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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 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 The Motor Disorder of Multiple System Atrophy JNNP 56:1239-1242, Quinn,N.P.&Marsden,C.D., 1993 Brain MRI and Electrophysiologic Abnormalities in Preclinical and Clinical Adrenomyeloneuropathy Neurol 42:85-91, Aubourg,P.,et al, 1992 Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases Neurol 42:312-319, Manetto,V.,et al, 1992 Primary Lateral Sclerosis, Clin Features, Neuropath & Dx Criteria Brain 115:495-520, Pringle,C.E.,et al, 1992 Neuronal Intranuclear Inclusion Disease in a Child:Diagnosis by Rectal Biopsy Ann Neurol 27:103-106, Goutieres,F.,et al, 1990 Post-encephalitic Parkinsonism:Current Experience JNNP 44:670-676, Rail,D.,et al, 1981 Showing articles 0 to 9 of 9