Ceylaner S - Search Results

1

Molecular diagnosis of maturity-onset diabetes of the young (MODY) in Turkish children by using targeted next-generation sequencing.

Anık A, Çatlı G, Abacı A, Sarı E, Yeşilkaya E, Korkmaz HA, Demir K, Altıncık A, Tuhan HÜ, Kızıldağ S, Özkan B, Ceylaner S, Böber E. Anık A, et al. Among authors: ceylaner s. J Pediatr Endocrinol Metab. 2015 Nov 1;28(11-12):1265-71. doi: 10.1515/jpem-2014-0430. J Pediatr Endocrinol Metab. 2015. PMID: 26226118

2

A Mutation in INSR in a Child Presenting with Severe Acanthosis Nigricans.

Tuhan H, Ceylaner S, Nalbantoğlu Ö, Acar S, Abacı A, Böber E, Demir K. Tuhan H, et al. Among authors: ceylaner s. J Clin Res Pediatr Endocrinol. 2017 Dec 15;9(4):371-374. doi: 10.4274/jcrpe.4577. Epub 2017 Jun 30. J Clin Res Pediatr Endocrinol. 2017. PMID: 28663160 Free PMC article.

3

A novel missense mutation in HSD17B3 gene in a 46, XY adolescent presenting with primary amenorrhea and virilization at puberty.

Tuhan HU, Anik A, Catli G, Ceylaner S, Dundar B, Bober E, Abaci A. Tuhan HU, et al. Among authors: ceylaner s. Clin Chim Acta. 2015 Jan 1;438:154-6. doi: 10.1016/j.cca.2014.07.025. Epub 2014 Jul 24. Clin Chim Acta. 2015. PMID: 25064799

4

Maturity onset diabetes of youth (MODY) in Turkish children: sequence analysis of 11 causative genes by next generation sequencing.

Ağladıoğlu SY, Aycan Z, Çetinkaya S, Baş VN, Önder A, Peltek Kendirci HN, Doğan H, Ceylaner S. Ağladıoğlu SY, et al. Among authors: ceylaner s. J Pediatr Endocrinol Metab. 2016 Apr;29(4):487-96. doi: 10.1515/jpem-2015-0039. J Pediatr Endocrinol Metab. 2016. PMID: 26669242

5

Molecular and clinical findings of Turkish patients with hereditary fructose intolerance.

Gunduz M, Ünal-Uzun Ö, Koç N, Ceylaner S, Özaydın E, Kasapkara ÇS. Gunduz M, et al. Among authors: ceylaner s. J Pediatr Endocrinol Metab. 2021 Jun 23;34(8):1017-1022. doi: 10.1515/jpem-2021-0303. Print 2021 Aug 26. J Pediatr Endocrinol Metab. 2021. PMID: 34162028

6

Niemann-Pick type C disease with a novel intronic mutation: three Turkish cases from the same family.

Kılıç Yıldırım G, Yarar C, Şeker Yılmaz B, Ceylaner S. Kılıç Yıldırım G, et al. Among authors: ceylaner s. J Pediatr Endocrinol Metab. 2021 Dec 10;35(4):535-541. doi: 10.1515/jpem-2021-0052. Print 2022 Apr 26. J Pediatr Endocrinol Metab. 2021. PMID: 34883004

7

Three cases of Wolfram syndrome with different clinical aspects.

Çamtosun E, Şıklar Z, Kocaay P, Ceylaner S, Flanagan SE, Ellard S, Berberoğlu M. Çamtosun E, et al. Among authors: ceylaner s. J Pediatr Endocrinol Metab. 2015 Mar;28(3-4):433-8. doi: 10.1515/jpem-2014-0139. J Pediatr Endocrinol Metab. 2015. PMID: 25210753

8

Cystinosis in Eastern Turkey.

Doğan M, Bulan K, Kaba S, Cesur Y, Ceylaner S, Ustyol L. Doğan M, et al. Among authors: ceylaner s. J Pediatr Endocrinol Metab. 2016 Aug 1;29(8):965-9. doi: 10.1515/jpem-2014-0477. J Pediatr Endocrinol Metab. 2016. PMID: 27269891

9

Primary systemic carnitine deficiency: a Turkish case with a novel homozygous SLC22A5 mutation and 14 years follow-up.

Yilmaz BS, Kor D, Mungan NO, Erdem S, Ceylaner S. Yilmaz BS, et al. Among authors: ceylaner s. J Pediatr Endocrinol Metab. 2015 Sep;28(9-10):1179-81. doi: 10.1515/jpem-2014-0528. J Pediatr Endocrinol Metab. 2015. PMID: 26030785

10

Clinical findings in five Turkish patients with citrin deficiency and identification of a novel mutation on SLC25A13.

Köse MD, Kagnici M, Özdemir TR, Erdur CB, Erdemir G, Karakoyun M, Guzin Y, Ceylaner S, Genel F. Köse MD, et al. Among authors: ceylaner s. J Pediatr Endocrinol Metab. 2020 Jan 28;33(1):157-163. doi: 10.1515/jpem-2019-0377. J Pediatr Endocrinol Metab. 2020. PMID: 31809266

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