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European Journal of Human Genetics : EJHG|January 13, 2011
Dutch myotonic dystrophy type 2 patients and a North-African DM2 family carry the common European founder haplotypeMarieke J H Coenen, Alide A Tieleman, Mascha M V A P Schijvenaars, et al.Neuromuscular Disorders : NMD|May 19, 2019
Muscle fiber dysfunction contributes to weakness in inclusion body myositisSaskia Lassche, Anke Rietveld, Arend Heerschap, et al.Neuroimage. Clinical|December 8, 2018
Structural white matter networks in myotonic dystrophy type 1Maud van Dorst, Kees Okkersen, Roy P C Kessels, et al.Journal of Neuromuscular Diseases|October 6, 2025
Immunohistological and electron microscopy profile of unique TIRM-MRI guided muscle biopsies of FSHD patientsAnna Greco, Benno Kusters, Ritse Mann, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 26, 2023
Respiratory function in LAMA2-related muscular dystrophy and SELENON-related congenital myopathy, a 1.5-year natural history studyKarlijn Bouman, Jeroen L M van Doorn, Jan T Groothuis, et al.European Journal of Neurology|May 1, 2009
Optimizing referral of patients with neuromuscular disorders to allied health careA J Pieterse, E H C Cup, R P Akkermans, et al.Stem Cell Research & Therapy|September 15, 2024
Ameliorated cellular hallmarks of myotonic dystrophy in hybrid myotubes from patient and unaffected donor cellsRenée H L Raaijmakers, C Rosanne M Ausems, Marieke Willemse, et al.Neuromuscular Disorders : NMD|August 22, 2006
A case of neuromuscular mimicryMaaike M Bos, Sebastiaan Overeem, Baziel G M van Engelen, et al.Journal of Neurology, Neurosurgery, and Psychiatry|February 13, 2009
Redefining the clinical phenotypes of non-dystrophic myotonic syndromesJ Trip, G Drost, H B Ginjaar, et al.Neuromuscular Disorders : NMD|November 6, 2017
Involvement of pelvic girdle and proximal leg muscles in early oculopharyngeal muscular dystrophyB M van der Sluijs, S Lassche, G J Knuiman, et al.Pageof 84