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David A Dyment

Showing results (41-50 of 120) with videos related to

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Journal of Neurology|December 17, 2009
Prevalence of MS in Iranian immigrants to British Columbia, CanadaColleen Guimond, David A Dyment, Sreeram V Ramagopalan, et al.
BMC Neurology|November 18, 2010
Congenital abnormalities and multiple sclerosisSreeram V Ramagopalan, Colleen Guimond, Maria Criscuoli, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Outcome of over 1500 matches through the Matchmaker Exchange for rare disease gene discovery: The 2-year experience of Care4Rare CanadaMatthew Osmond, Taila Hartley, David A Dyment, et al.
American Journal of Human Genetics|November 4, 2022
Care4Rare Canada: Outcomes from a decade of network science for rare disease gene discoveryKym M Boycott, Taila Hartley, Kristin D Kernohan, et al.
Human Molecular Genetics|December 23, 2008
Epigenetics in multiple sclerosis susceptibility: difference in transgenerational risk localizes to the major histocompatibility complexMichael J Chao, Sreeram V Ramagopalan, Blanca M Herrera, et al.
American Journal of Medical Genetics. Part A|May 20, 2022
A 79-kb paternally inherited 7q32.2 microdeletion involving MEST in a patient with a Silver-Russell syndrome-like phenotypeKrista Marie Vincent, Dimitri J Stavropoulos, Melanie Beaulieu-Bergeron, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 3, 2024
IRF2BPL-Related Disorder, Causing Neurodevelopmental Disorder with Regression, Abnormal Movements, Loss of Speech and Seizures (NEDAMSS) Is Characterized by Pathology Consistent with DRPLASunita Venkateswaran, Jean Michaud, Yoko Ito, et al.
Neurology. Genetics|January 16, 2019
Lysosomal dysfunction in <i>TMEM106B</i> hypomyelinating leukodystrophyYoko Ito, Taila Hartley, Stephen Baird, et al.
Human Molecular Genetics|August 14, 2003
Significant linkage to migraine with aura on chromosome 11q24Zameel M Cader, Sandra Noble-Topham, David A Dyment, et al.
Human Molecular Genetics|September 22, 2017
SHORT syndrome due to a novel de novo mutation in PRKCE (Protein Kinase Cɛ) impairing TORC2-dependent AKT activationDiana Alcantara, Frances Elmslie, Martine Tetreault, et al.
Pageof 12

Showing results (41-50 of 120) with videos related to

Sort By:
Pageof 12
Journal of Neurology|December 17, 2009
Prevalence of MS in Iranian immigrants to British Columbia, CanadaColleen Guimond, David A Dyment, Sreeram V Ramagopalan, et al.
BMC Neurology|November 18, 2010
Congenital abnormalities and multiple sclerosisSreeram V Ramagopalan, Colleen Guimond, Maria Criscuoli, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Outcome of over 1500 matches through the Matchmaker Exchange for rare disease gene discovery: The 2-year experience of Care4Rare CanadaMatthew Osmond, Taila Hartley, David A Dyment, et al.
American Journal of Human Genetics|November 4, 2022
Care4Rare Canada: Outcomes from a decade of network science for rare disease gene discoveryKym M Boycott, Taila Hartley, Kristin D Kernohan, et al.
Human Molecular Genetics|December 23, 2008
Epigenetics in multiple sclerosis susceptibility: difference in transgenerational risk localizes to the major histocompatibility complexMichael J Chao, Sreeram V Ramagopalan, Blanca M Herrera, et al.
American Journal of Medical Genetics. Part A|May 20, 2022
A 79-kb paternally inherited 7q32.2 microdeletion involving MEST in a patient with a Silver-Russell syndrome-like phenotypeKrista Marie Vincent, Dimitri J Stavropoulos, Melanie Beaulieu-Bergeron, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 3, 2024
IRF2BPL-Related Disorder, Causing Neurodevelopmental Disorder with Regression, Abnormal Movements, Loss of Speech and Seizures (NEDAMSS) Is Characterized by Pathology Consistent with DRPLASunita Venkateswaran, Jean Michaud, Yoko Ito, et al.
Neurology. Genetics|January 16, 2019
Lysosomal dysfunction in <i>TMEM106B</i> hypomyelinating leukodystrophyYoko Ito, Taila Hartley, Stephen Baird, et al.
Human Molecular Genetics|August 14, 2003
Significant linkage to migraine with aura on chromosome 11q24Zameel M Cader, Sandra Noble-Topham, David A Dyment, et al.
Human Molecular Genetics|September 22, 2017
SHORT syndrome due to a novel de novo mutation in PRKCE (Protein Kinase Cɛ) impairing TORC2-dependent AKT activationDiana Alcantara, Frances Elmslie, Martine Tetreault, et al.
Pageof 12