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Brain : a Journal of Neurology
|
February 16, 2013
Glucocerebrosidase mutations influence the natural history of Parkinson's disease in a community-based incident cohort
Sophie E Winder-Rhodes, Jonathan R Evans, Maria Ban, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 23, 2018
PDE10A and ADCY5 mutations linked to molecular and microstructural basal ganglia pathology
Flavia Niccolini, Niccolo E Mencacci, Tayyabah Yousaf, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 17, 2017
PREDICT-PD: An online approach to prospectively identify risk indicators of Parkinson's disease
Alastair J Noyce, Lea R'Bibo, Luisa Peress, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 3, 2013
Genotype and phenotype in Parkinson's disease: lessons in heterogeneity from deep brain stimulation
Aikaterina Angeli, Niccolo E Mencacci, Raquel Duran, et al.
Human Molecular Genetics
|
July 10, 2015
The CACNA1B R1389H variant is not associated with myoclonus-dystonia in a large European multicentric cohort
Niccolo E Mencacci, Léa R'bibo, Sara Bandres-Ciga, et al.
Cells
|
April 13, 2023
Loss-of-Function Variants in <i>DRD1</i> in Infantile Parkinsonism-Dystonia
Kimberley M Reid, Dora Steel, Sanjana Nair, et al.
JAMA Neurology
|
March 6, 2013
Parkin disease: a clinicopathologic entity?
Karen M Doherty, Laura Silveira-Moriyama, Laura Parkkinen, et al.
Annals of Neurology
|
February 21, 2013
Mutations in the autoregulatory domain of β-tubulin 4a cause hereditary dystonia
Joshua Hersheson, Niccolo E Mencacci, Mary Davis, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
December 11, 2012
The glucocerobrosidase E326K variant predisposes to Parkinson's disease, but does not cause Gaucher's disease
Raquel Duran, Niccolo E Mencacci, Aikaterini V Angeli, et al.
Research Square
|
October 7, 2024
The <i>LRRK2</i> p.L1795F variant causes Parkinson's disease in the European population
Lara M Lange, Kristin Levine, Susan H Fox, et al.
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of 3
Search research articles
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Showing results (11-20 of 29) with videos related to
Sort By:
Page
of 3
Brain : a Journal of Neurology
|
February 16, 2013
Glucocerebrosidase mutations influence the natural history of Parkinson's disease in a community-based incident cohort
Sophie E Winder-Rhodes, Jonathan R Evans, Maria Ban, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 23, 2018
PDE10A and ADCY5 mutations linked to molecular and microstructural basal ganglia pathology
Flavia Niccolini, Niccolo E Mencacci, Tayyabah Yousaf, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 17, 2017
PREDICT-PD: An online approach to prospectively identify risk indicators of Parkinson's disease
Alastair J Noyce, Lea R'Bibo, Luisa Peress, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 3, 2013
Genotype and phenotype in Parkinson's disease: lessons in heterogeneity from deep brain stimulation
Aikaterina Angeli, Niccolo E Mencacci, Raquel Duran, et al.
Human Molecular Genetics
|
July 10, 2015
The CACNA1B R1389H variant is not associated with myoclonus-dystonia in a large European multicentric cohort
Niccolo E Mencacci, Léa R'bibo, Sara Bandres-Ciga, et al.
Cells
|
April 13, 2023
Loss-of-Function Variants in <i>DRD1</i> in Infantile Parkinsonism-Dystonia
Kimberley M Reid, Dora Steel, Sanjana Nair, et al.
JAMA Neurology
|
March 6, 2013
Parkin disease: a clinicopathologic entity?
Karen M Doherty, Laura Silveira-Moriyama, Laura Parkkinen, et al.
Annals of Neurology
|
February 21, 2013
Mutations in the autoregulatory domain of β-tubulin 4a cause hereditary dystonia
Joshua Hersheson, Niccolo E Mencacci, Mary Davis, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
December 11, 2012
The glucocerobrosidase E326K variant predisposes to Parkinson's disease, but does not cause Gaucher's disease
Raquel Duran, Niccolo E Mencacci, Aikaterini V Angeli, et al.
Research Square
|
October 7, 2024
The <i>LRRK2</i> p.L1795F variant causes Parkinson's disease in the European population
Lara M Lange, Kristin Levine, Susan H Fox, et al.
Page
of 3