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JAMA Neurology
|
February 7, 2018
Quality of Care for Veterans With Transient Ischemic Attack and Minor Stroke
Dawn M Bravata, Laura J Myers, Greg Arling, et al.
Archives of Neurology
|
November 10, 2010
SNCA variant associated with Parkinson disease and plasma alpha-synuclein level
Ignacio F Mata, Min Shi, Pinky Agarwal, et al.
Neurology
|
June 29, 2018
Independent home use of a brain-computer interface by people with amyotrophic lateral sclerosis
Jonathan R Wolpaw, Richard S Bedlack, Domenic J Reda, 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.
Proceedings of the National Academy of Sciences of the United States of America
|
March 3, 2004
Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset
Nancy S Wexler, Judith Lorimer, Julie Porter, et al.
Neurology
|
December 4, 2016
A randomized, double-blind, placebo-controlled trial of coenzyme Q10 in Huntington disease
Andrew McGarry, Michael McDermott, Karl Kieburtz, et al.
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of 3
Search research articles
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Showing results (21-30 of 27) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 27 results.
JAMA Neurology
|
February 7, 2018
Quality of Care for Veterans With Transient Ischemic Attack and Minor Stroke
Dawn M Bravata, Laura J Myers, Greg Arling, et al.
Archives of Neurology
|
November 10, 2010
SNCA variant associated with Parkinson disease and plasma alpha-synuclein level
Ignacio F Mata, Min Shi, Pinky Agarwal, et al.
Neurology
|
June 29, 2018
Independent home use of a brain-computer interface by people with amyotrophic lateral sclerosis
Jonathan R Wolpaw, Richard S Bedlack, Domenic J Reda, 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.
Proceedings of the National Academy of Sciences of the United States of America
|
March 3, 2004
Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset
Nancy S Wexler, Judith Lorimer, Julie Porter, et al.
Neurology
|
December 4, 2016
A randomized, double-blind, placebo-controlled trial of coenzyme Q10 in Huntington disease
Andrew McGarry, Michael McDermott, Karl Kieburtz, et al.
Page
of 3