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Page 1
Mutations in BTD gene causing biotinidase deficiency: a regional report.
Kasapkara ÇS, Akar M, Özbek MN, Tüzün H, Aldudak B, Baran RT, Tanyalçın T. Kasapkara ÇS, et al. Among authors: tuzun h. J Pediatr Endocrinol Metab. 2015 Mar;28(3-4):421-4. doi: 10.1515/jpem-2014-0056. J Pediatr Endocrinol Metab. 2015. PMID: 25423671
Clinical characteristics and molecular genetic analysis of 22 patients with neonatal diabetes from the South-Eastern region of Turkey: predominance of non-KATP channel mutations.
Demirbilek H, Arya VB, Ozbek MN, Houghton JA, Baran RT, Akar M, Tekes S, Tuzun H, Mackay DJ, Flanagan SE, Hattersley AT, Ellard S, Hussain K. Demirbilek H, et al. Among authors: tuzun h. Eur J Endocrinol. 2015 Jun;172(6):697-705. doi: 10.1530/EJE-14-0852. Epub 2015 Mar 9. Eur J Endocrinol. 2015. PMID: 25755231 Free PMC article.
Sirolimus-Induced Hepatitis in Two Patients with Hyperinsulinemic Hypoglycemia.
Haliloğlu B, Tüzün H, Flanagan SE, Çelik M, Kaya A, Ellard S, Özbek MN. Haliloğlu B, et al. Among authors: tuzun h. J Clin Res Pediatr Endocrinol. 2018 Jul 31;10(3):279-283. doi: 10.4274/jcrpe.5335. Epub 2017 Dec 8. J Clin Res Pediatr Endocrinol. 2018. PMID: 29217498 Free PMC article.
Folate deficiency in patients with classical galactosemia: A novel finding that needs to be considered for dietary treatments.
Çelik M, Özgün N, Akdeniz O, Fidan M, Tüzün H, İpek MŞ, Emecan M, Eminoğlu FT. Çelik M, et al. Among authors: tuzun h. Turk J Pediatr. 2018;60(5):540-546. doi: 10.24953/turkjped.2018.05.011. Turk J Pediatr. 2018. PMID: 30968626 Free article.
Celik M, Ozgun N, Akdeniz O, Fidan M, Tuzun H, Ipek MS, Emecan M, Eminoglu FT. Folate deficiency in patients with classical galactosemia: A novel finding that needs to be considered for dietary treatments. ...
Celik M, Ozgun N, Akdeniz O, Fidan M, Tuzun H, Ipek MS, Emecan M, Eminoglu FT. Folate deficiency in patients with classical ga …
71 results