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Page 1
Pediatric kidney care experience after the 2023 Turkey/Syria earthquake.
Bakkaloğlu SA, Delibaş A, Sürmeli Döven S, Taner S, Yavuz S, Erfidan G, Danacı Vatansever E, Aynacı F, Yilmaz K, Taşdemir M, Akacı O, Akıncı N, Güven S, Çiçek N, Dursun I, Keleşoğlu E, Sancaktar M, Alaygut D, Saygılı S, Yavaşcan Ö, Yılmaz A, Gülleroğlu K, Ertan P, Demir BK, Poyrazoğlu H, Pınarbaşı S, Gençler A, Baştuğ F, Günay N, Çeleğen K, Noyan A, Parmaksız G, Avcı B, Çaycı FŞ, Bayrakçı U, Özlü SG, Aksoy ÖY, Yel S, İnal GA, Köse S, Bayazıt AK, Atmış B, Sarıbaş E, Çağlı Ç, Tabel Y, Elmas AT, Zırhlı Selçuk Ş, Demircioğlu Kılıç B, Akbalık Kara M, Büyükçelik M, Balat A, Durucu Tiryaki B, Erdoğdu B, Aksu B, Mahmudova G, Dursun H, Candan C, Göknar N, Mutlubaş F, Çamlar SA, Başaran C, Akbulut BB, Düzova A, Gülhan B, Oruç Ç, Peru H, Alpay H, Türkkan ÖN, Gülmez R, Çelakıl M, Doğan K, Bilge I, Pehlivanoğlu C, Büyükkaragöz B, Leventoğlu E, Alpman N, Zeybek C, Tülpar S, Çiçek Gülşan RY, Kara A, Gürgöze MK, Önder Akyol EN, Özdemir Atikel Y, Pul S, Sönmez F, Yıldız G, Akman S, Elmacı M, Küçük N, Yüksel S, Kavaz A, Nalçacıoğlu H, Alparslan C, Dinçel N, Elhan AH, Sever L. Bakkaloğlu SA, et al. Among authors: mutlubas f. Nephrol Dial Transplant. 2024 Feb 7:gfae033. doi: 10.1093/ndt/gfae033. Online ahead of print. Nephrol Dial Transplant. 2024. PMID: 38327222
Clinical outcome in children with Henoch-Schönlein nephritis.
Mir S, Yavascan O, Mutlubas F, Yeniay B, Sonmez F. Mir S, et al. Among authors: mutlubas f. Pediatr Nephrol. 2007 Jan;22(1):64-70. doi: 10.1007/s00467-006-0278-0. Epub 2006 Sep 21. Pediatr Nephrol. 2007. PMID: 17024391
A novel homozygous W99G mutation in CLDN-16 gene causing familial hypomagnesemic hypercalciuric nephrocalcinosis in Turkish siblings.
Alparslan C, Öncel EP, Akbay S, Alaygut D, Mutlubaş F, Tatlı M, Konrad M, Yavaşcan Ö, Kasap-Demir B. Alparslan C, et al. Among authors: mutlubas f. Turk J Pediatr. 2018;60(1):76-80. doi: 10.24953/turkjped.2018.01.011. Turk J Pediatr. 2018. PMID: 30102483 Free article.
Alparslan C, Oncel EP, Akbay S, Alaygut D, Mutlubas F, Tatli M, Konrad M, Yavascan O, Kasap-Demir B. A novel homozygous W99G mutation in CLDN-16 gene causing familial hypomagnesemic hypercalciuric nephrocalcinosis in Turkish siblings. ...
Alparslan C, Oncel EP, Akbay S, Alaygut D, Mutlubas F, Tatli M, Konrad M, Yavascan O, Kasap-Demir B. A novel homozygous W99G m …
A rare cause of neonatal hypertension: Congenital mesoblastic nephroma.
Soyaltın E, Alaygut D, Alparslan C, Özdemir T, Çamlar SA, Mutlubaş F, Kasap-Demir B, Yavaşcan Ö. Soyaltın E, et al. Among authors: mutlubas f. Turk J Pediatr. 2018;60(2):198-200. doi: 10.24953/turkjped.2018.02.014. Turk J Pediatr. 2018. PMID: 30325129 Free article.
Soyaltin E, Alaygut D, Alparslan C, Ozdemir T, Arslansoyu-Camlar S, Mutlubas F, Kasap-Demir B, Yavascan O. A rare cause of neonatal hypertension: Congenital mesoblastic nephroma. ...
Soyaltin E, Alaygut D, Alparslan C, Ozdemir T, Arslansoyu-Camlar S, Mutlubas F, Kasap-Demir B, Yavascan O. A rare cause of neo …
Periumbilical swelling, erythema, and discharge in a girl: Questions.
Alaygut D, Soyaltin E, Camlar SA, Tekin A, Sayan A, Ozdemir T, Alparslan C, Mutlubas F, Yavascan O, Demir BK. Alaygut D, et al. Among authors: mutlubas f. Pediatr Nephrol. 2020 Mar;35(3):409-410. doi: 10.1007/s00467-019-04353-0. Epub 2019 Sep 16. Pediatr Nephrol. 2020. PMID: 31529152 No abstract available.
59 results