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TypeTitleAuthor(s)YearViews
PS1 Alzheimer's disease family with spastic paraplegia: The search for a gene modifierRogaeva, E; Bergeron, C; Sato, C; Moliaka, I; Kawarai, T; Toulina, A; Song, YQ; Kolesnikova, T; Orlacchio, A; Bernardi, G; St GeorgeHyslop, PH200390
 
Alleles at the Nicastrin locus modify presenilin 1-deficiency phenotypeRozmahel, R; Mount, HTJ; Chen, F; Nguyen, V; Huang, J; Erdebil, S; Liauw, J; Yu, G; Hasegawa, H; Gu, Y; Song, YQ; Schmidt, SD; Nixon, RA; Mathews, PM; Bergeron, C; Fraser, P; Westaway, D; St GeorgeHyslop, P2002116
 
A Novel PS1 Case of Variant Alzheimer’s Disease with Spastic Paraplegia: The Search for a Gene-ModifierRogaeva, EA; Moliaka, I; Toshitaka, K; Sato, C; Medeiros, H; Song, Y; Liang, Y; Kolesnikova, T; Bergeron, C; St George-Hyslop, PH200299
 
Low frequency of TAU mutations and further genetic heterogeneity in FTDKawarai, T; Rogaeva, E; Song, Y; Moliaka, Y; Medeiros, H; Liang, Y; Sato, C; Ling, S; Fong, M; Kolesnikova, T; Bergeron, C; Lang, AE; Paterson, AD; Orlacchio, A; Bernardi, G; Rockwood, K; Allegri, R; Rainero, I; Pinessi, L; Cappa, G; Kertesz, A; Bruni, AC; Freedman, M; Ahern, GL; Tuite, P; Fornazzari, L; St George-Hyslop, P200292
 
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