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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. Among authors: may s. Mov Disord. 2007 Mar 15;22(4):546-9. doi: 10.1002/mds.21343. Mov Disord. 2007. PMID: 17230458 Free article.
Potential outcome measures and trial design issues for multiple system atrophy.
May S, Gilman S, Sowell BB, Thomas RG, Stern MB, Colcher A, Tanner CM, Huang N, Novak P, Reich SG, Jankovic J, Ondo WG, Low PA, Sandroni P, Lipp A, Marshall FJ, Wooten F, Shults CW; North American Multiple System Atrophy Study Group. May S, et al. Mov Disord. 2007 Dec;22(16):2371-7. doi: 10.1002/mds.21734. Mov Disord. 2007. PMID: 17914727 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. Among authors: may sj. 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.
GREGoR: Accelerating Genomics for Rare Diseases.
Dawood M, Heavner B, Wheeler MM, Ungar RA, LoTempio J, Wiel L, Berger S, Bernstein JA, Chong JX, Délot EC, Eichler EE, Gibbs RA, Lupski JR, Shojaie A, Talkowski ME, Wagner AH, Wei CL, Wellington C, Wheeler MT, Members GP, Carvalho CMB, Gifford CA, May S, Miller DE, Rehm HL, Sedlazeck FJ, Vilain E, O'Donnell-Luria A, Posey JE, Chadwick LH, Bamshad MJ, Montgomery SB, Diseases GRTETGOR, Consortium. Dawood M, et al. Among authors: may s. ArXiv [Preprint]. 2024 Dec 18:arXiv:2412.14338v1. ArXiv. 2024. PMID: 39764392 Free PMC article. Preprint.
1,505 results