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Neurology|July 19, 2022

Natural History Study of STXBP1-Developmental and Epileptic Encephalopathy Into AdulthoodHannah Stamberger, David Crosiers, Ganna Balagura, et al.

Nature Genetics|January 13, 2009

15q13.3 microdeletions increase risk of idiopathic generalized epilepsyIngo Helbig, Heather C Mefford, Andrew J Sharp, et al.

Neurology|March 22, 2022

Spectrum of Phenotypic, Genetic, and Functional Characteristics in Patients With Epilepsy With <i>KCNC2</i> Pathogenic VariantsNiklas Schwarz, Simone Seiffert, Manuela Pendziwiat, et al.

Neurology|August 14, 2016

Phenotypic spectrum of GABRA1: From generalized epilepsies to severe epileptic encephalopathiesKatrine Johannesen, Carla Marini, Siona Pfeffer, et al.

Nature Communications|October 31, 2019

Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3Rahel T Florian, Florian Kraft, Elsa Leitão, et al.

Epilepsia|February 20, 2020

From theory to practice: Critical points in the 2017 ILAE classification of epileptic seizures and epilepsiesAndré Palmini, Naoki Akamatsu, Thomas Bast, et al.

Seizure|March 11, 2020

Could the 2017 ILAE and the four-dimensional epilepsy classifications be merged to a new "Integrated Epilepsy Classification"?Felix Rosenow, Naoki Akamatsu, Thomas Bast, et al.

Brain : a Journal of Neurology|September 10, 2013

Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1ADalia Kasperaviciute, Claudia B Catarino, Mar Matarin, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 4, 2020

NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patternsHannah Stamberger, Trine B Hammer, Elena Gardella, et al.

Human Molecular Genetics|September 6, 2012

Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32, , Michael Steffens, et al.

Pageof 31

Search research articles

Showing results (301-310 of 310) with videos related to

Sort By:

Pageof 31

You have reached the last page of results.This site can display upto 310 results.

Neurology|July 19, 2022

Natural History Study of STXBP1-Developmental and Epileptic Encephalopathy Into AdulthoodHannah Stamberger, David Crosiers, Ganna Balagura, et al.

Nature Genetics|January 13, 2009

15q13.3 microdeletions increase risk of idiopathic generalized epilepsyIngo Helbig, Heather C Mefford, Andrew J Sharp, et al.

Neurology|March 22, 2022

Spectrum of Phenotypic, Genetic, and Functional Characteristics in Patients With Epilepsy With <i>KCNC2</i> Pathogenic VariantsNiklas Schwarz, Simone Seiffert, Manuela Pendziwiat, et al.

Neurology|August 14, 2016

Phenotypic spectrum of GABRA1: From generalized epilepsies to severe epileptic encephalopathiesKatrine Johannesen, Carla Marini, Siona Pfeffer, et al.

Nature Communications|October 31, 2019

Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3Rahel T Florian, Florian Kraft, Elsa Leitão, et al.

Epilepsia|February 20, 2020

From theory to practice: Critical points in the 2017 ILAE classification of epileptic seizures and epilepsiesAndré Palmini, Naoki Akamatsu, Thomas Bast, et al.

Seizure|March 11, 2020

Could the 2017 ILAE and the four-dimensional epilepsy classifications be merged to a new "Integrated Epilepsy Classification"?Felix Rosenow, Naoki Akamatsu, Thomas Bast, et al.

Brain : a Journal of Neurology|September 10, 2013

Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1ADalia Kasperaviciute, Claudia B Catarino, Mar Matarin, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 4, 2020

NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patternsHannah Stamberger, Trine B Hammer, Elena Gardella, et al.

Human Molecular Genetics|September 6, 2012

Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32, , Michael Steffens, et al.

Pageof 31