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Showing articles 0 to 8 of 8 Filter Applied: cerebellar atrophy,primary (Click to remove) Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches Lancet Neurol 18:1136-1146, Shribman,S.,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 A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes Ann Neurol 77:1-7, Scripko, P.,et al, 2015 Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis NEJM 364:1062-1074, Case 8-2011, 2011 A 23-Year-Old Man With Seizures and Visual Deficit Neurol 70:73-78, Boustany,R.-M.,et al, 2008 Cerebellar Ataxia With Anti-Glutamic Acid Decarboxylase Antibodies Arch Neurol 58:225-230, Honorat,J.,et al, 2001 CAG Repeat Number Correlates with the Rate of Brainstem and Cerebellar Atrophy in Machado-Joseph Disease Neurol 51:882-884, Abe,Y.,et al, 1998 Idiopathic Cerebellar Ataxia of Late Onset:Natural History and MRI Morphology JNNP 53:297-305, Klockgether,T.,et al, 1990 Showing articles 0 to 8 of 8