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Gerald Pfeffer

Showing results (71-80 of 93) with videos related to

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Epilepsia|January 3, 2025
Detecting somatic variants in purified brain DNA obtained from surgically implanted depth electrodes in epilepsyRumika Mascarenhas, Daria Merrikh, Maryam Khanbabaei, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|July 28, 2020
Response to Provincial Governments' Decisions Regarding Monitoring for Adults with Spinal Muscular AtrophyVictoria L Hodgkinson, Kristine Chapman, Aaron Izenberg, et al.
Frontiers in Neurology|February 15, 2021
Association Between BDNF Val66Met Polymorphism and Mild Behavioral Impairment in Patients With Parkinson's DiseaseMehrafarin Ramezani, Jennifer A Ruskey, Kristina Martens, et al.
Brain : a Journal of Neurology|May 12, 2012
Titin mutation segregates with hereditary myopathy with early respiratory failureGerald Pfeffer, Hannah R Elliott, Helen Griffin, et al.
Journal of Clinical Neurology (Seoul, Korea)|January 10, 2026
The Oral Microbiome in Amyotrophic Lateral Sclerosis Shows Differentially Abundant Organisms in Limb Versus Bulbar Onset Disease: A Binational StudySarah M Jacob, Bugyeong Son, Sahar Bagheri, et al.
Scientific Reports|March 2, 2021
Investigating the relationship between the SNCA gene and cognitive abilities in idiopathic Parkinson's disease using machine learningMehrafarin Ramezani, Pauline Mouches, Eunjin Yoon, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|January 26, 2026
Kerri L Schellenberg, Gudrun Caspar-Bell, Colin Ellis, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|September 22, 2025
Best practice recommendations for the clinical care of spinal bulbar muscular atrophyKerri L Schellenberg, Gudrun Caspar-Bell, Colin Ellis, et al.
JAMA Neurology|November 25, 2014
Clonal expansion of secondary mitochondrial DNA deletions associated with spinocerebellar ataxia type 28Gráinne S Gorman, Gerald Pfeffer, Helen Griffin, et al.
Journal of Neuromuscular Diseases|April 19, 2021
A Canadian Adult Spinal Muscular Atrophy Outcome Measures Toolkit: Results of a National Consensus using a Modified Delphi MethodJeremy Slayter, Victoria Hodgkinson, Josh Lounsberry, et al.
Pageof 10

Showing results (71-80 of 93) with videos related to

Sort By:
Pageof 10
Epilepsia|January 3, 2025
Detecting somatic variants in purified brain DNA obtained from surgically implanted depth electrodes in epilepsyRumika Mascarenhas, Daria Merrikh, Maryam Khanbabaei, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|July 28, 2020
Response to Provincial Governments' Decisions Regarding Monitoring for Adults with Spinal Muscular AtrophyVictoria L Hodgkinson, Kristine Chapman, Aaron Izenberg, et al.
Frontiers in Neurology|February 15, 2021
Association Between BDNF Val66Met Polymorphism and Mild Behavioral Impairment in Patients With Parkinson's DiseaseMehrafarin Ramezani, Jennifer A Ruskey, Kristina Martens, et al.
Brain : a Journal of Neurology|May 12, 2012
Titin mutation segregates with hereditary myopathy with early respiratory failureGerald Pfeffer, Hannah R Elliott, Helen Griffin, et al.
Journal of Clinical Neurology (Seoul, Korea)|January 10, 2026
The Oral Microbiome in Amyotrophic Lateral Sclerosis Shows Differentially Abundant Organisms in Limb Versus Bulbar Onset Disease: A Binational StudySarah M Jacob, Bugyeong Son, Sahar Bagheri, et al.
Scientific Reports|March 2, 2021
Investigating the relationship between the SNCA gene and cognitive abilities in idiopathic Parkinson's disease using machine learningMehrafarin Ramezani, Pauline Mouches, Eunjin Yoon, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|January 26, 2026
Kerri L Schellenberg, Gudrun Caspar-Bell, Colin Ellis, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|September 22, 2025
Best practice recommendations for the clinical care of spinal bulbar muscular atrophyKerri L Schellenberg, Gudrun Caspar-Bell, Colin Ellis, et al.
JAMA Neurology|November 25, 2014
Clonal expansion of secondary mitochondrial DNA deletions associated with spinocerebellar ataxia type 28Gráinne S Gorman, Gerald Pfeffer, Helen Griffin, et al.
Journal of Neuromuscular Diseases|April 19, 2021
A Canadian Adult Spinal Muscular Atrophy Outcome Measures Toolkit: Results of a National Consensus using a Modified Delphi MethodJeremy Slayter, Victoria Hodgkinson, Josh Lounsberry, et al.
Pageof 10