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Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data.
Khan NL, Jain S, Lynch JM, Pavese N, Abou-Sleiman P, Holton JL, Healy DG, Gilks WP, Sweeney MG, Ganguly M, Gibbons V, Gandhi S, Vaughan J, Eunson LH, Katzenschlager R, Gayton J, Lennox G, Revesz T, Nicholl D, Bhatia KP, Quinn N, Brooks D, Lees AJ, Davis MB, Piccini P, Singleton AB, Wood NW. Khan NL, et al. Among authors: revesz t. Brain. 2005 Dec;128(Pt 12):2786-96. doi: 10.1093/brain/awh667. Epub 2005 Nov 4. Brain. 2005. PMID: 16272164
PINK1 protein in normal human brain and Parkinson's disease.
Gandhi S, Muqit MM, Stanyer L, Healy DG, Abou-Sleiman PM, Hargreaves I, Heales S, Ganguly M, Parsons L, Lees AJ, Latchman DS, Holton JL, Wood NW, Revesz T. Gandhi S, et al. Among authors: revesz t. Brain. 2006 Jul;129(Pt 7):1720-31. doi: 10.1093/brain/awl114. Epub 2006 May 15. Brain. 2006. PMID: 16702191
Neuropathology of primary adult-onset dystonia.
Holton JL, Schneider SA, Ganesharajah T, Gandhi S, Strand C, Shashidharan P, Barreto J, Wood NW, Lees AJ, Bhatia KP, Revesz T. Holton JL, et al. Among authors: revesz t. Neurology. 2008 Feb 26;70(9):695-9. doi: 10.1212/01.wnl.0000302175.76229.f0. Neurology. 2008. PMID: 18299520
Hyposmia in G2019S LRRK2-related parkinsonism: clinical and pathologic data.
Silveira-Moriyama L, Guedes LC, Kingsbury A, Ayling H, Shaw K, Barbosa ER, Bonifati V, Quinn NP, Abou-Sleiman P, Wood NW, Petrie A, Sampaio C, Ferreira JJ, Holton J, Revesz T, Lees AJ. Silveira-Moriyama L, et al. Among authors: revesz t. Neurology. 2008 Sep 23;71(13):1021-6. doi: 10.1212/01.wnl.0000326575.20829.45. Neurology. 2008. PMID: 18809839
A clinico-pathological study of subtypes in Parkinson's disease.
Selikhova M, Williams DR, Kempster PA, Holton JL, Revesz T, Lees AJ. Selikhova M, et al. Among authors: revesz t. Brain. 2009 Nov;132(Pt 11):2947-57. doi: 10.1093/brain/awp234. Epub 2009 Sep 16. Brain. 2009. PMID: 19759203
LRRK2 expression in idiopathic and G2019S positive Parkinson's disease subjects: a morphological and quantitative study.
Sharma S, Bandopadhyay R, Lashley T, Renton AE, Kingsbury AE, Kumaran R, Kallis C, Vilariño-Güell C, O'Sullivan SS, Lees AJ, Revesz T, Wood NW, Holton JL. Sharma S, et al. Among authors: revesz t. Neuropathol Appl Neurobiol. 2011 Dec;37(7):777-90. doi: 10.1111/j.1365-2990.2011.01187.x. Neuropathol Appl Neurobiol. 2011. PMID: 21696411
A common LRRK2 mutation in idiopathic Parkinson's disease.
Gilks WP, Abou-Sleiman PM, Gandhi S, Jain S, Singleton A, Lees AJ, Shaw K, Bhatia KP, Bonifati V, Quinn NP, Lynch J, Healy DG, Holton JL, Revesz T, Wood NW. Gilks WP, et al. Among authors: revesz t. Lancet. 2005 Jan 29-Feb 4;365(9457):415-6. doi: 10.1016/S0140-6736(05)17830-1. Lancet. 2005. PMID: 15680457
559 results