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Showing articles 0 to 9 of 9

Filter Applied: pyramidal tract dysfunction (Click to remove)

Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006

Dysarthria in Acute Ischemic Stroke
Neurol 56:1021-1027, Urban,P.P.,et al, 2001

Presence of Diarrhea and Absence of Tendon Xanthomas in Patients With Cerebrotendinous Xanthomatosis
Arch Neurol 57:520-524, Verrips,A.,et al, 2000

Clinical Correlates of Vascular Parkinsonism
Arch Neurol 56:98-102, Winikates,J.&Jancovic,J., 1999

Disequilibrium in Patients with Atherosclerosis; Relevance of Pontine Ischemic Rarefaction
Neurol 51:570-573, Kwa,V.I.H.,et al, 1998

Asymmetrical Skin Temperature in Ischemic Stroke
Stroke 26:1543-1547, Korpelainen,J.T.,et al, 1995

Clinicopath Conf
Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992

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 9 of 9