Adelheid Kruel-Wiemer
Kehl, BW 77694, Germany
Last Updated: 09/26/2026
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Found 25 publications
Gene-specific long-term course, neurodevelopmental outcome and quality of life in patients with LIS1/PAFAH1B1-, DCX-, DYNC1H1-, TUBA1A- and TUBG1-related lissencephaly.
Journal: Orphanet journal of rare diseases
Published: August 05, 2025
Sturge Weber syndrome in a multinational pediatric cohort: a systematic analysis of different types.
Sturge Weber syndrome in a multinational pediatric cohort: a systematic analysis of different types.
Journal: Orphanet journal of rare diseases
Published: January 24, 2025
The natural history of pediatric Sturge-Weber Syndrome: A multinational cross-sectional study.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: August 02, 2024
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.
Journal: Expert review of clinical pharmacology
Published: April 01, 2021
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.
Journal: Orphanet journal of rare diseases
Published: November 21, 2020
Expectations and knowledge of cannabidiol therapy for childhood epilepsy - A German caregiver survey.
Journal: Epilepsy & behavior : E&B
Published: May 27, 2020
Cannabidiol Interacts Significantly with Everolimus-Report of a Patient with Tuberous Sclerosis Complex.
Journal: Neuropediatrics
Published: September 21, 2019
Congenital Lymphatic Malformation and Aortic Aneurysm in a Patient with TSC2 Mutation.
Journal: Neuropediatrics
Published: September 11, 2019
Last Updated: 09/26/2026