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LRBA deficiency: a rare cause of type 1 diabetes, colitis, and severe immunodeficiency.
Kardelen AD, Kara M, Güller D, Ozturan EK, Abalı ZY, Ceylaner S, Kıykım A, Cantez S, Torun SH, Poyrazoglu S, Bas F, Darendelıler F. Kardelen AD, et al. Among authors: abali zy. Hormones (Athens). 2021 Jun;20(2):389-394. doi: 10.1007/s42000-020-00257-z. Epub 2020 Nov 5. Hormones (Athens). 2021. PMID: 33155142 Review.
Clinical and Hormonal Profiles Correlate With Molecular Characteristics in Patients With 11β-Hydroxylase Deficiency.
Yildiz M, Isik E, Abali ZY, Keskin M, Ozbek MN, Bas F, Ucakturk SA, Buyukinan M, Onal H, Kara C, Storbeck KH, Darendeliler F, Cayir A, Unal E, Anik A, Demirbilek H, Cetin T, Dursun F, Catli G, Turan S, Falhammar H, Baris T, Yaman A, Haklar G, Bereket A, Guran T. Yildiz M, et al. Among authors: abali zy. J Clin Endocrinol Metab. 2021 Aug 18;106(9):e3714-e3724. doi: 10.1210/clinem/dgab225. J Clin Endocrinol Metab. 2021. PMID: 33830237
Clinical, biochemical and genetic features with nonclassical 21-hydroxylase deficiency and final height.
Savaş-Erdeve Ş, Çetinkaya S, Abalı ZY, Poyrazoğlu Ş, Baş F, Berberoğlu M, Sıklar Z, Korkmaz Ö, Buluş D, Akbaş ED, Güran T, Böber E, Akın O, Yılmaz GC, Aycan Z. Savaş-Erdeve Ş, et al. Among authors: abali zy. J Pediatr Endocrinol Metab. 2017 Jul 26;30(7):759-766. doi: 10.1515/jpem-2017-0088. J Pediatr Endocrinol Metab. 2017. PMID: 28672743
19 results