Yıldız Y - Search Results

1

Long-term clinical evaluation of patients with alpha-mannosidosis - A multicenter study.

Köse E, Kasapkara ÇS, İnci A, Yıldız Y, Sürücü Kara İ, Kahraman AB, Tümer L, Dursun A, Eminoğlu FT. Köse E, et al. Among authors: yildiz y. Eur J Med Genet. 2024 Apr;68:104927. doi: 10.1016/j.ejmg.2024.104927. Epub 2024 Feb 19. Eur J Med Genet. 2024. PMID: 38382588 Free article.

2

Partial hydatidiform mole in a phenylketonuria patient treated with sapropterin dihydrochloride.

Yildiz Y, Dursun A, Tokatli A, Coskun T, Sivri S. Yildiz Y, et al. Gynecol Endocrinol. 2017 Jan;33(1):19-20. doi: 10.1080/09513590.2016.1247796. Epub 2016 Nov 29. Gynecol Endocrinol. 2017. PMID: 27898272

3

Late-diagnosed phenylketonuria in an eight-year-old boy with dyslexia and attention-deficit hyperactivity disorder.

Yıldız Y, Dursun A, Tokatlı A, Coşkun T, Sivri HS. Yıldız Y, et al. Turk J Pediatr. 2016;58(1):94-96. doi: 10.24953/turkjped.2016.01.014. Turk J Pediatr. 2016. PMID: 27922243 Free article.

4

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. Pediatr Neurol. 2019 Oct;99:69-75. doi: 10.1016/j.pediatrneurol.2019.06.015. Epub 2019 Jun 28. Pediatr Neurol. 2019. PMID: 31331668

5

Cognitive and behavioral impairment in mild hyperphenylalaninemia.

Evinç SG, Pektaş E, Foto-Özdemir D, Yıldız Y, Karaboncuk Y, Bilginer-Gürbüz B, Dursun A, Tokatlı A, Coskun T, Öktem F, Sivri HS. Evinç SG, et al. Among authors: yildiz y. Turk J Pediatr. 2018;60(6):617-624. doi: 10.24953/turkjped.2018.06.001. Turk J Pediatr. 2018. PMID: 31365197 Free article.

Evinc SG, Pektas E, Foto-Ozdemir D, Yildiz Y, Karaboncuk Y, Bilginer-Gurbuz B, Dursun A, Tokatli A, Coskun T, Oktem F, Sivri HS. ...

Evinc SG, Pektas E, Foto-Ozdemir D, Yildiz Y, Karaboncuk Y, Bilginer-Gurbuz B, Dursun A, Tokatli A, Coskun T, Oktem F, …

6

Erratum to 'Determinants of Riboflavin Responsiveness in Multiple Acyl-CoA Dehydrogenase Deficiency' [Pediatric Neurology 99 (2019) 69-75].

Yıldız Y, Talim B, Haliloglu G, Topaloglu H, Akçören Z, Dursun A, Sivri HS, Coşkun T, Tokatlı A. Yıldız Y, et al. Pediatr Neurol. 2020 Feb;103:91. doi: 10.1016/j.pediatrneurol.2019.11.001. Epub 2019 Dec 6. Pediatr Neurol. 2020. PMID: 31818519 No abstract available.

7

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. 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

8

Predictors of acute metabolic decompensation in children with maple syrup urine disease at the emergency department.

Yıldız Y, Akcan Yıldız L, Dursun A, Tokatlı A, Coşkun T, Tekşam Ö, Sivri HS. Yıldız Y, et al. Eur J Pediatr. 2020 Jul;179(7):1107-1114. doi: 10.1007/s00431-020-03602-x. Epub 2020 Feb 11. Eur J Pediatr. 2020. PMID: 32048023

9

Oral health status of children with phenylketonuria.

Ballikaya E, Yildiz Y, Sivri HS, Tokatli A, Dursun A, Olmez S, Coskun T, Uzamis Tekcicek M. Ballikaya E, et al. Among authors: yildiz y. J Pediatr Endocrinol Metab. 2020 Mar 26;33(3):361-365. doi: 10.1515/jpem-2019-0439. J Pediatr Endocrinol Metab. 2020. PMID: 32049652

10

Recurrent Postinfectious Rhabdomyolysis in a 5-Year-Old Girl.

Torun EG, Yildiz Y, Yazici MU, Çolak FK, Kasapkara CS. Torun EG, et al. Among authors: yildiz y. Klin Padiatr. 2021 Jul;233(4):203-205. doi: 10.1055/a-1263-1402. Epub 2020 Oct 9. Klin Padiatr. 2021. PMID: 33036056 English. No abstract available.

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