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Berge Minassian

Showing results (1-10 of 20) with videos related to

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Genes|February 24, 2024
Progressive Myoclonus Epilepsy: A Scoping Review of Diagnostic, Phenotypic and Therapeutic AdvancesVincent Zimmern, Berge Minassian
Frontiers in Neurology|March 7, 2022
A Review of Targeted Therapies for Monogenic Epilepsy SyndromesVincent Zimmern, Berge Minassian, Christian Korff
Handbook of Clinical Neurology|April 30, 2013
Neuronal ceroid lipofuscinosesBrigitte Chabrol, Catherine Caillaud, Berge Minassian
Biochemical Society Transactions|October 28, 2021
LUBAC: a new player in polyglucosan body diseaseAndrew Aboujaoude, Berge Minassian, Sharmistha Mitra
Clinical Case Reports|July 8, 2016
Infantile spasms with periventricular nodular heterotopia, unbalanced chromosomal translocation 3p26.2 -10p15.1 and 6q22.31 duplicationKevin Jones, Shelly K Weiss, Berge Minassian
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 7, 2024
Mitochondrial encephalopathies and myopathies: Our tertiary center's experienceCan Ozlu, Souad Messahel, Berge Minassian, et al.
Advances in Neurology|October 29, 2004
Progressive myoclonus epilepsies: EPM1, EPM2A, EPM2BElayne M Chan, Danielle M Andrade, Silvana Franceschetti, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|August 22, 2025
Sleep architecture and qEEG patterns in PME type 1 diagnosisEmma Pophal, Mohamed Taha, Emily Doll, et al.
Plos One|September 27, 2023
Unraveling the role of non-coding rare variants in epilepsyAlexandre Girard, Claudia Moreau, Jacques L Michaud, et al.
Neurology|June 17, 2018
Ocular phenotype and electroretinogram abnormalities in Lafora disease: A "window to the brain"Ajoy Vincent, Angelo Macrì, Anupreet Tumber, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Genes|February 24, 2024
Progressive Myoclonus Epilepsy: A Scoping Review of Diagnostic, Phenotypic and Therapeutic AdvancesVincent Zimmern, Berge Minassian
Frontiers in Neurology|March 7, 2022
A Review of Targeted Therapies for Monogenic Epilepsy SyndromesVincent Zimmern, Berge Minassian, Christian Korff
Handbook of Clinical Neurology|April 30, 2013
Neuronal ceroid lipofuscinosesBrigitte Chabrol, Catherine Caillaud, Berge Minassian
Biochemical Society Transactions|October 28, 2021
LUBAC: a new player in polyglucosan body diseaseAndrew Aboujaoude, Berge Minassian, Sharmistha Mitra
Clinical Case Reports|July 8, 2016
Infantile spasms with periventricular nodular heterotopia, unbalanced chromosomal translocation 3p26.2 -10p15.1 and 6q22.31 duplicationKevin Jones, Shelly K Weiss, Berge Minassian
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 7, 2024
Mitochondrial encephalopathies and myopathies: Our tertiary center's experienceCan Ozlu, Souad Messahel, Berge Minassian, et al.
Advances in Neurology|October 29, 2004
Progressive myoclonus epilepsies: EPM1, EPM2A, EPM2BElayne M Chan, Danielle M Andrade, Silvana Franceschetti, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|August 22, 2025
Sleep architecture and qEEG patterns in PME type 1 diagnosisEmma Pophal, Mohamed Taha, Emily Doll, et al.
Plos One|September 27, 2023
Unraveling the role of non-coding rare variants in epilepsyAlexandre Girard, Claudia Moreau, Jacques L Michaud, et al.
Neurology|June 17, 2018
Ocular phenotype and electroretinogram abnormalities in Lafora disease: A "window to the brain"Ajoy Vincent, Angelo Macrì, Anupreet Tumber, et al.
Pageof 2