Search details
1.
Adaptive human immunity drives remyelination in a mouse model of demyelination.
Brain
; 140(4): 967-980, 2017 Apr 01.
Article
in English
| MEDLINE | ID: mdl-28334918
2.
Power estimation for non-standardized multisite studies.
Neuroimage
; 134: 281-294, 2016 07 01.
Article
in English
| MEDLINE | ID: mdl-27039700
3.
MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis.
Brain
; 136(Pt 6): 1778-82, 2013 Jun.
Article
in English
| MEDLINE | ID: mdl-23739915
4.
Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1.
PLoS Genet
; 7(7): e1002171, 2011 Jul.
Article
in English
| MEDLINE | ID: mdl-21779176
5.
Closing the case of APOE in multiple sclerosis: no association with disease risk in over 29 000 subjects.
J Med Genet
; 49(9): 558-62, 2012 Sep.
Article
in English
| MEDLINE | ID: mdl-22972946
6.
Tyrosine kinase 2 variant influences T lymphocyte polarization and multiple sclerosis susceptibility.
Brain
; 134(Pt 3): 693-703, 2011 Mar.
Article
in English
| MEDLINE | ID: mdl-21354972
7.
Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk.
J Med Genet
; 50(3): 140-3, 2013 Mar.
Article
in English
| MEDLINE | ID: mdl-23315543
8.
Linkage disequilibrium screening for multiple sclerosis implicates JAG1 and POU2AF1 as susceptibility genes in Europeans.
J Neuroimmunol
; 179(1-2): 108-16, 2006 Oct.
Article
in English
| MEDLINE | ID: mdl-16934875
9.
Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients.
G3 (Bethesda)
; 6(7): 2073-9, 2016 07 07.
Article
in English
| MEDLINE | ID: mdl-27194806
10.
Genetic analysis of multiple sclerosis in Europeans: French data.
J Neuroimmunol
; 143(1-2): 74-8, 2003 Oct.
Article
in English
| MEDLINE | ID: mdl-14575918
11.
IFIH1-GCA-KCNH7 locus is not associated with genetic susceptibility to multiple sclerosis in French patients.
Eur J Hum Genet
; 17(6): 844-7, 2009 Jun.
Article
in English
| MEDLINE | ID: mdl-19156166
12.
Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis.
Nat Genet
; 42(6): 469-70; author reply 470-1, 2010 Jun.
Article
in English
| MEDLINE | ID: mdl-20502484
13.
Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60.
Am J Hum Genet
; 70(5): 1328-32, 2002 May.
Article
in English
| MEDLINE | ID: mdl-11898127
14.
Genetic interaction of CTLA-4 with HLA-DR15 in multiple sclerosis patients.
Ann Neurol
; 54(1): 119-22, 2003 Jul.
Article
in English
| MEDLINE | ID: mdl-12838528
15.
Investigation of seven proposed regions of linkage in multiple sclerosis: an American and French collaborative study.
Neurogenetics
; 5(1): 45-8, 2004 Feb.
Article
in English
| MEDLINE | ID: mdl-14595552
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