Peter Van den Bergh
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Explore the profile of Peter Van den Bergh including associated specialties, affiliations and a list of published articles.
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53
Citations
1880
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Recent Articles
1.
Arends S, Drenthen J, de Koning L, Van den Bergh P, Hadden R, Kuwabara S, et al.
Eur J Neurol
. 2024 Jul;
31(9):e16335.
PMID: 38965709
Background And Purpose: Various electrodiagnostic criteria have been developed in Guillain-Barré syndrome (GBS). Their performance in a broad representation of GBS patients has not been evaluated. Motor conduction data from...
2.
De Wel B, Iterbeke L, Huysmans L, Peeters R, Goosens V, Dubuisson N, et al.
Eur J Neurol
. 2024 Mar;
31(7):e16282.
PMID: 38504654
Background And Purpose: Because Becker muscular dystrophy (BMD) is a heterogeneous disease and only few studies have evaluated adult patients, it is currently still unclear which outcome measures should be...
3.
Topf A, Cox D, Zaharieva I, Di Leo V, Sarparanta J, Jonson P, et al.
Nat Genet
. 2024 Mar;
56(3):395-407.
PMID: 38429495
In digenic inheritance, pathogenic variants in two genes must be inherited together to cause disease. Only very few examples of digenic inheritance have been described in the neuromuscular disease field....
4.
Carrington G, Hau A, Kosta S, Dugdale H, Muntoni F, DAmico A, et al.
JCI Insight
. 2023 Oct;
8(21.
PMID: 37788100
Myosin heavy chains encoded by MYH7 and MYH2 are abundant in human skeletal muscle and important for muscle contraction. However, it is unclear how mutations in these genes disrupt myosin...
5.
Lemmers R, Butterfield R, van der Vliet P, De Bleecker J, van der Pol L, Dunn D, et al.
Brain
. 2023 Sep;
147(2):414-426.
PMID: 37703328
Facioscapulohumeral dystrophy (FSHD) has a unique genetic aetiology resulting in partial chromatin relaxation of the D4Z4 macrosatellite repeat array on 4qter. This D4Z4 chromatin relaxation facilitates inappropriate expression of the...
6.
Allen N, ORahelly M, Eymard B, Chouchane M, Hahn A, Kearns G, et al.
Brain
. 2023 May;
146(10):4233-4246.
PMID: 37186601
In utero exposure to maternal antibodies targeting the fetal acetylcholine receptor isoform (fAChR) can impair fetal movement, leading to arthrogryposis multiplex congenita (AMC). Fetal AChR antibodies have also been implicated...
7.
Al-Hakem H, Doets A, Stino A, Zivkovic S, Andersen H, Willison H, et al.
Neurology
. 2023 Apr;
100(23):e2386-e2397.
PMID: 37076309
Background And Objectives: To investigate CSF findings in relation to clinical and electrodiagnostic subtypes, severity, and outcome of Guillain-Barré syndrome (GBS) based on 1,500 patients in the International GBS Outcome...
8.
Leonhard S, van der Eijk A, Andersen H, Antonini G, Arends S, Attarian S, et al.
Neurology
. 2022 Aug;
99(12):e1299-e1313.
PMID: 35981895
Background And Objectives: Infections play a key role in the development of Guillain-Barré syndrome (GBS) and have been associated with specific clinical features and disease severity. The clinical variation of...
9.
Aleksovska K, Kobulashvili T, Costa J, Zimmermann G, Ritchie K, Reinhard C, et al.
Eur J Neurol
. 2022 Mar;
29(6):1571-1586.
PMID: 35318776
Background And Purpose: Rare diseases affect up to 29 million people in the European Union, and almost 50% of them affect the nervous system or muscles. Delays in diagnosis and...
10.
Arends S, Drenthen J, Van den Bergh P, Franssen H, Hadden R, Islam B, et al.
Clin Neurophysiol
. 2022 Jan;
138:231-240.
PMID: 35078730
Objective: To describe the heterogeneity of electrodiagnostic (EDx) studies in Guillain-Barré syndrome (GBS) patients collected as part of the International GBS Outcome Study (IGOS). Methods: Prospectively collected clinical and EDx...