Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: Dyskinesias and COMT[original query] |
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COMT genotype and effectiveness of entacapone in patients with fluctuating Parkinson's disease. Neurology 2002 Feb 58 (4): 564-7. Lee M S, Kim H S, Cho E K, Lim J H, Rinne J |
Genetic polymorphism of catechol-O-methyltransferase and levodopa pharmacokinetic-pharmacodynamic pattern in patients with Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society 2005 Jun 20 (6): 734-9. Contin Manuela, Martinelli Paolo, Mochi Mirella, Riva Roberto, Albani Fiorenzo, Baruzzi Agosti |
The association of functional catechol-O-methyltransferase haplotypes with risk of Parkinson's disease, levodopa treatment response, and complications. Pharmacogenetics and genomics 2008 Sep 18 (9): 815-21. Bialecka Monika, Kurzawski Mateusz, Klodowska-Duda Gabriela, Opala Grzegorz, Tan Eng-King, Drozdzik Mar |
Catechol-O-methyltransferase Val158Met and the risk of dyskinesias in Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society 2012 Jan 27 (1): 132-5. de Lau Lonneke M L, Verbaan Dagmar, Marinus Johan, Heutink Peter, van Hilten Jacobus |
Influence of single nucleotide polymorphisms in COMT, MAO-A and BDNF genes on dyskinesias and levodopa use in Parkinson's disease. Neuro-degenerative diseases 2014 13 (1): 24-8. Cheshire Perdita, Bertram Kelly, Ling Helen, O'Sullivan Sean S, Halliday Glenda, McLean Catriona, Bras Jose, Foltynie Tom, Storey Elsdon, Williams David |
Association of Catechol-O-Methyltransferase and monoamine oxidase B gene polymorphisms with motor complications in parkinson's disease in a Chinese population. Parkinsonism & related disorders 2014 Oct 20 (10): 1041-5. Hao Hongying, Shao Ming, An Jing, Chen Chushuang, Feng Xiuli, Xie Shu, Gu Zhuqin, Chan Piu, |
Catechol-O-methyltransferase Val158Met polymorphism influences prefrontal executive function in early Parkinson's disease. Journal of the neurological sciences 2016 Oct 369 347-53. Zhang Youwen, Feng Shujun, Nie Kun, Zhao Xin, Gan Rong, Wang Limin, Zhao Jiehao, Tang Hongmei, Gao Liang, Zhu Ruiming, Wang Lijuan, Zhang Yu |
Exome-wide association study of levodopa-induced dyskinesia in Parkinson's disease. Scientific reports 2021 10 11 (1): 19582. König Eva, Nicoletti Alessandra, Pattaro Cristian, Annesi Grazia, Melotti Roberto, Gialluisi Alessandro, Schwienbacher Christine, Picard Anne, Blankenburg Hagen, Pichler Irene, Modugno Nicola, Ciullo Marina, Esposito Teresa, Domingues Francisco S, Hicks Andrew A, Zappia Mario, Pramstaller Peter |
Functional MAOB Gene Intron 13 Polymorphism Predicts Dyskinesia in Parkinson's Disease. Parkinson's disease 2022 2022 5597503. Löhle Matthias, Mangone Graziella, Hermann Wiebke, Hausbrand Denise, Wolz Martin, Mende Julia, Reichmann Heinz, Hermann Andreas, Corvol Jean-Christophe, Storch Alexand |
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