Yiş U - Search Results

1

Childhood onset limb-girdle muscular dystrophies in the Aegean part of Turkey.

Yiş U, Diniz G, Hazan F, Daimagüler HS, Baysal BT, Baydan F, Akinci G, Ünalp A, Aktan G, Bayram E, Hiz S, Paketçi C, Okur D, Özer E, Danyeli AE, Polat M, Uyanik G, Çirak S. Yiş U, et al. Acta Myol. 2018 Sep 1;37(3):210-220. eCollection 2018 Sep. Acta Myol. 2018. PMID: 30838351 Free PMC article.

2

A case of Walker-Warburg syndrome resulting from a homozygous POMT1 mutation.

Yis U, Uyanik G, Kurul S, Dirik E, Ozer E, Gross C, Hehr U. Yis U, et al. Eur J Paediatr Neurol. 2007 Jan;11(1):46-9. doi: 10.1016/j.ejpn.2006.10.007. Epub 2006 Dec 11. Eur J Paediatr Neurol. 2007. PMID: 17161965

3

Homocysteine levels in epileptic children receiving antiepileptic drugs.

Kurul S, Unalp A, Yiş U. Kurul S, et al. Among authors: yis u. J Child Neurol. 2007 Dec;22(12):1389-92. doi: 10.1177/0883073807307081. J Child Neurol. 2007. PMID: 18174557

4

Unusual findings in Leigh syndrome caused by T8993C mutation.

Yiş U, Seneca S, Dirik E, Kurul SH, Ozer E, Cakmakçi H, De Meirleir L. Yiş U, et al. Eur J Paediatr Neurol. 2009 Nov;13(6):550-2. doi: 10.1016/j.ejpn.2008.10.009. Epub 2008 Nov 30. Eur J Paediatr Neurol. 2009. PMID: 19046652

5

Oxidant status in children after febrile seizures.

Güneş S, Dirik E, Yiş U, Seçkin E, Kuralay F, Köse S, Unalp A. Güneş S, et al. Among authors: yis u. Pediatr Neurol. 2009 Jan;40(1):47-9. doi: 10.1016/j.pediatrneurol.2008.09.006. Pediatr Neurol. 2009. PMID: 19068254

6

Temporary diazepam responsive apneic attacks and congenital myasthenic syndrome.

Yis U, Kurul SH, Oztura I, Ozden O, Akinci G, Dirik E. Yis U, et al. J Child Neurol. 2009 Jul;24(7):895-8. doi: 10.1177/0883073808331083. Epub 2009 Mar 16. J Child Neurol. 2009. PMID: 19289695

7

Diagnostic value of proton MR spectroscopy and diffusion-weighted MR imaging in childhood inherited neurometabolic brain diseases and review of the literature.

Cakmakci H, Pekcevik Y, Yis U, Unalp A, Kurul S. Cakmakci H, et al. Among authors: yis u. Eur J Radiol. 2010 Jun;74(3):e161-71. doi: 10.1016/j.ejrad.2009.05.048. Epub 2009 Jun 21. Eur J Radiol. 2010. PMID: 19540689 Review.

8

Clinical, pathological and radiological survey of patients with Leigh syndrome.

Yis U, Hiz Kurul S, Dirik E, Cakmakçi H, Ozer E. Yis U, et al. Minerva Pediatr. 2009 Aug;61(4):371-8. Minerva Pediatr. 2009. PMID: 19752846

9

Two cases with megalencephalic leukoencephalopathy with subcortical cysts and MLC1 mutations in the Turkish population.

Yiş U, Scheper GC, Uran N, Unalp A, Cakmakçi H, Hiz-Kurul S, Dirik E, van der Knaap MS. Yiş U, et al. Turk J Pediatr. 2010 Mar-Apr;52(2):179-83. Turk J Pediatr. 2010. PMID: 20560255

10

Fukutin mutations in non-Japanese patients with congenital muscular dystrophy: less severe mutations predominate in patients with a non-Walker-Warburg phenotype.

Yis U, Uyanik G, Heck PB, Smitka M, Nobel H, Ebinger F, Dirik E, Feng L, Kurul SH, Brocke K, Unalp A, Özer E, Cakmakci H, Sewry C, Cirak S, Muntoni F, Hehr U, Morris-Rosendahl DJ. Yis U, et al. Neuromuscul Disord. 2011 Jan;21(1):20-30. doi: 10.1016/j.nmd.2010.08.007. Epub 2010 Oct 18. Neuromuscul Disord. 2011. PMID: 20961758

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