Otfried M. Debus
Muenster, NW 48153, Germany
Last Updated: 09/26/2026
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Found 10 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
Anaplerotic Therapy Using Triheptanoin in Two Brothers Suffering from Aconitase 2 Deficiency.
Journal: Metabolites
Published: March 10, 2024
Music Therapy Supports Children with Neurological Diseases during Physical Therapy Interventions.
Journal: International journal of environmental research and public health
Published: December 13, 2021
A mutation in the neonatal isoform of SCN2A causes neonatal-onset epilepsy.
Journal: American journal of medical genetics. Part A
Published: February 13, 2021
The Translational Medicine Professional: A Bridge Between Bench and Bedside?
Journal: Frontiers in medicine
Published: July 15, 2018
The earlier, the better
Journal: Kinderkrankenschwester : Organ der Sektion Kinderkrankenpflege
Published: August 28, 2015
LIS1-associated classic lissencephaly: A retrospective, multicenter survey of the epileptogenic phenotype and response to antiepileptic drugs.
Journal: Brain & development
Published: August 06, 2015
Expanding the clinical and molecular spectrum of thiamine pyrophosphokinase deficiency: a treatable neurological disorder caused by TPK1 mutations.
Journal: Molecular genetics and metabolism
Published: June 28, 2014
Showing 1-10 of 10
Last Updated: 09/26/2026