Yiş U - Search Results

1

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

2

Primary lymphedema in a four year old boy.

Yis U, Dirik E. Yis U, et al. Indian Pediatr. 2005 Jul;42(7):726-7. Indian Pediatr. 2005. PMID: 16085981 Free article. No abstract available.

3

Parental attitude of mothers, iron deficiency anemia, and breath-holding spells.

Hüdaoglu O, Dirik E, Yiş U, Kurul S. Hüdaoglu O, et al. Among authors: yis u. Pediatr Neurol. 2006 Jul;35(1):18-20. doi: 10.1016/j.pediatrneurol.2005.12.006. Pediatr Neurol. 2006. PMID: 16814080

4

Aorta coarctation presenting with intracranial aneurysm rupture.

Hüdaoğlu O, Kurul S, Cakmakci H, Men S, Yiş U, Dirik E. Hüdaoğlu O, et al. Among authors: yis u. J Paediatr Child Health. 2006 Jul-Aug;42(7-8):477-9. doi: 10.1111/j.1440-1754.2006.00903.x. J Paediatr Child Health. 2006. PMID: 16898890

5

Nonconvulsive status epilepticus and neurodevelopmental delay.

Dirik E, Yiş U, Hüdaoglu O, Kurul S. Dirik E, et al. Among authors: yis u. Pediatr Neurol. 2006 Sep;35(3):209-12. doi: 10.1016/j.pediatrneurol.2006.02.007. Pediatr Neurol. 2006. PMID: 16939862

6

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

7

Basilar artery thrombosis in a child heterozygous for prothrombin gene G20210A mutation.

Hüdaoglu O, Kurul S, Yis U, Dirik E, Cakmakçi H, Men S. Hüdaoglu O, et al. Among authors: yis u. J Child Neurol. 2007 Mar;22(3):329-31. doi: 10.1177/0883073807299861. J Child Neurol. 2007. PMID: 17621506

8

Spinocerebellar ataxia type 2 in a Turkish family.

Dirik E, Yiş U, Başak N, Soydan E, Hüdaoğlu O, Ozgönül F. Dirik E, et al. Among authors: yis u. J Child Neurol. 2007 Jul;22(7):891-4. doi: 10.1177/0883073807304702. J Child Neurol. 2007. PMID: 17715286

9

Recurrent attacks of status epilepticus as predominant symptom in 3-methylcrotonyl-CoA carboxylase deficiency.

Dirik E, Yiş U, Paşaoğlu G, Chambaz C, Baumgartner MR. Dirik E, et al. Among authors: yis u. Brain Dev. 2008 Mar;30(3):218-20. doi: 10.1016/j.braindev.2007.08.005. Epub 2007 Sep 14. Brain Dev. 2008. PMID: 17869468

10

Differential diagnosis of muscular hypotonia in infants: the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VI).

Yiş U, Dirik E, Chambaz C, Steinmann B, Giunta C. Yiş U, et al. Neuromuscul Disord. 2008 Mar;18(3):210-4. doi: 10.1016/j.nmd.2007.11.006. Epub 2007 Dec 26. Neuromuscul Disord. 2008. PMID: 18155911

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