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Arthritis and Rheumatism
|
April 12, 2011
C8orf13-BLK is a genetic risk locus for systemic sclerosis and has additive effects with BANK1: results from a large french cohort and meta-analysis
Baptiste Coustet, Philippe Dieudé, Mickael Guedj, et al.
Genetic Epidemiology
|
November 30, 2007
Multistage designs in the genomic era: providing balance in complex disease studies
Marie-Pierre Dubé, Silke Schmidt, Elizabeth Hauser, et al.
International Journal of Cancer
|
October 11, 2014
Genes involved in the WNT and vesicular trafficking pathways are associated with melanoma predisposition
Maider Ibarrola-Villava, Rajiv Kumar, Eduardo Nagore, et al.
The Journal of Rheumatology
|
March 3, 2011
Association study of ITGAM, ITGAX, and CD58 autoimmune risk loci in systemic sclerosis: results from 2 large European Caucasian cohorts
Baptiste Coustet, Sandeep K Agarwal, Pravitt Gourh, et al.
Genetic Epidemiology
|
November 30, 2007
Multiple testing in the genomics era: findings from Genetic Analysis Workshop 15, Group 15
Lisa J Martin, Jessica G Woo, Christy L Avery, et al.
The Journal of Rheumatology
|
March 17, 2012
Independent replication and meta analysis of association studies establish TNFSF4 as a susceptibility gene preferentially associated with the subset of anticentromere-positive patients with systemic sclerosis
Baptiste Coustet, Matthieu Bouaziz, Philippe Dieudé, et al.
Orphanet Journal of Rare Diseases
|
December 19, 2014
An exploratory randomised double-blind and placebo-controlled phase 2 study of a combination of baclofen, naltrexone and sorbitol (PXT3003) in patients with Charcot-Marie-Tooth disease type 1A
Shahram Attarian, Jean-Michel Vallat, Laurent Magy, et al.
Orphanet Journal of Rare Diseases
|
July 9, 2016
Erratum to: An exploratory randomised double-blind and placebo-controlled phase 2 study of a combination of baclofen, naltrexone and sorbitol (PXT3003) in patients with Charcot-Marie-Tooth disease type 1A
Shahram Attarian, Jean-Michel Vallat, Laurent Magy, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 28) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 28 results.
Arthritis and Rheumatism
|
April 12, 2011
C8orf13-BLK is a genetic risk locus for systemic sclerosis and has additive effects with BANK1: results from a large french cohort and meta-analysis
Baptiste Coustet, Philippe Dieudé, Mickael Guedj, et al.
Genetic Epidemiology
|
November 30, 2007
Multistage designs in the genomic era: providing balance in complex disease studies
Marie-Pierre Dubé, Silke Schmidt, Elizabeth Hauser, et al.
International Journal of Cancer
|
October 11, 2014
Genes involved in the WNT and vesicular trafficking pathways are associated with melanoma predisposition
Maider Ibarrola-Villava, Rajiv Kumar, Eduardo Nagore, et al.
The Journal of Rheumatology
|
March 3, 2011
Association study of ITGAM, ITGAX, and CD58 autoimmune risk loci in systemic sclerosis: results from 2 large European Caucasian cohorts
Baptiste Coustet, Sandeep K Agarwal, Pravitt Gourh, et al.
Genetic Epidemiology
|
November 30, 2007
Multiple testing in the genomics era: findings from Genetic Analysis Workshop 15, Group 15
Lisa J Martin, Jessica G Woo, Christy L Avery, et al.
The Journal of Rheumatology
|
March 17, 2012
Independent replication and meta analysis of association studies establish TNFSF4 as a susceptibility gene preferentially associated with the subset of anticentromere-positive patients with systemic sclerosis
Baptiste Coustet, Matthieu Bouaziz, Philippe Dieudé, et al.
Orphanet Journal of Rare Diseases
|
December 19, 2014
An exploratory randomised double-blind and placebo-controlled phase 2 study of a combination of baclofen, naltrexone and sorbitol (PXT3003) in patients with Charcot-Marie-Tooth disease type 1A
Shahram Attarian, Jean-Michel Vallat, Laurent Magy, et al.
Orphanet Journal of Rare Diseases
|
July 9, 2016
Erratum to: An exploratory randomised double-blind and placebo-controlled phase 2 study of a combination of baclofen, naltrexone and sorbitol (PXT3003) in patients with Charcot-Marie-Tooth disease type 1A
Shahram Attarian, Jean-Michel Vallat, Laurent Magy, et al.
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of 3