I J M de Groot
Overview
Explore the profile of I J M de Groot including associated specialties, affiliations and a list of published articles.
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Articles
21
Citations
226
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Recent Articles
1.
van de Velde N, Krom Y, Bongers J, Hoek R, Ikelaar N, van der Holst M, et al.
J Neuromuscul Dis
. 2024 Jul;
11(5):1095-1109.
PMID: 39031379
Background: Duchenne and Becker muscular dystrophy lack curative treatments. Registers can facilitate therapy development, serving as a platform to study epidemiology, assess clinical trial feasibility, identify eligible candidates, collect real-world...
2.
Houwen-van Opstal S, van den Elzen Y, Jansen M, Willemsen M, Cup E, de Groot I
J Neuromuscul Dis
. 2020 Jun;
7(4):467-475.
PMID: 32568104
Background: To retard shortening of finger flexors in patients with Duchenne muscular dystrophy (DMD), hand orthoses are prescribed. However, many patients do not wear the orthoses regularly. To optimize orthotic...
3.
Es M, Erasmus C, Houwen S, de Groot I, Voet N, van den Engel-Hoek L
J Pediatr Rehabil Med
. 2020 Mar;
13(1):17-23.
PMID: 32176663
Purpose: Regardless of age or disease stage, children with neuromuscular disorders (NMD) are at risk of developing dysphagia and/or dysarthria. It is important to screen these children regularly in order...
4.
Peeters L, Kingma I, van Dieen J, de Groot I
J Neuroeng Rehabil
. 2019 Mar;
16(1):44.
PMID: 30917845
Background: Performing daily activities independently becomes more difficult in time for patients with Duchenne muscular dystrophy (DMD) due to muscle weakness. When performing seated daily activities, the trunk plays an...
5.
Ricotti V, Selby V, Ridout D, Domingos J, Decostre V, Mayhew A, et al.
Neuromuscul Disord
. 2019 Mar;
29(4):261-268.
PMID: 30852071
The field of translational research in Duchenne muscular dystrophy (DMD) has been transformed in the last decade by a number of therapeutic targets, mostly studied in ambulant patients. A paucity...
6.
Peeters L, Kingma I, Faber G, van Dieen J, de Groot I
Exp Brain Res
. 2018 Nov;
237(1):289.
PMID: 30443670
The authors inadvertently submitted a wrong figure part for publication. Figure 8b should be as follows.
7.
Peeters L, Kingma I, Faber G, van Dieen J, de Groot I
Exp Brain Res
. 2018 May;
236(7):2023-2036.
PMID: 29737378
Development of trunk and head supportive devices for children with neuromuscular disorders requires detailed information about pelvis, trunk and head movement in interaction with upper extremity movement, as these are...
8.
van den Engel-Hoek L, Knuijt S, van Gerven M, Lagarde M, Groothuis J, de Groot I, et al.
J Oral Rehabil
. 2017 Jan;
44(3):155-162.
PMID: 28054362
In patients with mitochondrial disease, fatigue and muscle problems are the most common complaints. They also experience these complaints during mastication. To measure endurance of continuous mastication in patients with...
9.
van den Bergen J, Ginjaar H, van Essen A, Pangalila R, de Groot I, Wijkstra P, et al.
J Neuromuscul Dis
. 2016 Nov;
1(1):99-109.
PMID: 27858664
Background: Duchenne muscular dystrophy (DMD) is a progressive muscle disease. No curative therapy is currently available, but in recent decades standards of care have improved. These improvements include the use...
10.
van den Engel-Hoek L, de Groot I, Sie L, van Bruggen H, de Groot S, Erasmus C, et al.
Neuromuscul Disord
. 2016 May;
26(6):354-60.
PMID: 27132120
Dysphagia in Duchenne muscular dystrophy (DMD) worsens with age, with increasingly effortful mastication. The aims of this study were to describe mastication problems in consecutive stages in a group of...