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Results:
1-7
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Results: 7
Authors:
Farrer, M
Destee, A
Levecque, C
Singleton, A
Engelender, S
Becquet, E
Mouroux, V
Richard, F
Defebvre, L
Crook, R
Hernandez, D
Ross, CA
Hardy, J
Amouyel, P
Chartier-Harlin, MC
Citation: M. Farrer et al., Genetic analysis of synphilin-1 in familial Parkinson's disease, NEUROBIOL D, 8(2), 2001, pp. 317-323
Authors:
Levecque, C
Destee, A
Mouroux, V
Becquet, E
Defebvre, L
Amouyel, P
Chartier-Harlin, MC
Citation: C. Levecque et al., No genetic association of the Ubiquitin Carboxy-terminal Hydrolase-L1 geneS18Y polymorphism with familial Parkinson's disease, J NEURAL TR, 108(8-9), 2001, pp. 979-984
Authors:
Dujardin, K
Defebvre, L
Grunberg, C
Becquet, E
Destee, A
Citation: K. Dujardin et al., Memory and executive function in sporadic and familial Parkinson's disease, BRAIN, 124, 2001, pp. 389-398
Authors:
Farrer, M
Destee, T
Becquet, E
Wavrant-De Vrieze, F
Mouroux, V
Richard, F
Defebvre, L
Lincoln, S
Hardy, J
Amouyel, S
Chartier-Harlin, MC
Citation: M. Farrer et al., Linkage exclusion in French families with probable Parkinson's disease, MOVEMENT D, 15(6), 2000, pp. 1075-1083
Authors:
Lincoln, S
Crook, R
Chartier-Harlin, MC
Gwinn-Hardy, K
Baker, M
Mouroux, V
Richard, F
Becquet, E
Amouyel, P
Destee, A
Hardy, J
Farrer, M
Citation: S. Lincoln et al., No pathogenic mutations in the beta-synuclein gene in Parkinson's disease, NEUROSCI L, 269(2), 1999, pp. 107-109
Authors:
Lincoln, S
Gwinn-Hardy, K
Goudreau, J
Chartier-Harlin, MC
Baker, M
Mouroux, V
Richard, F
Destee, A
Becquet, E
Amouyel, P
Lynch, T
Hardy, J
Farrer, M
Citation: S. Lincoln et al., No pathogenic mutations in the persyn gene in Parkinson's disease, NEUROSCI L, 259(1), 1999, pp. 65-66
Authors:
Dujardin, K
Duhamel, A
Becquet, E
Grunberg, C
Defebvre, L
Destee, A
Citation: K. Dujardin et al., Neuropsychological abnormalities in first degree relatives of patients with familial Parkinson's disease, J NE NE PSY, 67(3), 1999, pp. 323-328
Risultati:
1-7
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