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Journal of Neurology, Neurosurgery, and Psychiatry
|
April 27, 2021
Real-life survey of pitfalls and successes of precision medicine in genetic epilepsies
Simona Balestrini, Daniela Chiarello, Maria Gogou, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 2, 2022
The Genetic Landscape of Complex Childhood-Onset Hyperkinetic Movement Disorders
Belén Pérez-Dueñas, Kathleen Gorman, Anna Marcé-Grau, et al.
Nature Reviews. Neurology
|
September 8, 2020
International consensus recommendations on the diagnostic work-up for malformations of cortical development
Renske Oegema, Tahsin Stefan Barakat, Martina Wilke, et al.
Epilepsia
|
January 31, 2013
Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significance
Federico Zara, Nicola Specchio, Pasquale Striano, et al.
Molecular Genetics & Genomic Medicine
|
September 22, 2016
Targeted sequencing of 351 candidate genes for epileptic encephalopathy in a large cohort of patients
Carolien G F de Kovel, Eva H Brilstra, Marjan J A van Kempen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 5, 2025
COL4A1 and COL4A2-related disorders: Clinical features, diagnostic guidelines, and management
Diana Tambala, Rachel Vassar, John Snow, et al.
BMJ Open
|
June 18, 2016
Efficacy of ketamine in refractory convulsive status epilepticus in children: a protocol for a sequential design, multicentre, randomised, controlled, open-label, non-profit trial (KETASER01)
Anna Rosati, Lucrezia Ilvento, Manuela L'Erario, 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.
Epilepsia
|
May 30, 2020
Phenotypic and genetic spectrum of epilepsy with myoclonic atonic seizures
Shan Tang, Laura Addis, Anna Smith, et al.
Brain : a Journal of Neurology
|
June 30, 2022
Monoallelic and biallelic mutations in RELN underlie a graded series of neurodevelopmental disorders
Nataliya Di Donato, Renzo Guerrini, Charles J Billington, et al.
Page
of 62
Search research articles
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Showing results (481-490 of 611) with videos related to
Sort By:
Page
of 62
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 27, 2021
Real-life survey of pitfalls and successes of precision medicine in genetic epilepsies
Simona Balestrini, Daniela Chiarello, Maria Gogou, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 2, 2022
The Genetic Landscape of Complex Childhood-Onset Hyperkinetic Movement Disorders
Belén Pérez-Dueñas, Kathleen Gorman, Anna Marcé-Grau, et al.
Nature Reviews. Neurology
|
September 8, 2020
International consensus recommendations on the diagnostic work-up for malformations of cortical development
Renske Oegema, Tahsin Stefan Barakat, Martina Wilke, et al.
Epilepsia
|
January 31, 2013
Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significance
Federico Zara, Nicola Specchio, Pasquale Striano, et al.
Molecular Genetics & Genomic Medicine
|
September 22, 2016
Targeted sequencing of 351 candidate genes for epileptic encephalopathy in a large cohort of patients
Carolien G F de Kovel, Eva H Brilstra, Marjan J A van Kempen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 5, 2025
COL4A1 and COL4A2-related disorders: Clinical features, diagnostic guidelines, and management
Diana Tambala, Rachel Vassar, John Snow, et al.
BMJ Open
|
June 18, 2016
Efficacy of ketamine in refractory convulsive status epilepticus in children: a protocol for a sequential design, multicentre, randomised, controlled, open-label, non-profit trial (KETASER01)
Anna Rosati, Lucrezia Ilvento, Manuela L'Erario, 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.
Epilepsia
|
May 30, 2020
Phenotypic and genetic spectrum of epilepsy with myoclonic atonic seizures
Shan Tang, Laura Addis, Anna Smith, et al.
Brain : a Journal of Neurology
|
June 30, 2022
Monoallelic and biallelic mutations in RELN underlie a graded series of neurodevelopmental disorders
Nataliya Di Donato, Renzo Guerrini, Charles J Billington, et al.
Page
of 62