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Human Mutation
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July 11, 2012
Use of support vector machines for disease risk prediction in genome-wide association studies: concerns and opportunities
Florian Mittag, Finja Büchel, Mohamad Saad, et al.
Brain : a Journal of Neurology
|
October 8, 2020
Mitochondrial damage-associated inflammation highlights biomarkers in PRKN/PINK1 parkinsonism
Max Borsche, Inke R König, Sylvie Delcambre, et al.
Brain : a Journal of Neurology
|
April 17, 2026
Blood mtDNA markers of mitochondrial subtype and early-onset Parkinson's disease biology
Anne Grünewald, Felix Knab, Milan Zimmermann, et al.
NPJ Parkinson'S Disease
|
July 27, 2021
Alpha-synuclein research: defining strategic moves in the battle against Parkinson's disease
Luis M A Oliveira, Thomas Gasser, Robert Edwards, et al.
Archives of Neurology
|
January 12, 2005
A rare truncating mutation in ADH1C (G78Stop) shows significant association with Parkinson disease in a large international sample
Silvia Buervenich, Andrea Carmine, Dagmar Galter, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 17, 2005
Alpha-synuclein and Parkinson's disease: implications from the screening of more than 1,900 patients
Daniela Berg, Marc Niwar, Sylvia Maass, et al.
Nature
|
March 18, 2016
The contribution of China's emissions to global climate forcing
Bengang Li, Thomas Gasser, Philippe Ciais, et al.
Molecular Psychiatry
|
July 8, 2021
PIAS2-mediated blockade of IFN-β signaling: a basis for sporadic Parkinson disease dementia
Joana Magalhaes, Emilie Tresse, Patrick Ejlerskov, et al.
Journal of Neuroinflammation
|
May 26, 2016
Inflammatory profile in LRRK2-associated prodromal and clinical PD
Kathrin Brockmann, Anja Apel, Claudia Schulte, et al.
Annals of Neurology
|
August 2, 2003
How much phenotypic variation can be attributed to parkin genotype?
Ebba Lohmann, Magali Periquet, Vincenzo Bonifati, et al.
Page
of 43
Search research articles
Search
Showing results (311-320 of 421) with videos related to
Sort By:
Page
of 43
Human Mutation
|
July 11, 2012
Use of support vector machines for disease risk prediction in genome-wide association studies: concerns and opportunities
Florian Mittag, Finja Büchel, Mohamad Saad, et al.
Brain : a Journal of Neurology
|
October 8, 2020
Mitochondrial damage-associated inflammation highlights biomarkers in PRKN/PINK1 parkinsonism
Max Borsche, Inke R König, Sylvie Delcambre, et al.
Brain : a Journal of Neurology
|
April 17, 2026
Blood mtDNA markers of mitochondrial subtype and early-onset Parkinson's disease biology
Anne Grünewald, Felix Knab, Milan Zimmermann, et al.
NPJ Parkinson'S Disease
|
July 27, 2021
Alpha-synuclein research: defining strategic moves in the battle against Parkinson's disease
Luis M A Oliveira, Thomas Gasser, Robert Edwards, et al.
Archives of Neurology
|
January 12, 2005
A rare truncating mutation in ADH1C (G78Stop) shows significant association with Parkinson disease in a large international sample
Silvia Buervenich, Andrea Carmine, Dagmar Galter, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 17, 2005
Alpha-synuclein and Parkinson's disease: implications from the screening of more than 1,900 patients
Daniela Berg, Marc Niwar, Sylvia Maass, et al.
Nature
|
March 18, 2016
The contribution of China's emissions to global climate forcing
Bengang Li, Thomas Gasser, Philippe Ciais, et al.
Molecular Psychiatry
|
July 8, 2021
PIAS2-mediated blockade of IFN-β signaling: a basis for sporadic Parkinson disease dementia
Joana Magalhaes, Emilie Tresse, Patrick Ejlerskov, et al.
Journal of Neuroinflammation
|
May 26, 2016
Inflammatory profile in LRRK2-associated prodromal and clinical PD
Kathrin Brockmann, Anja Apel, Claudia Schulte, et al.
Annals of Neurology
|
August 2, 2003
How much phenotypic variation can be attributed to parkin genotype?
Ebba Lohmann, Magali Periquet, Vincenzo Bonifati, et al.
Page
of 43