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List of works by Markus Wolff

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

scientific article published in 2021

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

scientific article published on 28 February 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

scientific article

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

scientific article published on 4 March 2017

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

scientific article published on May 25, 2012

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

scientific article published on 30 June 2020

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

scientific article published on 01 December 2019

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

scientific article published on 06 March 2013

Targeted next generation sequencing as a diagnostic tool in epileptic disorders ⬇️

scientific article published on May 21, 2012

The landscape of epilepsy-related GATOR1 variants

scientific article published on 10 August 2018

The phenotype of SCN8A developmental and epileptic encephalopathy

scientific article published on 31 August 2018

The phenotypic spectrum of SCN8A encephalopathy

scientific article

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