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A multicenter, matched case-control analysis comparing burden-of-illness in Dravet syndrome to refractory epilepsy and seizure remission in patients and caregivers in Germany

scientific article published on 27 June 2019

Auditory stimulation during sleep suppresses spike activity in benign epilepsy with centrotemporal spikes

artículo científico publicado en 2021

Burden-of-illness and cost-driving factors in Dravet syndrome patients and carers: A prospective, multicenter study from Germany

artículo científico publicado en 2019

Correction to: The landscape of epilepsy-related GATOR1 variants

scientific article published on 01 July 2019

Correction: The landscape of epilepsy-related GATOR1 variants

scientific article published on 01 August 2019

GRIN2B mutations in West syndrome and intellectual disability with focal epilepsy

artículo científico publicado en 2014

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders.

artículo científico publicado en 2017

Interstitial 9q34.11–q34.13 deletion in a patient with severe intellectual disability, hydrocephalus, and cleft lip/palate

artículo científico publicado el 25 de mayo de 2012

Late diagnosis of human immunodeficiency virus infection is linked to higher rates of epilepsy in children in the Eastern Cape of South Africa

artículo científico publicado en 2020

Phenotypic spectrum and genetics of SCN2A-related disorders, treatment options, and outcomes in epilepsy and beyond

artículo científico publicado en 2019

Plasma Exchange Is Effective in a 13-Year-Old Girl with Steroid-Resistant Bilateral Optic Neuritis

artículo científico publicado el 6 de marzo de 2013

Targeted next generation sequencing as a diagnostic tool in epileptic disorders

artículo científico publicado el 21 de mayo de 2012

The landscape of epilepsy-related GATOR1 variants

artículo científico publicado en 2018

The phenotype of SCN8A developmental and epileptic encephalopathy

artículo científico publicado en 2018

The phenotypic spectrum of SCN8A encephalopathy

artículo científico publicado en 2015