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Showing articles 0 to 8 of 8 Filter Applied: next-generation sequencing (Click to remove) Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019 Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023 Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists Neurol 100:766-783, Manini,A.,&Pantoni,L., 2023 Clinical Metagenomic Sequencing for Diagnosis of Meningitis and Encephalitis NEJM 380:2327-2340, Wilson, M.R.,et al, 2019 Ehlers-Danlos Syndromes BMJ 366:I4966, Ghali, N.,et al, 2019 Congenital Myasthenic Syndromes in Adult Neurology Clinic Neurol 91:e1770-e1777, Kao, J.C.,et al, 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 Dystonia in Children and Adolescents: A Systematic Review and a New Diagnostic Algorithm JNNP 86:774-781, Van Egmond, M.E.,et al, 2015 Showing articles 0 to 8 of 8