Sarah Herdewyn
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Explore the profile of Sarah Herdewyn including associated specialties, affiliations and a list of published articles.
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10
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154
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Recent Articles
1.
Adams L, Lamquet S, Linussio J, Van Nieuwenhuysen T, Vodolazkaia A, Mukovnikova M, et al.
Case Rep Neurol
. 2025 Feb;
17(1):9-15.
PMID: 39981031
Introduction: Botulism is a rare but potentially life-threatening syndrome caused by botulinum neurotoxin. The classic presentation of botulism is the acute onset of bilateral cranial neuropathies associated with symmetric descending...
2.
Smeets N, Gheldof A, Dequeker B, Poleur M, Slootjes S, Van Parijs V, et al.
Pediatr Neurol
. 2024 Jul;
158:57-65.
PMID: 38964204
Background: Congenital myasthenic syndromes (CMS) are a group of genetic disorders characterized by impaired neuromuscular transmission. CMS typically present at a young age with fatigable muscle weakness, often with an...
3.
Exome Sequencing and Multigene Panel Testing in 1,411 Patients With Adult-Onset Neurologic Disorders
Schuermans N, Verdin H, Ghijsels J, Hellemans M, Debackere E, Bogaert E, et al.
Neurol Genet
. 2023 May;
9(3):e200071.
PMID: 37152446
Background And Objectives: Owing to their extensive clinical and molecular heterogeneity, hereditary neurologic diseases in adults are difficult to diagnose. The current knowledge about the diagnostic yield and clinical utility...
4.
Janssens L, De Puydt J, Milazzo M, Symoens S, De Bleecker J, Herdewyn S
Neuromuscul Disord
. 2022 Oct;
32(11-12):864-869.
PMID: 36283893
Malignant hyperthermia is a life-threatening disorder, which can be prevented by avoiding certain anesthetic agents. Pathogenic variants in the skeletal muscle ryanodine receptor 1-gene are linked to malignant hyperthermia. We...
5.
Van Assche S, Parmentier H, Varkas G, Peene I, Herdewyn S
BMC Neurol
. 2022 Sep;
22(1):368.
PMID: 36153490
Background: Autoimmune Syndrome Induced by Adjuvants (ASIA) is a concept introduced by Shoenfeld to group various disease entities believed to be triggered by an infection, silicone exposure or other external...
6.
Beel S, Herdewyn S, Fazal R, De Decker M, Moisse M, Robberecht W, et al.
Mol Neurodegener
. 2018 Oct;
13(1):55.
PMID: 30326935
Background: TAR DNA binding protein 43 (TDP-43) is the main disease protein in most patients with amyotrophic lateral sclerosis (ALS) and about 50% of patients with frontotemporal dementia (FTD). TDP-43...
7.
Herdewyn S, Cirillo C, Van Den Bosch L, Robberecht W, Vanden Berghe P, Van Damme P
Mol Neurodegener
. 2014 Jun;
9:24.
PMID: 24938805
Background: Intraneuronal inclusions of TAR DNA-binding protein 43 (TDP-43) have been found in the majority of Amyotrophic Lateral Sclerosis (ALS) patients. Mutations in the gene encoding TDP-43 cause familial ALS....
8.
Debray S, Race V, Crabbe V, Herdewyn S, Matthijs G, Goris A, et al.
Neurobiol Aging
. 2013 Jul;
34(12):2890.e7-2890.e12.
PMID: 23870417
We determined the frequency of C9orf72 repeat expansions in a large cohort of Belgian patients with familial (fALS) and sporadic (sALS) amyotrophic lateral sclerosis (ALS). In total, 119 patients with...
9.
De Muynck L, Herdewyn S, Beel S, Scheveneels W, Van Den Bosch L, Robberecht W, et al.
Neurobiol Aging
. 2013 May;
34(11):2541-7.
PMID: 23706646
Progranulin (PGRN) is a growth factor involved in wound healing, inflammation, tumor growth, and neurodegeneration. Mutations in the gene encoding PGRN give rise to shortage of PGRN and cause familial...
10.
Herdewyn S, De Muynck L, Van Den Bosch L, Robberecht W, Van Damme P
Neurobiol Aging
. 2013 Apr;
34(10):2302-3.
PMID: 23608112
Motor neuron degeneration in amyotrophic lateral sclerosis (ALS) is familial in 10% of patients, with mutations in SOD1 and C9orf72 being the most frequent cause. There is convincing evidence for...