Human Genome Epidemiology Literature Finder
Records 1 - 6 (of 6 Records) |
Query Trace: Dystonia and PINK1[original query] |
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Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypes. Neurology 2005 Jul 65 (1): 87-95. Bonifati V, Rohé C F, Breedveld G J, Fabrizio E, De Mari M, Tassorelli C, Tavella A, Marconi R, Nicholl D J, Chien H F, Fincati E, Abbruzzese G, Marini P, De Gaetano A, Horstink M W, Maat-Kievit J A, Sampaio C, Antonini A, Stocchi F, Montagna P, Toni V, Guidi M, Dalla Libera A, Tinazzi M, De Pandis F, Fabbrini G, Goldwurm S, de Klein A, Barbosa E, Lopiano L, Martignoni E, Lamberti P, Vanacore N, Meco G, Oostra B A, |
GCH1 in early-onset Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society 2009 Oct 24 (14): 2070-5. Cobb Stephanie A, Wider Christian, Ross Owen A, Mata Ignacio F, Adler Charles H, Rajput Alex, Rajput Ali H, Wu Ruey-Meei, Hauser Robert, Josephs Keith A, Carr Jonathan, Gwinn Katrina, Heckman Michael G, Aasly Jan O, Lynch Timothy, Uitti Ryan J, Wszolek Zbigniew K, Kapatos Gregory, Farrer Matthew |
Systematic review and UK-based study of PARK2 (parkin), PINK1, PARK7 (DJ-1) and LRRK2 in early-onset Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society 2012 Oct 27 (12): 1522-9. Kilarski Laura L, Pearson Justin P, Newsway Victoria, Majounie Elisa, Knipe M Duleeka W, Misbahuddin Anjum, Chinnery Patrick F, Burn David J, Clarke Carl E, Marion Marie-Helene, Lewthwaite Alistair J, Nicholl David J, Wood Nicholas W, Morrison Karen E, Williams-Gray Caroline H, Evans Jonathan R, Sawcer Stephen J, Barker Roger A, Wickremaratchi Mirdhu M, Ben-Shlomo Yoav, Williams Nigel M, Morris Huw |
Genetic variants of PARK genes in Korean patients with early-onset Parkinson's disease. Neurobiology of aging 2019 03 75 224.e9-224.e15. Youn Jinyoung, Lee Chung, Oh Eungseok, Park Jinse, Kim Ji Sun, Kim Hee-Tae, Cho Jin Whan, Park Woong-Yang, Jang Wooyoung, Ki Chang-Se |
Levodopa-induced dyskinesia in early-onset Parkinson's disease (EOPD) associates with glucocerebrosidase mutation: A next-generation sequencing study in EOPD patients in Thailand. PloS one 2023 10 18 (10): e0293516. Sekh Thanprasertsuk, Prasit Phowthongkum, Thitipong Hopetrungraung, Chalalai Poorirerngpoom, Tikumphorn Sathirapatya, Patsorn Wichit, Onanong Phokaewvarangkul, Kornkiat Vongpaisarnsin, Saknan Bongsebandhu-Phubhakdi, Roongroj Bhidayasi |
Clinical and genetic profile of patients with dystonia: An experience from a tertiary neurology center from India. Parkinsonism & related disorders 2024 1 120 105986. Debjyoti Dhar, Vikram V Holla, Riyanka Kumari, Ravi Yadav, Nitish Kamble, Babylakshmi Muthusamy, Pramod Kumar P |
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- Page last updated:Jun 17, 2024
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