Corinne G C Horlings
Overview
Explore the profile of Corinne G C Horlings including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
36
Citations
497
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Kleinveld V, Bruijnes J, Labrecque S, Jeurissen-Bekkering D, Faber C, Horlings C
Brain Behav
. 2024 Nov;
14(11):e70162.
PMID: 39552113
Introduction: Myotonic dystrophy type 1 (DM1) patients might represent a high-risk population for severe COVID-19 disease, as cardiopulmonary symptoms are part of the clinical spectrum of DM1. The COVID-19 pandemic...
2.
Kools J, Vincenten S, van Engelen B, Voet N, Merkies I, Horlings C, et al.
Muscle Nerve
. 2024 Nov;
71(1):55-62.
PMID: 39508285
Introduction/aims: The number of clinical trials in facioscapulohumeral muscular dystrophy (FSHD) is expected to increase in the near future. There is a need for clinical outcome assessments (COAs) that can...
3.
Deenen J, Horlings C, Voermans N, van Doorn P, Faber C, van der Kooi A, et al.
Neuromuscul Disord
. 2024 Aug;
42:27-35.
PMID: 39116821
Most neuromuscular disorders are rare, but as a group they are not. Nevertheless, epidemiological data of specific neuromuscular disorders are scarce, especially on the incidence. We applied a capture-recapture approach...
4.
Vosse B, de Jong J, la Fontaine L, Horlings C, van Kuijk S, Cobben N, et al.
J Neuromuscul Dis
. 2024 Aug;
11(5):1123-1130.
PMID: 39093078
Background: Chronic respiratory failure often occurs in myotonic dystrophy type 1 (DM1) and can be treated with noninvasive home mechanical ventilation (HMV). Treatment adherence with HMV is often suboptimal in...
5.
Kleinveld V, Keritam O, Horlings C, Cetin H, Wanschitz J, Hotter A, et al.
Muscle Nerve
. 2024 Feb;
69(4):422-427.
PMID: 38334356
Introduction/aims: The clinical presentation of multifocal motor neuropathy (MMN) may mimic early amyotrophic lateral sclerosis (ALS) with predominant lower motor neuron (LMN) involvement, posing a diagnostic challenge. Both diseases have...
6.
Kroon R, Kalf J, Swart B, Heskamp L, Rooy J, van Engelen B, et al.
Neurology
. 2024 Jan;
102(1):e207833.
PMID: 38165364
Background And Objectives: Oculopharyngeal muscular dystrophy (OPMD) is a rare progressive neuromuscular disease. MRI is one of the techniques that is used in neuromuscular disorders to evaluate muscle alterations. The...
7.
Kleinveld V, Platzgummer S, Wanschitz J, Horlings C, Loscher W
Brain Sci
. 2023 May;
13(4).
PMID: 37190588
(1) Background: This study aims to assess the diagnostic accuracy of parameters based on a combination of transcranial magnetic stimulation (TMS) and electrical stimulation (ES) in the differentiation between idiopathic...
8.
Joosten I, Horlings C, Vosse B, Wagner A, Bovenkerk D, Evertz R, et al.
Muscle Nerve
. 2022 Dec;
67(2):130-137.
PMID: 36484161
Introduction/aims: Although the extent of muscle weakness and organ complications has not been well studied in patients with late-onset myotonic dystrophy type 1 (DM1), adult-onset DM1 is associated with severe...
9.
Kroon R, Kalf J, Meijers R, Swart B, Cameron I, Doorduin J, et al.
Muscle Nerve
. 2022 Jul;
66(4):453-461.
PMID: 35859342
Introduction/aims: Oculopharyngeal muscular dystrophy (OPMD) is a late-onset, progressive muscle disease. Quantitative muscle ultrasound (QMUS) assesses structural changes in muscles and is a sensitive biomarker in neuromuscular disorders. Our aim...
10.
Joosten I, Janssen C, Horlings C, Uijl D, Evertz R, van Engelen B, et al.
Europace
. 2022 Jul;
25(1):156-163.
PMID: 35851806
Aims: To evaluate the clinical effectiveness of routine 24 h Holter monitoring to screen for conduction disturbances and arrhythmias in patients with myotonic dystrophy type 1 (DM1). Methods And Results:...