Association of Catechol-O-Methyltransferase Gene Polymorphisms and Haplotypes in the Levodopa-Induced Adverse Events in Subjects with Parkinson’s Disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
Clinical Biochemistry
Link
https://link.springer.com/content/pdf/10.1007/s12291-022-01046-8.pdf
Reference43 articles.
1. Cacabelos R. Parkinson’s disease: from pathogenesis to pharmacogenomics. Int J Mol Sci. 2017;18:E551.
2. Chaudhuri KR, Schapira AH. Non-motor symptoms of Parkinson’s disease: dopaminergic pathophysiology and treatment. Lancet Neurol. 2009;8:464–74.
3. Hauser RA, Auinger P, Oakes D. Levodopa response in early Parkinson’s disease. Mov Disord. 2009;24:2328–36.
4. Katzenschlager R, Lees AJ. Treatment of Parkinson’s disease: levodopa as the first choice. J Neurol. 2002;249(2):II19–24.
5. Schumacher-Schuh AF, Altmann V, Rieck M, Tovo-Rodrigues L, Monte TL, Callegari-Jacques SM, Medeiros MS, Rieder CR, Hutz MH. Association of common genetic variants of HOMER1 gene with levodopa adverse effects in Parkinson’s disease patients. Pharmacogenomics J. 2014;14:289–94.
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