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Showing articles 0 to 8 of 8 Filter Applied: pyramidal tract dysfunction (Click to remove) Aicardi-Gouti�res Syndrome Br Med Bull 89:183-201, Orcesi, S.,et al, 2009 Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006 Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases Neurol 42:312-319, Manetto,V.,et al, 1992 Clinicopath Conf Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992 Hallervorden-Spatz Syndrome and Brain Iron Metabolism Arch Neurol 48:1285-1293, Swaiman,K.F., 1991 Acute Extrapyramidal Syndrome in Methylmalonic Acidemia:"Metabolic Stroke"Involving the Globus Pallidus J Pediatr 113:1022-1027, Heidenreich,R.,et al, 1988 Post-encephalitic Parkinsonism:Current Experience JNNP 44:670-676, Rail,D.,et al, 1981 Autosomal Dominant System Degeneration in Portugese Families of the Azores Islands Neurol 28:703, Coutinho,P.,et al, 1978 Showing articles 0 to 8 of 8