Search research articles
Contact Us
Filters
Showing results (1-10 of 9) with videos related to
Page
of 1
Sort By:
Anesthesia and Analgesia
|
August 5, 2025
Augmented Reality in Airway Management: A Scoping Review
Andrew Hart, Matthew Zemel, Laurence Henson, et al.
Neurology
|
July 31, 2015
Intragenic deletions of ALDH7A1 in pyridoxine-dependent epilepsy caused by Alu-Alu recombination
Heather 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 disability
Gemma 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 WDR45
Gemma 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 encephalopathy
Borislav 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 encephalopathy
Borislav Dejanovic, Tania Djémié, Nora Grünewald, et al.
Neurology. Genetics
|
April 12, 2016
Epileptic spasms are a feature of DEPDC5 mTORopathy
Gemma 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 Seizures
Gemma 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.
Page
of 1
Search research articles
Search
Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
Anesthesia and Analgesia
|
August 5, 2025
Augmented Reality in Airway Management: A Scoping Review
Andrew Hart, Matthew Zemel, Laurence Henson, et al.
Neurology
|
July 31, 2015
Intragenic deletions of ALDH7A1 in pyridoxine-dependent epilepsy caused by Alu-Alu recombination
Heather 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 disability
Gemma 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 WDR45
Gemma 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 encephalopathy
Borislav 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 encephalopathy
Borislav Dejanovic, Tania Djémié, Nora Grünewald, et al.
Neurology. Genetics
|
April 12, 2016
Epileptic spasms are a feature of DEPDC5 mTORopathy
Gemma 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 Seizures
Gemma 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.
Page
of 1