Search research articles
Contact Us
Filters
Showing results (101-110 of 128) with videos related to
Page
of 13
Sort By:
Epilepsia
|
July 6, 2017
Response to the numbering of seizure types
Robert S Fisher, J Helen Cross, Carol D'Souza, et al.
Brain : a Journal of Neurology
|
September 19, 2019
KCNT1 epilepsy with migrating focal seizures shows a temporal sequence with poor outcome, high mortality and SUDEP
Mathieu Kuchenbuch, Giulia Barcia, Nicole Chemaly, et al.
Nature Genetics
|
August 13, 2013
GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction
Gaetan Lesca, Gabrielle Rudolf, Nadine Bruneau, et al.
Human Genetics
|
July 3, 2016
Identity by descent fine mapping of familial adult myoclonus epilepsy (FAME) to 2p11.2-2q11.2
Lyndal Henden, Saskia Freytag, Zaid Afawi, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
June 8, 2021
CACNA1A-associated epilepsy: Electroclinical findings and treatment response on seizures in 18 patients
Marie Le Roux, Magalie Barth, Sophie Gueden, et al.
Human Molecular Genetics
|
February 19, 2015
Galanin pathogenic mutations in temporal lobe epilepsy
Michel Guipponi, Amina Chentouf, Kristin E B Webling, et al.
European Journal of Human Genetics : EJHG
|
May 30, 2020
Biallelic PDE2A variants: a new cause of syndromic paroxysmal dyskinesia
Diane Doummar, Christel Dentel, Romane Lyautey, et al.
Seizure
|
May 17, 2020
EEG in fitness to drive evaluations in people with epilepsy - Considerable variations across Europe
Rune Markhus, Oliver Henning, Ellen Molteberg, et al.
Seizure
|
April 23, 2016
Current practices in long-term video-EEG monitoring services: A survey among partners of the E-PILEPSY pilot network of reference for refractory epilepsy and epilepsy surgery
Teia Kobulashvili, Julia Höfler, Judith Dobesberger, et al.
Brain : a Journal of Neurology
|
December 14, 2018
GRIN2A-related disorders: genotype and functional consequence predict phenotype
Vincent Strehlow, Henrike O Heyne, Danique R M Vlaskamp, et al.
Page
of 13
Search research articles
Search
Showing results (101-110 of 128) with videos related to
Sort By:
Page
of 13
Epilepsia
|
July 6, 2017
Response to the numbering of seizure types
Robert S Fisher, J Helen Cross, Carol D'Souza, et al.
Brain : a Journal of Neurology
|
September 19, 2019
KCNT1 epilepsy with migrating focal seizures shows a temporal sequence with poor outcome, high mortality and SUDEP
Mathieu Kuchenbuch, Giulia Barcia, Nicole Chemaly, et al.
Nature Genetics
|
August 13, 2013
GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction
Gaetan Lesca, Gabrielle Rudolf, Nadine Bruneau, et al.
Human Genetics
|
July 3, 2016
Identity by descent fine mapping of familial adult myoclonus epilepsy (FAME) to 2p11.2-2q11.2
Lyndal Henden, Saskia Freytag, Zaid Afawi, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
June 8, 2021
CACNA1A-associated epilepsy: Electroclinical findings and treatment response on seizures in 18 patients
Marie Le Roux, Magalie Barth, Sophie Gueden, et al.
Human Molecular Genetics
|
February 19, 2015
Galanin pathogenic mutations in temporal lobe epilepsy
Michel Guipponi, Amina Chentouf, Kristin E B Webling, et al.
European Journal of Human Genetics : EJHG
|
May 30, 2020
Biallelic PDE2A variants: a new cause of syndromic paroxysmal dyskinesia
Diane Doummar, Christel Dentel, Romane Lyautey, et al.
Seizure
|
May 17, 2020
EEG in fitness to drive evaluations in people with epilepsy - Considerable variations across Europe
Rune Markhus, Oliver Henning, Ellen Molteberg, et al.
Seizure
|
April 23, 2016
Current practices in long-term video-EEG monitoring services: A survey among partners of the E-PILEPSY pilot network of reference for refractory epilepsy and epilepsy surgery
Teia Kobulashvili, Julia Höfler, Judith Dobesberger, et al.
Brain : a Journal of Neurology
|
December 14, 2018
GRIN2A-related disorders: genotype and functional consequence predict phenotype
Vincent Strehlow, Henrike O Heyne, Danique R M Vlaskamp, et al.
Page
of 13