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Showing articles 0 to 15 of 15

Filter Applied: genetic neurologic disorders (Click to remove)

Multiple Sclerosis
NEJM 343:938-952, Noseworthy,J.H. et al, 2000

Ion Channel Diseases:Episodic Disorders of the Nervous System
Semin Neurol 19:363-369, Ptacek,L.J., 1999

Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
JNNP 65:427-431, Hanna,M.G.,et al, 1998

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

Conjugal Multiple Sclerosis:A Clinical and Laboratory Study
Neurol 41:1320-1321, Finelli,P.F., 1991

Localization of Idiopathic Generalized Epilepsy on Chromosome 6p in Families of Juvenile Myoclonic epilepsy patients
Neurol 41:1651-1655, Durner,M.,et al, 1991

Narcolspey
NEJM 323:389-394, Aldrich,M.S., 1990

Risk Factors for Multiple Sclerosis:Race or Place? Editorial
JNNP 53:821-823, 903, 906990., Compston,A., 1990

Familial Patterns of Narcolepsy
lancet 2:1376-1379, Guilleminault,C.,et al, 1989

Genetic Factors in Myasthenia Gravis:A Family Study
Neurol 38:38-42, Kerzin-Storrar,L.,et al, 1988

Narcolepsy & Immunity
BMJ 292:359-360, Parkes,J.D.,et al, 1986

The Genetics of Susceptibility to Multiple Sclerosis
Epidemiol Rev 4:45-65, Spielman,R.S.&Nathanson,N., 1982

A Family with Hereditary Ataxia:HLA Typing
Neurol 30:12-20, Nino,H.E.,et al, 1980

Spinocerebellar Ataxia & HLA Linkage:Risk Prediction by HLA Typing
NEJM 296:1138, Jackson,J.F.,et al, 1977

Cause of Weakness in Myasthenia Gravis
NEJM 294:722, Grob,D., 1976



Showing articles 0 to 15 of 15