Human Genome Epidemiology Literature Finder
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Records 1 - 10 (of 10 Records) |
| Query Trace: Multiple System Atrophy and LRRK2[original query] |
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| Analysis of 14 LRRK2 mutations in Parkinson's plus syndromes and late-onset Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society 2006 Jul 21 (7): 997-1001. Tan E K, Skipper Lisa, Chua Eva, Wong Meng-Cheong, Pavanni Ratnagopal, Bonnard Carine, Kolatkar Prasanna, Liu Jian-J |
| G2019S mutation in the leucine-rich repeat kinase 2 gene is not associated with multiple system atrophy. Movement disorders : official journal of the Movement Disorder Society 2007 Mar 22 (4): 546-9. Ozelius Laurie J, Foroud Tatiana, May Susanne, Senthil Geetha, Sandroni Paola, Low Phillip A, Reich Stephen, Colcher Amy, Stern Matthew B, Ondo William G, Jankovic Joseph, Huang Neng, Tanner Caroline M, Novak Peter, Gilman Sid, Marshall Frederick J, Wooten G Frederick, Chelimsky Thomas C, Shults Clifford W, |
| Analysis of the LRRK2 Gly2385Arg variant in primary dystonia and multiple system atrophy in Taiwan. Parkinsonism & related disorders 2008 14 (5): 393-6. Lu Chin-Song, Chang Hsiu-Chen, Weng Yi-Hsin, Chen Rou-Shayn, Bonifati Vincenzo, Wu-Chou Yah-Hu |
| Screening for the LRRK2 G2019S and codon-1441 mutations in a pathological series of parkinsonian syndromes and frontotemporal lobar degeneration. Journal of the neurological sciences 2008 Jul 270 (1-2): 94-8. Gaig Carles, Ezquerra Mario, Martí Maria José, Valldeoriola Francesc, Muñoz Esteban, Lladó Albert, Rey Maria Jesús, Cardozo Adriana, Molinuevo José Luis, Tolosa Eduar |
| The G2019S LRRK2 Mutation is Rare in Korean Patients with Parkinson's Disease and Multiple System Atrophy. Journal of clinical neurology (Seoul, Korea) 2009 Mar 5 (1): 29-32. Cho Jin-Whan, Kim Sung-Yeon, Park Sung-Sup, Jeon Beom |
| LRRK2 exonic variants and risk of multiple system atrophy. Neurology 2014 Dec 83 (24): 2256-61. Heckman Michael G, Schottlaender Lucia, Soto-Ortolaza Alexandra I, Diehl Nancy N, Rayaprolu Sruti, Ogaki Kotaro, Fujioka Shinsuke, Murray Melissa E, Cheshire William P, Uitti Ryan J, Wszolek Zbigniew K, Farrer Matthew J, Sailer Anna, Singleton Andrew B, Chinnery Patrick F, Keogh Michael J, Gentleman Steve M, Holton Janice L, Aoife Kiely, Mann David M A, Al-Sarraj Safa, Troakes Claire, Dickson Dennis W, Houlden Henry, Ross Owen |
| MAPT haplotype diversity in multiple system atrophy. Parkinsonism & related disorders 2016 09 30 40-5. Labbé Catherine, Heckman Michael G, Lorenzo-Betancor Oswaldo, Murray Melissa E, Ogaki Kotaro, Soto-Ortolaza Alexandra I, Walton Ronald L, Fujioka Shinsuke, Koga Shunsuke, Uitti Ryan J, van Gerpen Jay A, Petersen Ronald C, Graff-Radford Neill R, Younkin Steven G, Boeve Bradley F, Cheshire William P, Low Phillip A, Sandroni Paola, Coon Elizabeth A, Singer Wolfgang, Wszolek Zbigniew K, Dickson Dennis W, Ross Owen |
| LRRK2 protective haplotype and full sequencing study in REM sleep behavior disorder. Parkinsonism & related disorders 2018 Mar . Ouled Amar Bencheikh Bouchra, Ruskey Jennifer A, Arnulf Isabelle, Dauvilliers Yves, Monaca Christelle Charley, De Cock Valérie Cochen, Gagnon Jean-François, Spiegelman Dan, Hu Michele T M, Högl Birgit, Stefani Ambra, Ferini-Strambi Luigi, Plazzi Giuseppe, Antelmi Elena, Young Peter, Heidbreder Anna, Mollenhauer Brit, Sixel-Döring Friederike, Trenkwalder Claudia, Oertel Wolfgang, Montplaisir Jacques Y, Postuma Ronald B, Rouleau Guy A, Gan-Or Z |
| Clinicopathologic and genetic features of multiple system atrophy with Lewy body disease. Brain pathology (Zurich, Switzerland) 2020 4 30 (4): 766-778. Koga Shunsuke, Li Fuyao, Zhao Na, Roemer Shanu F, Ferman Tanis J, Wernick Anna I, Walton Ronald L, Faroqi Ayman H, Graff-Radford Neill R, Cheshire William P, Ross Owen A, Dickson Dennis |
| Investigation of Somatic Mutations in Human Brains Targeting Genes Associated With Parkinson's Disease. Frontiers in neurology 2020 11 11 570424. Leija-Salazar Melissa, Pittman Alan, Mokretar Katya, Morris Huw, Schapira Anthony H, Proukakis Christ |
- Page last reviewed:Feb 1, 2023
- Page last updated:Jun 02, 2023
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