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Dysphagia and Dysarthria in Children with Neuromuscular Diseases, a Prevalence Study
Kooi-van Es M, Erasmus CE, de Swart BJM, et al.
Journal of Neuromuscular Diseases, 2020
Clinical, morphological and genetic characterization of Brody disease: an international study of 40 patients
Molenaar JP, Verhoeven JI, Rodenburg RJ, et al.
Brain : a journal of neurology, 2020, 143, 2, p 452
Ophthalmological findings in facioscapulohumeral dystrophy
Goselink RJM, Schreur V, van Kernebeek CR, et al.
Brain communications, 2020, 1, 1
Early onset as a marker for disease severity in facioscapulohumeral muscular dystrophy
Goselink RJM, Goselink RJM, Mul K, et al.
Neurology, 2019, 92, 4
Panel-Based Exome Sequencing for Neuromuscular Disorders as a Diagnostic Service
Westra D, Schouten MI, Stunnenberg BC, et al.
Journal of Neuromuscular Diseases, 2019, 6, 2, p 241
Functional impairments, fatigue and quality of life in RYR1-related myopathies: A questionnaire study
van Ruitenbeek E, Custers JAE, Verhaak C, et al.
Neuromuscular disorders : NMD, 2019, 29, 1, p 30
A 22-year follow-up reveals a variable disease severity in early-onset facioscapulohumeral dystrophy
Goselink RJM, van Kernebeek CR, Mul K, et al.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society, 2018
Facioscapulohumeral Dystrophy in Childhood: A Nationwide Natural History Study
Goselink RJM, Goselink RJM, Schreuder THA, et al.
Annals of neurology, 2018, 84, 5, p 627
Early onset facioscapulohumeral dystrophy - a systematic review using individual patient data
Goselink RJM, Voermans NC, Okkersen K, et al.
Neuromuscular disorders : NMD, 2017, 27, 12, p 1077
Facioscapulohumeral dystrophy in children: design of a prospective, observational study on natural history, predictors and clinical impact (iFocus FSHD)
Goselink RJ, Schreuder TH, Mul K, et al.
BMC neurology, 2016, 16, 138
Dystrophic changes in masticatory muscles related chewing problems and malocclusions in Duchenne muscular dystrophy
van den Engel-Hoek L, de Groot IJ, Sie LT, et al.
Neuromuscular disorders : NMD, 2016, 26, 6, p 354
Primary cataract as a key to recognition of myotonic dystrophy type 1
Voermans NC, Erasmus CE, Ockeloen CW, et al.
European journal of ophthalmology, 2015, 25, 4, p e46
Feeding and swallowing disorders in Pediatric Neuromuscular diseases : An overview
van den Engel-Hoek L, De Groot IJM, de Swart BJM, et al.
Journal of Neuromuscular Diseases, 2015, 2, 4, p. 357-369
Dysphagia in spinal muscular atrophy type II. More than a bulbar problem ?
van den Engel-Hoek L, Erasmus CE, van Bruggen HW, et al.
Neurology, 2009, 73, 21, p. 1787-1791
Is head balance a major determinant for swallowing problems in patients with spinal muscular atrophy type 2 ?
van den Engel-Hoek L, de Swart BJM, Erasmus CE
Journal of child neurology, 2008, 23, 8, p. 919-921
