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G2019S mutation in the leucine-rich repeat kinase 2 gene is not associated with multiple system atrophy.
Ozelius LJ, Foroud T, May S, Senthil G, Sandroni P, Low PA, Reich S, Colcher A, Stern MB, Ondo WG, Jankovic J, Huang N, Tanner CM, Novak P, Gilman S, Marshall FJ, Wooten GF, Chelimsky TC, Shults CW; North American Multiple System Atrophy Study Group. Ozelius LJ, et al. Mov Disord. 2007 Mar 15;22(4):546-9. doi: 10.1002/mds.21343. Mov Disord. 2007. PMID: 17230458 Free article.
The North American Multiple System Atrophy Study Group.
Gilman S, May SJ, Shults CW, Tanner CM, Kukull W, Lee VM, Masliah E, Low P, Sandroni P, Trojanowski JQ, Ozelius L, Foroud T; North American Multiple System Atrophy Study Group. Gilman S, et al. J Neural Transm (Vienna). 2005 Dec;112(12):1687-94. doi: 10.1007/s00702-005-0381-6. J Neural Transm (Vienna). 2005. PMID: 16284910 Free article. Review.
LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews.
Ozelius LJ, Senthil G, Saunders-Pullman R, Ohmann E, Deligtisch A, Tagliati M, Hunt AL, Klein C, Henick B, Hailpern SM, Lipton RB, Soto-Valencia J, Risch N, Bressman SB. Ozelius LJ, et al. N Engl J Med. 2006 Jan 26;354(4):424-5. doi: 10.1056/NEJMc055509. N Engl J Med. 2006. PMID: 16436782 No abstract available.
Clinical expression of LRRK2 G2019S mutations in the elderly.
San Luciano M, Lipton RB, Wang C, Katz M, Zimmerman ME, Sanders AE, Ozelius LJ, Bressman SB, Saunders-Pullman R. San Luciano M, et al. Among authors: ozelius lj. Mov Disord. 2010 Nov 15;25(15):2571-6. doi: 10.1002/mds.23330. Mov Disord. 2010. PMID: 20721910 Free PMC article.
289 results