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David K Simon

Showing results (51-60 of 98) with videos related to

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BMC Medical Genetics|April 2, 2010
Maternal inheritance and mitochondrial DNA variants in familial Parkinson's diseaseDavid K Simon, Nathan Pankratz, Diane K Kissell, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 16, 2004
Evaluation of the role of Nurr1 in a large sample of familial Parkinson's diseaseWilliam C Nichols, Sean K Uniacke, Nathan Pankratz, et al.
Environmental Health Perspectives|September 3, 2010
Association of cumulative lead exposure with Parkinson's diseaseMarc G Weisskopf, Jennifer Weuve, Huiling Nie, et al.
Neurobiology of Aging|October 26, 2005
Somatic mitochondrial DNA mutations in single neurons and gliaIppolita Cantuti-Castelvetri, Michael T Lin, Kangni Zheng, et al.
Neurobiology of Aging|December 17, 2003
Somatic mitochondrial DNA mutations in cortex and substantia nigra in aging and Parkinson's diseaseDavid K Simon, Michael T Lin, Leiya Zheng, et al.
Annals of Neurology|June 22, 2012
Somatic mitochondrial DNA mutations in early Parkinson and incidental Lewy body diseaseMichael T Lin, Ippolita Cantuti-Castelvetri, Kangni Zheng, et al.
Neurogenetics|May 21, 2003
A heteroplasmic mitochondrial complex I gene mutation in adult-onset dystoniaDavid K Simon, Jennifer Friedman, Xandra O Breakefield, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 4, 2007
Rapid and reliable detection of exon rearrangements in various movement disorders genes by multiplex ligation-dependent probe amplificationAna Djarmati, Miodrag Guzvić, Anne Grünewald, et al.
Plos One|December 9, 2014
No sex differences in use of dopaminergic medication in early Parkinson disease in the US and Canada - baseline findings of a multicenter trialChizoba C Umeh, Adriana Pérez, Erika F Augustine, et al.
Ageing Research Reviews|September 24, 2023
Ferroptosis in Parkinson's disease: Molecular mechanisms and therapeutic potentialXv-Shen Ding, Li Gao, Zheng Han, et al.
Pageof 10

Showing results (51-60 of 98) with videos related to

Sort By:
Pageof 10
BMC Medical Genetics|April 2, 2010
Maternal inheritance and mitochondrial DNA variants in familial Parkinson's diseaseDavid K Simon, Nathan Pankratz, Diane K Kissell, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 16, 2004
Evaluation of the role of Nurr1 in a large sample of familial Parkinson's diseaseWilliam C Nichols, Sean K Uniacke, Nathan Pankratz, et al.
Environmental Health Perspectives|September 3, 2010
Association of cumulative lead exposure with Parkinson's diseaseMarc G Weisskopf, Jennifer Weuve, Huiling Nie, et al.
Neurobiology of Aging|October 26, 2005
Somatic mitochondrial DNA mutations in single neurons and gliaIppolita Cantuti-Castelvetri, Michael T Lin, Kangni Zheng, et al.
Neurobiology of Aging|December 17, 2003
Somatic mitochondrial DNA mutations in cortex and substantia nigra in aging and Parkinson's diseaseDavid K Simon, Michael T Lin, Leiya Zheng, et al.
Annals of Neurology|June 22, 2012
Somatic mitochondrial DNA mutations in early Parkinson and incidental Lewy body diseaseMichael T Lin, Ippolita Cantuti-Castelvetri, Kangni Zheng, et al.
Neurogenetics|May 21, 2003
A heteroplasmic mitochondrial complex I gene mutation in adult-onset dystoniaDavid K Simon, Jennifer Friedman, Xandra O Breakefield, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 4, 2007
Rapid and reliable detection of exon rearrangements in various movement disorders genes by multiplex ligation-dependent probe amplificationAna Djarmati, Miodrag Guzvić, Anne Grünewald, et al.
Plos One|December 9, 2014
No sex differences in use of dopaminergic medication in early Parkinson disease in the US and Canada - baseline findings of a multicenter trialChizoba C Umeh, Adriana Pérez, Erika F Augustine, et al.
Ageing Research Reviews|September 24, 2023
Ferroptosis in Parkinson's disease: Molecular mechanisms and therapeutic potentialXv-Shen Ding, Li Gao, Zheng Han, et al.
Pageof 10