Karen Schluter-Muller

Neuruppin, BB 16816, Germany

Last Updated: 09/26/2026

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Found 13 publications

Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes.

Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes.

Journal: medRxiv : the preprint server for health sciences

Published: March 03, 2023

Efficacy, Retention and Tolerability of Everolimus in Patients with Tuberous Sclerosis Complex: A Survey-Based Study on Patients' Perspectives.

Efficacy, Retention and Tolerability of Everolimus in Patients with Tuberous Sclerosis Complex: A Survey-Based Study on Patients' Perspectives.

Journal: CNS drugs

Published: June 21, 2021

Prescription patterns of antiseizure drugs in tuberous sclerosis complex (TSC)-associated epilepsy: a multicenter cohort study from Germany and review of the literature.

Prescription patterns of antiseizure drugs in tuberous sclerosis complex (TSC)-associated epilepsy: a multicenter cohort study from Germany and review of the literature.

Journal: Expert review of clinical pharmacology

Published: April 01, 2021

Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications.

Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications.

Journal: Brain : a journal of neurology

Published: March 12, 2021

Health-related quality of life in children and adolescents with tuberous sclerosis complex and their caregivers: A multicentre cohort study from Germany.

Health-related quality of life in children and adolescents with tuberous sclerosis complex and their caregivers: A multicentre cohort study from Germany.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

Published: March 11, 2021

Direct and indirect costs and cost-driving factors of Tuberous sclerosis complex in children, adolescents, and caregivers: a multicenter cohort study.

Direct and indirect costs and cost-driving factors of Tuberous sclerosis complex in children, adolescents, and caregivers: a multicenter cohort study.

Journal: Orphanet journal of rare diseases

Published: November 21, 2020

Stiripentol fails to lower plasma oxalate in a dialysis-dependent PH1 patient.

Stiripentol fails to lower plasma oxalate in a dialysis-dependent PH1 patient.

Journal: Pediatric nephrology (Berlin, Germany)

Published: January 18, 2020

Correction: The landscape of epilepsy-related GATOR1 variants.

Correction: The landscape of epilepsy-related GATOR1 variants.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: September 29, 2018

Postmarketing experience with brivaracetam in the treatment of focal epilepsy in children and adolescents.

Postmarketing experience with brivaracetam in the treatment of focal epilepsy in children and adolescents.

Journal: Epilepsy & behavior : E&B

Published: September 08, 2018

Correction to: The landscape of epilepsy-related GATOR1 variants.

Correction to: The landscape of epilepsy-related GATOR1 variants.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: August 31, 2018

Use of brivaracetam in genetic generalized epilepsies and for acute, intravenous treatment of absence status epilepticus.

Use of brivaracetam in genetic generalized epilepsies and for acute, intravenous treatment of absence status epilepticus.

Journal: Epilepsia

Published: May 31, 2018

Efficacy, Retention, and Tolerability of Brivaracetam in Patients With Epileptic Encephalopathies: A Multicenter Cohort Study From Germany.

Efficacy, Retention, and Tolerability of Brivaracetam in Patients With Epileptic Encephalopathies: A Multicenter Cohort Study From Germany.

Journal: Frontiers in neurology

Published: May 08, 2018

Showing 1-12 of 13

Last Updated: 09/26/2026