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Clinica Chimica Acta; International Journal of Clinical Chemistry
|
March 10, 2015
Autoimmune peripheral neuropathies
Pierre R Bourque, Jodi Warman Chardon, Rami Massie
Neurology
|
September 19, 2019
Teaching NeuroImages: Sneddon syndrome
Ahmad Almutlaq, Mohammed Alshurem, Myriam Levesque-Roy, et al.
Journal of the Neurological Sciences
|
February 5, 2022
Scapuloperoneal syndrome with mitochondrial DNA deletion
Émilie Pichette, Erin O'Ferrall, Jason Karamchandani, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
August 18, 2017
Traduction française de l'échelle Charcot-Marie-Tooth Disease Pediatric Scale
Cynthia Gagnon, Rami Massie, Marjolaine Tremblay, et al.
Journal of Neuropathology and Experimental Neurology
|
September 2, 2017
A New Mutation in FIG4 Causes a Severe Form of CMT4J Involving TRPV4 in the Pathogenic Cascade
Benoit J Gentil, Erin O'Ferrall, Colin Chalk, et al.
Current Cardiology Reports
|
June 25, 2025
Beyond the Heart: Exploring Extracardiac Manifestations in Cardiac Amyloidosis for Early Diagnosis
Marcus Saldanha, Lu Kun Chen, Joshua Solomon, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
January 24, 2022
Breakthrough of Granulomatosis with Polyangiitis-Associated CNS Vasculitis Amidst Adequate B-cell Depletion
Samantha Rivet, David Pellerin, Rami Massie, et al.
Muscle & Nerve
|
December 8, 2020
Temporal evolution of nerve conduction study abnormalities in anti-myelin-associated glycoprotein neuropathy
Pierre R Bourque, Josée Masson-Roy, Jodi Warman-Chardon, et al.
American Journal of Medical Genetics. Part A
|
December 2, 2023
An adult patient with Tatton-Brown-Rahman syndrome caused by a novel DNMT3A variant and axonal polyneuropathy
Al-Alya AlSabah, Mohammed Alsalmi, Rami Massie, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
January 27, 2026
The genetics of autosomal recessive ALS: a review of the common forms and their phenotypes
Matti D Allen, Vanessa Diab, Nastasija Lezaic, et al.
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Search research articles
Search
Showing results (11-20 of 39) with videos related to
Sort By:
Page
of 4
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
March 10, 2015
Autoimmune peripheral neuropathies
Pierre R Bourque, Jodi Warman Chardon, Rami Massie
Neurology
|
September 19, 2019
Teaching NeuroImages: Sneddon syndrome
Ahmad Almutlaq, Mohammed Alshurem, Myriam Levesque-Roy, et al.
Journal of the Neurological Sciences
|
February 5, 2022
Scapuloperoneal syndrome with mitochondrial DNA deletion
Émilie Pichette, Erin O'Ferrall, Jason Karamchandani, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
August 18, 2017
Traduction française de l'échelle Charcot-Marie-Tooth Disease Pediatric Scale
Cynthia Gagnon, Rami Massie, Marjolaine Tremblay, et al.
Journal of Neuropathology and Experimental Neurology
|
September 2, 2017
A New Mutation in FIG4 Causes a Severe Form of CMT4J Involving TRPV4 in the Pathogenic Cascade
Benoit J Gentil, Erin O'Ferrall, Colin Chalk, et al.
Current Cardiology Reports
|
June 25, 2025
Beyond the Heart: Exploring Extracardiac Manifestations in Cardiac Amyloidosis for Early Diagnosis
Marcus Saldanha, Lu Kun Chen, Joshua Solomon, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
January 24, 2022
Breakthrough of Granulomatosis with Polyangiitis-Associated CNS Vasculitis Amidst Adequate B-cell Depletion
Samantha Rivet, David Pellerin, Rami Massie, et al.
Muscle & Nerve
|
December 8, 2020
Temporal evolution of nerve conduction study abnormalities in anti-myelin-associated glycoprotein neuropathy
Pierre R Bourque, Josée Masson-Roy, Jodi Warman-Chardon, et al.
American Journal of Medical Genetics. Part A
|
December 2, 2023
An adult patient with Tatton-Brown-Rahman syndrome caused by a novel DNMT3A variant and axonal polyneuropathy
Al-Alya AlSabah, Mohammed Alsalmi, Rami Massie, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
January 27, 2026
The genetics of autosomal recessive ALS: a review of the common forms and their phenotypes
Matti D Allen, Vanessa Diab, Nastasija Lezaic, et al.
Page
of 4