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JAMA Neurology
|
April 5, 2013
Neuropathologic basis of age-associated brain atrophy
Deniz Erten-Lyons, Hiroko H Dodge, Randall Woltjer, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 27, 2005
Parkinson's disease and LRRK2: frequency of a common mutation in U.S. movement disorder clinics
Denise M Kay, Cyrus P Zabetian, Stewart A Factor, et al.
North Carolina Medical Journal
|
July 10, 2020
Academic-Practice Partnership for Caregiver Training and Support: The Duke Elder Family/Caregiver Training (DEFT) Center
Cristina C Hendrix, Doreen Matters, Tamara Griffin, et al.
American Journal of Medical Genetics. Part A
|
August 21, 2007
Narrowing the DYT6 dystonia region and evidence for locus heterogeneity in the Amish-Mennonites
Rachel Saunders-Pullman, Deborah Raymond, Geetha Senthil, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 25, 2004
Distribution, type, and origin of Parkin mutations: review and case studies
Katja Hedrich, Cordula Eskelson, Beth Wilmot, et al.
Nature Genetics
|
June 20, 2006
PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron
Neil V Morgan, Shawn K Westaway, Jenny E V Morton, et al.
Neurology
|
October 5, 2012
GBA mutations increase risk for Lewy body disease with and without Alzheimer disease pathology
Debby Tsuang, James B Leverenz, Oscar L Lopez, et al.
JAMA Neurology
|
February 15, 2013
APOE ε4 increases risk for dementia in pure synucleinopathies
Debby Tsuang, James B Leverenz, Oscar L Lopez, et al.
Plos Genetics
|
September 5, 2014
Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias
Gary W Beecham, Kara Hamilton, Adam C Naj, et al.
Archives of Neurology
|
August 11, 2010
Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes
Gyungah Jun, Adam C Naj, Gary W Beecham, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 23) with videos related to
Sort By:
Page
of 3
JAMA Neurology
|
April 5, 2013
Neuropathologic basis of age-associated brain atrophy
Deniz Erten-Lyons, Hiroko H Dodge, Randall Woltjer, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 27, 2005
Parkinson's disease and LRRK2: frequency of a common mutation in U.S. movement disorder clinics
Denise M Kay, Cyrus P Zabetian, Stewart A Factor, et al.
North Carolina Medical Journal
|
July 10, 2020
Academic-Practice Partnership for Caregiver Training and Support: The Duke Elder Family/Caregiver Training (DEFT) Center
Cristina C Hendrix, Doreen Matters, Tamara Griffin, et al.
American Journal of Medical Genetics. Part A
|
August 21, 2007
Narrowing the DYT6 dystonia region and evidence for locus heterogeneity in the Amish-Mennonites
Rachel Saunders-Pullman, Deborah Raymond, Geetha Senthil, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 25, 2004
Distribution, type, and origin of Parkin mutations: review and case studies
Katja Hedrich, Cordula Eskelson, Beth Wilmot, et al.
Nature Genetics
|
June 20, 2006
PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron
Neil V Morgan, Shawn K Westaway, Jenny E V Morton, et al.
Neurology
|
October 5, 2012
GBA mutations increase risk for Lewy body disease with and without Alzheimer disease pathology
Debby Tsuang, James B Leverenz, Oscar L Lopez, et al.
JAMA Neurology
|
February 15, 2013
APOE ε4 increases risk for dementia in pure synucleinopathies
Debby Tsuang, James B Leverenz, Oscar L Lopez, et al.
Plos Genetics
|
September 5, 2014
Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias
Gary W Beecham, Kara Hamilton, Adam C Naj, et al.
Archives of Neurology
|
August 11, 2010
Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes
Gyungah Jun, Adam C Naj, Gary W Beecham, et al.
Page
of 3