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Results: 1-7 |
Results: 7
Genetic analysis of synphilin-1 in familial Parkinson's disease
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
No genetic association of the Ubiquitin Carboxy-terminal Hydrolase-L1 geneS18Y polymorphism with familial Parkinson's disease
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
Linkage exclusion in French families with probable Parkinson's disease
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
A new GTP-cyclohydrolase I mutation in an unusual dopa-responsive dystonia, familial form
Authors: Brique, S Destee, A Lambert, JC Mouroux, V Delacourte, A Amouyel, P Chartier-Harlin, MC
Citation: S. Brique et al., A new GTP-cyclohydrolase I mutation in an unusual dopa-responsive dystonia, familial form, NEUROREPORT, 10(3), 1999, pp. 487-491
No pathogenic mutations in the beta-synuclein gene in Parkinson's disease
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
No pathogenic mutations in the persyn gene in Parkinson's disease
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
The risk of developing Alzheimer's disease associated with the APOE promoter polymorphisms
Authors: Lambert, JC Berr, C Pasquier, F Delacourte, A Frigard, B Cottel, D Perez-Tur, J Mouroux, V Mohr, M Cecyre, D Galasko, D Lendon, C Poirier, J Hardy, J Mann, D Amouyel, P Chartier-Harlin, MC
Citation: Jc. Lambert et al., The risk of developing Alzheimer's disease associated with the APOE promoter polymorphisms, ALZHEIMER'S DISEASE AND RELATED DISORDERS, 1999, pp. 47-52
Risultati: 1-7 |