المؤلفون: Hans Timmerman, A.A. Tieleman, Oliver H.G. Wilder-Smith, Judith van Vliet, Aad Verrips, Baziel G.M. van Engelen, Robert van Dongen

المصدر: van Vliet, J, Tieleman, A A, Verrips, A, Timmerman, H, van Dongen, R T M, van Engelen, B G M & Wilder-Smith, O H G 2018, ' Qualitative and Quantitative Aspects of Pain in Patients With Myotonic Dystrophy Type 2 ', Journal of Pain, vol. 19, no. 8, pp. 920-930 . https://doi.org/10.1016/j.jpain.2018.03.006Test
Journal of Pain, 19, 920-930
Journal of Pain, 19, 8, pp. 920-930

مصطلحات موضوعية: Adult, Male, Pain Threshold, musculoskeletal diseases, medicine.medical_specialty, Fibromyalgia, Central sensitization, Myotonic dystrophy type 2, quantitative sensory testing, Anxiety, Healthcare improvement science Radboud Institute for Health Sciences [Radboudumc 18], 03 medical and health sciences, All institutes and research themes of the Radboud University Medical Center, 0302 clinical medicine, Quality of life, Surveys and Questionnaires, Internal medicine, Humans, Myotonic Dystrophy, Medicine, pain, In patient, Muscle, Skeletal, Aged, 030203 arthritis & rheumatology, Central Nervous System Sensitization, fibromyalgia syndrome, Depression, business.industry, Catastrophization, Quantitative sensory testing, central sensitization, Middle Aged, Disorders of movement Donders Center for Medical Neuroscience [Radboudumc 3], medicine.disease, Disease control, Anesthesiology and Pain Medicine, Neurology, Hyperalgesia, Quality of Life, Female, Neurology (clinical), medicine.symptom, business, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b64c530ca8aea05bf21eed3418c86743Test
https://doi.org/10.1016/j.jpain.2018.03.006Test

المؤلفون: Mascha M.V.A.P. Schijvenaars, Baziel G.M. van Engelen, A.A. Tieleman, Laura P.W. Ranum, Marieke J H Coenen, Maike Leferink, Hans Scheffer

المصدر: European Journal of Human Genetics, 19, 5, pp. 567-70
European Journal of Human Genetics, 19, 567-70

مصطلحات موضوعية: musculoskeletal diseases, Population, Functional Neurogenomics Human Movement & Fatigue [DCN 2], Genomic disorders and inherited multi-system disorders Functional Neurogenomics [IGMD 3], Biology, Myotonic dystrophy, Polymorphism, Single Nucleotide, Article, Polymorphism (computer science), Genetics, medicine, Humans, Myotonic Dystrophy, Allele, education, Genomic disorders and inherited multi-system disorders Molecular epidemiology [IGMD 3], Genetics (clinical), Netherlands, education.field_of_study, Haplotype, RNA-Binding Proteins, medicine.disease, Founder Effect, Morocco, Haplotypes, Microsatellite, Trinucleotide repeat expansion, Founder effect, Myotonic Disorders

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9665d6336bad3899b727c970cacb4602Test
https://hdl.handle.net/2066/96834Test