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CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne
|
June 9, 2016
Myotonic dystrophy type 1
Cam-Tu Emilie Nguyen, Craig Campbell
Mcgill Journal of Medicine : MJM : an International Forum for the Advancement of Medical Sciences by Students
|
June 5, 2008
Interventional radiology: from idea to device to patient
Anthony Ciarallo, Cam-Tu Emilie Nguyen, Lawrence Stein
Pediatric Neurology
|
November 5, 2018
Twinkle-Associated Mitochondrial DNA Depletion
Salma Remtulla, Cam-Tu Emilie Nguyen, Chitra Prasad, et al.
Journal of Neuromuscular Diseases
|
June 23, 2019
A Phenotypic Description of Congenital Myotonic Dystrophy using PhenoStacks
Madhavi Prasad, Michael Glueck, Delia Ceballos-Saenz, et al.
Neurology(R) Neuroimmunology & Neuroinflammation
|
December 22, 2023
CNS Inflammation as the First Sign of Complement Factor I Deficiency: A Severe Myelitis Treated With Intense Immunotherapy and Eculizumab
Valérie Massey, Cam-Tu Emilie Nguyen, Tine François, et al.
HGG Advances
|
January 20, 2022
Variants in <i>LSM7</i> impair LSM complexes assembly, neurodevelopment in zebrafish and may be associated with an ultra-rare neurological disease
Alexa Derksen, Hung-Yu Shih, Diane Forget, et al.
Journal of Child Neurology
|
May 24, 2023
The Experience of Parents of Children With Genetically Determined Leukoencephalopathies With the Health Care System: A Qualitative Study
Pouneh Amir Yazdani, Marie-Lou St-Jean, Sara Matovic, et al.
Journal of Child Neurology
|
January 5, 2022
Experience of Parents of Children with Genetically Determined Leukoencephalopathies Regarding the Adapted Health Care Services During the COVID-19 Pandemic
Pouneh Amir Yazdani, Marie-Lou St-Jean, Sara Matovic, et al.
Multiple Sclerosis and Related Disorders
|
June 15, 2023
Clinical course, imaging, and pathological features of 45 adult and pediatric cases of myelin oligodendrocyte glycoprotein antibody-associated disease
Hayet Boudjani, Giulia Fadda, Gabrielle Dufort, et al.
Neurology
|
November 12, 2025
Urine Sorbitol and Xylitol for the Diagnosis of Sorbitol Dehydrogenase Deficiency-Related Neuropathy
Jordan Elliott Bontrager, Amy L White, Karlla W Brigatti, et al.
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Search research articles
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Showing results (1-10 of 13) with videos related to
Sort By:
Page
of 2
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne
|
June 9, 2016
Myotonic dystrophy type 1
Cam-Tu Emilie Nguyen, Craig Campbell
Mcgill Journal of Medicine : MJM : an International Forum for the Advancement of Medical Sciences by Students
|
June 5, 2008
Interventional radiology: from idea to device to patient
Anthony Ciarallo, Cam-Tu Emilie Nguyen, Lawrence Stein
Pediatric Neurology
|
November 5, 2018
Twinkle-Associated Mitochondrial DNA Depletion
Salma Remtulla, Cam-Tu Emilie Nguyen, Chitra Prasad, et al.
Journal of Neuromuscular Diseases
|
June 23, 2019
A Phenotypic Description of Congenital Myotonic Dystrophy using PhenoStacks
Madhavi Prasad, Michael Glueck, Delia Ceballos-Saenz, et al.
Neurology(R) Neuroimmunology & Neuroinflammation
|
December 22, 2023
CNS Inflammation as the First Sign of Complement Factor I Deficiency: A Severe Myelitis Treated With Intense Immunotherapy and Eculizumab
Valérie Massey, Cam-Tu Emilie Nguyen, Tine François, et al.
HGG Advances
|
January 20, 2022
Variants in <i>LSM7</i> impair LSM complexes assembly, neurodevelopment in zebrafish and may be associated with an ultra-rare neurological disease
Alexa Derksen, Hung-Yu Shih, Diane Forget, et al.
Journal of Child Neurology
|
May 24, 2023
The Experience of Parents of Children With Genetically Determined Leukoencephalopathies With the Health Care System: A Qualitative Study
Pouneh Amir Yazdani, Marie-Lou St-Jean, Sara Matovic, et al.
Journal of Child Neurology
|
January 5, 2022
Experience of Parents of Children with Genetically Determined Leukoencephalopathies Regarding the Adapted Health Care Services During the COVID-19 Pandemic
Pouneh Amir Yazdani, Marie-Lou St-Jean, Sara Matovic, et al.
Multiple Sclerosis and Related Disorders
|
June 15, 2023
Clinical course, imaging, and pathological features of 45 adult and pediatric cases of myelin oligodendrocyte glycoprotein antibody-associated disease
Hayet Boudjani, Giulia Fadda, Gabrielle Dufort, et al.
Neurology
|
November 12, 2025
Urine Sorbitol and Xylitol for the Diagnosis of Sorbitol Dehydrogenase Deficiency-Related Neuropathy
Jordan Elliott Bontrager, Amy L White, Karlla W Brigatti, et al.
Page
of 2