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Epigenetics|April 24, 2012
Correlation analysis of clinical parameters with epigenetic modifications in the DUX4 promoter in FSHDJudit Balog, Peter E Thijssen, Jessica C de Greef, et al.Journal of Neurology, Neurosurgery, and Psychiatry|January 20, 2006
Ptosis aggravates dysphagia in oculopharyngeal muscular dystrophyB J M de Swart, B M van der Sluijs, A M C Vos, et al.Neuromuscular Disorders : NMD|September 27, 2008
Clinical and molecular overlap between myopathies and inherited connective tissue diseasesN C Voermans, C G Bönnemann, P A Huijing, et al.Journal of Exposure Science & Environmental Epidemiology|July 5, 2007
Risk management measures for chemicals in consumer products: documentation, assessment, and communication across the supply chainYuri Bruinen de Bruin, Pertti Bert Hakkinen, Majlinda Lahaniatis, et al.Annals of Neurology|July 17, 1998
Genetic characteristics of myoadenylate deaminase deficiencyH T Verzijl, B G van Engelen, J A Luyten, et al.Plos One|July 9, 2025
Signals of complexity and fragmentation in accelerometer dataEls Weinans, Jerrald L Rector, Sarah Charman, et al.Molecular Therapy. Methods & Clinical Development|October 26, 2019
Intrinsic Myogenic Potential of Skeletal Muscle-Derived Pericytes from Patients with Myotonic Dystrophy Type 1Cornelia Rosanne Maria Ausems, Renée Henrica Lamberta Raaijmakers, Walterus Johannes Antonius Adriana van den Broek, et al.Disability and Rehabilitation|September 14, 2007
Development of a tool to guide referral of patients with neuromuscular disorders to allied health services. Part twoAllan J Pieterse, Edith H C Cup, Simone Knuijt, et al.European Neurology|June 26, 2003
Successful treatment of dermatomyositis and polymyositis with anti-tumor-necrosis-factor-alpha: preliminary observationsG J D Hengstman, F H J van den Hoogen, P Barrera, et al.BMC Neurology|July 15, 2011
Living with myotonic dystrophy; what can be learned from couples? A qualitative studyEdith H C Cup, Astrid Kinébanian, Ton Satink, et al.Pageof 84