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Simon Harvey

Showing results (121-130 of 133) with videos related to

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Neurology. Genetics|May 5, 2018
Somatic <i>GNAQ</i> mutation in the <i>forme fruste</i> of Sturge-Weber syndromeMichael S Hildebrand, A Simon Harvey, Stephen Malone, et al.
Annals of Clinical and Translational Neurology|May 23, 2015
Familial cortical dysplasia type IIA caused by a germline mutation in DEPDC5Thomas Scerri, Jessica R Riseley, Greta Gillies, et al.
Neurology|May 5, 2021
One-Stage, Limited-Resection Epilepsy Surgery for Bottom-of-Sulcus DysplasiaEmma Macdonald-Laurs, Wirginia J Maixner, Catherine A Bailey, et al.
Annals of Neurology|August 19, 2015
Familial cortical dysplasia caused by mutation in the mammalian target of rapamycin regulator NPRL3Joe C Sim, Thomas Scerri, Miriam Fanjul-Fernández, et al.
American Journal of Human Genetics|July 26, 2016
Mutations of the Sonic Hedgehog Pathway Underlie Hypothalamic Hamartoma with Gelastic EpilepsyMichael S Hildebrand, Nicole G Griffin, John A Damiano, et al.
Epilepsia Open|August 24, 2019
Epidemiology and etiology of infantile developmental and epileptic encephalopathies in TasmaniaTyson L Ware, Shannon R Huskins, Bronwyn E Grinton, et al.
Brain Communications|July 3, 2026
Late-onset epileptic spasms: presentation, aetiology and outcomeSameer Dal, Emma Macdonald-Laurs, Simone Mandelstam, et al.
Brain Communications|March 19, 2021
Cerebrospinal fluid liquid biopsy for detecting somatic mosaicism in brainZimeng Ye, Zac Chatterton, Jahnvi Pflueger, et al.
Human Molecular Genetics|February 9, 2022
Sporadic hypothalamic hamartoma is a ciliopathy with somatic and bi-allelic contributionsTimothy E Green, Joshua E Motelow, Mark F Bennett, et al.
Epilepsia|January 21, 2021
The severe epilepsy syndromes of infancy: A population-based studyKatherine B Howell, Jeremy L Freeman, Mark T Mackay, et al.
Pageof 14

Showing results (121-130 of 133) with videos related to

Sort By:
Pageof 14
Neurology. Genetics|May 5, 2018
Somatic <i>GNAQ</i> mutation in the <i>forme fruste</i> of Sturge-Weber syndromeMichael S Hildebrand, A Simon Harvey, Stephen Malone, et al.
Annals of Clinical and Translational Neurology|May 23, 2015
Familial cortical dysplasia type IIA caused by a germline mutation in DEPDC5Thomas Scerri, Jessica R Riseley, Greta Gillies, et al.
Neurology|May 5, 2021
One-Stage, Limited-Resection Epilepsy Surgery for Bottom-of-Sulcus DysplasiaEmma Macdonald-Laurs, Wirginia J Maixner, Catherine A Bailey, et al.
Annals of Neurology|August 19, 2015
Familial cortical dysplasia caused by mutation in the mammalian target of rapamycin regulator NPRL3Joe C Sim, Thomas Scerri, Miriam Fanjul-Fernández, et al.
American Journal of Human Genetics|July 26, 2016
Mutations of the Sonic Hedgehog Pathway Underlie Hypothalamic Hamartoma with Gelastic EpilepsyMichael S Hildebrand, Nicole G Griffin, John A Damiano, et al.
Epilepsia Open|August 24, 2019
Epidemiology and etiology of infantile developmental and epileptic encephalopathies in TasmaniaTyson L Ware, Shannon R Huskins, Bronwyn E Grinton, et al.
Brain Communications|July 3, 2026
Late-onset epileptic spasms: presentation, aetiology and outcomeSameer Dal, Emma Macdonald-Laurs, Simone Mandelstam, et al.
Brain Communications|March 19, 2021
Cerebrospinal fluid liquid biopsy for detecting somatic mosaicism in brainZimeng Ye, Zac Chatterton, Jahnvi Pflueger, et al.
Human Molecular Genetics|February 9, 2022
Sporadic hypothalamic hamartoma is a ciliopathy with somatic and bi-allelic contributionsTimothy E Green, Joshua E Motelow, Mark F Bennett, et al.
Epilepsia|January 21, 2021
The severe epilepsy syndromes of infancy: A population-based studyKatherine B Howell, Jeremy L Freeman, Mark T Mackay, et al.
Pageof 14