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Dystrophic changes in masticatory muscles, related chewing problems and malocclusions in duchenne muscular dystrophy

Neuromuscular disorders : NMD, 2016-06, Vol.26 (6), p.354-360

2016

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Predictive factors for masticatory performance in Duchenne muscular dystrophy

Neuromuscular disorders : NMD, 2014-08, Vol.24 (8), p.684-692

2014

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D.P.26 3D kinematic and EMG study of the arm function in boys with DMD: A pilot study

Neuromuscular disorders : NMD, 2012-10, Vol.22 (9), p.826-826

2012

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Reliability of the walking energy cost test and the six-minute walk test in boys with Duchenne muscular dystrophy

Neuromuscular disorders : NMD, 2014-03, Vol.24 (3), p.216-221

2014

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S.P.13 Exploring arm function in FSHD by means of questionnaires

Neuromuscular disorders : NMD, 2012-10, Vol.22 (9), p.879-879

2012

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S.P.12 Investigating arm function in boys with DMD by means of an international questionnaire

Neuromuscular disorders : NMD, 2012-10, Vol.22 (9), p.879-879

2012

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S.P.14 Exploring arm function in persons with LGMD by means of questionnaires

Neuromuscular disorders : NMD, 2012-10, Vol.22 (9), p.879-880

2012

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D.P.28 Arm function in FSHD studied with 3D movement kinematics and EMG

Neuromuscular disorders : NMD, 2012-10, Vol.22 (9), p.826-826

2012

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D.P.27 Arm function in LGMD studied with 3D movement kinematics and EMG

Neuromuscular disorders : NMD, 2012-10, Vol.22 (9), p.826-826

2012

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P.7.15 What can we learn from an assisted bicycle training in a symptomatic girl with Duchenne muscular dystrophy? A case study

Neuromuscular disorders : NMD, 2013-10, Vol.23 (9), p.778-778

2013

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S.P.45 ENERGETIC, a multidisciplinary self-management group program for reconditioning and managing fatigue

Neuromuscular disorders : NMD, 2012-10, Vol.22 (9), p.896-897

2012

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P1.55 Assisted bicycle training delays physical deterioration in boys with Duchenne muscular dystrophy: Results of the randomized controlled trial “no use is disuse”

Neuromuscular disorders : NMD, 2011-10, Vol.21 (9), p.658-658

2011

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G.P.9.04 Dysphagia in spinal muscular atrophy type II, more than a bulbar problem?

Neuromuscular disorders : NMD, 2009-09, Vol.19 (8), p.595-595

2009

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T.P.3.01 Glucocorticoids influence therapeutic efficacy of idebenone (Catena® ) on peak expiratory flow in patients with Duchenne muscular dystrophy (DMD)

Neuromuscular disorders : NMD, 2009-09, Vol.19 (8), p.610-610

2009

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Respiratory and upper limb function as outcome measures in ambulant and non-ambulant subjects with Duchenne muscular dystrophy: A prospective multicentre study

Neuromuscular disorders : NMD, 2019-04, Vol.29 (4), p.261-268

2019

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Don't forget the trunk in Duchenne muscular dystrophy patients: more muscle weakness and compensation than expected

Journal of neuroengineering and rehabilitation, 2019-03, Vol.16 (1), p.44-44, Article 44

2019

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Reduced mandibular range of motion in Duchenne Muscular Dystrophy: predictive factors

Journal of oral rehabilitation, 2015-06, Vol.42 (6), p.430-438

2015

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Critical illness polyneuropathy: a summary of the literature on rehabilitation outcome

Disability and rehabilitation, 2000, Vol.22 (17), p.808-810

Van Der Schaaf, A. Beelen, I. J. M. De Groot, M.

