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The Lancet. Neurology
|
September 10, 2013
Incidence and mechanisms of cardiorespiratory arrests in epilepsy monitoring units (MORTEMUS): a retrospective study
Philippe 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 study
Philippe 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 properties
Karen 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 trends
Dorothée 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 epilepsy
Mikko Muona, Samuel F Berkovic, Leanne M Dibbens, et al.
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of 10
Search research articles
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Showing results (91-100 of 95) with videos related to
Sort By:
Page
of 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 study
Philippe 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 study
Philippe 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 properties
Karen 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 trends
Dorothée 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 epilepsy
Mikko Muona, Samuel F Berkovic, Leanne M Dibbens, et al.
Page
of 10