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Jeremy L Freeman

Showing results (111-120 of 123) with videos related to

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Annals of Neurology|December 23, 2011
Rare copy number variants are an important cause of epileptic encephalopathiesHeather C Mefford, Simone C Yendle, Cynthia Hsu, 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.
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.
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.
The Australian and New Zealand Journal of Psychiatry|April 6, 2017
The Anorexia Nervosa Genetics Initiative: Study description and sample characteristics of the Australian and New Zealand armKatherine M Kirk, Felicity C Martin, Amy Mao, 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.
Nature Genetics|May 28, 2013
Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1Gemma L Carvill, Sinéad B Heavin, Simone C Yendle, et al.
Human Mutation|September 13, 2019
Expanding the genetic and phenotypic relevance of KCNB1 variants in developmental and epileptic encephalopathies: 27 new patients and overview of the literatureClaire Bar, Giulia Barcia, Mélanie Jennesson, et al.
Pageof 13

Showing results (111-120 of 123) with videos related to

Sort By:
Pageof 13
Annals of Neurology|December 23, 2011
Rare copy number variants are an important cause of epileptic encephalopathiesHeather C Mefford, Simone C Yendle, Cynthia Hsu, 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.
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.
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.
The Australian and New Zealand Journal of Psychiatry|April 6, 2017
The Anorexia Nervosa Genetics Initiative: Study description and sample characteristics of the Australian and New Zealand armKatherine M Kirk, Felicity C Martin, Amy Mao, 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.
Nature Genetics|May 28, 2013
Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1Gemma L Carvill, Sinéad B Heavin, Simone C Yendle, et al.
Human Mutation|September 13, 2019
Expanding the genetic and phenotypic relevance of KCNB1 variants in developmental and epileptic encephalopathies: 27 new patients and overview of the literatureClaire Bar, Giulia Barcia, Mélanie Jennesson, et al.
Pageof 13