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Franck Kalume

Showing results (1-10 of 28) with videos related to

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Respiratory Physiology & Neurobiology|July 16, 2013
Sudden unexpected death in Dravet syndrome: respiratory and other physiological dysfunctionsFranck Kalume
Epilepsia|April 6, 2011
Insights into pathophysiology and therapy from a mouse model of Dravet syndromeJohn C Oakley, Franck Kalume, William A Catterall
The Journal of Physiology|March 3, 2010
NaV1.1 channels and epilepsyWilliam A Catterall, Franck Kalume, John C Oakley
Neurobiology of Disease|November 4, 2020
Disordered autonomic function during exposure to moderate heat or exercise in a mouse model of Dravet syndromeNikhil Sahai, Angela M Bard, Orrin Devinsky, et al.
Seminars in Cell & Developmental Biology|June 7, 2021
Sleep timing and the circadian clock in mammals: Past, present and the road aheadRaymond E A Sanchez, Franck Kalume, Horacio O de la Iglesia
Journal of Neuroscience Methods|July 3, 2019
A more efficient conditional mouse model of Dravet syndrome: Implications for epigenetic selection and sex-dependent behaviorsAaron D Williams, Franck Kalume, Ruth E Westenbroek, et al.
Journal of Neuroscience Research|June 16, 2004
Molecular mimicry: cross-reactive antibodies from patients with immune-mediated neurologic disease inhibit neuronal firingFranck Kalume, Sang Min Lee, Yvette Morcos, et al.
Journal of Neuropathology and Experimental Neurology|February 7, 2016
Brain Aggregates: An Effective In Vitro Cell Culture System Modeling Neurodegenerative DiseasesMisol Ahn, Franck Kalume, Rose Pitstick, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 24, 2009
Temperature- and age-dependent seizures in a mouse model of severe myoclonic epilepsy in infancyJohn C Oakley, Franck Kalume, Frank H Yu, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 12, 2007
Reduced sodium current in Purkinje neurons from Nav1.1 mutant mice: implications for ataxia in severe myoclonic epilepsy in infancyFranck Kalume, Frank H Yu, Ruth E Westenbroek, et al.
Pageof 3

Showing results (1-10 of 28) with videos related to

Sort By:
Pageof 3
Respiratory Physiology & Neurobiology|July 16, 2013
Sudden unexpected death in Dravet syndrome: respiratory and other physiological dysfunctionsFranck Kalume
Epilepsia|April 6, 2011
Insights into pathophysiology and therapy from a mouse model of Dravet syndromeJohn C Oakley, Franck Kalume, William A Catterall
The Journal of Physiology|March 3, 2010
NaV1.1 channels and epilepsyWilliam A Catterall, Franck Kalume, John C Oakley
Neurobiology of Disease|November 4, 2020
Disordered autonomic function during exposure to moderate heat or exercise in a mouse model of Dravet syndromeNikhil Sahai, Angela M Bard, Orrin Devinsky, et al.
Seminars in Cell & Developmental Biology|June 7, 2021
Sleep timing and the circadian clock in mammals: Past, present and the road aheadRaymond E A Sanchez, Franck Kalume, Horacio O de la Iglesia
Journal of Neuroscience Methods|July 3, 2019
A more efficient conditional mouse model of Dravet syndrome: Implications for epigenetic selection and sex-dependent behaviorsAaron D Williams, Franck Kalume, Ruth E Westenbroek, et al.
Journal of Neuroscience Research|June 16, 2004
Molecular mimicry: cross-reactive antibodies from patients with immune-mediated neurologic disease inhibit neuronal firingFranck Kalume, Sang Min Lee, Yvette Morcos, et al.
Journal of Neuropathology and Experimental Neurology|February 7, 2016
Brain Aggregates: An Effective In Vitro Cell Culture System Modeling Neurodegenerative DiseasesMisol Ahn, Franck Kalume, Rose Pitstick, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 24, 2009
Temperature- and age-dependent seizures in a mouse model of severe myoclonic epilepsy in infancyJohn C Oakley, Franck Kalume, Frank H Yu, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 12, 2007
Reduced sodium current in Purkinje neurons from Nav1.1 mutant mice: implications for ataxia in severe myoclonic epilepsy in infancyFranck Kalume, Frank H Yu, Ruth E Westenbroek, et al.
Pageof 3