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Retrospective evaluation of patients with X-linked adrenoleukodystrophy with a wide range of clinical presentations: a single center experience.
Olgac A, Kasapkara ÇS, Derinkuyu B, Yüksel D, Çetinkaya S, Aksoy A, Ceylaner S, Güleray N, Yeşilipek A, Aydın Hİ, Orgun LT, Kılıç M. Olgac A, et al. Among authors: kasapkara cs. J Pediatr Endocrinol Metab. 2021 Jun 24;34(9):1169-1179. doi: 10.1515/jpem-2021-0032. Print 2021 Sep 27. J Pediatr Endocrinol Metab. 2021. PMID: 34162029 Clinical Trial.
PMM2-CDG and sensorineural hearing loss.
Kasapkara ÇS, Barış Z, Kılıç M, Yüksel D, Keldermans L, Matthijs G, Jaeken J. Kasapkara ÇS, et al. J Inherit Metab Dis. 2017 Sep;40(5):629-630. doi: 10.1007/s10545-017-0073-z. Epub 2017 Jul 31. J Inherit Metab Dis. 2017. PMID: 28762107 No abstract available.
A new NBIA patient from Turkey with homozygous C19ORF12 mutation.
Kasapkara ÇS, Tümer L, Gregory A, Ezgü F, İnci A, Derinkuyu BE, Fox R, Rogers C, Hayflick S. Kasapkara ÇS, et al. Acta Neurol Belg. 2019 Dec;119(4):623-625. doi: 10.1007/s13760-018-1026-5. Epub 2018 Oct 8. Acta Neurol Belg. 2019. PMID: 30298423 Free PMC article. No abstract available.
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: kasapkara cs. 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: kasapkara cs. 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.
91 results