Yalcinkaya C - Search Results

1

Tezen D, Gunduz A, Erdemir Kiziltan M, Yalcinkaya C, Kiziltan G. Tezen D, et al. Among authors: yalcinkaya c. Neurol Sci. 2022 Dec;43(12):6947-6950. doi: 10.1007/s10072-022-06394-0. Epub 2022 Sep 16. Neurol Sci. 2022. PMID: 36112278

2

Clinical characteristics of 49 patients with psychogenic movement disorders in a tertiary clinic in Turkey.

Ertan S, Uluduz D, Ozekmekçi S, Kiziltan G, Ertan T, Yalçinkaya C, Ozkara C. Ertan S, et al. Among authors: yalcinkaya c. Mov Disord. 2009 Apr 15;24(5):759-62. doi: 10.1002/mds.22114. Mov Disord. 2009. PMID: 19205065

3

Familial microhydranencephaly, a family that does not map to 16p13.13-p12.2: relationship with hereditary fetal brain degeneration and fetal brain disruption sequence.

Behunova J, Zavadilikova E, Bozoglu TM, Gunduz A, Tolun A, Yalcinkaya C. Behunova J, et al. Among authors: yalcinkaya c. Clin Dysmorphol. 2010 Jul;19(3):107-118. doi: 10.1097/MCD.0b013e32833946e9. Clin Dysmorphol. 2010. PMID: 20375726

4

Dysembryoplastic neuroepithelial tumors and gangliogliomas: clinical results of 52 patients.

Ozlen F, Gunduz A, Asan Z, Tanriverdi T, Ozkara C, Yeni N, Yalcinkaya C, Ozyurt E, Uzan M. Ozlen F, et al. Among authors: yalcinkaya c. Acta Neurochir (Wien). 2010 Oct;152(10):1661-71. doi: 10.1007/s00701-010-0696-4. Epub 2010 Jun 5. Acta Neurochir (Wien). 2010. PMID: 20526635

5

Novel NDE1 homozygous mutation resulting in microhydranencephaly and not microlyssencephaly.

Guven A, Gunduz A, Bozoglu TM, Yalcinkaya C, Tolun A. Guven A, et al. Among authors: yalcinkaya c. Neurogenetics. 2012 Aug;13(3):189-94. doi: 10.1007/s10048-012-0326-9. Epub 2012 Apr 15. Neurogenetics. 2012. PMID: 22526350

6

Cerebrotendinous xanthomatosis: the effectiveness of high-dose piracetam for the treatment of cerebellar and sensorial ataxia.

Uygunoglu U, Gunduz A, Menku SF, Yilmaz B, Hatipoglu E, Yalcinkaya C, Saip S, Apaydin H. Uygunoglu U, et al. Among authors: yalcinkaya c. Cerebellum. 2014 Dec;13(6):787-90. doi: 10.1007/s12311-014-0587-y. Cerebellum. 2014. PMID: 25084753 No abstract available.

7

Progression of myoclonus subtypes in subacute sclerosing panencephalitis.

Ser MH, Gündüz A, Demirbilek V, Yalçınkaya C, Nalbantoğlu M, Coşkun T, Kızıltan M. Ser MH, et al. Among authors: yalcinkaya c. Neurophysiol Clin. 2021 Dec;51(6):533-540. doi: 10.1016/j.neucli.2021.07.001. Epub 2021 Nov 10. Neurophysiol Clin. 2021. PMID: 34772596

8

Photosensitive absence epilepsy with myoclonias and heterozygosity for succinic semialdehyde dehydrogenase (SSADH) deficiency.

Dervent A, Gibson KM, Pearl PL, Salomons GS, Jakobs C, Yalcinkaya C. Dervent A, et al. Among authors: yalcinkaya c. Clin Neurophysiol. 2004 Jun;115(6):1417-22. doi: 10.1016/j.clinph.2004.01.002. Clin Neurophysiol. 2004. PMID: 15134710

9

Functional deficiencies of sulfite oxidase: Differential diagnoses in neonates presenting with intractable seizures and cystic encephalomalacia.

Sass JO, Gunduz A, Araujo Rodrigues Funayama C, Korkmaz B, Dantas Pinto KG, Tuysuz B, Yanasse Dos Santos L, Taskiran E, de Fátima Turcato M, Lam CW, Reiss J, Walter M, Yalcinkaya C, Camelo Junior JS. Sass JO, et al. Among authors: yalcinkaya c. Brain Dev. 2010 Aug;32(7):544-9. doi: 10.1016/j.braindev.2009.09.005. Epub 2009 Sep 29. Brain Dev. 2010. PMID: 19793632

10

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. Neuropediatrics. 2012 Jun;43(3):159-61. doi: 10.1055/s-0032-1313912. Epub 2012 May 19. Neuropediatrics. 2012. PMID: 22610664

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