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Ali H Rajput

Showing results (51-60 of 78) with videos related to

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Neurobiology of Disease|August 9, 2015
Accumulation of amyloid-β in the cerebellar cortex of essential tremor patientsEric Béliveau, Cyntia Tremblay, Émilie Aubry-Lafontaine, et al.
NPJ Parkinson'S Disease|May 7, 2026
High molecular weight insoluble parkin in the substantia nigra of patients with idiopathic Parkinson's diseaseCyntia Tremblay, Laura Pshevorskiy, Rosalie J Cottez, et al.
Journal of Magnetic Resonance Imaging : JMRI|June 1, 2010
Brain iron detected by SWI high pass filtered phase calibrated with synchrotron X-ray fluorescenceKarla Hopp, Bogdan F Gh Popescu, Richard P E McCrea, et al.
Brain : a Journal of Neurology|November 12, 2009
Brain alpha-synuclein accumulation in multiple system atrophy, Parkinson's disease and progressive supranuclear palsy: a comparative investigationJunchao Tong, Henry Wong, Mark Guttman, et al.
Brain : a Journal of Neurology|November 29, 2011
Defective dentate nucleus GABA receptors in essential tremorSarah Paris-Robidas, Elodie Brochu, Marion Sintes, et al.
Neurobiology of Aging|December 29, 2009
Metabotropic glutamate receptor type 5 in levodopa-induced motor complicationsBazoumana Ouattara, Laurent Grégoire, Marc Morissette, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 6, 2014
Genetic variability of the retromer cargo recognition complex in parkinsonismEmil K Gustavsson, Ilaria Guella, Joanne Trinh, et al.
Parkinsonism & Related Disorders|February 19, 2013
STX6 rs1411478 is not associated with increased risk of Parkinson's diseaseJoanne Trinh, Carles Vilariño-Güell, Alan Donald, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 14, 2014
DNAJC13 genetic variants in parkinsonismEmil K Gustavsson, Joanne Trinh, Ilaria Guella, et al.
European Journal of Human Genetics : EJHG|August 14, 2014
VPS35 and DNAJC13 disease-causing variants in essential tremorAlex Rajput, Jay P Ross, Cecily Q Bernales, et al.
Pageof 8

Showing results (51-60 of 78) with videos related to

Sort By:
Pageof 8
Neurobiology of Disease|August 9, 2015
Accumulation of amyloid-β in the cerebellar cortex of essential tremor patientsEric Béliveau, Cyntia Tremblay, Émilie Aubry-Lafontaine, et al.
NPJ Parkinson'S Disease|May 7, 2026
High molecular weight insoluble parkin in the substantia nigra of patients with idiopathic Parkinson's diseaseCyntia Tremblay, Laura Pshevorskiy, Rosalie J Cottez, et al.
Journal of Magnetic Resonance Imaging : JMRI|June 1, 2010
Brain iron detected by SWI high pass filtered phase calibrated with synchrotron X-ray fluorescenceKarla Hopp, Bogdan F Gh Popescu, Richard P E McCrea, et al.
Brain : a Journal of Neurology|November 12, 2009
Brain alpha-synuclein accumulation in multiple system atrophy, Parkinson's disease and progressive supranuclear palsy: a comparative investigationJunchao Tong, Henry Wong, Mark Guttman, et al.
Brain : a Journal of Neurology|November 29, 2011
Defective dentate nucleus GABA receptors in essential tremorSarah Paris-Robidas, Elodie Brochu, Marion Sintes, et al.
Neurobiology of Aging|December 29, 2009
Metabotropic glutamate receptor type 5 in levodopa-induced motor complicationsBazoumana Ouattara, Laurent Grégoire, Marc Morissette, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 6, 2014
Genetic variability of the retromer cargo recognition complex in parkinsonismEmil K Gustavsson, Ilaria Guella, Joanne Trinh, et al.
Parkinsonism & Related Disorders|February 19, 2013
STX6 rs1411478 is not associated with increased risk of Parkinson's diseaseJoanne Trinh, Carles Vilariño-Güell, Alan Donald, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 14, 2014
DNAJC13 genetic variants in parkinsonismEmil K Gustavsson, Joanne Trinh, Ilaria Guella, et al.
European Journal of Human Genetics : EJHG|August 14, 2014
VPS35 and DNAJC13 disease-causing variants in essential tremorAlex Rajput, Jay P Ross, Cecily Q Bernales, et al.
Pageof 8