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Showing articles 0 to 12 of 12 Filter Applied: pyramidal tract dysfunction (Click to remove) 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 Multiple-System Atrophy NEJM 372:249-263, Fanciulli, A. & Wenning, G.K., 2015 Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006 Clinicopathological Study of 35 Cases of Multiple System Atrophy JNNP 58:160-166, Wenning,G.K.,et al, 1995 Asymmetrical Skin Temperature in Ischemic Stroke Stroke 26:1543-1547, Korpelainen,J.T.,et al, 1995 The Motor Disorder of Multiple System Atrophy JNNP 56:1239-1242, Quinn,N.P.&Marsden,C.D., 1993 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 Neurologic Aspects of Cobalamin Deficiency Medicine 70:229-245, Healton,E.B.,et al, 1991 Neurological Complications in Infants & Children with Acquired Immune Deficiency Syndrome Ann Neurol 18:560-566, Belman,A.L.,et al, 1985 Chronic Meningitis Medicine 55:341, Ellner,J.J.,et al, 1976 Mollaret's Meningitis & Differential Diagnosis of Recurrent Meningitis Am J Med 52:128, Hermans,P.,et al, 1972 Showing articles 0 to 12 of 12