Filters: Author is Breteler, Monique M B [Clear All Filters]
de Lau LM, Koudstaal PJ, Hofman A, Breteler MM. Serum uric acid levels and the risk of Parkinson disease. Ann Neurol. 2005;58(5):797-800.
de Lau LM, Koudstaal PJ, van Meurs JB, Uitterlinden AG, Hofman A, Breteler MM. Methylenetetrahydrofolate reductase C677T genotype and PD. Ann Neurol. 2005;57(6):927-30.
Martinez M, Brice A, Vaughan JR, Zimprich A, Breteler MM, Meco G, et al. Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease. Am J Med Genet B Neuropsychiatr Genet. 2005;136B(1):72-4.
Dekker MC, Giesbergen PC, Njajou OT, van Swieten JC, Hofman A, Breteler MM, et al. Mutations in the hemochromatosis gene (HFE), Parkinson's disease and parkinsonism. Neurosci Lett. 2003;348(2):117-9.
Valente E, Brancati F, Ferraris A, Graham EA, Davis MB, Breteler MM, et al. PARK6-linked parkinsonism occurs in several European families. Ann Neurol. 2002;51(1):14-8.

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