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Movement Disorders : Official Journal of the Movement Disorder Society
|
November 3, 2023
Frequency of Hereditary and GBA1-Related Parkinsonism in Latin America: A Systematic Review and Meta-Analysis
Paula Saffie Awad, Daniel Teixeira-Dos-Santos, Bruno Lopes Santos-Lobato, et al.
Reviews in the Neurosciences
|
November 5, 2020
Genetic parkinsonisms and cancer: a systematic review and meta-analysis
Andrea Sturchio, Alok K Dwivedi, Joaquin A Vizcarra, et al.
NPJ Parkinson'S Disease
|
September 5, 2020
Multivariate prediction of dementia in Parkinson's disease
Thanaphong Phongpreecha, Brenna Cholerton, Ignacio F Mata, et al.
Neurogenetics
|
September 21, 2005
Lrrk2 pathogenic substitutions in Parkinson's disease
Ignacio F Mata, Jennifer M Kachergus, Julie P Taylor, et al.
Parkinsonism & Related Disorders
|
August 17, 2005
Clinical traits of LRRK2-associated Parkinson's disease in Ireland: a link between familial and idiopathic PD
David Gosal, Owen A Ross, Joe Wiley, et al.
Parkinsonism & Related Disorders
|
February 25, 2011
The UCHL1 S18Y polymorphism and Parkinson's disease in a Japanese population
Katherine W Snapinn, Eric B Larson, Hideshi Kawakami, et al.
Parkinsonism & Related Disorders
|
February 16, 2019
The distribution and risk effect of GBA variants in a large cohort of PD patients from Colombia and Peru
Carlos Velez-Pardo, Oswaldo Lorenzo-Betancor, Marlene Jimenez-Del-Rio, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
July 20, 2024
Assessing the lack of diversity in genetics research across neurodegenerative diseases: A systematic review of the GWAS Catalog and literature
Caroline Jonson, Kristin S Levine, Julie Lake, et al.
Medrxiv : the Preprint Server for Health Sciences
|
January 23, 2024
Assessing the lack of diversity in genetics research across neurodegenerative diseases: a systematic review of the GWAS Catalog and literature
Caroline Jonson, Kristin S Levine, Julie Lake, et al.
Journal of Molecular Neuroscience : MN
|
January 1, 2013
Mutational screening of PARKIN identified a 3' UTR variant (rs62637702) associated with Parkinson's disease
Lorena de Mena, L Luís Samaranch, Eliecer Coto, et al.
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of 13
Search research articles
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Showing results (61-70 of 128) with videos related to
Sort By:
Page
of 13
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 3, 2023
Frequency of Hereditary and GBA1-Related Parkinsonism in Latin America: A Systematic Review and Meta-Analysis
Paula Saffie Awad, Daniel Teixeira-Dos-Santos, Bruno Lopes Santos-Lobato, et al.
Reviews in the Neurosciences
|
November 5, 2020
Genetic parkinsonisms and cancer: a systematic review and meta-analysis
Andrea Sturchio, Alok K Dwivedi, Joaquin A Vizcarra, et al.
NPJ Parkinson'S Disease
|
September 5, 2020
Multivariate prediction of dementia in Parkinson's disease
Thanaphong Phongpreecha, Brenna Cholerton, Ignacio F Mata, et al.
Neurogenetics
|
September 21, 2005
Lrrk2 pathogenic substitutions in Parkinson's disease
Ignacio F Mata, Jennifer M Kachergus, Julie P Taylor, et al.
Parkinsonism & Related Disorders
|
August 17, 2005
Clinical traits of LRRK2-associated Parkinson's disease in Ireland: a link between familial and idiopathic PD
David Gosal, Owen A Ross, Joe Wiley, et al.
Parkinsonism & Related Disorders
|
February 25, 2011
The UCHL1 S18Y polymorphism and Parkinson's disease in a Japanese population
Katherine W Snapinn, Eric B Larson, Hideshi Kawakami, et al.
Parkinsonism & Related Disorders
|
February 16, 2019
The distribution and risk effect of GBA variants in a large cohort of PD patients from Colombia and Peru
Carlos Velez-Pardo, Oswaldo Lorenzo-Betancor, Marlene Jimenez-Del-Rio, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
July 20, 2024
Assessing the lack of diversity in genetics research across neurodegenerative diseases: A systematic review of the GWAS Catalog and literature
Caroline Jonson, Kristin S Levine, Julie Lake, et al.
Medrxiv : the Preprint Server for Health Sciences
|
January 23, 2024
Assessing the lack of diversity in genetics research across neurodegenerative diseases: a systematic review of the GWAS Catalog and literature
Caroline Jonson, Kristin S Levine, Julie Lake, et al.
Journal of Molecular Neuroscience : MN
|
January 1, 2013
Mutational screening of PARKIN identified a 3' UTR variant (rs62637702) associated with Parkinson's disease
Lorena de Mena, L Luís Samaranch, Eliecer Coto, et al.
Page
of 13