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Showing articles 0 to 8 of 8 Filter Applied: paraparesis,familial spastic (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 Ears of the Lynx Magnetic Resonance Imaging Sign Ann Neurol 88:16-17, Baghbanian, S.M.,et al, 2020 "Ears of the Lynx" MRI Sign is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia AJNR 40:199-203, Pascual, B.,et al, 2019 SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases Eur J Hum Genet 24:1016-1021, Choquet,K.,et al, 2016 X-Linked Pure Familial Spastic Paraparesis Arch Neurol 52:665-669, Cambi,F.,et al, 1995 MR Imaging of the Spinal Cord in 23 Subjects with ALD-AMN Complex AJR 158:413-416, Snyder,R.D.,et al, 1992 Hereditary Motor and Sensory Neuropathies and Hereditary Spastic Paraplegia:A Magnetic Stimulation Study Ann Neurol 28:43-49, Claus,D.,et al, 1990 Showing articles 0 to 8 of 8