Coskun T - Search Results

1

Brown-Vialetto-Van Laere syndrome: two siblings with a new mutation and dramatic therapeutic effect of high-dose riboflavin.

Horoz OO, Mungan NO, Yildizdas D, Hergüner Ö, Ceylaner S, Kör D, Waterham H, Coskun T. Horoz OO, et al. Among authors: coskun t. J Pediatr Endocrinol Metab. 2016 Feb;29(2):227-31. doi: 10.1515/jpem-2015-0198. J Pediatr Endocrinol Metab. 2016. PMID: 26444347

2

Recommendations on phenylketonuria in Turkey.

Coşkun T, Çoker M, Mungan NÖ, Özel HG, Sivri HS. Coşkun T, et al. Turk J Pediatr. 2022;64(3):413-434. doi: 10.24953/turkjped.2021.4098. Turk J Pediatr. 2022. PMID: 35899555 Free article.

3

Erratum to `Recommendations on phenylketonuria in Turkey` [Turk J Pediatr 2022; 64: 413-434].

Coşkun T, Çoker M, Mungan NÖ, Özel HG, Sivri HS. Coşkun T, et al. Turk J Pediatr. 2022;64(6):1175. Turk J Pediatr. 2022. PMID: 36583907 No abstract available.

4

A newborn with VLCAD deficiency. Clinical, biochemical, and histopathological findings.

Aliefendioğlu D, Dursun A, Coşkun T, Akçören Z, Wanders RJ, Waterham HR. Aliefendioğlu D, et al. Among authors: coskun t. Eur J Pediatr. 2007 Oct;166(10):1077-80. doi: 10.1007/s00431-006-0350-6. Epub 2007 Jan 6. Eur J Pediatr. 2007. PMID: 17206456

5

Genotypes and estimated prevalence of phosphomannomutase 2 deficiency in Turkey differ significantly from those in Europe.

Yıldız Y, Arslan M, Çelik G, Kasapkara ÇS, Ceylaner S, Dursun A, Sivri HS, Coşkun T, Tokatlı A. Yıldız Y, et al. Among authors: coskun t. Am J Med Genet A. 2020 Apr;182(4):705-712. doi: 10.1002/ajmg.a.61488. Epub 2020 Jan 25. Am J Med Genet A. 2020. PMID: 31981409

6

Deoxyguanosine kinase deficiency: a report of four patients.

Ünal Ö, Hişmi B, Kılıç M, Gülşen HH, Coşkun T, Sivri SH, Dursun A, Yüce A, Tokatlı A. Ünal Ö, et al. Among authors: coskun t. J Pediatr Endocrinol Metab. 2017 May 24;30(6):697-702. doi: 10.1515/jpem-2016-0268. J Pediatr Endocrinol Metab. 2017. PMID: 28493820

7

Determinants of Riboflavin Responsiveness in Multiple Acyl-CoA Dehydrogenase Deficiency.

Yıldız Y, Talim B, Haliloglu G, Topaloglu H, Akçören Z, Dursun A, Sivri HS, Coşkun T, Tokatlı A. Yıldız Y, et al. Among authors: coskun t. Pediatr Neurol. 2019 Oct;99:69-75. doi: 10.1016/j.pediatrneurol.2019.06.015. Epub 2019 Jun 28. Pediatr Neurol. 2019. PMID: 31331668

8

Hereditary fructose intolerance in a patient with phenylketonuria.

Coşkun T, Ozalp I, Tekinalp G. Coşkun T, et al. Turk J Pediatr. 1991 Jul-Sep;33(3):181-4. Turk J Pediatr. 1991. PMID: 1792698

9

Frequency of the IVS-10nt546 mutation in 44 Turkish phenylketonuria patients.

Ozgüç M, Ozalp I, Coşkun T, Yilmaz E, Erdem H, Ayter S. Ozgüç M, et al. Among authors: coskun t. Turk J Pediatr. 1993 Jan-Mar;35(1):11-4. Turk J Pediatr. 1993. PMID: 7901929

10

Neurophysiological studies of patients with classical phenylketonuria: evaluation of results of IQ scores, EEG and evoked potentials.

Coşkun T, Topçu M, Ustündağ I, Ozalp I, Renda Y, Ciğer A, Nurlu G. Coşkun T, et al. Turk J Pediatr. 1993 Jan-Mar;35(1):1-10. Turk J Pediatr. 1993. PMID: 8236512

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