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Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society
|
March 1, 1991
Environmental-occupational risk factors and familial associations in multiple system atrophy: a preliminary investigation
L E Nee, M R Gomez, J Dambrosia, et al.
Advances in Neurology
|
January 1, 1982
Heterogeneity and variability in Tourette syndrome
E D Caine, R J Polinsky, C L Ludlow, et al.
Journal of the Neurological Sciences
|
February 13, 2001
Platelet APP isoform ratios in asymptomatic young adults expressing an AD-related presenilin-1 mutation
F Baskin, R N Rosenberg, L Iyer, et al.
Human Genetics
|
June 1, 1991
Exclusion of linkage to the pericentromeric region of chromosome 21 in the Canadian pedigree with familial Alzheimer disease
S M Pulst, P Fain, V Cohn, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
September 1, 1985
Parkinson's disease and Alzheimer's disease: hypersensitivity to X rays in cultured cell lines
J H Robbins, F Otsuka, R E Tarone, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
June 1, 1987
Dominantly inherited Alzheimer's disease: cerebral glucose metabolism
R J Polinsky, H Noble, G Di Chiro, et al.
Mutation Research
|
January 1, 1986
Alzheimer disease fibroblasts are hypersensitive to the lethal effects of a DNA-damaging chemical
D A Scudiero, R J Polinsky, R A Brumback, et al.
Journal of Clinical Psychopharmacology
|
November 1, 1981
A double-blind controlled trial of lithium carbonate primary anorexia nervosa
H A Gross, M H Ebert, V B Faden, et al.
Neurology
|
June 13, 2001
An atypical intronic deletion widens the spectrum of mutations in hereditary spastic paraplegia
J J Higgins, J M Loveless, S Goswami, et al.
Neurology
|
January 1, 1996
Mutations in American families with spinocerebellar ataxia (SCA) type 3: SCA3 is allelic to Machado-Joseph disease
J J Higgins, L E Nee, O Vasconcelos, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 47) with videos related to
Sort By:
Page
of 5
Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society
|
March 1, 1991
Environmental-occupational risk factors and familial associations in multiple system atrophy: a preliminary investigation
L E Nee, M R Gomez, J Dambrosia, et al.
Advances in Neurology
|
January 1, 1982
Heterogeneity and variability in Tourette syndrome
E D Caine, R J Polinsky, C L Ludlow, et al.
Journal of the Neurological Sciences
|
February 13, 2001
Platelet APP isoform ratios in asymptomatic young adults expressing an AD-related presenilin-1 mutation
F Baskin, R N Rosenberg, L Iyer, et al.
Human Genetics
|
June 1, 1991
Exclusion of linkage to the pericentromeric region of chromosome 21 in the Canadian pedigree with familial Alzheimer disease
S M Pulst, P Fain, V Cohn, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
September 1, 1985
Parkinson's disease and Alzheimer's disease: hypersensitivity to X rays in cultured cell lines
J H Robbins, F Otsuka, R E Tarone, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
June 1, 1987
Dominantly inherited Alzheimer's disease: cerebral glucose metabolism
R J Polinsky, H Noble, G Di Chiro, et al.
Mutation Research
|
January 1, 1986
Alzheimer disease fibroblasts are hypersensitive to the lethal effects of a DNA-damaging chemical
D A Scudiero, R J Polinsky, R A Brumback, et al.
Journal of Clinical Psychopharmacology
|
November 1, 1981
A double-blind controlled trial of lithium carbonate primary anorexia nervosa
H A Gross, M H Ebert, V B Faden, et al.
Neurology
|
June 13, 2001
An atypical intronic deletion widens the spectrum of mutations in hereditary spastic paraplegia
J J Higgins, J M Loveless, S Goswami, et al.
Neurology
|
January 1, 1996
Mutations in American families with spinocerebellar ataxia (SCA) type 3: SCA3 is allelic to Machado-Joseph disease
J J Higgins, L E Nee, O Vasconcelos, et al.
Page
of 5