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FUS mutations in frontotemporal lobar degeneration with amyotrophic lateral sclerosis.
Published in:
2010
By:
- Broustal O;
- Camuzat A;
- Guillot-Noël L;
- Guy N;
- Millecamps S;
- Deffond D;
- Lacomblez L;
- Golfier V;
- Hannequin D;
- Salachas F;
- Camu W;
- Didic M;
- Dubois B;
- Meininger V;
- Le Ber I;
- Brice A;
- French clinical and genetic research network on FTD/FTD-MND
Publication type:
Journal Article
Genetic burden in multiple sclerosis families.
Published in:
Genes & Immunity, 2013, v. 14, n. 7, p. 434, doi. 10.1038/gene.2013.37
By:
- Isobe, N;
- Damotte, V;
- Lo Re, V;
- Ban, M;
- Pappas, D;
- Guillot-Noel, L;
- Rebeix, I;
- Compston, A;
- Mack, T;
- Cozen, W;
- Fontaine, B;
- Hauser, S L;
- Oksenberg, J R;
- Sawcer, S;
- Gourraud, P-A
Publication type:
Article
A gene pathway analysis highlights the role of cellular adhesion molecules in multiple sclerosis susceptibility.
Published in:
Genes & Immunity, 2014, v. 15, n. 2, p. 126, doi. 10.1038/gene.2013.70
By:
- Damotte, V;
- Guillot-Noel, L;
- Patsopoulos, N A;
- Madireddy, L;
- El Behi, M;
- De Jager, P L;
- Baranzini, S E;
- Cournu-Rebeix, I;
- Fontaine, B
Publication type:
Article
Investigation of sex-specific effects of apolipoprotein E on severity of EAE and MS.
Published in:
2015
By:
- Schrewe, L.;
- Lill, C. M.;
- T. Liu;
- Salmen, A.;
- Gerdes, L. A.;
- Guillot-Noel, L.;
- Akkad, D. A.;
- Blaschke, P.;
- Graetz, C.;
- Hoffjan, S.;
- Kroner, A.;
- Demir, S.;
- Böhme, A.;
- Rieckmann, P.;
- El Ali, A.;
- Hagemann, N.;
- Hermann, D. M.;
- Cournu-Rebeix, I.;
- Zipp, F.;
- Kümpfel, T.
Publication type:
journal article

Found: 4

FUS mutations in frontotemporal lobar degeneration with amyotrophic lateral sclerosis.

Genetic burden in multiple sclerosis families.

A gene pathway analysis highlights the role of cellular adhesion molecules in multiple sclerosis susceptibility.

Investigation of sex-specific effects of apolipoprotein E on severity of EAE and MS.