The DJ-1 concentration in cerebrospinal fluid does not differentiate among parkinsonian syndromes

Parkinsonism & Related Disorders - Tập 18 Số 7 - Trang 899-901 - 2012
Lisette Salvesen1,2,3, Sára Bech1,4,2, Annemette Løkkegaard1,2, Lena E. Hjermind1,4,5, Jørgen E. Nielsen4,5, Bente Pakkenberg3, Julia T. Tanassi6, Niels H. H. Heegaard6, Kristian Winge1,2
1Bispebjerg Movement Disorders Biobank, Bispebjerg University Hospital, Copenhagen, Denmark
2Department of Neurology, Bispebjerg University Hospital, Copenhagen, Denmark
3Research Laboratory for Stereology and Neuroscience, Bispebjerg University Hospital, Bispebjerg Bakke 23, 2400 Copenhagen, Region Hovedstaden, Denmark
4Department of Cellular and Molecular Medicine, Section of Neurogenetics, University of Copenhagen, Copenhagen, Denmark
5Memory Disorders Research Group, Department of Neurology, Rigshospitalet University Hospital, Copenhagen, Denmark
6Department of Clinical Biochemistry and Immunology, Statens Serum Institut, Copenhagen, Denmark

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Tài liệu tham khảo

Bonifati, 2003, Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism, Science, 299, 256, 10.1126/science.1077209

Batelli, 2008, DJ-1 modulates α-synuclein aggregation state in a cellular model of oxidative stress: relevance for Parkinson’s disease and involvement of HSP70, PLoS ONE, 3, e1884, 10.1371/journal.pone.0001884

Shi, 2011, Cerebrospinal fluid biomarkers for Parkinson disease diagnosis and progression, Ann Neurol, 69, 570, 10.1002/ana.22311

Hong, 2010, DJ-1 and α-synuclein in human cerebrospinal fluid as biomarkers of Parkinson’s disease, Brain, 133, 713, 10.1093/brain/awq008

Teunissen, 2009, A consensus protocol for the standardization of cerebrospinal fluid collection and biobanking, Neurology, 73, 1914, 10.1212/WNL.0b013e3181c47cc2

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Parkinsonism & Related Disorders

Tập 18 Số 7

899-901

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