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Page 1
Two novel missense mutations in nonketotic hyperglycinemia.
Yilmaz BS, Kor D, Ceylaner S, Mert GG, Incecik F, Kartal E, Mungan NO. Yilmaz BS, et al. Among authors: ceylaner s. J Child Neurol. 2015 May;30(6):789-92. doi: 10.1177/0883073814535499. Epub 2014 May 16. J Child Neurol. 2015. PMID: 24838951
Giant axonal disease: Report of eight cases.
Incecik F, Herguner OM, Ceylaner S, Zorludemir S, Altunbasak S. Incecik F, et al. Among authors: ceylaner s. Brain Dev. 2015 Sep;37(8):803-7. doi: 10.1016/j.braindev.2014.12.002. Epub 2014 Dec 19. Brain Dev. 2015. PMID: 25533284
Microcephaly and developmental delay caused by short-chain acyl-CoA dehydrogenase deficiency.
Kılıç M, Şenel S, Karaer K, Ceylaner S. Kılıç M, et al. Among authors: ceylaner s. Turk J Pediatr. 2017;59(6):708-710. doi: 10.24953/turkjped.2017.06.016. Turk J Pediatr. 2017. PMID: 30035407 Free article.
Kilic M, Senel S, Karaer K, Ceylaner S. Microcephaly and developmental delay caused by short-chain acyl-CoA dehydrogenase deficiency. ...
Kilic M, Senel S, Karaer K, Ceylaner S. Microcephaly and developmental delay caused by short-chain acyl-CoA dehydrogena …
Mild hypotonia and recurrent seizures in an 8-month-old boy: Questions.
Özlü SG, Kasapkara CS, Ceylaner S, Nergız ME, Alan B, Yılmaz S, Kurt ANÇ. Özlü SG, et al. Among authors: ceylaner s. Pediatr Nephrol. 2019 Oct;34(10):1727-1728. doi: 10.1007/s00467-019-04231-9. Epub 2019 Mar 22. Pediatr Nephrol. 2019. PMID: 30903373
Mild hypotonia and recurrent seizures in an 8-month-old boy: Answers.
Özlü SG, Kasapkara CS, Ceylaner S, Erat Nergız M, Alan B, Yılmaz S, Çıtak Kurt AN. Özlü SG, et al. Among authors: ceylaner s. Pediatr Nephrol. 2019 Oct;34(10):1729-1731. doi: 10.1007/s00467-019-04236-4. Epub 2019 Mar 22. Pediatr Nephrol. 2019. PMID: 30903374 No abstract available.
249 results