Browsing by Author Lew, M.

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Issue DateTitleAuthor(s)Citation
2005BDNF genetic variants are associated with onset age of familial Parkinson disease: GenePD StudyNicholson, Garth; et, al; Golbe, L. I.; Karamohamed, S.; Klein, C.; Latourelle, J.C.; Lew, M.; Perlmutter, J. S.; Racette, B. A.; Shill, H.; Wooten, G. F.; Concord Clinical School: ANZAC Research InstituteBDNF genetic variants are associated with onset age of familial Parkinson disease: GenePD Study, NEUROLOGY 2005, vol.65,(11),2005,pp 1823-1825
2008The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD studyCorbett, Alastair; Nicholson, Garth; et al, Not Known; Golbe, Lawrence I.; Growdon, J; Klein, Christine; Latourelle, J.C.; Lew, M.; Mark, Margery H.; Suchowersky, Oksana; Sun, Mei; Watts, Ray L; Wooten, Frederick; Concord Clinical School: Medicine; Concord Clinical School: ANZAC Research InstituteThe Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD study, B M C Medicine, vol.6,(32),2008,pp 32-1-32-7
2008Huntington CAG repeat size does not modify onset age in familial Parkinson's disease: the GenePD studyCorbett, Alastair; Nicholson, Garth; et al, Not Known; Golbe, Lawrence I.; Growdon, J; Klein, Christine; Latourelle, J.C.; Lew, M.; MacDonald, M E; Mark, Margery H.; McNicoll, Christopher F; Suchowersky, Oksana; Wooten, G. F.; Concord Clinical School: Medicine; Concord Clinical School: ANZAC Research InstituteHuntington CAG repeat size does not modify onset age in familial Parkinson's disease: the GenePD study, Movement Disorders, vol.23,(11),2008,pp 1596-1601
2008Replication of association between ELAVL4 and Parkinson disease: the GenePD studyCorbett, Alastair; Nicholson, Garth; DeStefano, Anita; et al, Not Known; Golbe, L. I.; Growdon, J; Klein, Christine; Latourelle, J.C.; Lew, M.; Mark, Margery H.; Suchowersky, Oksana; Watts, Ray L; Wooten, G. F.; Concord Clinical School: Medicine; Concord Clinical School: ANZAC Research InstituteReplication of association between ELAVL4 and Parkinson disease: the GenePD study, Human Genetics, vol.124,(1),2008,pp 95-99