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Anne Lortie

Showing results (41-50 of 51) with videos related to

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Human Molecular Genetics|May 1, 2014
The genetic landscape of infantile spasmsJacques L Michaud, Mathieu Lachance, Fadi F Hamdan, et al.
American Journal of Medical Genetics. Part A|February 5, 2008
A novel locus for idiopathic generalized epilepsy in French-Canadian families maps to 10p11Peter Kinirons, Dominique J Verlaan, Marie-Pierre Dubé, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|September 22, 2007
Near-infrared spectroscopy as an alternative to the Wada test for language mapping in children, adults and special populationsAnne Gallagher, Martin Thériault, Ed Maclin, et al.
Annals of Neurology|June 27, 2009
De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsyFadi F Hamdan, Amélie Piton, Julie Gauthier, et al.
Pediatrics|June 3, 2015
Recovery From Central Nervous System Acute Demyelination in ChildrenJulia O'Mahony, Ruth Ann Marrie, Audrey Laporte, et al.
American Journal of Human Genetics|May 13, 2014
Mutations in DOCK7 in individuals with epileptic encephalopathy and cortical blindnessIsabelle Perrault, Fadi F Hamdan, Marlène Rio, et al.
The Lancet. Neurology|April 5, 2011
Clinical, environmental, and genetic determinants of multiple sclerosis in children with acute demyelination: a prospective national cohort studyBrenda Banwell, Amit Bar-Or, Douglas L Arnold, et al.
Journal of Clinical Immunology|July 9, 2020
Neuroinflammatory Disease as an Isolated Manifestation of Hemophagocytic LymphohistiocytosisAnnaliesse Blincoe, Maximilian Heeg, Patrick K Campbell, et al.
American Journal of Human Genetics|April 30, 2019
Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human NeuronsScott Bell, Justine Rousseau, Huashan Peng, et al.
The Lancet. Neurology|July 24, 2018
Rare coding variants in genes encoding GABA<sub>A</sub> receptors in genetic generalised epilepsies: an exome-based case-control studyPatrick May, Simon Girard, Merle Harrer, et al.
Pageof 6

Showing results (41-50 of 51) with videos related to

Sort By:
Pageof 6
Human Molecular Genetics|May 1, 2014
The genetic landscape of infantile spasmsJacques L Michaud, Mathieu Lachance, Fadi F Hamdan, et al.
American Journal of Medical Genetics. Part A|February 5, 2008
A novel locus for idiopathic generalized epilepsy in French-Canadian families maps to 10p11Peter Kinirons, Dominique J Verlaan, Marie-Pierre Dubé, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|September 22, 2007
Near-infrared spectroscopy as an alternative to the Wada test for language mapping in children, adults and special populationsAnne Gallagher, Martin Thériault, Ed Maclin, et al.
Annals of Neurology|June 27, 2009
De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsyFadi F Hamdan, Amélie Piton, Julie Gauthier, et al.
Pediatrics|June 3, 2015
Recovery From Central Nervous System Acute Demyelination in ChildrenJulia O'Mahony, Ruth Ann Marrie, Audrey Laporte, et al.
American Journal of Human Genetics|May 13, 2014
Mutations in DOCK7 in individuals with epileptic encephalopathy and cortical blindnessIsabelle Perrault, Fadi F Hamdan, Marlène Rio, et al.
The Lancet. Neurology|April 5, 2011
Clinical, environmental, and genetic determinants of multiple sclerosis in children with acute demyelination: a prospective national cohort studyBrenda Banwell, Amit Bar-Or, Douglas L Arnold, et al.
Journal of Clinical Immunology|July 9, 2020
Neuroinflammatory Disease as an Isolated Manifestation of Hemophagocytic LymphohistiocytosisAnnaliesse Blincoe, Maximilian Heeg, Patrick K Campbell, et al.
American Journal of Human Genetics|April 30, 2019
Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human NeuronsScott Bell, Justine Rousseau, Huashan Peng, et al.
The Lancet. Neurology|July 24, 2018
Rare coding variants in genes encoding GABA<sub>A</sub> receptors in genetic generalised epilepsies: an exome-based case-control studyPatrick May, Simon Girard, Merle Harrer, et al.
Pageof 6