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Genome Medicine
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January 14, 2018
Correction to: Linkage, whole genome sequence, and biological data implicate variants in RAB10 in Alzheimer's disease resilience
Perry G Ridge, Celeste M Karch, Simon Hsu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 25, 2022
MED27, SLC6A7, and MPPE1 Variants in a Complex Neurodevelopmental Disorder with Severe Dystonia
Kimberley M Reid, Robert Spaull, Smrithi Salian, et al.
Annals of Neurology
|
May 29, 2009
SNCA variants are associated with increased risk for multiple system atrophy
Sonja W Scholz, Henry Houlden, Claudia Schulte, et al.
Brain : a Journal of Neurology
|
March 17, 2025
Genome-wide association study of neuropathological features in Lewy body disease
Rebecca R Valentino, Shunsuke Koga, Alexandra I Soto-Beasley, et al.
Neurobiology of Aging
|
June 13, 2017
NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases
Cornelis Blauwendraat, Faraz Faghri, Lasse Pihlstrom, et al.
BMC Neurology
|
April 20, 2017
Study protocol: Insight 46 - a neuroscience sub-study of the MRC National Survey of Health and Development
Christopher A Lane, Thomas D Parker, Dave M Cash, et al.
Human Molecular Genetics
|
June 29, 2014
Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies
Jose Bras, Rita Guerreiro, Lee Darwent, et al.
Neurobiology of Aging
|
January 21, 2014
Missense variant in TREML2 protects against Alzheimer's disease
Bruno A Benitez, Sheng Chih Jin, Rita Guerreiro, et al.
Neurobiology of Aging
|
December 9, 2015
Genome-wide analysis of genetic correlation in dementia with Lewy bodies, Parkinson's and Alzheimer's diseases
Rita Guerreiro, Valentina Escott-Price, Lee Darwent, et al.
Brain : a Journal of Neurology
|
July 5, 2014
Parkinson's disease in GTP cyclohydrolase 1 mutation carriers
Niccolò E Mencacci, Ioannis U Isaias, Martin M Reich, et al.
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Search research articles
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Showing results (91-100 of 118) with videos related to
Sort By:
Page
of 12
Genome Medicine
|
January 14, 2018
Correction to: Linkage, whole genome sequence, and biological data implicate variants in RAB10 in Alzheimer's disease resilience
Perry G Ridge, Celeste M Karch, Simon Hsu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 25, 2022
MED27, SLC6A7, and MPPE1 Variants in a Complex Neurodevelopmental Disorder with Severe Dystonia
Kimberley M Reid, Robert Spaull, Smrithi Salian, et al.
Annals of Neurology
|
May 29, 2009
SNCA variants are associated with increased risk for multiple system atrophy
Sonja W Scholz, Henry Houlden, Claudia Schulte, et al.
Brain : a Journal of Neurology
|
March 17, 2025
Genome-wide association study of neuropathological features in Lewy body disease
Rebecca R Valentino, Shunsuke Koga, Alexandra I Soto-Beasley, et al.
Neurobiology of Aging
|
June 13, 2017
NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases
Cornelis Blauwendraat, Faraz Faghri, Lasse Pihlstrom, et al.
BMC Neurology
|
April 20, 2017
Study protocol: Insight 46 - a neuroscience sub-study of the MRC National Survey of Health and Development
Christopher A Lane, Thomas D Parker, Dave M Cash, et al.
Human Molecular Genetics
|
June 29, 2014
Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies
Jose Bras, Rita Guerreiro, Lee Darwent, et al.
Neurobiology of Aging
|
January 21, 2014
Missense variant in TREML2 protects against Alzheimer's disease
Bruno A Benitez, Sheng Chih Jin, Rita Guerreiro, et al.
Neurobiology of Aging
|
December 9, 2015
Genome-wide analysis of genetic correlation in dementia with Lewy bodies, Parkinson's and Alzheimer's diseases
Rita Guerreiro, Valentina Escott-Price, Lee Darwent, et al.
Brain : a Journal of Neurology
|
July 5, 2014
Parkinson's disease in GTP cyclohydrolase 1 mutation carriers
Niccolò E Mencacci, Ioannis U Isaias, Martin M Reich, et al.
Page
of 12