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Showing articles 0 to 8 of 8 Filter Applied: exome sequencing (Click to remove) A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability Neurol 104:e210290, Voloshyna-Farber, E.Y.,et al, 2025 A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia Neurol 104:e213593, Pence, K.L. &Clark, R.A., 2025 A 62-Year-Old Man with Progressive Limb Weakness, Involuntary Movements, and HyperCKemia JAMA Neurol 82L:1286-1287, Liu,Y.,et al, 2025 A 13-Year-Old Boy with Subacute-Onset Spastic Gait JAMA Neurol 78:e1-e2, Xie, N.,et al, 2021 GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy Ann Neurol 86:962-968,809, Okubo, M.,et al, 2019 A Child with Arthrogryposis Neurol 91:e995-e998, Irumudomom, O. & Ghosh, P.S., 2018 SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases Eur J Hum Genet 24:1016-1021, Choquet,K.,et al, 2016 Heterozygous de-Novo Mutations in ATP1A3 in Patients with Alternating Hemiplegia of Childhood:A Whole-Exome Sequencing Gene-Identification Study Lancet Neurol 11:764-773, Rosewich,H.,et al, 2012 Showing articles 0 to 8 of 8