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2017 2
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2019 3
2020 1
2021 1
2023 0
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Page 1
Molecular Diagnosis of Monogenic Diabetes and Their Clinical/Laboratory Features in Turkish Children.
Gökşen D, Yeşilkaya E, Özen S, Kor Y, Eren E, Korkmaz Ö, Berberoğlu M, Karagüzel G, Er E, Abacı A, Evliyaoğlu O, Akbaş ED, Ünal E, Bolu S, Nalbantoğlu Ö, Anık A, Tayfun M, Büyükinan M, Abalı S, Can Yılmaz G, Kor D, Söbü E, Şıklar Z, Polat R, Darcan Ş. Gökşen D, et al. Among authors: akbas ed. J Clin Res Pediatr Endocrinol. 2021 Nov 25;13(4):433-438. doi: 10.4274/jcrpe.galenos.2021.2021.0056. Epub 2021 Jul 8. J Clin Res Pediatr Endocrinol. 2021. PMID: 34250910 Free PMC article.
Autoimmune Limbic Encephalitis Associated with Type 1 Diabetes Mellitus.
Akın O, Kılınç Uğurlu A, Akbaş ED, Döğer E, Akbaş Y, Bideci A, Yüce Ö, Gücüyener K, Çamurdan MO, Karabacak N, Cinaz P. Akın O, et al. Among authors: akbas ed. J Clin Res Pediatr Endocrinol. 2017 Dec 15;9(4):387-388. doi: 10.4274/jcrpe.3818. Epub 2017 Jul 17. J Clin Res Pediatr Endocrinol. 2017. PMID: 28720552 Free PMC article. No abstract available.
Clinical Characteristics and Long-term Follow-up of Patients with Diabetes Due To PTF1A Enhancer Mutations.
Demirbilek H, Cayir A, Flanagan SE, Yıldırım R, Kor Y, Gurbuz F, Haliloğlu B, Yıldız M, Baran RT, Akbas ED, Demiral M, Ünal E, Arslan G, Vuralli D, Buyukyilmaz G, Al-Khawaga S, Saeed A, Al Maadheed M, Khalifa A, Onal H, Yuksel B, Ozbek MN, Bereket A, Hattersley AT, Hussain K, De Franco E. Demirbilek H, et al. Among authors: akbas ed. J Clin Endocrinol Metab. 2020 Dec 1;105(12):e4351-9. doi: 10.1210/clinem/dgaa613. J Clin Endocrinol Metab. 2020. PMID: 32893856 Free PMC article.
Clinical and Laboratory Characteristics of Hyperprolactinemia in Children and Adolescents: National Survey.
Eren E, Törel Ergür A, İşgüven ŞP, Çelebi Bitkin E, Berberoğlu M, Şıklar Z, Baş F, Yel S, Baş S, Söbü E, Bereket A, Turan S, Sağlam H, Atay Z, Ercan O, Güran T, Atabek ME, Korkmaz HA, Kılınç Uğurlu A, Akıncı A, Döğer E, Şimşek E, Akbaş ED, Abacı A, Gül Ü, Acar S, Mengen Uçaktürk E, Yıldız M, Ünal E, Tarım Ö. Eren E, et al. Among authors: akbas ed. J Clin Res Pediatr Endocrinol. 2019 May 28;11(2):149-156. doi: 10.4274/jcrpe.galenos.2018.2018.0206. Epub 2018 Nov 5. J Clin Res Pediatr Endocrinol. 2019. PMID: 30396878 Free PMC article.
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: akbas ed. J Pediatr Endocrinol Metab. 2017 Jul 26;30(7):759-766. doi: 10.1515/jpem-2017-0088. J Pediatr Endocrinol Metab. 2017. PMID: 28672743
Genotype-phenotype correlation, gonadal malignancy risk, gender preference, and testosterone/dihydrotestosterone ratio in steroid 5-alpha-reductase type 2 deficiency: a multicenter study from Turkey.
Abacı A, Çatlı G, Kırbıyık Ö, Şahin NM, Abalı ZY, Ünal E, Şıklar Z, Mengen E, Özen S, Güran T, Kara C, Yıldız M, Eren E, Nalbantoğlu Ö, Güven A, Çayır A, Akbaş ED, Kor Y, Çürek Y, Aycan Z, Baş F, Darcan Ş, Berberoğlu M. Abacı A, et al. Among authors: akbas ed. J Endocrinol Invest. 2019 Apr;42(4):453-470. doi: 10.1007/s40618-018-0940-y. Epub 2018 Aug 21. J Endocrinol Invest. 2019. PMID: 30132287