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Deepak Gill

Showing results (51-60 of 97) with videos related to

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Developmental Medicine and Child Neurology|February 22, 2025
Pathogenic variants in chromatin-related genes: Linking immune dysregulation to neuroregression and acute neuropsychiatric disordersRussell C Dale, Shekeeb Mohammad, Velda X Han, et al.
Developmental Medicine and Child Neurology|June 14, 2022
Exome sequencing for patients with developmental and epileptic encephalopathies in clinical practiceIngrid E Scheffer, Caitlin A Bennett, Deepak Gill, et al.
Child Neuropsychology : a Journal on Normal and Abnormal Development in Childhood and Adolescence|May 5, 2023
Repeat testing enhances long-term verbal memory in children with epilepsySamantha Joplin, Michael Gascoigne, Belinda Barton, et al.
Epilepsy & Behavior : E&B|March 8, 2022
Accelerated long-term forgetting in children with temporal lobe epilepsy: A timescale investigation of material specificity and executive skillsSamantha Joplin, Michael Gascoigne, Belinda Barton, et al.
Developmental Medicine and Child Neurology|January 28, 2016
Eye movement disorders are an early manifestation of CACNA1A mutations in childrenEsther M Tantsis, Deepak Gill, Lyn Griffiths, et al.
Developmental Medicine and Child Neurology|December 17, 2013
Atypical multifocal Dravet syndrome lacks generalized seizures and may show later cognitive declineYoung Ok Kim, Susannah Bellows, Jacinta M McMahon, et al.
Epilepsia|November 24, 2015
Postencephalitic epilepsy and drug-resistant epilepsy after infectious and antibody-associated encephalitis in childhood: Clinical and etiologic risk factorsSekhar C Pillai, Shekeeb S Mohammad, Yael Hacohen, et al.
European Journal of Human Genetics : EJHG|February 23, 2012
Expanding the molecular basis and phenotypic spectrum of X-linked Joubert syndrome associated with OFD1 mutationsMichael Field, Ingrid E Scheffer, Deepak Gill, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 13, 2023
"Somewhere to turn to with my questions": A pre-post pilot of an information linker service for caregivers who have a child with a Developmental and Epileptic EncephalopathyEden G Robertson, Natalie J Roberts, Fleur Le Marne, et al.
Epilepsia Open|October 30, 2021
Infantile-onset myoclonic developmental and epileptic encephalopathy: A new RARS2 phenotypeGuillem de Valles-Ibáñez, Michael S Hildebrand, Melanie Bahlo, et al.
Pageof 10

Showing results (51-60 of 97) with videos related to

Sort By:
Pageof 10
Developmental Medicine and Child Neurology|February 22, 2025
Pathogenic variants in chromatin-related genes: Linking immune dysregulation to neuroregression and acute neuropsychiatric disordersRussell C Dale, Shekeeb Mohammad, Velda X Han, et al.
Developmental Medicine and Child Neurology|June 14, 2022
Exome sequencing for patients with developmental and epileptic encephalopathies in clinical practiceIngrid E Scheffer, Caitlin A Bennett, Deepak Gill, et al.
Child Neuropsychology : a Journal on Normal and Abnormal Development in Childhood and Adolescence|May 5, 2023
Repeat testing enhances long-term verbal memory in children with epilepsySamantha Joplin, Michael Gascoigne, Belinda Barton, et al.
Epilepsy & Behavior : E&B|March 8, 2022
Accelerated long-term forgetting in children with temporal lobe epilepsy: A timescale investigation of material specificity and executive skillsSamantha Joplin, Michael Gascoigne, Belinda Barton, et al.
Developmental Medicine and Child Neurology|January 28, 2016
Eye movement disorders are an early manifestation of CACNA1A mutations in childrenEsther M Tantsis, Deepak Gill, Lyn Griffiths, et al.
Developmental Medicine and Child Neurology|December 17, 2013
Atypical multifocal Dravet syndrome lacks generalized seizures and may show later cognitive declineYoung Ok Kim, Susannah Bellows, Jacinta M McMahon, et al.
Epilepsia|November 24, 2015
Postencephalitic epilepsy and drug-resistant epilepsy after infectious and antibody-associated encephalitis in childhood: Clinical and etiologic risk factorsSekhar C Pillai, Shekeeb S Mohammad, Yael Hacohen, et al.
European Journal of Human Genetics : EJHG|February 23, 2012
Expanding the molecular basis and phenotypic spectrum of X-linked Joubert syndrome associated with OFD1 mutationsMichael Field, Ingrid E Scheffer, Deepak Gill, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 13, 2023
"Somewhere to turn to with my questions": A pre-post pilot of an information linker service for caregivers who have a child with a Developmental and Epileptic EncephalopathyEden G Robertson, Natalie J Roberts, Fleur Le Marne, et al.
Epilepsia Open|October 30, 2021
Infantile-onset myoclonic developmental and epileptic encephalopathy: A new RARS2 phenotypeGuillem de Valles-Ibáñez, Michael S Hildebrand, Melanie Bahlo, et al.
Pageof 10