Resultats de la cerca - Singleton Andrew

Cell population-specific expression analysis of human cerebellum per Kuhn Alexandre, Kumar Azad, Beilina Alexandra, Dillman Allissa, Cookson Mark R, Singleton Andrew B

Obtenir text complet

A common genetic factor for Parkinson disease in ethnic Chinese population in Taiwan per Hardy John, Chen Chiung-Mei, Fung Hon-Chung, Singleton Andrew B, Wu Yih-Ru

Obtenir text complet

Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2 per Calado Ana, Dias Margarida, Januario Cristina, Morgadinho Ana, Ribeiro Maria, Guerreiro Rita, Bras Jose, Semedo Cristina, Oliveira Catarina, Hardy John, Singleton Andrew

Obtenir text complet

Association of HFE common mutations with Parkinson's disease, Alzheimer's disease and mild cognitive impairment in a Portuguese cohort per Morgadinho Ana S, Santiago Beatriz, Januario Cristina, Santana Isabel, Bras Jose M, Guerreiro Rita J, Ribeiro Maria H, Hardy John, Singleton Andrew, Oliveira Catarina

Obtenir text complet

Lack of evidence for a genetic association between <it>FGF20 </it>and Parkinson's disease in Finnish and Greek patients per Hadjigeorgiou George M, Papadimitriou Alexandros, Peuralinna Terhi, Dardiotis Euthimios, Hellström Olli, Gourbali Vanesa, Eerola Johanna, Xiromerisiou Georgia, Clarimon Jordi, Tienari Pentti J, Singleton Andrew B

Obtenir text complet

Analysis of <it>IFT74 </it>as a candidate gene for chromosome 9p-linked ALS-FTD per Rogaeva Ekaterina, Hutton Michael L, Adamson Jennifer, Wassermann Eric M, Huey Edward D, Holtzman David M, Fung Hon, Chiò Adriano, Pickering-Brown Stuart, Berger Stephen, Greenway Matthew J, Greggio Elisa, Cairns Nigel J, Cookson Mark R, Jain Shushant, Schymick Jennifer, Momeni Parastoo, St George-Hyslop Peter, Rothstein Jeffrey D, Hardiman Orla, Grafman Jordan, Singleton Andrew, Hardy John, Traynor Bryan J

Obtenir text complet