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Showing articles 0 to 6 of 6 Filter Applied: gene (Click to remove) Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019 FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018 Amyotrophic Lateral Sclerosis NEJM 377:162-172, Brown, R.H.,et al, 2017 GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease Neurol 77:1287-1294, Prust, M.,et al, 2011 Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996 Phenotype of Chromosome 14-Linked Familial Alzheimer's Disease in a Large Kindred Ann Neurol 36:368-378, Lampe,T.H.,et al, 1994 Showing articles 0 to 6 of 6