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Plos One
|
September 7, 2012
Creation of an open-access, mutation-defined fibroblast resource for neurological disease research
Selina Wray, Matthew Self, , et al.
BMC Medicine
|
November 7, 2008
The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD study
Jeanne C Latourelle, Mei Sun, Mark F Lew, 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.
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.
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of 7
Search research articles
Search
Showing results (61-70 of 64) with videos related to
Sort By:
Page
of 7
You have reached the last page of results.
This site can display upto 64 results.
Plos One
|
September 7, 2012
Creation of an open-access, mutation-defined fibroblast resource for neurological disease research
Selina Wray, Matthew Self, , et al.
BMC Medicine
|
November 7, 2008
The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD study
Jeanne C Latourelle, Mei Sun, Mark F Lew, 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.
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 7