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Showing articles 0 to 10 of 10 Filter Applied: lysosomal storage disease (Click to remove) Prevalence of Fabry Disease in Patients with Cryptogenic Stroke: A Prospective Study Lancet 366:1794-1796,1754, Rolfs,A.,et al, 2006 Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation JNNP 69: 5-12, Gray,R.G.F. et al, 2000 Niemann-Pick Type C Disease www.UpToDate.com, Nov, Schiffmann, R., 2026 AAV9-Mediated Gene Therapy for Infantile-Onset Pompes Disease NEJM 392:2438-2446, 2477, Ma,X.,et al, 2025 A 65-Year-Old Woman with Isolated Macroglossia as the Initial Presentation of a Rare Disease Neurol 103:e210070, Lara,C.,et al, 2024 A 23-Year-Old Woman Presenting with Cognitive Impairment and Gait Disturbance Neurol 99:997-1003, Chaity,D.K.,et al, 2022 Adult-Onset Niemann-Pick Disease Type C: Rapid Treatment Initiation Advised but Early Diagnosis Remains Difficult Front Neurol doi.10.3398/jneur.2017.00108, Piroth,T.,et al, 2017 Psychosis in an Adolescent Girl: A Common Manifestation in Niemann-Pick Type C Disease Child Adolesc Pych Ment Health 8:20, Wouters,S.,et al, 2014 "Im fine; Im just waiting for my disease" The New and Growing Class of Presymptomatic Patients Neurol 77:522-523, Kwon, J.M.et al, 2011 Glycogen-Storage Disease Type II eMedicine, May 2, Ibrahim,J. &McGovern,M., 2006 Showing articles 0 to 10 of 10