Yildiz Y - Search Results

1

Brain MR patterns in inherited disorders of monoamine neurotransmitters: An analysis of 70 patients.

Kuseyri Hübschmann O, Mohr A, Friedman J, Manti F, Horvath G, Cortès-Saladelafont E, Mercimek-Andrews S, Yildiz Y, Pons R, Kulhánek J, Oppebøen M, Koht JA, Podzamczer-Valls I, Domingo-Jimenez R, Ibáñez S, Alcoverro-Fortuny O, Gómez-Alemany T, de Castro P, Alfonsi C, Zafeiriou DI, López-Laso E, Guder P, Santer R, Honzík T, Hoffmann GF, Garbade SF, Sivri HS, Leuzzi V, Jeltsch K, García-Cazorla A, Opladen T; International Working Group on Neurotransmitter Related Disorders (iNTD); Harting I. Kuseyri Hübschmann O, et al. Among authors: yildiz y. J Inherit Metab Dis. 2021 Jul;44(4):1070-1082. doi: 10.1002/jimd.12360. Epub 2021 Jan 28. J Inherit Metab Dis. 2021. PMID: 33443316 Free article.

2

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.

3

Post-mortem detection of FLAD1 mutations in 2 Turkish siblings with hypotonia in early infancy.

Yıldız Y, Olsen RKJ, Sivri HS, Akçören Z, Nygaard HH, Tokatlı A. Yıldız Y, et al. Neuromuscul Disord. 2018 Sep;28(9):787-790. doi: 10.1016/j.nmd.2018.05.009. Epub 2018 May 31. Neuromuscul Disord. 2018. PMID: 30061063

4

Oral health status in patients with mucopolysaccharidoses.

Ballıkaya E, Eymirli PS, Yıldız Y, Avcu N, Sivri HS, Uzamış-Tekçiçek M. Ballıkaya E, et al. Among authors: yildiz y. Turk J Pediatr. 2018;60(4):400-406. doi: 10.24953/turkjped.2018.04.007. Turk J Pediatr. 2018. PMID: 30859764 Free article.

Ballikaya E, Eymirli PS, Yildiz Y, Avcu N, Sivri HS, Uzamis-Tekcicek M. Oral health status in patients with mucopolysaccharidoses. ...

Ballikaya E, Eymirli PS, Yildiz Y, Avcu N, Sivri HS, Uzamis-Tekcicek M. Oral health status in patients with mucopolysaccharido …

5

Maternal phenylketonuria in Turkey: outcomes of 71 pregnancies and issues in management.

Yıldız Y, Sivri HS. Yıldız Y, et al. Eur J Pediatr. 2019 Jul;178(7):1005-1011. doi: 10.1007/s00431-019-03387-8. Epub 2019 May 3. Eur J Pediatr. 2019. PMID: 31053953

6

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

7

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.

8

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

9

Inborn errors of metabolism in the differential diagnosis of fatty liver disease.

Yıldız Y, Sivri HS. Yıldız Y, et al. Turk J Gastroenterol. 2020 Jan;31(1):3-16. doi: 10.5152/tjg.2019.19367. Turk J Gastroenterol. 2020. PMID: 32009609 Free PMC article. Review.

10

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

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