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Kishore R Kumar

Showing results (21-30 of 107) with videos related to

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Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|December 24, 2011
Peripheral neuropathy in hereditary spastic paraplegia due to spastin (SPG4) mutation--a neurophysiological study using excitability techniquesKishore R Kumar, Carolyn M Sue, David Burke, et al.
Neuropediatrics|May 8, 2019
A Novel Homozygous Mutation in the FUCA1 Gene Highlighting Fucosidosis as a Cause of Dystonia: Case Report and Literature ReviewGautam Wali, G M Wali, Carolyn M Sue, et al.
BMJ Case Reports|August 22, 2025
A diagnostic challenge: spinocerebellar ataxia type 6 presenting with dystonia and parkinsonismTal Jonatan Koren, Kate E Ahmad, Kishore R Kumar, et al.
Movement Disorders Clinical Practice|December 17, 2021
Long-Term Follow-Up and Evolution of <i>ADCY5</i>-From a Ballistic to Dystonic PhenotypeGurusidheshwar M Wali, Gautam Wali, Kishore R Kumar, et al.
Internal Medicine Journal|October 14, 2024
Muscular dystrophy as a cause of unilateral scapular wingingMitchell J Lycett, Seamus E Dalton, Kishore R Kumar, et al.
Acta Neuropathologica Communications|May 26, 2021
An update on the neurological short tandem repeat expansion disorders and the emergence of long-read sequencing diagnosticsSanjog R Chintalaphani, Sandy S Pineda, Ira W Deveson, et al.
Neurology|December 26, 2022
Author Response: Use of Whole-Genome Sequencing for Mitochondrial Disease DiagnosisRyan L Davis, Kishore R Kumar, Eloise C Watson, et al.
Muscle & Nerve|February 2, 2010
A novel CLCN1 mutation (G1652A) causing a mild phenotype of thomsen diseaseKishore R Kumar, Karl Ng, Himesha Vandebona, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|January 15, 2024
Genetic Testing of Movements Disorders: A Review of Clinical UtilityDennis Yeow, Laura I Rudaks, Sue-Faye Siow, et al.
Muscle & Nerve|May 25, 2011
Axonal hyperpolarization in inclusion-body myopathy, Paget disease of the bone, and frontotemporal dementia (IBMPFD)Kishore R Kumar, Christina Liang, Merilee Needham, et al.
Pageof 11

Showing results (21-30 of 107) with videos related to

Sort By:
Pageof 11
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|December 24, 2011
Peripheral neuropathy in hereditary spastic paraplegia due to spastin (SPG4) mutation--a neurophysiological study using excitability techniquesKishore R Kumar, Carolyn M Sue, David Burke, et al.
Neuropediatrics|May 8, 2019
A Novel Homozygous Mutation in the FUCA1 Gene Highlighting Fucosidosis as a Cause of Dystonia: Case Report and Literature ReviewGautam Wali, G M Wali, Carolyn M Sue, et al.
BMJ Case Reports|August 22, 2025
A diagnostic challenge: spinocerebellar ataxia type 6 presenting with dystonia and parkinsonismTal Jonatan Koren, Kate E Ahmad, Kishore R Kumar, et al.
Movement Disorders Clinical Practice|December 17, 2021
Long-Term Follow-Up and Evolution of <i>ADCY5</i>-From a Ballistic to Dystonic PhenotypeGurusidheshwar M Wali, Gautam Wali, Kishore R Kumar, et al.
Internal Medicine Journal|October 14, 2024
Muscular dystrophy as a cause of unilateral scapular wingingMitchell J Lycett, Seamus E Dalton, Kishore R Kumar, et al.
Acta Neuropathologica Communications|May 26, 2021
An update on the neurological short tandem repeat expansion disorders and the emergence of long-read sequencing diagnosticsSanjog R Chintalaphani, Sandy S Pineda, Ira W Deveson, et al.
Neurology|December 26, 2022
Author Response: Use of Whole-Genome Sequencing for Mitochondrial Disease DiagnosisRyan L Davis, Kishore R Kumar, Eloise C Watson, et al.
Muscle & Nerve|February 2, 2010
A novel CLCN1 mutation (G1652A) causing a mild phenotype of thomsen diseaseKishore R Kumar, Karl Ng, Himesha Vandebona, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|January 15, 2024
Genetic Testing of Movements Disorders: A Review of Clinical UtilityDennis Yeow, Laura I Rudaks, Sue-Faye Siow, et al.
Muscle & Nerve|May 25, 2011
Axonal hyperpolarization in inclusion-body myopathy, Paget disease of the bone, and frontotemporal dementia (IBMPFD)Kishore R Kumar, Christina Liang, Merilee Needham, et al.
Pageof 11