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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, Balasz-Chmielewska I, Benetti E, Cloarec S, Csaicsich D, Decramer S, Gellermann J, Guigonis V, Hogan J, Bayazit AK, Melk A, Nigmatullina N, Oh J, Ozaltin F, Ranchin B, Tsimaratos M, Trautmann A, Antignac C, Schaefer F, Dorval G; PodoNet Network. Kachmar J, et al. Among authors: ozaltin f. Kidney Int Rep. 2024 Jan 10;9(4):973-981. doi: 10.1016/j.ekir.2024.01.005. eCollection 2024 Apr. Kidney Int Rep. 2024. PMID: 38765578 Free PMC article.
Adolescence-onset atypical hemolytic uremic syndrome: is it different from infant-onset?
Celegen K, Gulhan B, Fidan K, Yuksel S, Yilmaz N, Yılmaz AC, Demircioğlu Kılıç B, Gokce I, Kavaz Tufan A, Kalyoncu M, Nalcacıoglu H, Ozlu SG, Kurt Sukur ED, Canpolat N, K Bayazit A, Çomak E, Tabel Y, Tulpar S, Celakil M, Bek K, Zeybek C, Duzova A, Ozcakar B, Topaloglu R, Soylemezoglu O, Ozaltin F. Celegen K, et al. Among authors: ozaltin f. Clin Exp Nephrol. 2024 May 5. doi: 10.1007/s10157-024-02505-7. Online ahead of print. Clin Exp Nephrol. 2024. PMID: 38704765
Variable phenotype and genotype of pediatric patients with HNF1B nephropathy.
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. Gülhan B, et al. Among authors: ozaltin f. Clin Nephrol. 2024 May 3. doi: 10.5414/CN111310. Online ahead of print. Clin Nephrol. 2024. PMID: 38699986
Management of pediatric hemolytic uremic syndrome.
Gülhan B, Özaltın F, Fidan K, Özçakar ZB, Söylemezoğlu O. Gülhan B, et al. Among authors: ozaltin f. Turk J Pediatr. 2024;66(1):1-16. doi: 10.24953/turkjped.2023.596. Turk J Pediatr. 2024. PMID: 38523374 Free article. Review.
COVID-19 in Children with Chronic Kidney Disease; Does it Differ Much?
Baltu D, Kurt-Sukur ED, Tastemel Ozturk T, Gulhan B, Ozaltin F, Duzova A, Topaloglu R. Baltu D, et al. Among authors: ozaltin f. Klin Padiatr. 2024 Jan 15. doi: 10.1055/a-2207-3153. Online ahead of print. Klin Padiatr. 2024. PMID: 38224686 English.
Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT).
Riedhammer KM, Nguyen TT, Koşukcu C, Calzada-Wack J, Li Y, Assia Batzir N, 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, Hrabe de Angelis M, Ćomić J, Akgün Doğan Ö, 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. Riedhammer KM, et al. Among authors: ozaltin f. Kidney Int. 2024 Apr;105(4):844-864. doi: 10.1016/j.kint.2023.11.032. Epub 2023 Dec 26. Kidney Int. 2024. PMID: 38154558 Free PMC article.
189 results