2000

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The Dutch Dystrophinopathy Database: A National Registry with Standardized Patient and Clinician Reported Real-World Data

Journal of neuromuscular diseases, 2024-09, Vol.11 (5), p.1095-1109

2024

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236th ENMC International Workshop Bone protective therapy in Duchenne muscular dystrophy: Determining the feasibility and standards of clinical trials Hoofddorp, The Netherlands, 1–3 June 2018

Neuromuscular disorders : NMD, 2019-03, Vol.29 (3), p.251-259

2019

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Early detection of dysphagia and dysarthria in children with neuromuscular disorders: Diagnostic accuracy of a Screeninglist for Physicians

Journal of pediatric rehabilitation medicine, 2020-01, Vol.13 (1), p.17-23

2020

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Facilitators and Barriers to Wearing Hand Orthoses by Adults with Duchenne Muscular Dystrophy: A Mixed Methods Study Design

Journal of neuromuscular diseases, 2020-01, Vol.7 (4), p.467-475

2020

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Normal height and weight in a series of ambulant Duchenne muscular dystrophy patients using the 10day on/10day off prednisone regimen

Neuromuscular disorders : NMD, 2012-06, Vol.22 (6), p.500-504

2012

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Forty-Five Years of Duchenne Muscular Dystrophy in The Netherlands

Journal of neuromuscular diseases, 2014, Vol.1 (1), p.99-109

2014

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Normal height and weight in a series of ambulant Duchenne muscular dystrophy patients using the 10 day on/10 day off prednisone regimen

Neuromuscular disorders : NMD, 2012-06, Vol.22 (6), p.500-504

2012

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Dystrophic changes in masticatory muscles, related chewing problems and malocclusions in duchenne muscular dystrophy

Predictive factors for masticatory performance in Duchenne muscular dystrophy

D.P.26 3D kinematic and EMG study of the arm function in boys with DMD: A pilot study

Reliability of the walking energy cost test and the six-minute walk test in boys with Duchenne muscular dystrophy

S.P.13 Exploring arm function in FSHD by means of questionnaires

S.P.12 Investigating arm function in boys with DMD by means of an international questionnaire

S.P.14 Exploring arm function in persons with LGMD by means of questionnaires

D.P.28 Arm function in FSHD studied with 3D movement kinematics and EMG

D.P.27 Arm function in LGMD studied with 3D movement kinematics and EMG

P.7.15 What can we learn from an assisted bicycle training in a symptomatic girl with Duchenne muscular dystrophy? A case study

S.P.45 ENERGETIC, a multidisciplinary self-management group program for reconditioning and managing fatigue

P1.55 Assisted bicycle training delays physical deterioration in boys with Duchenne muscular dystrophy: Results of the randomized controlled trial “no use is disuse”

G.P.9.04 Dysphagia in spinal muscular atrophy type II, more than a bulbar problem?

T.P.3.01 Glucocorticoids influence therapeutic efficacy of idebenone (Catena® ) on peak expiratory flow in patients with Duchenne muscular dystrophy (DMD)

Respiratory and upper limb function as outcome measures in ambulant and non-ambulant subjects with Duchenne muscular dystrophy: A prospective multicentre study

Don't forget the trunk in Duchenne muscular dystrophy patients: more muscle weakness and compensation than expected

Reduced mandibular range of motion in Duchenne Muscular Dystrophy: predictive factors

Critical illness polyneuropathy: a summary of the literature on rehabilitation outcome

The Dutch Dystrophinopathy Database: A National Registry with Standardized Patient and Clinician Reported Real-World Data

236th ENMC International Workshop Bone protective therapy in Duchenne muscular dystrophy: Determining the feasibility and standards of clinical trials Hoofddorp, The Netherlands, 1–3 June 2018

Early detection of dysphagia and dysarthria in children with neuromuscular disorders: Diagnostic accuracy of a Screeninglist for Physicians

Facilitators and Barriers to Wearing Hand Orthoses by Adults with Duchenne Muscular Dystrophy: A Mixed Methods Study Design

Normal height and weight in a series of ambulant Duchenne muscular dystrophy patients using the 10day on/10day off prednisone regimen

Forty-Five Years of Duchenne Muscular Dystrophy in The Netherlands

Normal height and weight in a series of ambulant Duchenne muscular dystrophy patients using the 10 day on/10 day off prednisone regimen

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