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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: alaygut d. 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: alaygut d. 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. ...
Soyaltin E, Alaygut D, Alparslan C, Ozdemir T, Arslansoyu-Camlar S, Mutlubas F, Kasap-Demir B, Yavascan O. ...
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. 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.
Periumbilical swelling, erythema, and discharge in a girl: Answers.
Alaygut D, Soyaltin E, Camlar SA, Tekin A, Sayan A, Ozdemir T, Alparslan C, Mutlubas F, Yavascan O, Demir BK. Alaygut D, et al. Pediatr Nephrol. 2020 Mar;35(3):411-413. doi: 10.1007/s00467-019-04354-z. Epub 2019 Sep 16. Pediatr Nephrol. 2020. PMID: 31529155 No abstract available.
92 results