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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: saygili s. 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.
Proteinuria in a patient with Graves' disease: Questions.
Dagdeviren Cakir A, Canpolat N, Saygili S, Kilicaslan I, Turan H, Ercan O, Evliyaoglu O. Dagdeviren Cakir A, et al. Among authors: saygili s. Pediatr Nephrol. 2019 Aug;34(8):1379-1381. doi: 10.1007/s00467-019-04220-y. Epub 2019 Mar 6. Pediatr Nephrol. 2019. PMID: 30843109 No abstract available.
Proteinuria in a patient with Graves' disease: Answers.
Dagdeviren Cakir A, Canpolat N, Saygili S, Kilicaslan I, Turan H, Ercan O, Evliyaoglu O. Dagdeviren Cakir A, et al. Among authors: saygili s. Pediatr Nephrol. 2019 Aug;34(8):1383-1385. doi: 10.1007/s00467-019-04221-x. Epub 2019 Mar 6. Pediatr Nephrol. 2019. PMID: 30843111 No abstract available.
A rare cause of proteinuria after kidney transplantation: Questions.
Göknar N, Saygılı S, Canpolat N, Özlük Y, Kılıçaslan I, Sever L, Çalışkan S. Göknar N, et al. Among authors: saygili s. Pediatr Nephrol. 2019 Nov;34(11):2331-2332. doi: 10.1007/s00467-019-04262-2. Epub 2019 Apr 30. Pediatr Nephrol. 2019. PMID: 31041518 No abstract available.
A rare cause of proteinuria after kidney transplantation: Answers.
Göknar N, Saygılı S, Canpolat N, Özlük Y, Kılıçaslan I, Sever L, Çalışkan S. Göknar N, et al. Among authors: saygili s. Pediatr Nephrol. 2019 Nov;34(11):2333-2335. doi: 10.1007/s00467-019-04263-1. Epub 2019 Apr 30. Pediatr Nephrol. 2019. PMID: 31041519 No abstract available.
COL4A3 mutation is an independent risk factor for poor prognosis in children with Alport syndrome.
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. Ozdemir G, et al. Among authors: saygili s. Pediatr Nephrol. 2020 Oct;35(10):1941-1952. doi: 10.1007/s00467-020-04574-8. Epub 2020 May 11. Pediatr Nephrol. 2020. PMID: 32394188
86 results