Publications by authors named "Charlotta Lind"

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Charlotta Lind

Tidsskr Nor Laegeforen· February 2015

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Altered enzymatic activity and allele frequency of OMI/HTRA2 in Alzheimer's disease.
Marie Westerlund, Homira Behbahani, Sandra Gellhaar, Charlotte Forsell, Andrea Carmine Belin, Charlotta Lind

FASEB J· April 2011

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Variations of the CAG trinucleotide repeat in DNA polymerase γ (POLG1) is associated with Parkinson's disease in Sweden.
Anna Anvret, Marie Westerlund, Olof Sydow, Thomas Willows, Charlotta Lind

Neurosci Lett· November 2010

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Possible involvement of a mitochondrial translation initiation factor 3 variant causing decreased mRNA levels in Parkinson's disease.
Anna Anvret, Caroline Ran, Marie Westerlund, Ann-Christin Thelander, Olof Sydow, Charlotta Lind

Parkinsons Dis· June 2010

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Association of a polymorphism in the ABCB1 gene with Parkinson's disease.
Marie Westerlund, Andrea Carmine Belin, Anna Anvret, Anna Håkansson, Hans Nissbrandt, Charlotta Lind

Parkinsonism Relat Disord· July 2009

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Food quality effects on copepod growth and development: implications for bioassays in ecotoxicological testing.
Ulrika Dahl, Charlotta Rubio Lind, Elena Gorokhova, Britta Eklund, Magnus Breitholtz

Ecotoxicol Environ Saf· February 2009

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Subthalamic stimulation for essential tremor. Short- and long-term results and critical target area.
Göran Lind, Gaston Schechtmann, Charlotta Lind, Jaleh Winter, Björn A Meyerson, Bengt Linderoth

Stereotact Funct Neurosurg· December 2008

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Cerebellar alpha-synuclein levels are decreased in Parkinson's disease and do not correlate with SNCA polymorphisms associated with disease in a Swedish material.
Marie Westerlund, Andrea Carmine Belin, Anna Anvret, Anna Håkansson, Hans Nissbrandt, Charlotta Lind

FASEB J· October 2008

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S18Y in ubiquitin carboxy-terminal hydrolase L1 (UCH-L1) associated with decreased risk of Parkinson's disease in Sweden.
Andrea Carmine Belin, Marie Westerlund, Olle Bergman, Hans Nissbrandt, Charlotta Lind

Parkinsonism Relat Disord· July 2007

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Association study of two genetic variants in mitochondrial transcription factor A (TFAM) in Alzheimer's and Parkinson's disease.
Andrea Carmine Belin, Behnosh F Björk, Marie Westerlund, Dagmar Galter, Olof Sydow, Charlotta Lind

Neurosci Lett· June 2007

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