Sarah Herdewyn
Gent, VLG, Belgium
Last Updated: 09/26/2026
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Found 12 publications
Botulism: An Overlooked Cause of Bulbar Weakness in Intensive Care - A Case Report.
Journal: Case reports in neurology
Published: July 05, 2024
Response to: The use of guidelines to assess the risk of malignant hyperthermia in individuals with a RYR1 variant.
Journal: Neuromuscular disorders : NMD
Published: January 18, 2024
Exome Sequencing and Multigene Panel Testing in 1,411 Patients With Adult-Onset Neurologic Disorders.
Journal: Neurology. Genetics
Published: October 19, 2022
Risk of malignant hyperthermia in patients carrying a variant in the skeletal muscle ryanodine receptor 1 gene.
Journal: Neuromuscular disorders : NMD
Published: June 22, 2022
Progranulin reduces insoluble TDP-43 levels, slows down axonal degeneration and prolongs survival in mutant TDP-43 mice.
Journal: Molecular neurodegeneration
Published: April 03, 2018
Prevention of intestinal obstruction reveals progressive neurodegeneration in mutant TDP-43 (A315T) mice.
Journal: Molecular neurodegeneration
Published: March 10, 2014
Frequency of C9orf72 repeat expansions in amyotrophic lateral sclerosis: a Belgian cohort study.
Journal: Neurobiology of aging
Published: June 10, 2013
Progranulin does not affect motor neuron degeneration in mutant SOD1 mice and rats.
Journal: Neurobiology of aging
Published: October 12, 2012
Whole-genome sequencing reveals a coding non-pathogenic variant tagging a non-coding pathogenic hexanucleotide repeat expansion in C9orf72 as cause of amyotrophic lateral sclerosis.
Journal: Human molecular genetics
Published: February 21, 2012
Showing 1-12 of 12
Last Updated: 09/26/2026