Publications by authors named "Maria Anvret"

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Association of a protective paraoxonase 1 (PON1) polymorphism in Parkinson's disease.
Andrea Carmine Belin, Caroline Ran, Anna Anvret, Silvia Paddock, Marie Westerlund, Maria Anvret

Neurosci Lett· July 2012

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A rare truncating mutation in ADH1C (G78Stop) shows significant association with Parkinson disease in a large international sample.
Silvia Buervenich, Andrea Carmine, Dagmar Galter, Haydeh N Shahabi, Bo Johnels, Maria Anvret

Arch Neurol· January 2005

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ALDH1 mRNA: presence in human dopamine neurons and decreases in substantia nigra in Parkinson's disease and in the ventral tegmental area in schizophrenia.
Dagmar Galter, Silvia Buervenich, Andrea Carmine, Maria Anvret, Lars Olson

Neurobiol Dis· December 2003

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Refined mapping of the Welander distal myopathy region on chromosome 2p13 positions the new candidate region telomeric of the DYSF locus.
Désirée von Tell, Carl E G Bruder, Louise V B Anderson, Maria Anvret, Gabrielle Ahlberg

Neurogenetics· August 2003

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NURR1 promoter polymorphisms: Parkinson's disease, schizophrenia, and personality traits.
Andrea Carmine, Silvia Buervenich, Dagmar Galter, Erik G Jönsson, Göran C Sedvall, Maria Anvret

Am J Med Genet B Neuropsychiatr Genet· July 2003

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CTLA4 dimorphisms and the multiple sclerosis phenotype.
Thomas Masterman, Arturs Ligers, Zhiping Zhang, Dennis Hellgren, Hugh Salter, Maria Anvret

J Neuroimmunol· October 2002

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Further evidence for an association of the paraoxonase 1 (PON1) Met-54 allele with Parkinson's disease.
Andrea Carmine, Silvia Buervenich, Olof Sydow, Maria Anvret, Lars Olson

Mov Disord· July 2002

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