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Matthew Zemel

Showing results (1-10 of 9) with videos related to

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Anesthesia and Analgesia|August 5, 2025
Augmented Reality in Airway Management: A Scoping ReviewAndrew Hart, Matthew Zemel, Laurence Henson, et al.
Neurology|July 31, 2015
Intragenic deletions of ALDH7A1 in pyridoxine-dependent epilepsy caused by Alu-Alu recombinationHeather C Mefford, Matthew Zemel, Eileen Geraghty, et al.
Developmental Medicine and Child Neurology|July 11, 2021
Genetic convergence of developmental and epileptic encephalopathies and intellectual disabilityGemma L Carvill, Sandra Jansen, Amy Lacroix, et al.
Epilepsia|November 25, 2017
Severe infantile onset developmental and epileptic encephalopathy caused by mutations in autophagy gene WDR45Gemma L Carvill, Aijie Liu, Simone Mandelstam, et al.
EMBO Molecular Medicine|November 29, 2015
Simultaneous impairment of neuronal and metabolic function of mutated gephyrin in a patient with epileptic encephalopathyBorislav Dejanovic, Tania Djémié, Nora Grünewald, et al.
EMBO Molecular Medicine|December 3, 2017
Simultaneous impairment of neuronal and metabolic function of mutated gephyrin in a patient with epileptic encephalopathyBorislav Dejanovic, Tania Djémié, Nora Grünewald, et al.
Neurology. Genetics|April 12, 2016
Epileptic spasms are a feature of DEPDC5 mTORopathyGemma L Carvill, Douglas E Crompton, Brigid M Regan, et al.
American Journal of Human Genetics|April 14, 2015
Mutations in the GABA Transporter SLC6A1 Cause Epilepsy with Myoclonic-Atonic SeizuresGemma L Carvill, Jacinta M McMahon, Amy Schneider, et al.
Neurology|October 28, 2022
Neurodevelopmental and Epilepsy Phenotypes in Individuals With Missense Variants in the Voltage-Sensing and Pore Domains of <i>KCNH5</i>Hannah C Happ, Lynette G Sadleir, Matthew Zemel, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Anesthesia and Analgesia|August 5, 2025
Augmented Reality in Airway Management: A Scoping ReviewAndrew Hart, Matthew Zemel, Laurence Henson, et al.
Neurology|July 31, 2015
Intragenic deletions of ALDH7A1 in pyridoxine-dependent epilepsy caused by Alu-Alu recombinationHeather C Mefford, Matthew Zemel, Eileen Geraghty, et al.
Developmental Medicine and Child Neurology|July 11, 2021
Genetic convergence of developmental and epileptic encephalopathies and intellectual disabilityGemma L Carvill, Sandra Jansen, Amy Lacroix, et al.
Epilepsia|November 25, 2017
Severe infantile onset developmental and epileptic encephalopathy caused by mutations in autophagy gene WDR45Gemma L Carvill, Aijie Liu, Simone Mandelstam, et al.
EMBO Molecular Medicine|November 29, 2015
Simultaneous impairment of neuronal and metabolic function of mutated gephyrin in a patient with epileptic encephalopathyBorislav Dejanovic, Tania Djémié, Nora Grünewald, et al.
EMBO Molecular Medicine|December 3, 2017
Simultaneous impairment of neuronal and metabolic function of mutated gephyrin in a patient with epileptic encephalopathyBorislav Dejanovic, Tania Djémié, Nora Grünewald, et al.
Neurology. Genetics|April 12, 2016
Epileptic spasms are a feature of DEPDC5 mTORopathyGemma L Carvill, Douglas E Crompton, Brigid M Regan, et al.
American Journal of Human Genetics|April 14, 2015
Mutations in the GABA Transporter SLC6A1 Cause Epilepsy with Myoclonic-Atonic SeizuresGemma L Carvill, Jacinta M McMahon, Amy Schneider, et al.
Neurology|October 28, 2022
Neurodevelopmental and Epilepsy Phenotypes in Individuals With Missense Variants in the Voltage-Sensing and Pore Domains of <i>KCNH5</i>Hannah C Happ, Lynette G Sadleir, Matthew Zemel, et al.
Pageof 1