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Kishore Raj Kumar

Showing results (1-10 of 29) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|August 12, 2015
Targeting glucocerebrosidase: Reduced enzymatic activity and Parkinson's diseaseKishore Raj Kumar
Movement Disorders : Official Journal of the Movement Disorder Society|May 27, 2015
Mutations in hippocalcin and autosomal recessive dystonia: a role for perturbed calcium signaling?Kishore Raj Kumar
BMJ Case Reports|June 21, 2011
Essential thrombocythaemia presenting with subclavian artery thrombosis and multiple embolic eventsKishore Raj Kumar, Michelle Kiley
Movement Disorders : Official Journal of the Movement Disorder Society|March 12, 2022
Harnessing Transcriptomics to Decipher Dystonia PathogenesisAvi Fellner, Kishore Raj Kumar
Frontiers in Neurology|January 25, 2021
Pallidal Deep Brain Stimulation for Monogenic Dystonia: The Effect of Gene on OutcomeStephen Tisch, Kishore Raj Kumar
Current Neurology and Neuroscience Reports|March 1, 2021
Challenges and Controversies in the Genetic Diagnosis of Hereditary Spastic ParaplegiaLydia Saputra, Kishore Raj Kumar
Brain Communications|July 9, 2024
Clinical phenotyping is key to differentiating <i>RFC1</i>-associated neuropathy from immune-mediated neuropathySue-Faye Siow, Kishore Raj Kumar
Movement Disorders : Official Journal of the Movement Disorder Society|September 27, 2015
ADCY5 identified as a novel cause of benign hereditary choreaKishore Raj Kumar, Victor S C Fung
Genes|March 25, 2022
Monogenic Parkinson's Disease: Genotype, Phenotype, Pathophysiology, and Genetic TestingFangzhi Jia, Avi Fellner, Kishore Raj Kumar
Frontiers in Neurology|October 15, 2021
Editorial: Genetics of Paroxysmal Movement DisordersAnna De Rosa, Bettina Balint, Kishore Raj Kumar
Pageof 3

Showing results (1-10 of 29) with videos related to

Sort By:
Pageof 3
Movement Disorders : Official Journal of the Movement Disorder Society|August 12, 2015
Targeting glucocerebrosidase: Reduced enzymatic activity and Parkinson's diseaseKishore Raj Kumar
Movement Disorders : Official Journal of the Movement Disorder Society|May 27, 2015
Mutations in hippocalcin and autosomal recessive dystonia: a role for perturbed calcium signaling?Kishore Raj Kumar
BMJ Case Reports|June 21, 2011
Essential thrombocythaemia presenting with subclavian artery thrombosis and multiple embolic eventsKishore Raj Kumar, Michelle Kiley
Movement Disorders : Official Journal of the Movement Disorder Society|March 12, 2022
Harnessing Transcriptomics to Decipher Dystonia PathogenesisAvi Fellner, Kishore Raj Kumar
Frontiers in Neurology|January 25, 2021
Pallidal Deep Brain Stimulation for Monogenic Dystonia: The Effect of Gene on OutcomeStephen Tisch, Kishore Raj Kumar
Current Neurology and Neuroscience Reports|March 1, 2021
Challenges and Controversies in the Genetic Diagnosis of Hereditary Spastic ParaplegiaLydia Saputra, Kishore Raj Kumar
Brain Communications|July 9, 2024
Clinical phenotyping is key to differentiating <i>RFC1</i>-associated neuropathy from immune-mediated neuropathySue-Faye Siow, Kishore Raj Kumar
Movement Disorders : Official Journal of the Movement Disorder Society|September 27, 2015
ADCY5 identified as a novel cause of benign hereditary choreaKishore Raj Kumar, Victor S C Fung
Genes|March 25, 2022
Monogenic Parkinson's Disease: Genotype, Phenotype, Pathophysiology, and Genetic TestingFangzhi Jia, Avi Fellner, Kishore Raj Kumar
Frontiers in Neurology|October 15, 2021
Editorial: Genetics of Paroxysmal Movement DisordersAnna De Rosa, Bettina Balint, Kishore Raj Kumar
Pageof 3