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Patrick A Dion

Showing results (81-90 of 188) with videos related to

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Movement Disorders Clinical Practice|October 27, 2018
Case-Control and Family-Based Association Study of Specific <i>PTPRD</i> Variants in Restless Legs SyndromeZiv Gan-Or, Sirui Zhou, Amelie Johnson, et al.
Parkinsonism & Related Disorders|May 16, 2019
Genome-wide estimates of heritability and genetic correlations in essential tremorMonica Diez-Fairen, Sara Bandres-Ciga, Gabrielle Houle, et al.
Molecular Psychiatry|June 14, 2018
Missense variants in ATP1A3 and FXYD gene family are associated with childhood-onset schizophreniaBoris Chaumette, Vladimir Ferrafiat, Amirthagowri Ambalavanan, et al.
Nanoscale|November 28, 2024
Gold nanoclusters Au<sub>25</sub>AcCys<sub>18</sub> normalize intracellular ROS without increasing cytoplasmic alarmin acHMGB1 abundance in human microglia and neuronsIssan Zhang, Dusica Maysinger, Maja Beus, et al.
Translational Psychiatry|November 1, 2025
De novo variant analysis of childhood-onset obsessive-compulsive disorder in the French-Canadian populationKate Bornais, Jay P Ross, Zoe Schmilovich, et al.
Neurobiology of Aging|February 6, 2018
Association study of essential tremor genetic loci in Parkinson's diseaseJay P Ross, Sadaf Mohtashami, Etienne Leveille, et al.
European Journal of Medical Genetics|August 12, 2015
Identification of a novel homozygous SPG7 mutation by whole exome sequencing in a Greek family with a complicated form of hereditary spastic paraplegiaHussein Daoud, Eleni Merkouri Papadima, Bouchra Ouled Amar Bencheikh, et al.
Annals of Human Genetics|October 23, 2009
A mutation that creates a pseudoexon in SOD1 causes familial ALSPaul N Valdmanis, Veronique V Belzil, James Lee, et al.
Molecular Therapy. Nucleic Acids|March 5, 2019
RNA-Based Therapy Utilizing Oculopharyngeal Muscular Dystrophy Transcript Knockdown and ReplacementAida Abu-Baker, Nawwaf Kharma, Jonathan Perreault, et al.
Archives of Neurology|January 12, 2011
Resequencing of 29 candidate genes in patients with familial and sporadic amyotrophic lateral sclerosisHussein Daoud, Paul N Valdmanis, Francois Gros-Louis, et al.
Pageof 19

Showing results (81-90 of 188) with videos related to

Sort By:
Pageof 19
Movement Disorders Clinical Practice|October 27, 2018
Case-Control and Family-Based Association Study of Specific <i>PTPRD</i> Variants in Restless Legs SyndromeZiv Gan-Or, Sirui Zhou, Amelie Johnson, et al.
Parkinsonism & Related Disorders|May 16, 2019
Genome-wide estimates of heritability and genetic correlations in essential tremorMonica Diez-Fairen, Sara Bandres-Ciga, Gabrielle Houle, et al.
Molecular Psychiatry|June 14, 2018
Missense variants in ATP1A3 and FXYD gene family are associated with childhood-onset schizophreniaBoris Chaumette, Vladimir Ferrafiat, Amirthagowri Ambalavanan, et al.
Nanoscale|November 28, 2024
Gold nanoclusters Au<sub>25</sub>AcCys<sub>18</sub> normalize intracellular ROS without increasing cytoplasmic alarmin acHMGB1 abundance in human microglia and neuronsIssan Zhang, Dusica Maysinger, Maja Beus, et al.
Translational Psychiatry|November 1, 2025
De novo variant analysis of childhood-onset obsessive-compulsive disorder in the French-Canadian populationKate Bornais, Jay P Ross, Zoe Schmilovich, et al.
Neurobiology of Aging|February 6, 2018
Association study of essential tremor genetic loci in Parkinson's diseaseJay P Ross, Sadaf Mohtashami, Etienne Leveille, et al.
European Journal of Medical Genetics|August 12, 2015
Identification of a novel homozygous SPG7 mutation by whole exome sequencing in a Greek family with a complicated form of hereditary spastic paraplegiaHussein Daoud, Eleni Merkouri Papadima, Bouchra Ouled Amar Bencheikh, et al.
Annals of Human Genetics|October 23, 2009
A mutation that creates a pseudoexon in SOD1 causes familial ALSPaul N Valdmanis, Veronique V Belzil, James Lee, et al.
Molecular Therapy. Nucleic Acids|March 5, 2019
RNA-Based Therapy Utilizing Oculopharyngeal Muscular Dystrophy Transcript Knockdown and ReplacementAida Abu-Baker, Nawwaf Kharma, Jonathan Perreault, et al.
Archives of Neurology|January 12, 2011
Resequencing of 29 candidate genes in patients with familial and sporadic amyotrophic lateral sclerosisHussein Daoud, Paul N Valdmanis, Francois Gros-Louis, et al.
Pageof 19