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Donald S Higgins

Showing results (21-30 of 27) with videos related to

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JAMA Neurology|February 7, 2018
Quality of Care for Veterans With Transient Ischemic Attack and Minor StrokeDawn 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 levelIgnacio 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 sclerosisJonathan 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 diseaseIgnacio 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 studyAlexis 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 onsetNancy S Wexler, Judith Lorimer, Julie Porter, et al.
Neurology|December 4, 2016
A randomized, double-blind, placebo-controlled trial of coenzyme Q10 in Huntington diseaseAndrew McGarry, Michael McDermott, Karl Kieburtz, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 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 StrokeDawn 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 levelIgnacio 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 sclerosisJonathan 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 diseaseIgnacio 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 studyAlexis 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 onsetNancy S Wexler, Judith Lorimer, Julie Porter, et al.
Neurology|December 4, 2016
A randomized, double-blind, placebo-controlled trial of coenzyme Q10 in Huntington diseaseAndrew McGarry, Michael McDermott, Karl Kieburtz, et al.
Pageof 3