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European Journal of Neurology
|
October 10, 2018
Management of psychogenic non-epileptic seizures: a multidisciplinary approach
S Gasparini, E Beghi, E Ferlazzo, et al.
Neurology. Genetics
|
March 4, 2021
Genotype-phenotype correlations in patients with de novo <i>KCNQ2</i> pathogenic variants
Federica Malerba, Giulio Alberini, Ganna Balagura, et al.
Brain : a Journal of Neurology
|
October 21, 2017
Rare GABRA3 variants are associated with epileptic seizures, encephalopathy and dysmorphic features
Cristina Elena Niturad, Dorit Lev, Vera M Kalscheuer, et al.
Epilepsia
|
October 21, 2016
Symptomatic and presumed symptomatic focal epilepsies in childhood: An observational, prospective multicentre study
Marilena Vecchi, Carmen Barba, Debora De Carlo, et al.
Neurology. Genetics
|
June 3, 2022
Epilepsy Course and Developmental Trajectories in <i>STXBP1</i>-DEE
Ganna Balagura, Julie Xian, Antonella Riva, et al.
Brain : a Journal of Neurology
|
March 19, 2015
CHD2 variants are a risk factor for photosensitivity in epilepsy
Elizabeth C Galizia, Candace T Myers, Costin Leu, et al.
Neurology
|
February 12, 2016
STXBP1 encephalopathy: A neurodevelopmental disorder including epilepsy
Hannah Stamberger, Marina Nikanorova, Marjolein H Willemsen, et al.
European Journal of Heart Failure
|
December 18, 2025
Contemporary medical therapy for heart failure across the ejection fraction spectrum: The OPTIPHARM-HF registry
Riccardo M Inciardi, Maurizio Volterrani, Gianluigi Savarese, 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.
Page
of 36
Search research articles
Search
Showing results (351-360 of 359) with videos related to
Sort By:
Page
of 36
You have reached the last page of results.
This site can display upto 359 results.
European Journal of Neurology
|
October 10, 2018
Management of psychogenic non-epileptic seizures: a multidisciplinary approach
S Gasparini, E Beghi, E Ferlazzo, et al.
Neurology. Genetics
|
March 4, 2021
Genotype-phenotype correlations in patients with de novo <i>KCNQ2</i> pathogenic variants
Federica Malerba, Giulio Alberini, Ganna Balagura, et al.
Brain : a Journal of Neurology
|
October 21, 2017
Rare GABRA3 variants are associated with epileptic seizures, encephalopathy and dysmorphic features
Cristina Elena Niturad, Dorit Lev, Vera M Kalscheuer, et al.
Epilepsia
|
October 21, 2016
Symptomatic and presumed symptomatic focal epilepsies in childhood: An observational, prospective multicentre study
Marilena Vecchi, Carmen Barba, Debora De Carlo, et al.
Neurology. Genetics
|
June 3, 2022
Epilepsy Course and Developmental Trajectories in <i>STXBP1</i>-DEE
Ganna Balagura, Julie Xian, Antonella Riva, et al.
Brain : a Journal of Neurology
|
March 19, 2015
CHD2 variants are a risk factor for photosensitivity in epilepsy
Elizabeth C Galizia, Candace T Myers, Costin Leu, et al.
Neurology
|
February 12, 2016
STXBP1 encephalopathy: A neurodevelopmental disorder including epilepsy
Hannah Stamberger, Marina Nikanorova, Marjolein H Willemsen, et al.
European Journal of Heart Failure
|
December 18, 2025
Contemporary medical therapy for heart failure across the ejection fraction spectrum: The OPTIPHARM-HF registry
Riccardo M Inciardi, Maurizio Volterrani, Gianluigi Savarese, 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.
Page
of 36