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The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
November 2, 2022
New <i>SOD1</i> Mutation Causing Rapid Amyotrophic Lateral Sclerosis with Nerve Root Enhancement
Tefani Perera, Caralyn Bencsik, Gerald Pfeffer, et al.
Neurology
|
July 29, 2009
Biopsy-proven immune reconstitution syndrome in a patient with AIDS and cerebral toxoplasmosis
Gerald Pfeffer, Alister Prout, John Hooge, et al.
Journal of Neuromuscular Diseases
|
October 21, 2025
Conference proceedings from the Western Canadian Neuromuscular Conference (WCNMC) - September 27-29, 2024, Calgary, Canada
Gordon Jewett, Collin Luk, Homira Osman, et al.
Ebiomedicine
|
October 22, 2019
Neuropathy due to impaired axonal transport of non-fragmented mitochondria in MYH14 mutation carriers-Authors' reply
Gerald Pfeffer, A Micheil Innes, Timothy E Shutt
Current Opinion in Neurology
|
September 7, 2023
Therapeutic developments for valosin-containing protein mediated multisystem proteinopathy
Victoria Boock, Bhaskar Roy, Gerald Pfeffer, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
July 3, 2025
Tofersen Treatment Normalizes Neurofilament Levels in Autosomal Recessive <i>SOD1</i> Amyotrophic Lateral Sclerosis
Bram De Wel, Theodore Mobach, Gerald Pfeffer, et al.
Nutrients
|
July 14, 2023
The Role of Vitamin D in Neuroprotection in Multiple Sclerosis: An Update
Amarpreet Sangha, Michaela Quon, Gerald Pfeffer, et al.
Journal of Neurology
|
November 8, 2014
Diagnosis of muscle diseases presenting with early respiratory failure
Gerald Pfeffer, Marcus Povitz, G John Gibson, et al.
Brain : a Journal of Neurology
|
February 17, 2024
Higher than expected incident cases of spinal bulbar muscular atrophy in western Canada
Ryan Lamont, Malcolm King, Alexandra King, et al.
Movement Disorders Clinical Practice
|
June 3, 2026
The m.14484T>C MT-ND6 Mutation Presenting with a Hereditary Spastic-Paraparesis Phenotype
Gabriel Amorelli, Christelle Nilles, Gerald Pfeffer, et al.
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Search research articles
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Showing results (11-20 of 93) with videos related to
Sort By:
Page
of 10
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
November 2, 2022
New <i>SOD1</i> Mutation Causing Rapid Amyotrophic Lateral Sclerosis with Nerve Root Enhancement
Tefani Perera, Caralyn Bencsik, Gerald Pfeffer, et al.
Neurology
|
July 29, 2009
Biopsy-proven immune reconstitution syndrome in a patient with AIDS and cerebral toxoplasmosis
Gerald Pfeffer, Alister Prout, John Hooge, et al.
Journal of Neuromuscular Diseases
|
October 21, 2025
Conference proceedings from the Western Canadian Neuromuscular Conference (WCNMC) - September 27-29, 2024, Calgary, Canada
Gordon Jewett, Collin Luk, Homira Osman, et al.
Ebiomedicine
|
October 22, 2019
Neuropathy due to impaired axonal transport of non-fragmented mitochondria in MYH14 mutation carriers-Authors' reply
Gerald Pfeffer, A Micheil Innes, Timothy E Shutt
Current Opinion in Neurology
|
September 7, 2023
Therapeutic developments for valosin-containing protein mediated multisystem proteinopathy
Victoria Boock, Bhaskar Roy, Gerald Pfeffer, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
July 3, 2025
Tofersen Treatment Normalizes Neurofilament Levels in Autosomal Recessive <i>SOD1</i> Amyotrophic Lateral Sclerosis
Bram De Wel, Theodore Mobach, Gerald Pfeffer, et al.
Nutrients
|
July 14, 2023
The Role of Vitamin D in Neuroprotection in Multiple Sclerosis: An Update
Amarpreet Sangha, Michaela Quon, Gerald Pfeffer, et al.
Journal of Neurology
|
November 8, 2014
Diagnosis of muscle diseases presenting with early respiratory failure
Gerald Pfeffer, Marcus Povitz, G John Gibson, et al.
Brain : a Journal of Neurology
|
February 17, 2024
Higher than expected incident cases of spinal bulbar muscular atrophy in western Canada
Ryan Lamont, Malcolm King, Alexandra King, et al.
Movement Disorders Clinical Practice
|
June 3, 2026
The m.14484T>C MT-ND6 Mutation Presenting with a Hereditary Spastic-Paraparesis Phenotype
Gabriel Amorelli, Christelle Nilles, Gerald Pfeffer, et al.
Page
of 10