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Evaluation of vitamin D levels in children and adolescents after the first year of the COVID-19 pandemic: 1-year results of a secondary-level state hospital.
Arch Pediatr. 2024 Apr;31(3):179-182. doi: 10.1016/j.arcped.2023.11.001. Epub 2024 Mar 26.
Arch Pediatr. 2024.
PMID: 38538466
Changes in the presentation of newly diagnosed type 1 diabetes in children during the COVID-19 pandemic in a tertiary center in Southern Turkey.
Dilek SÖ, Gürbüz F, Turan İ, Celiloğlu C, Yüksel B.
Dilek SÖ, et al.
J Pediatr Endocrinol Metab. 2021 Jul 22;34(10):1303-1309. doi: 10.1515/jpem-2021-0287. Print 2021 Oct 26.
J Pediatr Endocrinol Metab. 2021.
PMID: 34291625
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Increased Severe Cases and New-Onset Type 1 Diabetes Among Children Presenting With Diabetic Ketoacidosis During First Year of COVID-19 Pandemic in Turkey.
Kiral E, Kirel B, Havan M, Keskin M, Karaoglan M, Yildirim A, Kangin M, Talay MN, Urun T, Altug U, Kesici S, Tufan E, Kacmaz E, Bozan G, Azapagasi E, Uysal Yazici M, Ozturk Z, Yesilbas O, Karaguzel G, Kaya G, Barlas U, Duyu M, Boyraz M, Sevketoglu E, Akcay N, Hancili S, Guven A, Dursun O, Ulgen Tekerek N, Ozcifci G, Yazici P, Turanli E, Kendirli T, Kahveci F, Yetimakman AF, Citak A, Şik G, Bingol I, Aygun F, Durak C, Yilmaz R, Bugrul F, Sari Y, Tekguç H, Albayrak H, Yener N, Agin H, Soydan E, Yildizdas D, Dilek SO, Yalindag N, Incekoy-Girgin F, Alacakir N, Tutunculer F, Arslanaoglu MO, Aydin C, Bilgin M, Simsek E, Dinleyici EC.
Kiral E, et al. Among authors: dilek so.
Front Pediatr. 2022 Jun 29;10:926013. doi: 10.3389/fped.2022.926013. eCollection 2022.
Front Pediatr. 2022.
PMID: 35844756
Free PMC article.
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Natural history of ENPP1 deficiency: Nationwide Turkish Cohort Study of autosomal-recessive hypophosphataemic rickets type 2.
Dursun F, Turan İ, Bitkin EÇ, Bayramoğlu E, Çayır A, Erdeve ŞS, Çakır EDP, Çamtosun E, Dilek SO, Kırmızıbekmez H, Eser M, Türkyılmaz A, Karagüzel G.
Dursun F, et al. Among authors: dilek so.
Clin Endocrinol (Oxf). 2024 Feb 7. doi: 10.1111/cen.15028. Online ahead of print.
Clin Endocrinol (Oxf). 2024.
PMID: 38324408
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Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism.
Kotan LD, Ternier G, Cakir AD, Emeksiz HC, Turan I, Delpouve G, Kardelen AD, Ozcabi B, Isik E, Mengen E, Cakir EDP, Yuksel A, Agladioglu SY, Dilek SO, Evliyaoglu O, Darendeliler F, Gurbuz F, Akkus G, Yuksel B, Giacobini P, Topaloglu AK.
Kotan LD, et al. Among authors: dilek so.
Genet Med. 2021 Jun;23(6):1008-1016. doi: 10.1038/s41436-020-01087-5. Epub 2021 Jan 25.
Genet Med. 2021.
PMID: 33495532
Free PMC article.
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