Demirbilek V - Search Results

1

Recessive LAMC3 mutations cause malformations of occipital cortical development.

Barak T, Kwan KY, Louvi A, Demirbilek V, Saygı S, Tüysüz B, Choi M, Boyacı H, Doerschner K, Zhu Y, Kaymakçalan H, Yılmaz S, Bakırcıoğlu M, Cağlayan AO, Oztürk AK, Yasuno K, Brunken WJ, Atalar E, Yalçınkaya C, Dinçer A, Bronen RA, Mane S, Ozçelik T, Lifton RP, Sestan N, Bilgüvar K, Günel M. Barak T, et al. Among authors: demirbilek v. Nat Genet. 2011 Jun;43(6):590-4. doi: 10.1038/ng.836. Epub 2011 May 15. Nat Genet. 2011. PMID: 21572413 Free PMC article.

2

Four Turkish families with hyperekplexia: A missense mutation and the exon 1-7 deletion in the GLRA1 gene.

Tezen D, Şimşir G, Çokar Ö, Demirbilek V, Başak AN, Yapıcı Z. Tezen D, et al. Among authors: demirbilek v. Parkinsonism Relat Disord. 2022 Dec;105:128-131. doi: 10.1016/j.parkreldis.2022.11.011. Epub 2022 Nov 15. Parkinsonism Relat Disord. 2022. PMID: 36434917

3

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: demirbilek v. J Child Neurol. 2010 Oct;25(10):1265-8. doi: 10.1177/0883073809357241. Epub 2010 Jan 28. J Child Neurol. 2010. PMID: 20110217

4

Chromosome 14q11.2-q21.1 duplication: a rare cause of West syndrome.

Çetin ÖE, Yalçınkaya C, Karaman B, Demirbilek V, Tüysüz B. Çetin ÖE, et al. Among authors: demirbilek v. Epileptic Disord. 2018 Jun 1;20(3):219-224. doi: 10.1684/epd.2018.0972. Epileptic Disord. 2018. PMID: 29905153

5

Early Diagnostic Signs and the Natural History of Typical Findings in Cohen Syndrome.

Güneş N, Alkaya DU, Demirbilek V, Yalçınkaya C, Tüysüz B. Güneş N, et al. Among authors: demirbilek v. J Pediatr. 2023 Jan;252:93-100. doi: 10.1016/j.jpeds.2022.08.052. Epub 2022 Sep 5. J Pediatr. 2023. PMID: 36067876

6

A study on visual evoked responses in childhood epilepsy with occipital paroxysms.

Demirbilek V, Dervent A, Korkmaz B, Erkol G, Yalçinkaya C. Demirbilek V, et al. Seizure. 2000 Jun;9(4):270-3. doi: 10.1053/seiz.2000.0399. Seizure. 2000. PMID: 10880287 Free article.

7

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: demirbilek v. J Child Neurol. 2000 Oct;15(10):690-3. doi: 10.1177/088307380001501010. J Child Neurol. 2000. PMID: 11063084

8

A rare finding in epilepsy with myoclonic absences: focal seizure.

Çetin ÖE, Abanoz Y, Kıvrak E, Yalçınkaya C, Demirbilek V. Çetin ÖE, et al. Among authors: demirbilek v. Childs Nerv Syst. 2016 Nov;32(11):2053-2055. doi: 10.1007/s00381-016-3235-7. Epub 2016 Sep 5. Childs Nerv Syst. 2016. PMID: 27596001 No abstract available.

9

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: demirbilek v. 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

10

Serum Levels of Neuropeptides in Epileptic Encephalopathy With Spike-and-Wave Activation in Sleep.

Atacan Yaşgüçlükal M, Ayça S, Demirbilek V, Saltık S, Yalçınkaya C, Erdoğan Döventaş Y, Çokar Ö. Atacan Yaşgüçlükal M, et al. Among authors: demirbilek v. Pediatr Neurol. 2023 Jul;144:110-114. doi: 10.1016/j.pediatrneurol.2023.04.017. Epub 2023 Apr 28. Pediatr Neurol. 2023. PMID: 37229878

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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

49 results

Search Page

Filters