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Gerald Pfeffer

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The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|December 16, 2010
Multisystem disorder in late-onset chronic progressive external ophthalmoplegiaGerald Pfeffer, Sandra Sirrs, N Kevin Wade, et al.
Brain : a Journal of Neurology|November 26, 2013
Reply: Hereditary myopathy with early respiratory failure is caused by mutations in the titin FN3 119 domainGerald Pfeffer, Helen Griffin, Angela Pyle, et al.
Brain : a Journal of Neurology|May 19, 2016
Emerging therapies for mitochondrial disordersHelen Nightingale, Gerald Pfeffer, David Bargiela, et al.
Parkinsonism & Related Disorders|October 16, 2023
Novel RAB39B variant associated intellectual disability and levodopa-responsive young-onset parkinsonismAli Abusrair, Adriana Mititelu, Gerald Pfeffer, et al.
Neurology. Genetics|August 13, 2019
Systematic review and meta-analysis of cardiac involvement in mitochondrial myopathyAsfia Quadir, Carly Sabine Pontifex, Helen Lee Robertson, et al.
The Cochrane Database of Systematic Reviews|April 20, 2012
Treatment for mitochondrial disordersGerald Pfeffer, Kari Majamaa, Douglass M Turnbull, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|February 18, 2020
Fentanyl Overdose Causing Hippocampal Ischaemia Followed by Delayed LeukoencephalopathyAaron R Switzer, Benjamin Beland, Justyna R Sarna, et al.
Multiple Sclerosis and Related Disorders|September 29, 2019
Long noncoding RNAs associated with phenotypic severity in multiple sclerosisMehul Gupta, Kristina Martens, Luanne M Metz, et al.
Frontiers in Neurology|January 28, 2021
Case Report: Calpainopathy Presenting After Bone Marrow Transplantation, With Studies of Donor Genetic Content in Various Tissue TypesKristina Martens, Jamie Leckie, Daniel Fok, et al.
International Journal of Molecular Sciences|June 19, 2024
Valosin-Containing Protein (VCP): A Review of Its Diverse Molecular Functions and Clinical PhenotypesCarly S Pontifex, Mashiat Zaman, Roberto D Fanganiello, et al.
Pageof 10

Showing results (21-30 of 93) with videos related to

Sort By:
Pageof 10
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|December 16, 2010
Multisystem disorder in late-onset chronic progressive external ophthalmoplegiaGerald Pfeffer, Sandra Sirrs, N Kevin Wade, et al.
Brain : a Journal of Neurology|November 26, 2013
Reply: Hereditary myopathy with early respiratory failure is caused by mutations in the titin FN3 119 domainGerald Pfeffer, Helen Griffin, Angela Pyle, et al.
Brain : a Journal of Neurology|May 19, 2016
Emerging therapies for mitochondrial disordersHelen Nightingale, Gerald Pfeffer, David Bargiela, et al.
Parkinsonism & Related Disorders|October 16, 2023
Novel RAB39B variant associated intellectual disability and levodopa-responsive young-onset parkinsonismAli Abusrair, Adriana Mititelu, Gerald Pfeffer, et al.
Neurology. Genetics|August 13, 2019
Systematic review and meta-analysis of cardiac involvement in mitochondrial myopathyAsfia Quadir, Carly Sabine Pontifex, Helen Lee Robertson, et al.
The Cochrane Database of Systematic Reviews|April 20, 2012
Treatment for mitochondrial disordersGerald Pfeffer, Kari Majamaa, Douglass M Turnbull, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|February 18, 2020
Fentanyl Overdose Causing Hippocampal Ischaemia Followed by Delayed LeukoencephalopathyAaron R Switzer, Benjamin Beland, Justyna R Sarna, et al.
Multiple Sclerosis and Related Disorders|September 29, 2019
Long noncoding RNAs associated with phenotypic severity in multiple sclerosisMehul Gupta, Kristina Martens, Luanne M Metz, et al.
Frontiers in Neurology|January 28, 2021
Case Report: Calpainopathy Presenting After Bone Marrow Transplantation, With Studies of Donor Genetic Content in Various Tissue TypesKristina Martens, Jamie Leckie, Daniel Fok, et al.
International Journal of Molecular Sciences|June 19, 2024
Valosin-Containing Protein (VCP): A Review of Its Diverse Molecular Functions and Clinical PhenotypesCarly S Pontifex, Mashiat Zaman, Roberto D Fanganiello, et al.
Pageof 10