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Neurology
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June 23, 2012
Randomized trial of deep brain stimulation for Parkinson disease: thirty-six-month outcomes
Frances M Weaver, Kenneth A Follett, Matthew Stern, et al.
Plos Genetics
|
August 31, 2011
Genome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffee
Taye H Hamza, Honglei Chen, Erin M Hill-Burns, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 2, 2012
Common variation in the LRRK2 gene is a risk factor for Parkinson's disease
Ignacio F Mata, Harvey Checkoway, Carolyn M Hutter, et al.
Molecular Neurodegeneration
|
September 25, 2015
The RAB39B p.G192R mutation causes X-linked dominant Parkinson's disease
Ignacio F Mata, Yongwoo Jang, Chun-Hyung Kim, et al.
The Lancet. Neurology
|
October 21, 2006
Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study
Alexis Elbaz, Lorene M Nelson, Haydeh Payami, et al.
Annals of Neurology
|
May 3, 2021
Genomewide Association Studies of LRRK2 Modifiers of Parkinson's Disease
Dongbing Lai, Babak Alipanahi, Pierre Fontanillas, et al.
The New England Journal of Medicine
|
January 26, 2017
Genetic Drivers of Kidney Defects in the DiGeorge Syndrome
Esther Lopez-Rivera, Yangfan P Liu, Miguel Verbitsky, et al.
JAMA
|
July 6, 2016
Effect of Deutetrabenazine on Chorea Among Patients With Huntington Disease: A Randomized Clinical Trial
, Samuel Frank, Claudia M Testa, et al.
JAMA Neurology
|
November 17, 2015
Clinical-Genetic Associations in the Prospective Huntington at Risk Observational Study (PHAROS): Implications for Clinical Trials
, Kevin Michael Biglan, Ira Shoulson, et al.
Page
of 9
Search research articles
Search
Showing results (81-90 of 89) with videos related to
Sort By:
Page
of 9
You have reached the last page of results.
This site can display upto 89 results.
Neurology
|
June 23, 2012
Randomized trial of deep brain stimulation for Parkinson disease: thirty-six-month outcomes
Frances M Weaver, Kenneth A Follett, Matthew Stern, et al.
Plos Genetics
|
August 31, 2011
Genome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffee
Taye H Hamza, Honglei Chen, Erin M Hill-Burns, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 2, 2012
Common variation in the LRRK2 gene is a risk factor for Parkinson's disease
Ignacio F Mata, Harvey Checkoway, Carolyn M Hutter, et al.
Molecular Neurodegeneration
|
September 25, 2015
The RAB39B p.G192R mutation causes X-linked dominant Parkinson's disease
Ignacio F Mata, Yongwoo Jang, Chun-Hyung Kim, et al.
The Lancet. Neurology
|
October 21, 2006
Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study
Alexis Elbaz, Lorene M Nelson, Haydeh Payami, et al.
Annals of Neurology
|
May 3, 2021
Genomewide Association Studies of LRRK2 Modifiers of Parkinson's Disease
Dongbing Lai, Babak Alipanahi, Pierre Fontanillas, et al.
The New England Journal of Medicine
|
January 26, 2017
Genetic Drivers of Kidney Defects in the DiGeorge Syndrome
Esther Lopez-Rivera, Yangfan P Liu, Miguel Verbitsky, et al.
JAMA
|
July 6, 2016
Effect of Deutetrabenazine on Chorea Among Patients With Huntington Disease: A Randomized Clinical Trial
, Samuel Frank, Claudia M Testa, et al.
JAMA Neurology
|
November 17, 2015
Clinical-Genetic Associations in the Prospective Huntington at Risk Observational Study (PHAROS): Implications for Clinical Trials
, Kevin Michael Biglan, Ira Shoulson, et al.
Page
of 9