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Alcohol dehydrogenase alleles in Parkinson's disease.
Buervenich S, Sydow O, Carmine A, Zhang Z, Anvret M, Olson L. Buervenich S, et al. Among authors: anvret m. Mov Disord. 2000 Sep;15(5):813-8. doi: 10.1002/1531-8257(200009)15:5<813::aid-mds1008>3.0.co;2-y. Mov Disord. 2000. PMID: 11009184
NURR1 promoter polymorphisms: Parkinson's disease, schizophrenia, and personality traits.
Carmine A, Buervenich S, Galter D, Jönsson EG, Sedvall GC, Farde L, Gustavsson JP, Bergman H, Chowdari KV, Nimgaonkar VL, Anvret M, Sydow O, Olson L. Carmine A, et al. Among authors: anvret m. Am J Med Genet B Neuropsychiatr Genet. 2003 Jul 1;120B(1):51-7. doi: 10.1002/ajmg.b.20033. Am J Med Genet B Neuropsychiatr Genet. 2003. PMID: 12815740
A rare truncating mutation in ADH1C (G78Stop) shows significant association with Parkinson disease in a large international sample.
Buervenich S, Carmine A, Galter D, Shahabi HN, Johnels B, Holmberg B, Ahlberg J, Nissbrandt H, Eerola J, Hellström O, Tienari PJ, Matsuura T, Ashizawa T, Wüllner U, Klockgether T, Zimprich A, Gasser T, Hanson M, Waseem S, Singleton A, McMahon FJ, Anvret M, Sydow O, Olson L. Buervenich S, et al. Among authors: anvret m. Arch Neurol. 2005 Jan;62(1):74-8. doi: 10.1001/archneur.62.1.74. Arch Neurol. 2005. PMID: 15642852
Association of a protective paraoxonase 1 (PON1) polymorphism in Parkinson's disease.
Belin AC, Ran C, Anvret A, Paddock S, Westerlund M, Håkansson A, Nissbrandt H, Söderkvist P, Dizdar N, Ahmadi A, Anvret M, Willows T, Sydow O, Galter D. Belin AC, et al. Among authors: anvret m. Neurosci Lett. 2012 Jul 26;522(1):30-5. doi: 10.1016/j.neulet.2012.06.007. Epub 2012 Jun 13. Neurosci Lett. 2012. PMID: 22704918
146 results