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Science Translational Medicine
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April 1, 2016
Familial autoinflammation with neutrophilic dermatosis reveals a regulatory mechanism of pyrin activation
Seth L Masters, Vasiliki Lagou, Isabelle Jéru, et al.
Human Molecular Genetics
|
November 16, 2013
No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis
An Goris, Jessica van Setten, Frank Diekstra, et al.
Nature Communications
|
March 29, 2019
Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusions
Montse Olivé, Martin Engvall, Gianina Ravenscroft, et al.
Neurobiology of Aging
|
May 20, 2014
Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study
Perry T C van Doormaal, Nicola Ticozzi, Cinzia Gellera, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 25, 2009
The role of the CD58 locus in multiple sclerosis
Philip L De Jager, Clare Baecher-Allan, Lisa M Maier, et al.
Nature Genetics
|
May 27, 2010
Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis
, David R Booth, Robert N Heard, et al.
Neurology
|
July 18, 2014
Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12
Laura L Kilarski, Sefanja Achterberg, William J Devan, et al.
Brain : a Journal of Neurology
|
January 25, 2015
Genetic variants are major determinants of CSF antibody levels in multiple sclerosis
An Goris, Ine Pauwels, Marte W Gustavsen, et al.
G3 (Bethesda, Md.)
|
May 20, 2016
Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients
A Dessa Sadovnick, Anthony L Traboulsee, Cecily Q Bernales, et al.
Neuroimage
|
April 5, 2016
Power estimation for non-standardized multisite studies
Anisha Keshavan, Friedemann Paul, Mona K Beyer, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 86) with videos related to
Sort By:
Page
of 9
Science Translational Medicine
|
April 1, 2016
Familial autoinflammation with neutrophilic dermatosis reveals a regulatory mechanism of pyrin activation
Seth L Masters, Vasiliki Lagou, Isabelle Jéru, et al.
Human Molecular Genetics
|
November 16, 2013
No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis
An Goris, Jessica van Setten, Frank Diekstra, et al.
Nature Communications
|
March 29, 2019
Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusions
Montse Olivé, Martin Engvall, Gianina Ravenscroft, et al.
Neurobiology of Aging
|
May 20, 2014
Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study
Perry T C van Doormaal, Nicola Ticozzi, Cinzia Gellera, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 25, 2009
The role of the CD58 locus in multiple sclerosis
Philip L De Jager, Clare Baecher-Allan, Lisa M Maier, et al.
Nature Genetics
|
May 27, 2010
Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis
, David R Booth, Robert N Heard, et al.
Neurology
|
July 18, 2014
Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12
Laura L Kilarski, Sefanja Achterberg, William J Devan, et al.
Brain : a Journal of Neurology
|
January 25, 2015
Genetic variants are major determinants of CSF antibody levels in multiple sclerosis
An Goris, Ine Pauwels, Marte W Gustavsen, et al.
G3 (Bethesda, Md.)
|
May 20, 2016
Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients
A Dessa Sadovnick, Anthony L Traboulsee, Cecily Q Bernales, et al.
Neuroimage
|
April 5, 2016
Power estimation for non-standardized multisite studies
Anisha Keshavan, Friedemann Paul, Mona K Beyer, et al.
Page
of 9