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Showing articles 0 to 12 of 12 Filter Applied: lysosomal storage disease (Click to remove) Pes Cavus and Neuropathy Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019 Clinicopathologic Conference, Tay-Sacks Disease (GM2, Gangliosidosis) NEJM 370:1830-1841, Case 14-2014, 2014 Glycogen-Storage Disease Type II eMedicine, May 2, Ibrahim,J. &McGovern,M., 2006 Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype NEJM 347:672-680, Case 27-2002, 2002 Follow-up of Nine Patients with Hurler Syndrome After Bone Marrow Transplantation J Pediatr 133:119-125, 71998., Guffon,N.,et al, 1998 Fucosidosis Revisited:A Review of 77 Patients Am J Med Genet 38:111-131, Willems,P.J.,et al, 1991 Long-Term Effects of Antidarsagene Autotemcel for Metachromatic Leukodystrophy NEJM 392:1609-1620, Fumagalli,F.,et al, 2025 A 23-Year-Old Woman Presenting with Cognitive Impairment and Gait Disturbance Neurol 99:997-1003, Chaity,D.K.,et al, 2022 Hematopoietic Stem - and Progenitor-Cell Gene Therapy for Hurler Syndrome NEJM 385:1929-1940, Gentner, B.,et al, 2021 Enzyme Replacement Therapy With Agalsidase Alfa in Patients With Fabrys Disease: An Analysis of Registry Data Lancet 374:1986-1996, 1950, Mehta,A.,et al, 2009 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 Mucolipidosis Type IV; Characteristic MRI Findings Neurol 51:565-569, Frei,K.P.,et al, 1998 Showing articles 0 to 12 of 12