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David Dyment

Showing results (1-10 of 33) with videos related to

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Autoimmune Diseases|July 13, 2011
Multiple sclerosisSreeram Ramagopalan, David Dyment, Rachel Farrell, et al.
American Journal of Medical Genetics. Part A|June 21, 2023
Missense variant in SRCAP with distinct DNA methylation signature associated with non-FLHS SRCAP-related neurodevelopmental disorderAlexandre White-Brown, Sanaa Choufani, , et al.
Frontiers in Cell and Developmental Biology|January 2, 2023
Genetically unresolved case of Rauch-Steindl syndrome diagnosed by its wolf-hirschhorn associated DNA methylation episignatureHaley McConkey, Alexandre White-Brown, Jennifer Kerkhof, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|August 24, 2017
Pointed rhythmic theta waves: a unique EEG pattern in KCNQ2-related neonatal epileptic encephalopathySarah Grace Buttle, Erick Sell, David Dyment, et al.
Genome|December 10, 2003
Different patterns of gene silencing in position-effect variegationVett K Lloyd, David Dyment, Donald A R Sinclair, et al.
Brain : a Journal of Neurology|February 15, 2018
Reply: The recurrent mutation in TMEM106B also causes hypomyelinating leukodystrophy in China and is a CpG hotspotCas Simons, David Dyment, Marjo S van der Knaap, et al.
Child Neurology Open|August 29, 2018
Atypical Rett Syndrome and Intractable Epilepsy With Novel <i>GRIN2B</i> MutationPaulina Kyriakopoulos, Vanda McNiven, Melissa T Carter, et al.
Journal of Genetic Counseling|February 3, 2026
The personal utility of genetic testing in children with epilepsySneha Gupta, Heather Leduc-Pessah, Nick Barrowman, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|November 14, 2018
Development of Criteria for Epilepsy Genetic Testing in Ontario, CanadaPuneet Jain, Danielle Andrade, Elizabeth Donner, et al.
JIMD Reports|September 26, 2015
Detailed Biochemical and Bioenergetic Characterization of FBXL4-Related Encephalomyopathic Mitochondrial DNA DepletionGhadi Antoun, Skye McBride, Jason R Vanstone, et al.
Pageof 4

Showing results (1-10 of 33) with videos related to

Sort By:
Pageof 4
Autoimmune Diseases|July 13, 2011
Multiple sclerosisSreeram Ramagopalan, David Dyment, Rachel Farrell, et al.
American Journal of Medical Genetics. Part A|June 21, 2023
Missense variant in SRCAP with distinct DNA methylation signature associated with non-FLHS SRCAP-related neurodevelopmental disorderAlexandre White-Brown, Sanaa Choufani, , et al.
Frontiers in Cell and Developmental Biology|January 2, 2023
Genetically unresolved case of Rauch-Steindl syndrome diagnosed by its wolf-hirschhorn associated DNA methylation episignatureHaley McConkey, Alexandre White-Brown, Jennifer Kerkhof, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|August 24, 2017
Pointed rhythmic theta waves: a unique EEG pattern in KCNQ2-related neonatal epileptic encephalopathySarah Grace Buttle, Erick Sell, David Dyment, et al.
Genome|December 10, 2003
Different patterns of gene silencing in position-effect variegationVett K Lloyd, David Dyment, Donald A R Sinclair, et al.
Brain : a Journal of Neurology|February 15, 2018
Reply: The recurrent mutation in TMEM106B also causes hypomyelinating leukodystrophy in China and is a CpG hotspotCas Simons, David Dyment, Marjo S van der Knaap, et al.
Child Neurology Open|August 29, 2018
Atypical Rett Syndrome and Intractable Epilepsy With Novel <i>GRIN2B</i> MutationPaulina Kyriakopoulos, Vanda McNiven, Melissa T Carter, et al.
Journal of Genetic Counseling|February 3, 2026
The personal utility of genetic testing in children with epilepsySneha Gupta, Heather Leduc-Pessah, Nick Barrowman, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|November 14, 2018
Development of Criteria for Epilepsy Genetic Testing in Ontario, CanadaPuneet Jain, Danielle Andrade, Elizabeth Donner, et al.
JIMD Reports|September 26, 2015
Detailed Biochemical and Bioenergetic Characterization of FBXL4-Related Encephalomyopathic Mitochondrial DNA DepletionGhadi Antoun, Skye McBride, Jason R Vanstone, et al.
Pageof 4