Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: Tremor and SNCA[original query] |
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Genetic variants of a-synuclein are not associated with essential tremor. Movement disorders : official journal of the Movement Disorder Society 2011 Dec 26 (14): 2552-6. Ross Owen A, Conneely Karen N, Wang Tao, Vilarino-Guell Carles, Soto-Ortolaza Alexandra I, Rajput Alex, Wszolek Zbigniew K, Uitti Ryan J, Louis Elan D, Clark Lorraine N, Farrer Matthew J, Testa Claudia |
SNCA variants rs2736990 and rs356220 as risk factors for Parkinson's disease but not for amyotrophic lateral sclerosis and multiple system atrophy in a Chinese population. Neurobiology of aging 2014 Dec 35 (12): 2882.e1-6. Guo Xiao Yan, Chen Yong Ping, Song Wei, Zhao Bi, Cao Bei, Wei Qian Qian, Ou Ru Wei, Yang Yuan, Yuan Li Xing, Shang Hui-Fa |
a-Synuclein rs356219 polymorphisms in patients with Gaucher disease and Parkinson disease. Neuroscience letters 2014 Sep 580 104-7. Altarescu Gheona, Ioscovich Daniel, Alcalay Roy N, Zimran Ari, Elstein Debor |
Frequency of the ASP620ASN mutation in VPS35 and Arg1205His mutation in EIF4G1 in familial Parkinson's disease from South Italy. Neurobiology of aging 2014 Oct 35 (10): 2422.e1-2. Gagliardi Monica, Annesi Grazia, Tarantino Patrizia, Nicoletti Giuseppe, Quattrone Al |
Association of Parkinson disease risk loci with mild parkinsonian signs in older persons. JAMA neurology 2014 Apr 71 (4): 429-35. Shulman Joshua M, Yu Lei, Buchman Aron S, Evans Denis A, Schneider Julie A, Bennett David A, De Jager Philip |
Common variant rs356182 near SNCA defines a Parkinson's disease endophenotype. Annals of clinical and translational neurology 2017 Jan 4 (1): 15-25. Cooper Christine A, Jain Nimansha, Gallagher Michael D, Weintraub Daniel, Xie Sharon X, Berlyand Yosef, Espay Alberto J, Quinn Joseph, Edwards Karen L, Montine Thomas, Van Deerlin Vivianna M, Trojanowski John, Zabetian Cyrus P, Chen-Plotkin Alice |
Somatic copy number gains of ?-synuclein (SNCA) in Parkinson's disease and multiple system atrophy brains. Brain : a journal of neurology 2018 6 141 (8): 2419-2431. Mokretar Katya, Pease Daniel, Taanman Jan-Willem, Soenmez Aynur, Ejaz Ayesha, Lashley Tammaryn, Ling Helen, Gentleman Steve, Houlden Henry, Holton Janice L, Schapira Anthony H V, Nacheva Elizabeth, Proukakis Christ |
Genetic Risk Factors for Essential Tremor: A Review. Tremor and other hyperkinetic movements (New York, N.Y.) 2020 Jun 10 4. Siokas Vasileios, Aloizou Athina-Maria, Tsouris Zisis, Liampas Ioannis, Aslanidou Paraskevi, Dastamani Metaxia, Brotis Alexandros G, Bogdanos Dimitrios P, Hadjigeorgiou Georgios M, Dardiotis Efthimi |
Characterization of molecular biomarkers in cerebrospinal fluid and serum of E46K-SNCA mutation carriers. Parkinsonism & related disorders 2022 2 96 29-35. Murueta-Goyena Ane, Cipriani Raffaela, Carmona-Abellán Mar, Acera Marian, Ayo Naia, Del Pino Rocío, Tijero Beatriz, Fernández-Valle Tamara, Gabilondo Iñigo, Zallo Fátima, Matute Carlos, Sánchez-Pernaute Rosario, Khurana Vikram, Cavaliere Fabio, Capetillo-Zarate Estibaliz, Gómez-Esteban Juan Carl |
Genetic screening of Filipinos suspected with familial Parkinson's disease: A pilot study. Parkinsonism & related disorders 2023 2 108 105319. Caritativo Erin Camille A, Yu Jeryl Ritzi T, Bautista Juan Miguel P, Nishioka Kenya, Jamora Roland Dominic G, Yalung Patrick M, Ng Arlene R, Hattori Nobuta |
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- Page last updated:Jun 11, 2024
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