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Arielle Crespel

Showing results (91-100 of 95) with videos related to

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The Lancet. Neurology|September 10, 2013
Incidence and mechanisms of cardiorespiratory arrests in epilepsy monitoring units (MORTEMUS): a retrospective studyPhilippe Ryvlin, Lina Nashef, Samden D Lhatoo, et al.
The Lancet. Neurology|November 24, 2025
Seizure-related biomarkers of sudden unexpected death in epilepsy (SUDEP) in drug-resistant focal epilepsy (REPO<sub>2</sub>MSE): a prospective, multicentre case-control studyPhilippe Ryvlin, Margaux Huot, Luc Valton, et al.
Annals of Neurology|April 6, 2017
Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K<sup>+</sup> channel propertiesKaren L Oliver, Silvana Franceschetti, Carol J Milligan, et al.
Epilepsy & Behavior : E&B|June 13, 2013
Consensus on diagnosis and management of JME: From founder's observations to current trendsDorothée G A Kasteleijn-Nolst Trenité, Bettina Schmitz, Dieter Janz, et al.
Nature Genetics|November 18, 2014
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsyMikko Muona, Samuel F Berkovic, Leanne M Dibbens, et al.
Pageof 10

Showing results (91-100 of 95) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 95 results.
The Lancet. Neurology|September 10, 2013
Incidence and mechanisms of cardiorespiratory arrests in epilepsy monitoring units (MORTEMUS): a retrospective studyPhilippe Ryvlin, Lina Nashef, Samden D Lhatoo, et al.
The Lancet. Neurology|November 24, 2025
Seizure-related biomarkers of sudden unexpected death in epilepsy (SUDEP) in drug-resistant focal epilepsy (REPO<sub>2</sub>MSE): a prospective, multicentre case-control studyPhilippe Ryvlin, Margaux Huot, Luc Valton, et al.
Annals of Neurology|April 6, 2017
Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K<sup>+</sup> channel propertiesKaren L Oliver, Silvana Franceschetti, Carol J Milligan, et al.
Epilepsy & Behavior : E&B|June 13, 2013
Consensus on diagnosis and management of JME: From founder's observations to current trendsDorothée G A Kasteleijn-Nolst Trenité, Bettina Schmitz, Dieter Janz, et al.
Nature Genetics|November 18, 2014
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsyMikko Muona, Samuel F Berkovic, Leanne M Dibbens, et al.
Pageof 10