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Human Mutation
|
June 3, 2021
Integrated in silico and experimental assessment of disease relevance of PCDH19 missense variants
Duyen H Pham, Melissa R Pitman, Raman Kumar, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 30, 2025
Bilateral frontal periventricular nodular heterotopia: a distinctive cortical malformation
Ine Hoogwijs, Simone A Mandelstam, George McGillivray, et al.
Ebiomedicine
|
April 29, 2023
CSF neopterin, quinolinic acid and kynurenine/tryptophan ratio are biomarkers of active neuroinflammation
Jingya Yan, Kavitha Kothur, Shekeeb Mohammad, et al.
Neurology
|
March 14, 2014
GABRA1 and STXBP1: novel genetic causes of Dravet syndrome
Gemma L Carvill, Sarah Weckhuysen, Jacinta M McMahon, et al.
American Journal of Medical Genetics. Part A
|
October 13, 2006
Polymicrogyria and deletion 22q11.2 syndrome: window to the etiology of a common cortical malformation
Nathaniel H Robin, Clare J Taylor, Donna M McDonald-McGinn, et al.
Annals of Neurology
|
August 3, 2024
Solving the Etiology of Developmental and Epileptic Encephalopathy with Spike-Wave Activation in Sleep (D/EE-SWAS)
Sindhu Viswanathan, Karen L Oliver, Brigid M Regan, et al.
Nature Genetics
|
May 28, 2013
Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1
Gemma L Carvill, Sinéad B Heavin, Simone C Yendle, et al.
Neurology
|
January 9, 2015
The phenotypic spectrum of SCN8A encephalopathy
Jan Larsen, Gemma L Carvill, Elena Gardella, et al.
Medrxiv : the Preprint Server for Health Sciences
|
December 3, 2025
Deep tissue sequencing improves genetic diagnostic yield in focal cortical dysplasia
Breana Galea, Joshua Reid, Samuel Gooley, et al.
Human Mutation
|
March 21, 2020
Damaging de novo missense variants in EEF1A2 lead to a developmental and degenerative epileptic-dyskinetic encephalopathy
Gemma L Carvill, Katherine L Helbig, Candace T Myers, et al.
Page
of 10
Search research articles
Search
Showing results (81-90 of 97) with videos related to
Sort By:
Page
of 10
Human Mutation
|
June 3, 2021
Integrated in silico and experimental assessment of disease relevance of PCDH19 missense variants
Duyen H Pham, Melissa R Pitman, Raman Kumar, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 30, 2025
Bilateral frontal periventricular nodular heterotopia: a distinctive cortical malformation
Ine Hoogwijs, Simone A Mandelstam, George McGillivray, et al.
Ebiomedicine
|
April 29, 2023
CSF neopterin, quinolinic acid and kynurenine/tryptophan ratio are biomarkers of active neuroinflammation
Jingya Yan, Kavitha Kothur, Shekeeb Mohammad, et al.
Neurology
|
March 14, 2014
GABRA1 and STXBP1: novel genetic causes of Dravet syndrome
Gemma L Carvill, Sarah Weckhuysen, Jacinta M McMahon, et al.
American Journal of Medical Genetics. Part A
|
October 13, 2006
Polymicrogyria and deletion 22q11.2 syndrome: window to the etiology of a common cortical malformation
Nathaniel H Robin, Clare J Taylor, Donna M McDonald-McGinn, et al.
Annals of Neurology
|
August 3, 2024
Solving the Etiology of Developmental and Epileptic Encephalopathy with Spike-Wave Activation in Sleep (D/EE-SWAS)
Sindhu Viswanathan, Karen L Oliver, Brigid M Regan, et al.
Nature Genetics
|
May 28, 2013
Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1
Gemma L Carvill, Sinéad B Heavin, Simone C Yendle, et al.
Neurology
|
January 9, 2015
The phenotypic spectrum of SCN8A encephalopathy
Jan Larsen, Gemma L Carvill, Elena Gardella, et al.
Medrxiv : the Preprint Server for Health Sciences
|
December 3, 2025
Deep tissue sequencing improves genetic diagnostic yield in focal cortical dysplasia
Breana Galea, Joshua Reid, Samuel Gooley, et al.
Human Mutation
|
March 21, 2020
Damaging de novo missense variants in EEF1A2 lead to a developmental and degenerative epileptic-dyskinetic encephalopathy
Gemma L Carvill, Katherine L Helbig, Candace T Myers, et al.
Page
of 10