Ertürk O - Search Results

1

Apraxia in Parkinson's disease and multiple system atrophy.

Uluduz D, Ertürk O, Kenangil G, Ozekmekçi S, Ertan S, Apaydin H, Erginöz E. Uluduz D, et al. Among authors: erturk o. Eur J Neurol. 2010 Mar;17(3):413-8. doi: 10.1111/j.1468-1331.2009.02905.x. Epub 2009 Dec 30. Eur J Neurol. 2010. PMID: 20050896

2

Efficacy of nebivolol and amitriptyline in the prophylaxis of cyclic vomiting syndrome: a case report.

Erturk O, Uluduz D, Karaali-Savrun F. Erturk O, et al. Neurologist. 2010 Sep;16(5):313-4. doi: 10.1097/NRL.0b013e3181b120a6. Neurologist. 2010. PMID: 20827121

3

Challenges in diagnosing SSPE.

Erturk O, Karslıgil B, Cokar O, Yapici Z, Demirbilek V, Gurses C, Yalcinkaya C, Gokyigit A, Direskeneli GS, Yentur S, Onal E, Yilmaz G, Dervent A. Erturk O, et al. Childs Nerv Syst. 2011 Dec;27(12):2041-4. doi: 10.1007/s00381-011-1603-x. Epub 2011 Oct 15. Childs Nerv Syst. 2011. PMID: 22002104

4

Prenatal unilateral cerebellar hypoplasia diagnosed as PHACE syndrome.

Erturk O, Uygunoglu U, Celkan T, Yalcinkaya C. Erturk O, et al. Childs Nerv Syst. 2016 Apr;32(4):587-8. doi: 10.1007/s00381-016-3027-0. Epub 2016 Jan 29. Childs Nerv Syst. 2016. PMID: 26825811 No abstract available.

5

Epilepsy Surgery in Children with Lesional Partial Epilepsies.

Erturk O, Ozkara C, Yalcinkaya C, Dervent A, Yeni SN, Demirbilek V, Unver O, Uysal S, Ozyurt E, Uzan M. Erturk O, et al. Turk Neurosurg. 2015;25(6):900-4. doi: 10.5137/1019-5149.JTN.11342-14.1. Turk Neurosurg. 2015. PMID: 26617140 Free article.

6

A novel GJC2 mutation associated with hypomyelination and Müllerian agenesis syndrome: coincidence or a new entity?

Yalcinkaya C, Erturk O, Tuysuz B, Yesil G, Verbeke JI, Keyser B, Stuhrmann M, Steinemann D, Sistermans EA, van der Knaap MS. Yalcinkaya C, et al. Among authors: erturk o. Neuropediatrics. 2012 Jun;43(3):159-61. doi: 10.1055/s-0032-1313912. Epub 2012 May 19. Neuropediatrics. 2012. PMID: 22610664

7

Mentalis muscle related reflexes.

Gündüz A, Uyanık Ö, Ertürk Ö, Sohtaoğlu M, Kızıltan ME. Gündüz A, et al. Among authors: erturk o. Neurol Sci. 2016 May;37(5):789-92. doi: 10.1007/s10072-015-2455-z. Epub 2015 Dec 31. Neurol Sci. 2016. PMID: 26721248

8

Novel VLDLR microdeletion identified in two Turkish siblings with pachygyria and pontocerebellar atrophy.

Kolb LE, Arlier Z, Yalcinkaya C, Ozturk AK, Moliterno JA, Erturk O, Bayrakli F, Korkmaz B, DiLuna ML, Yasuno K, Bilguvar K, Ozcelik T, Tuysuz B, State MW, Gunel M. Kolb LE, et al. Among authors: erturk o. Neurogenetics. 2010 Jul;11(3):319-25. doi: 10.1007/s10048-009-0232-y. Epub 2010 Jan 15. Neurogenetics. 2010. PMID: 20082205

9

Startle and blink reflex in high functioning autism.

Erturk O, Korkmaz B, Alev G, Demirbilek V, Kiziltan M. Erturk O, et al. Neurophysiol Clin. 2016 Jun;46(3):189-92. doi: 10.1016/j.neucli.2016.02.001. Epub 2016 Mar 17. Neurophysiol Clin. 2016. PMID: 26997128

10

Four novel SCN1A mutations in Turkish patients with severe myoclonic epilepsy of infancy (SMEI).

Arlier Z, Bayri Y, Kolb LE, Erturk O, Ozturk AK, Bayrakli F, Bilguvar K, Moliterno JA, Dervent A, Demirbilek V, Yalcinkaya C, Korkmaz B, Tuysuz B, Gunel M. Arlier Z, et al. Among authors: erturk o. J Child Neurol. 2010 Oct;25(10):1265-8. doi: 10.1177/0883073809357241. Epub 2010 Jan 28. J Child Neurol. 2010. PMID: 20110217

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