Results: 1-12 |
Results: 12

Authors: West, AB Zimprich, A Lockhart, PJ Farrer, M Singleton, A Holtom, B Lincoln, S Hofer, A Hill, L Muller-Myhsok, B Wszolek, ZK Hardy, J Gasser, T
Citation: Ab. West et al., Refinement of the PARK3 locus on chromosome 2p13 and the analysis of 14 candidate genes, EUR J HUM G, 9(9), 2001, pp. 659-666

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: Farrer, M Maraganore, DM Lockhart, P Singleton, A Lesnick, TG de Andrade, M West, A de Silva, R Hardy, J Hernandez, D
Citation: M. Farrer et al., alpha-synuclein gene haplotypes are associated with Parkinson's disease, HUM MOL GEN, 10(17), 2001, pp. 1847-1851

Authors: Farrer, M Chan, P Chen, R Tan, L Lincoln, S Hernandez, D Forno, L Gwinn-Hardy, K Petrucelli, L Hussey, J Singleton, A Tanner, C Hardy, J Langston, JW
Citation: M. Farrer et al., Lewy bodies and parkinsonism in families with parkin mutations, ANN NEUROL, 50(3), 2001, pp. 293-300

Authors: Rowlands, G Willis, S Singleton, A
Citation: G. Rowlands et al., Referrals and relationships: in-practice referrals meetings in a general practice, FAM PRACT, 18(4), 2001, pp. 399-406

Authors: Gwinn-Hardy, K Singleton, A O'Suilleabhain, P Boss, M Nicholl, D Adam, A Hussey, J Critchley, P Hardy, J Farrer, M
Citation: K. Gwinn-hardy et al., Spinocerebellar ataxia type 3 phenotypically resembling Parkinson disease in a black family, ARCH NEUROL, 58(2), 2001, pp. 296-299

Authors: Hardy, J Singleton, A
Citation: J. Hardy et A. Singleton, The future of genetic analysis of neurological disorders, NEUROBIOL D, 7(2), 2000, pp. 65-69

Authors: Gwinn-Hardy, K Chen, JY Liu, HC Liu, TY Boss, M Seltzer, W Adam, A Singleton, A Koroshetz, W Waters, C Hardy, J Farrer, M
Citation: K. Gwinn-hardy et al., Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese, NEUROLOGY, 55(6), 2000, pp. 800-805

Authors: De Jonghe, C Cruts, M Rogaeva, EA Tysoe, C Singleton, A Vanderstichele, H Meschino, W Dermaut, D Vanderhoeven, I Backhovens, H Vanmechelen, E Morris, CM Hardy, J Rubinsztein, DC St George-Hyslop, PH Van Broeckhoven, C
Citation: C. De Jonghe et al., Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimer's disease by increased A beta 42 secretion, HUM MOL GEN, 8(8), 1999, pp. 1529-1540

Authors: Singleton, A
Citation: A. Singleton, Opportunities, threats and myths in journals, LEARN PUBL, 12(2), 1999, pp. 97-105

Authors: Singleton, A Smith, F Harris, T Ross-Harper, R Hilton, S
Citation: A. Singleton et al., An evaluation of the Team Objective Structured Clinical Examination (TOSCE), MED EDUC, 33(1), 1999, pp. 34-41

Authors: Smith, F Singleton, A Teague, PA Ross-Harper, R Wilke, G Hilton, S
Citation: F. Smith et al., An evaluation of an educational group for general practitioner continuing education and development, MED TEACH, 20(6), 1998, pp. 572-578
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