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Literatur

Оглавление

Kasten M, Kertelge L, Bruggemann N et al. (2010) Nonmotor symptoms in genetic Parkinson disease. Archives of neurology 67(6): 670–6.

Lill CM, Mashychev A, Hartmann C et al. (2016) Launching the movement disorders society genetic mutation database (MDSGene). Movement disorders: official journal of the Movement Disorder Society 31(5): 607–9.

Lill CM, Roehr JT, McQueen MB et al. (2012) Comprehensive research synopsis and systematic meta-analyses in Parkinson’s disease genetics: The PDGene database. PLoS Genet 8(3): e1002548.

Noyce AJ, Bestwick JP, Silveira-Moriyama L et al. (2012) Meta-analysis of early nonmotor features and risk factors for Parkinson disease. Ann Neurol 72(6): 893–901.

Polymeropoulos MH, Lavedan C, Leroy E et al. (1997) Mutation in the alpha-synuclein gene identified in families with Parkinson’s disease. Science 276(5321): 2045–7.

Sidransky E, Lopez G (2012) The link between the GBA gene and parkinsonism. The Lancet Neurology 11(11): 986–98.

4 Prof. Dr. Kathrin Reetz, Oberärztin, Klinik für Neurologie, RWTH Aachen Universität.

Parkinson

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