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Page 1
Implication of FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT).
Riedhammer KM, Nguyen TT, Koşukcu C, Calzada-Wack J, Li Y, Saygılı S, Wimmers V, Kim GJ, Chrysanthou M, Bakey Z, Kraiger M, Sanz-Moreno A, Amarie OV, Rathkolb B, Klein-Rodewald T, Garrett L, Hölter SM, Seisenberger C, Haug S, 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, Ćalışkan S, Weber R, Bergmann C, Jeanpierre C, Saunier S, Lim TY, Hildebrandt F, Alhaddad B, Wu K, Antony D, Matschkal J, Schaaf C, Renders L, Schmaderer C, Meitinger T, Heemann U, Köttgen A, Arnold S, Ozaltin F, Schmidts M, Hoefele J. Riedhammer KM, et al. Among authors: agbas a. medRxiv [Preprint]. 2023 Mar 22:2023.03.21.23287206. doi: 10.1101/2023.03.21.23287206. medRxiv. 2023. Update in: Kidney Int. 2024 Apr;105(4):844-864. doi: 10.1016/j.kint.2023.11.032. PMID: 36993625 Free PMC article. Updated. Preprint.
A nationwide retrospective study in Turkish children with nephrocalcinosis.
Döven SS, Tülpar S, Baştuğ F, Yıldırım ZNY, Yılmaz EK, Çiçek N, Küçük N, Çomak E, Yazıcıoğlu B, Nalçacıoğlu H, Delibaş A, Uysal B, Ağbaş A, Gemici A, Günay N, Ertan P, Bıyıklı N, Hacıhamdioğlu DÖ, Elmacı AM, Atikel YÖ, Delebe EÖÇ, Sever FL, Gökçe İ, Öner N, Akman S, Aksu B, Atmış B, Yel S, Yılmaz A, Çelik B, Dursun İ, Alpay H. Döven SS, et al. Among authors: agbas a. Turk J Med Sci. 2021 Oct;51(5):2564-2569. doi: 10.3906/sag-2103-347. Epub 2021 Oct 21. Turk J Med Sci. 2021. PMID: 34174796 Free article.
Treatment and long-term outcome in primary distal renal tubular acidosis.
Lopez-Garcia SC, Emma F, Walsh SB, Fila M, Hooman N, Zaniew M, Bertholet-Thomas A, Colussi G, Burgmaier K, Levtchenko E, Sharma J, Singhal J, Soliman NA, Ariceta G, Basu B, Murer L, Tasic V, Tsygin A, Decramer S, Gil-Peña H, Koster-Kamphuis L, La Scola C, Gellermann J, Konrad M, Lilien M, Francisco T, Tramma D, Trnka P, Yüksel S, Caruso MR, Chromek M, Ekinci Z, Gambaro G, Kari JA, König J, Taroni F, Thumfart J, Trepiccione F, Winding L, Wühl E, Ağbaş A, Belkevich A, Vargas-Poussou R, Blanchard A, Conti G, Boyer O, Dursun I, Pınarbaşı AS, Melek E, Miglinas M, Novo R, Mallett A, Milosevic D, Szczepanska M, Wente S, Cheong HI, Sinha R, Gucev Z, Dufek S, Iancu D; European dRTA Consortium; Kleta R, Schaefer F, Bockenhauer D. Lopez-Garcia SC, et al. Among authors: agbas a. Nephrol Dial Transplant. 2019 Jun 1;34(6):981-991. doi: 10.1093/ndt/gfy409. Nephrol Dial Transplant. 2019. PMID: 30773598
Congenital erythropoietic porphyria.
Kürkçüoğlu M, Tunç B, Ağbaş A. Kürkçüoğlu M, et al. Among authors: agbas a. Turk J Pediatr. 1985 Jan-Mar;27(1):39-44. Turk J Pediatr. 1985. PMID: 3984055 No abstract available.
84 results