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Movement Disorders : Official Journal of the Movement Disorder Society
|
December 17, 1997
A gene (ETM) for essential tremor maps to chromosome 2p22-p25
J J Higgins, L T Pho, L E Nee
Neurology
|
February 5, 1999
A lack of the R406W tau mutation in progressive supranuclear palsy and corticobasal degeneration
J J Higgins, I Litvan, L E Nee, et al.
Neurology
|
December 31, 1997
An autosomal recessive disorder with posterior column ataxia and retinitis pigmentosa
J J Higgins, D H Morton, N Patronas, et al.
Alzheimer Disease and Associated Disorders
|
January 1, 1991
Familial Alzheimer disease: a large, multigeneration German kindred
P Frommelt, R Schnabel, W Kühne, et al.
Lancet (London, England)
|
November 3, 1998
Abeta-42 deposition precedes other changes in PS-1 Alzheimer's disease
C F Lippa, L E Nee, H Mori, et al.
Neuroscience
|
December 1, 1992
Studies of activated microglial cells and macrophages using Alzheimer's disease cerebrospinal fluid in adult rats with experimentally induced lesions
E A Ling, A Dahlström, R J Polinsky, et al.
Neurology
|
January 27, 1998
Progressive supranuclear gaze palsy is in linkage disequilibrium with the tau and not the alpha-synuclein gene
J J Higgins, I Litvan, L T Pho, et al.
Annals of Neurology
|
January 1, 1980
Gilles de la Tourette syndrome: clinical and family study of 50 cases
L E Nee, E D Caine, R J Polinsky, et al.
Archives of Neurology
|
April 1, 1983
A family with histologically confirmed Alzheimer's disease
L E Nee, R J Polinsky, R Eldridge, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 1, 1997
Evidence for a new spinocerebellar ataxia locus
J J Higgins, L T Pho, S E Ide, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 47) with videos related to
Sort By:
Page
of 5
Movement Disorders : Official Journal of the Movement Disorder Society
|
December 17, 1997
A gene (ETM) for essential tremor maps to chromosome 2p22-p25
J J Higgins, L T Pho, L E Nee
Neurology
|
February 5, 1999
A lack of the R406W tau mutation in progressive supranuclear palsy and corticobasal degeneration
J J Higgins, I Litvan, L E Nee, et al.
Neurology
|
December 31, 1997
An autosomal recessive disorder with posterior column ataxia and retinitis pigmentosa
J J Higgins, D H Morton, N Patronas, et al.
Alzheimer Disease and Associated Disorders
|
January 1, 1991
Familial Alzheimer disease: a large, multigeneration German kindred
P Frommelt, R Schnabel, W Kühne, et al.
Lancet (London, England)
|
November 3, 1998
Abeta-42 deposition precedes other changes in PS-1 Alzheimer's disease
C F Lippa, L E Nee, H Mori, et al.
Neuroscience
|
December 1, 1992
Studies of activated microglial cells and macrophages using Alzheimer's disease cerebrospinal fluid in adult rats with experimentally induced lesions
E A Ling, A Dahlström, R J Polinsky, et al.
Neurology
|
January 27, 1998
Progressive supranuclear gaze palsy is in linkage disequilibrium with the tau and not the alpha-synuclein gene
J J Higgins, I Litvan, L T Pho, et al.
Annals of Neurology
|
January 1, 1980
Gilles de la Tourette syndrome: clinical and family study of 50 cases
L E Nee, E D Caine, R J Polinsky, et al.
Archives of Neurology
|
April 1, 1983
A family with histologically confirmed Alzheimer's disease
L E Nee, R J Polinsky, R Eldridge, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 1, 1997
Evidence for a new spinocerebellar ataxia locus
J J Higgins, L T Pho, S E Ide, et al.
Page
of 5