Refine your research by the most used items
Author / Editor
- Brice, Alexis (4)
- Condroyer, Christel (3)
- Lesage, Suzanne (3)
- Tison, François (3)
- Anheim, Mathieu (2)
- Damier, Philippe (2)
- Durr, Alexandra (2)
- Dürr, Alexandra (2)
- Lohmann, Ebba (2)
- Pollak, Pierre (2)

Document type
Full text accessibility
Full text version
Subject
Highlights
Show items per page
Title | Authors / Editors | Date | |
---|---|---|---|
![]() |
EIF4G1 in familial Parkinson's disease: pathogenic mutations or rare benign variants? | Lesage, Suzanne; Condroyer, Christel; Klebe, Stephan; Lohmann, Ebba; ... Brice, Alexis | 2012 |
![]() |
FXTAS: new insights and the need for revised diagnostic criteria | Apartis, Emmanuelle; Blancher, Anne; Meissner, Wassilios G; Guyant-Maréchal, Lucie; ... Anheim, Mathieu | 2012 |
![]() |
Follow-up study of the GIGYF2 gene in French families with Parkinson's disease | Lesage, Suzanne; Condroyer, Christel; Lohman, Ebba; Troiano, André; ... Brice, Alexis | 2010 |
![]() |
Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans | Lesage, Suzanne; Patin, Etienne; Condroyer, Christel; Leutenegger, Anne-Louise; ... Brice, Alexis | 2010 |