Dürr, ARefine your research by the most used items
Author / Editor
- Brice, A (4)
- Lesage, S (4)
- Condroyer, C (3)
- Belarbi, S (2)
- Brefel-Courbon, C (2)
- French Parkinson's Disease Genetics Study Group (2)
- Lohmann, E (2)
- Pollak, Pierre (2)
- Tazir, M (2)
- Tison, F (2)
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remove all| Title | Authors / Editors | Date | |
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Mutations in the glucocerebrosidase gene confer a risk for Parkinson disease in North Africa | Lesage, S; Condroyer, C; Hecham, N; Anheim, M; ... Brice, A | 2011 |
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Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson's disease | Lesage, S; Condroyer, C; Lannuzel, A; Lohmann, E; ... Brice, A | 2009 |
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Low disease risk in relatives of north african lrrk2 Parkinson disease patients | Troiano, A R; Elbaz, A; Lohmann, E; Belarbi, S; ... Brice, A | 2010 |
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Identification of VPS35 mutations replicated in French families with Parkinson disease | Lesage, S; Condroyer, C; Klebe, S; Honoré, A; ... Brice, A | 2012 |
