Yüksel A - Search Results

1

Siblings with cystic leukoencephalopathy and megalencephaly.

Yalçinkaya C, Comu S, Koçer N, Yüksel A, Gündüz E, Demirbilek V, Ocal A. Yalçinkaya C, et al. Among authors: yuksel a. J Child Neurol. 2000 Oct;15(10):690-3. doi: 10.1177/088307380001501010. J Child Neurol. 2000. PMID: 11063084

2

Neuroimaging findings of four patients with Sandhoff disease.

Yüksel A, Yalçinkaya C, Işlak C, Gündüz E, Seven M. Yüksel A, et al. Pediatr Neurol. 1999 Aug;21(2):562-5. doi: 10.1016/s0887-8994(99)00041-7. Pediatr Neurol. 1999. PMID: 10465144

3

Epilepsy in vacuolating megalencephalic leukoencephalopathy with subcortical cysts.

Yalçinkaya C, Yüksel A, Comu S, Kiliç G, Cokar O, Dervent A. Yalçinkaya C, et al. Among authors: yuksel a. Seizure. 2003 Sep;12(6):388-96. doi: 10.1016/s1059-1311(02)00350-3. Seizure. 2003. PMID: 12915085 Free article.

4

Magnetic resonance imaging, magnetic resonance spectroscopy, and facial dysmorphism in a case of Lowe syndrome with novel OCRL1 gene mutation.

Yuksel A, Karaca E, Albayram MS. Yuksel A, et al. J Child Neurol. 2009 Jan;24(1):93-6. doi: 10.1177/0883073808321047. J Child Neurol. 2009. PMID: 19168822

5

Infantile-onset megalencephalic leucoencephalopathy in two siblings.

Soylu H, Yüksel A, Kutlu NO, Aydinli M, Seven M, Mocan H. Soylu H, et al. Among authors: yuksel a. J Paediatr Child Health. 2000 Dec;36(6):598-602. doi: 10.1046/j.1440-1754.2000.00522.x. J Paediatr Child Health. 2000. PMID: 11115041

6

Facial dysmorphism in Leigh syndrome with SURF-1 mutation and COX deficiency.

Yüksel A, Seven M, Cetincelik U, Yeşil G, Köksal V. Yüksel A, et al. Pediatr Neurol. 2006 Jun;34(6):486-9. doi: 10.1016/j.pediatrneurol.2005.10.020. Pediatr Neurol. 2006. PMID: 16765830

7

Changes in the antioxidant system in epileptic children receiving antiepileptic drugs: two-year prospective studies.

Yüksel A, Cengiz M, Seven M, Ulutin T. Yüksel A, et al. J Child Neurol. 2001 Aug;16(8):603-6. doi: 10.1177/088307380101600814. J Child Neurol. 2001. PMID: 11510935

8

Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disorders.

Travaglini L, Brancati F, Silhavy J, Iannicelli M, Nickerson E, Elkhartoufi N, Scott E, Spencer E, Gabriel S, Thomas S, Ben-Zeev B, Bertini E, Boltshauser E, Chaouch M, Cilio MR, de Jong MM, Kayserili H, Ogur G, Poretti A, Signorini S, Uziel G, Zaki MS; International JSRD Study Group; Johnson C, Attié-Bitach T, Gleeson JG, Valente EM. Travaglini L, et al. Eur J Hum Genet. 2013 Oct;21(10):1074-8. doi: 10.1038/ejhg.2012.305. Epub 2013 Feb 6. Eur J Hum Genet. 2013. PMID: 23386033 Free PMC article.

9

Therapeutic plasma exchange for malignant refractory status epilepticus: a case report.

Gedik AH, Demirkol D, Tatlı B, Bayraktar S, Alkan A, Karabocuoglu M, Yuksel A. Gedik AH, et al. Among authors: yuksel a. Pediatr Neurol. 2014 Apr;50(4):407-10. doi: 10.1016/j.pediatrneurol.2014.01.001. Epub 2014 Jan 4. Pediatr Neurol. 2014. PMID: 24630284

10

Marked improvement in Segawa syndrome after L-dopa and selegiline treatment.

Yosunkaya E, Karaca E, Basaran S, Seven M, Yüksel A. Yosunkaya E, et al. Among authors: yuksel a. Pediatr Neurol. 2010 May;42(5):348-50. doi: 10.1016/j.pediatrneurol.2010.01.008. Pediatr Neurol. 2010. PMID: 20399390

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