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Showing articles 0 to 10 of 10 Filter Applied: optic atrophy (Click to remove) Hallervorden-Spatz Syndrome and Brain Iron Metabolism Arch Neurol 48:1285-1293, Swaiman,K.F., 1991 Clinicopathological Conference Metachromatic Leukodystrophy (juvenile type) Case 7-1984, NEJM 310:445-4551984., , 1984 The Phenotypic Continuum of ATP1A3-Related Disorders Neurol 99:e1511-e1526, Vezyroglou,A., et al, 2022 Infantile Bilateral Striatal Necrosis Maps to Chromosome 19q Neurol 62:87-90, Basel-Vanagaite,L.,et al, 2004 Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities Ann Neurol 39:343-351, Rahman,S.,et al, 1996 Clinicopath Conf Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992 Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging Neurol 42:1220-1224, 1992,, Rando,T.A.,et al, 1992 Juvenile Metachromatic Leukodystrophy Arch Neurol 37:42-46, Haltia,T.,et al, 1980 Dominant Spinopontine Atrophy Arch Neurol 35:156, Pogacar,S.,et al, 1978 Progressive Rubella Panencephalitis Arch Neurol 33:722, Wolinsky,J.S.,et al, 1976 Showing articles 0 to 10 of 10