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Page 1
Familial Adult Myoclonic Epilepsy: Clinical and Genetic Approach to an Under-recognized Disease.
Noro Psikiyatr Ars. 2023 May 22;60(2):174-177. doi: 10.29399/npa.28252. eCollection 2023.
Noro Psikiyatr Ars. 2023.
PMID: 37287551
Free PMC article.
Review.
Adult-onset leukodystrophy with homozygous AARS2 mutation located in the aminoacylation domain.
Uzun GA.
Uzun GA.
Neurol India. 2019 May-Jun;67(3):871-872. doi: 10.4103/0028-3886.263237.
Neurol India. 2019.
PMID: 31347571
Free article.
No abstract available.
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Screening LGI1 in a cohort of 26 lateral temporal lobe epilepsy patients with auditory aura from Turkey detects a novel de novo mutation.
Kesim YF, Uzun GA, Yucesan E, Tuncer FN, Ozdemir O, Bebek N, Ozbek U, Iseri SA, Baykan B.
Kesim YF, et al. Among authors: uzun ga.
Epilepsy Res. 2016 Feb;120:73-8. doi: 10.1016/j.eplepsyres.2015.12.006. Epub 2015 Dec 12.
Epilepsy Res. 2016.
PMID: 26773249
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Analysis of Mutations in AARS2 in a Series of CSF1R-Negative Patients With Adult-Onset Leukoencephalopathy With Axonal Spheroids and Pigmented Glia.
Lynch DS, Zhang WJ, Lakshmanan R, Kinsella JA, Uzun GA, Karbay M, Tüfekçioglu Z, Hanagasi H, Burke G, Foulds N, Hammans SR, Bhattacharjee A, Wilson H, Adams M, Walker M, Nicoll JA, Chataway J, Fox N, Davagnanam I, Phadke R, Houlden H.
Lynch DS, et al. Among authors: uzun ga.
JAMA Neurol. 2016 Dec 1;73(12):1433-1439. doi: 10.1001/jamaneurol.2016.2229.
JAMA Neurol. 2016.
PMID: 27749956
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