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Genome Medicine|September 11, 2010
Copy number variation in Parkinson's diseaseMathias Toft, Owen A RossNeurobiology of Aging|October 21, 2018
No evidence for DNM3 as genetic modifier of age at onset in idiopathic Parkinson's diseaseVictoria Berge-Seidl, Lasse Pihlstrøm, Zbigniew K Wszolek, et al.Neuroscience Letters|February 28, 2007
Variants in the LRRK1 gene and susceptibility to Parkinson's disease in NorwayKristoffer Haugarvoll, Mathias Toft, Owen A Ross, et al.Archives of Neurology|September 13, 2006
Clinical heterogeneity of the LRRK2 G2019S mutationSpiridon Papapetropoulos, Carlos Singer, Owen A Ross, et al.Mechanisms of Ageing and Development|August 10, 2005
LRRK2 mutations are not common in Alzheimer's diseaseMathias Toft, Sigrid Botne Sando, Stacey Melquist, et al.Movement Disorders : Official Journal of the Movement Disorder Society|December 16, 2011
The Wilson films--MS tremorMathias ToftAmerican Journal of Human Genetics|August 7, 2004
Linkage disequilibrium and association of MAPT H1 in Parkinson diseaseLisa Skipper, Kristen Wilkes, Mathias Toft, et al.Neurogenetics|July 30, 2011
Genetic variability in SNCA and Parkinson's diseaseLasse Pihlstrøm, Mathias ToftTidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|April 3, 2004
[The genetics of Parkinson disease]Mathias Toft, Jan AaslyBMC Neurology|April 12, 2011
Aggravated stuttering following subthalamic deep brain stimulation in Parkinson's disease--two casesMathias Toft, Espen DietrichsPageof 49