Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: Tremor and GBA[original query] |
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Mutation analysis and genotype/phenotype relationships of Gaucher disease patients in Spain. Journal of human genetics 2007 52 (5): 391-6. Alfonso Pilar, Aznarez Sofía, Giralt Manuel, Pocovi Miguel, Giraldo Pilar, |
Mutations in the Parkinson's disease genes, Leucine Rich Repeat Kinase 2 (LRRK2) and Glucocerebrosidase (GBA), are not associated with essential tremor. Parkinsonism & related disorders 2010 Feb 16 (2): 132-5. Clark Lorraine N, Kisselev Sergey, Park Naeun, Ross Barbara, Verbitsky Miguel, Rios Eileen, Alcalay Roy N, Lee Joseph H, Louis Elan |
Genetic association study of glucocerebrosidase gene L444P mutation in essential tremor and multiple system atrophy in mainland China. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2012 Nov . Sun QY, Guo JF, Han WW, Zuo X, Wang L, Yao LY, Pan Q, Xia K, Yan XX, Tang BS |
Heterogeneity among patients with Parkinson's disease: cluster analysis and genetic association. Journal of the neurological sciences 2015 Apr 351 (1-2): 41-5. Ma Ling-Yan, Chan Piu, Gu Zhu-Qin, Li Fang-Fei, Feng T |
Effect of GBA Mutations on Phenotype of Parkinson's Disease: A Study on Chinese Population and a Meta-Analysis. Parkinson's disease 2015 2015 916971. Zhang Yuan, Sun Qi-Ying, Zhao Yu-Wen, Shu Li, Guo Ji-Feng, Xu Qian, Yan Xin-Xiang, Tang Bei-S |
Association of GBA Mutations and the E326K Polymorphism With Motor and Cognitive Progression in Parkinson Disease. JAMA neurology 2016 Oct 73 (10): 1217-1224. Davis Marie Y, Johnson Catherine O, Leverenz James B, Weintraub Daniel, Trojanowski John Q, Chen-Plotkin Alice, Van Deerlin Vivianna M, Quinn Joseph F, Chung Kathryn A, Peterson-Hiller Amie L, Rosenthal Liana S, Dawson Ted M, Albert Marilyn S, Goldman Jennifer G, Stebbins Glenn T, Bernard Bryan, Wszolek Zbigniew K, Ross Owen A, Dickson Dennis W, Eidelberg David, Mattis Paul J, Niethammer Martin, Yearout Dora, Hu Shu-Ching, Cholerton Brenna A, Smith Megan, Mata Ignacio F, Montine Thomas J, Edwards Karen L, Zabetian Cyrus |
Prodromal Clinical Markers of Parkinson disease in Gaucher Disease Individuals. European neurology 2016 Jun 76 (1-2): 19-21. Gatto Emilia M, Etcheverry Jose Luis, Sanguinetti Ana, Cesarini Martin, Fernandez Escobar Nicolas, Drelichman Guiller |
Clinical profiles associated with LRRK2 and GBA mutations in Brazilians with Parkinson's disease. Journal of the neurological sciences 2017 Oct 381 160-164. da Silva Camilla P, de M Abreu Gabriella, Cabello Acero Pedro H, Campos Mário, Pereira João S, de A Ramos Sarah R, Nascimento Caroline M, Voigt Danielle D, Rosso Ana Lucia, Araujo Leite Marco A, Vasconcellos Luiz Felipe R, Nicaretta Denise H, Della Coletta Marcus V, da Silva Delson José, Gonçalves Andressa P, Dos Santos Jussara M, Calassara Veluma, Valença Débora Cristina T, de M Martins Cyro J, Santos-Rebouças Cíntia B, Pimentel Márcia M |
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 |
A rare homozygous p.Arg87Trp variant of the GBA gene in Gaucher disease: A case report. Clinical case reports 2022 5 10 (5): e05846. Jilani Houweyda, Hsoumi Faten, Rejeb Imen, Elaribi Yasmina, Hizem Syrine, Sebai Molka, Rolfs Arndt, Benjemaa Lam |
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