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1A 22-year follow-up reveals a variable disease severity in early-onset facioscapulohumeral dystrophy
المؤلفون: Richard J.L.F. Lemmers, Oebele F. Brouwer, Nicol C. Voermans, Baziel G.M. van Engelen, George W. Padberg, Corrie E. Erasmus, Karlien Mul, Caroline R. van Kernebeek, Rianne J.M. Goselink, Silvère M. van der Maarel
المصدر: European Journal of Paediatric Neurology, 22(5), 782-785. ELSEVIER SCI LTD
European Journal of Paediatric Neurology, 22, 5, pp. 782-785
European Journal of Paediatric Neurology, 22, 782-785مصطلحات موضوعية: 0301 basic medicine, Adult, Male, Pediatrics, medicine.medical_specialty, Infantile FSHD, Adolescent, Hearing loss, Natural history, Other Research Donders Center for Medical Neuroscience [Radboudumc 0], Physical examination, Facioscapulohumeral dystrophy, DIAGNOSIS, 03 medical and health sciences, 0302 clinical medicine, Wheelchair, Intellectual disability, Medicine, Humans, Age of Onset, Variable disease severity, medicine.diagnostic_test, business.industry, Dystrophy, Early-onset FSHD, General Medicine, Middle Aged, Disorders of movement Donders Center for Medical Neuroscience [Radboudumc 3], medicine.disease, MUSCULAR-DYSTROPHY, Muscular Dystrophy, Facioscapulohumeral, Clinical trial, 030104 developmental biology, Phenotype, Pediatrics, Perinatology and Child Health, Female, Neurology (clinical), medicine.symptom, business, 030217 neurology & neurosurgery, Neuromuscular disorders, Follow-Up Studies
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca33a22fb1b90995a41c02f559f9f78cTest
https://doi.org/10.1016/j.ejpn.2018.04.013Test -
2دورية أكاديميةA 22-year follow-up reveals a variable disease severity in early-onset facioscapulohumeral dystrophy
المؤلفون: Goselink, R.J.M., Kernebeek, C.R. van, Mul, K., Lemmers, R.J.L.F., Maarel, S.M. van der, Brouwer, O.F., Voermans, N., Padberg, G.W., Erasmus, C.E., Engelen, B.G.M. van
المصدر: European Journal of Paediatric Neurology
مصطلحات موضوعية: Facioscapulohumeral dystrophy, Early-onset FSHD, Infantile FSHD, Neuromuscular disorders, Natural history
العلاقة: lumc-id: 57085600; https://hdl.handle.net/1887/95935Test