yabanoglu-Ciftci S, Nemutlu E, Eylem CC, Gök-Topak ED, Ulubayram K, Kır S, Gulhan B, Uçar G, Ozaltin F, Topaloglu R. Omic Studies on In Vitro Cystinosis Model: siRNA-Mediated CTNS Gene Silencing in HK-2 Cells. Lab Invest. 2024 Jan;104(1):100287.
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Baltu D, Kurt-Sukur ED, Tastemel Ozturk T, Gulhan B, Ozaltin F, Duzova A, Topaloglu R. COVID-19 in Children with Chronic Kidney Disease; Does it Differ Much? Klin Padiatr. 2024 Jan 15. doi: 10.1055/a-2207-3153.
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Riedhammer KM, Nguyen TT, Koşukcu C, Calzada-Wack J, Li Y, Batzir NA, Saygılı S, Wimmers V, Kim GJ, Chrysanthou M, Bakey Z, Sofrin-Drucker E, Kraiger M, Sanz-Moreno A, Amarie OV, Rathkolb B, Klein-Rodewald T, Garrett L, Hölter SM, Seisenberger C, Haug S, Schlosser P, Marschall S, Wurst W, Fuchs H, Gailus-Durner V, Wuttke M, de Angelis MH, Ćomić J, Doğan ÖA, Özlük Y, Taşdemir M, Ağbaş A, Canpolat N, Orenstein N, Çalışkan S, Weber RG, Bergmann C, Jeanpierre C, Saunier S, Lim TY, Hildebrandt F, Alhaddad B, Basel-Salmon L, Borovitz Y, Wu K, Antony D, Matschkal J, Schaaf CW, Renders L, Schmaderer C, Rogg M, Schell C, Meitinger T, Heemann U, Köttgen A, Arnold SJ, Ozaltin F, Schmidts M, Hoefele J. Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT). Kidney Int 2024; 105: 844-864.
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Gülhan B, Özaltın F, Fidan K, Özçakar ZB, Söylemezoğlu O. Management of pediatric hemolytic uremic syndrome. Turk J Pediatr. 2024;66(1):1-16.
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Kachmar J, Boyer O, Lipska-Zie˛tkiewicz B , Morinière V , Gribouval O , Heidet L , Balasz-Chmielewska I , Benetti E , Cloarec S , Csaicsich D , Decramer S , Gellermann J, Guigonis V, Hogan J, Karabay Bayazit A, Melk A, Nigmatullina N, Oh J, Ozaltin F, Ranchin B, Tsimaratos M, Trautmann A, Antignac C , Schaefer F and Dorval G ; on behalf of the PodoNet Network. Steroid-Resistant Nephrotic Syndrome due to NPHS2 Variants Is Not Associated With Posttransplant Recurrence. Kidney International Reports 2024; 9, 973–981.
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Gülhan B, Ekici O, Dursun İ, Göknar N, Yüksel S, Alaygut D, Özçakar ZB, Nalçacıoğlu H, Demircioğlu Kılıç B, Söylemezoğlu O, Duzova A, Topaloglu R, Ozaltin F. Variable phenotype and genotype of pediatric patients with HNF1B nephropathy. Clin Nephrol. 2024 May 3. doi: 10.5414/CN111310.
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