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Showing articles 0 to 9 of 9 Filter Applied: pyramidal tract dysfunction (Click to remove) Clinicopath Conf Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992 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 Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006 Clinical Correlates of Vascular Parkinsonism Arch Neurol 56:98-102, Winikates,J.&Jancovic,J., 1999 MR of Childhood Metachromatic Leukodystrophy AJNR 18:733-738, Kim,T.S.,et al, 1997 The Motor Disorder of Multiple System Atrophy JNNP 56:1239-1242, Quinn,N.P.&Marsden,C.D., 1993 Hallervorden-Spatz Syndrome and Brain Iron Metabolism Arch Neurol 48:1285-1293, Swaiman,K.F., 1991 Neuronal Intranuclear Inclusion Disease in a Child:Diagnosis by Rectal Biopsy Ann Neurol 27:103-106, Goutieres,F.,et al, 1990 The Acquired Immunodeficiency Syndrome (AIDS) Dementia Complex Ann Int Med 111:400-410, Ho,D.D.,et al, 1989 Showing articles 0 to 9 of 9