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Archives of Neurology|August 8, 2002
Clinical features and ATTCT repeat expansion in spinocerebellar ataxia type 10Raji P Grewal, Madhureeta Achari, Tohru Matsuura, et al.
The International Journal of Neuroscience|May 23, 2015
Autosomal dominant hereditary spastic paraplegia with axonal sensory motor polyneuropathy maps to chromosome 21q 22.3Leema Reddy Peddareddygari, Philip A Hanna, Robert P Igo, et al.
Case Reports in Neurology|October 11, 2016
Role of Therapeutic Plasma Exchange in Treatment of Tumefactive Multiple Sclerosis-Associated Low CD4 and CD8 LevelsKristen Lew, Nishith Mewada, Sahana Ramanujam, et al.
American Journal of Human Genetics|May 6, 2004
Somatic and germline instability of the ATTCT repeat in spinocerebellar ataxia type 10Tohru Matsuura, Ping Fang, Xi Lin, et al.
American Journal of Human Genetics|January 9, 2008
X-linked dominant scapuloperoneal myopathy is due to a mutation in the gene encoding four-and-a-half-LIM protein 1Catarina M Quinzii, Tuan H Vu, K Christopher Min, et al.
Circulation. Genomic and Precision Medicine|July 16, 2019
Subtype Specificity of Genetic Loci Associated With Stroke in 16 664 Cases and 32 792 ControlsMatthew Traylor, Christopher D Anderson, Loes C A Rutten-Jacobs, et al.
The Lancet. Neurology|March 28, 2021
Genetic basis of lacunar stroke: a pooled analysis of individual patient data and genome-wide association studiesMatthew Traylor, Elodie Persyn, Liisa Tomppo, et al.
Stroke|September 12, 2013
Stroke Genetics Network (SiGN) study: design and rationale for a genome-wide association study of ischemic stroke subtypesJames F Meschia, Donna K Arnett, Hakan Ay, et al.
Neurology|September 28, 2014
Agreement between TOAST and CCS ischemic stroke classification: the NINDS SiGN studyPatrick F McArdle, Steven J Kittner, Hakan Ay, et al.
Stroke|July 23, 2020
Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With StrokeKeith L Keene, Hyacinth I Hyacinth, Joshua C Bis, et al.
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