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Neurology. Genetics
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May 5, 2018
Somatic <i>GNAQ</i> mutation in the <i>forme fruste</i> of Sturge-Weber syndrome
Michael 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 DEPDC5
Thomas Scerri, Jessica R Riseley, Greta Gillies, et al.
Neurology
|
May 5, 2021
One-Stage, Limited-Resection Epilepsy Surgery for Bottom-of-Sulcus Dysplasia
Emma 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 NPRL3
Joe 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 Epilepsy
Michael 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 Tasmania
Tyson L Ware, Shannon R Huskins, Bronwyn E Grinton, et al.
Brain Communications
|
July 3, 2026
Late-onset epileptic spasms: presentation, aetiology and outcome
Sameer Dal, Emma Macdonald-Laurs, Simone Mandelstam, et al.
Brain Communications
|
March 19, 2021
Cerebrospinal fluid liquid biopsy for detecting somatic mosaicism in brain
Zimeng Ye, Zac Chatterton, Jahnvi Pflueger, et al.
Human Molecular Genetics
|
February 9, 2022
Sporadic hypothalamic hamartoma is a ciliopathy with somatic and bi-allelic contributions
Timothy E Green, Joshua E Motelow, Mark F Bennett, et al.
Epilepsia
|
January 21, 2021
The severe epilepsy syndromes of infancy: A population-based study
Katherine B Howell, Jeremy L Freeman, Mark T Mackay, et al.
Page
of 14
Search research articles
Search
Showing results (121-130 of 133) with videos related to
Sort By:
Page
of 14
Neurology. Genetics
|
May 5, 2018
Somatic <i>GNAQ</i> mutation in the <i>forme fruste</i> of Sturge-Weber syndrome
Michael 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 DEPDC5
Thomas Scerri, Jessica R Riseley, Greta Gillies, et al.
Neurology
|
May 5, 2021
One-Stage, Limited-Resection Epilepsy Surgery for Bottom-of-Sulcus Dysplasia
Emma 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 NPRL3
Joe 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 Epilepsy
Michael 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 Tasmania
Tyson L Ware, Shannon R Huskins, Bronwyn E Grinton, et al.
Brain Communications
|
July 3, 2026
Late-onset epileptic spasms: presentation, aetiology and outcome
Sameer Dal, Emma Macdonald-Laurs, Simone Mandelstam, et al.
Brain Communications
|
March 19, 2021
Cerebrospinal fluid liquid biopsy for detecting somatic mosaicism in brain
Zimeng Ye, Zac Chatterton, Jahnvi Pflueger, et al.
Human Molecular Genetics
|
February 9, 2022
Sporadic hypothalamic hamartoma is a ciliopathy with somatic and bi-allelic contributions
Timothy E Green, Joshua E Motelow, Mark F Bennett, et al.
Epilepsia
|
January 21, 2021
The severe epilepsy syndromes of infancy: A population-based study
Katherine B Howell, Jeremy L Freeman, Mark T Mackay, et al.
Page
of 14