Yiş U - Search Results

1

Identification of PCDH19 Gene Mutations/Deletions in Patients with Early Onset Epilepsy.

Gursoy S, Ataman E, Baysal BT, Özyılmaz B, Gençpınar P, Hız AS, Yiş U, Ünalp A, Dündar NO, Ülgenalp A, Erçal D. Gursoy S, et al. Among authors: yis u. Ann Indian Acad Neurol. 2020 Mar-Apr;23(2):206-210. doi: 10.4103/aian.AIAN_465_19. Epub 2020 Feb 25. Ann Indian Acad Neurol. 2020. PMID: 32189863 Free PMC article.

2

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

3

Long-standing fever and Angelman syndrome: report of two cases.

Yiş U, Giray O, Kurul SH, Bora E, Ulgenalp A, Erçal D, Dirik E. Yiş U, et al. J Paediatr Child Health. 2008 May;44(5):308-10. doi: 10.1111/j.1440-1754.2008.01302.x. J Paediatr Child Health. 2008. PMID: 18416709

4

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

5

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.

6

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

7

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

8

Measurement of the apparent diffusion coefficient in paediatric mitochondrial encephalopathy cases and a comparison of parenchymal changes associated with the disease using follow-up diffusion coefficient measurements.

Uysal F, Cakmakçı H, Yiş U, Ellidokuz H, Hız AS. Uysal F, et al. Among authors: yis u. Eur J Radiol. 2014 Jan;83(1):212-8. doi: 10.1016/j.ejrad.2013.06.031. Epub 2013 Oct 17. Eur J Radiol. 2014. PMID: 24176530

9

Importance of acylcarnitine profile analysis for disorders of lipid metabolism in adolescent patients with recurrent rhabdomyolysis: Report of two cases.

Topçu Y, Bayram E, Karaoğlu P, Yiş U, Kurul SH. Topçu Y, et al. Among authors: yis u. Ann Indian Acad Neurol. 2014 Oct;17(4):437-40. doi: 10.4103/0972-2327.144031. Ann Indian Acad Neurol. 2014. PMID: 25506168 Free PMC article.

10

Importance of acrocyanosis in delayed walking.

Yiş U, Polat İ, Karakaya P, Ayanoğlu M, Hiz AS. Yiş U, et al. J Pediatr Neurosci. 2015 Jan-Mar;10(1):80-1. doi: 10.4103/1817-1745.154368. J Pediatr Neurosci. 2015. PMID: 25878756 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

205 results

Search Page