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Neurology. Genetics
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November 23, 2016
De novo <i>FGF12</i> mutation in 2 patients with neonatal-onset epilepsy
Ilaria Guella, Linda Huh, Marna B McKenzie, et al.
American Journal of Human Genetics
|
August 5, 2017
De Novo Mutations in YWHAG Cause Early-Onset Epilepsy
Ilaria Guella, Marna B McKenzie, Daniel M Evans, et al.
American Journal of Human Genetics
|
July 4, 2017
Loss-of-Function and Gain-of-Function Mutations in KCNQ5 Cause Intellectual Disability or Epileptic Encephalopathy
Anna Lehman, Samrat Thouta, Grazia M S Mancini, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
April 2, 2025
The Current State of Care for Tuberous Sclerosis Complex in Canada
Robyn Whitney, Maryam Nabavi Nouri, Lauren Sham, et al.
Pediatrics
|
June 3, 2015
Recovery From Central Nervous System Acute Demyelination in Children
Julia O'Mahony, Ruth Ann Marrie, Audrey Laporte, et al.
Intensive Care Medicine
|
October 26, 2020
Neuromuscular blockade in patients with ARDS: a rapid practice guideline
Waleed Alhazzani, E Belley-Cote, M H Møller, et al.
The Journal of Clinical Investigation
|
April 10, 2018
Humanized mouse model of Rasmussen's encephalitis supports the immune-mediated hypothesis
Hania Kebir, Lionel Carmant, François Fontaine, et al.
Neurosurgery
|
June 30, 2015
Resective Epilepsy Surgery for Tuberous Sclerosis in Children: Determining Predictors of Seizure Outcomes in a Multicenter Retrospective Cohort Study
Aria Fallah, Shaun D Rodgers, Alexander G Weil, et al.
Malaria Journal
|
May 25, 2022
Recommendations for environmental risk assessment of gene drive applications for malaria vector control
John B Connolly, John D Mumford, Debora C M Glandorf, et al.
Frontiers in Neurology
|
June 6, 2019
Diagnostic Yield and Treatment Impact of Targeted Exome Sequencing in Early-Onset Epilepsy
Michelle Demos, Ilaria Guella, Conrado DeGuzman, et al.
Page
of 33
Search research articles
Search
Showing results (291-300 of 330) with videos related to
Sort By:
Page
of 33
Neurology. Genetics
|
November 23, 2016
De novo <i>FGF12</i> mutation in 2 patients with neonatal-onset epilepsy
Ilaria Guella, Linda Huh, Marna B McKenzie, et al.
American Journal of Human Genetics
|
August 5, 2017
De Novo Mutations in YWHAG Cause Early-Onset Epilepsy
Ilaria Guella, Marna B McKenzie, Daniel M Evans, et al.
American Journal of Human Genetics
|
July 4, 2017
Loss-of-Function and Gain-of-Function Mutations in KCNQ5 Cause Intellectual Disability or Epileptic Encephalopathy
Anna Lehman, Samrat Thouta, Grazia M S Mancini, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
April 2, 2025
The Current State of Care for Tuberous Sclerosis Complex in Canada
Robyn Whitney, Maryam Nabavi Nouri, Lauren Sham, et al.
Pediatrics
|
June 3, 2015
Recovery From Central Nervous System Acute Demyelination in Children
Julia O'Mahony, Ruth Ann Marrie, Audrey Laporte, et al.
Intensive Care Medicine
|
October 26, 2020
Neuromuscular blockade in patients with ARDS: a rapid practice guideline
Waleed Alhazzani, E Belley-Cote, M H Møller, et al.
The Journal of Clinical Investigation
|
April 10, 2018
Humanized mouse model of Rasmussen's encephalitis supports the immune-mediated hypothesis
Hania Kebir, Lionel Carmant, François Fontaine, et al.
Neurosurgery
|
June 30, 2015
Resective Epilepsy Surgery for Tuberous Sclerosis in Children: Determining Predictors of Seizure Outcomes in a Multicenter Retrospective Cohort Study
Aria Fallah, Shaun D Rodgers, Alexander G Weil, et al.
Malaria Journal
|
May 25, 2022
Recommendations for environmental risk assessment of gene drive applications for malaria vector control
John B Connolly, John D Mumford, Debora C M Glandorf, et al.
Frontiers in Neurology
|
June 6, 2019
Diagnostic Yield and Treatment Impact of Targeted Exome Sequencing in Early-Onset Epilepsy
Michelle Demos, Ilaria Guella, Conrado DeGuzman, et al.
Page
of 33