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Neurology|August 10, 2019
Genetic determinants of disease severity in the myotonic dystrophy type 1 OPTIMISTIC cohortSarah A Cumming, Cecilia Jimenez-Moreno, Kees Okkersen, et al.
European Neurology|January 31, 2008
Open-label trial of anti-TNF-alpha in dermato- and polymyositis treated concomitantly with methotrexateG J D Hengstman, J L De Bleecker, E Feist, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 1, 2024
Quality of life and support needs in children, adolescents, and young adults with facioscapulohumeral dystrophy, a mixed-method studyJildou N Dijkstra, Nathaniël B Rasing, Helena T M Boon, et al.
Acta Neurologica Belgica|January 13, 2024
Living with facioscapulohumeral muscular dystrophy during the first two COVID-19 outbreaks: a repeated patient survey in the NetherlandsJohanna C W Deenen, Joost Kools, Anna Greco, et al.
Frontiers in Cellular and Infection Microbiology|June 18, 2026
Endothelial glycocalyx injury in bacterial bloodstream infection: biological determinants and association with host response aberrationsHui Wang, Joe M Butler, Erik H A Michels, et al.
Neurology|August 12, 2021
Longitudinal Assessment of Strength, Functional Capacity, Oropharyngeal Function, and Quality of Life in Oculopharyngeal Muscular DystrophyRosemarie H M J M Kroon, Johanna G Kalf, Bert J M de Swart, et al.
BMJ Open|May 20, 2021
Identifying the critically ill paediatric oncology patient: a study protocol for a prospective observational cohort study for validation of a modified Bedside Paediatric Early Warning System score in hospitalised paediatric oncology patientsMarijn Soeteman, Teus H Kappen, Martine van Engelen, et al.
Heart (British Cardiac Society)|April 2, 2010
22q11.2 Deletion Syndrome is under-recognised in adult patients with tetralogy of Fallot and pulmonary atresiaKlaartje van Engelen, Ana Topf, Bernard D Keavney, et al.
Clinical Genetics|August 8, 2009
Neuromuscular features in Marfan syndromeN c Voermans, J Timmermans, N van Alfen, et al.
Neurology|February 19, 2024
Brody Disease, an Early-Onset Myopathy With Delayed Relaxation and Abnormal Gait: A Case Series of 9 ChildrenJamie I Verhoeven, Jasper Kramer, Juergen Seeger, et al.
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