المؤلفون: Fran H.P. Smulders, A.A. Tieleman, Joost Raaphorst, Joost Berends, Baziel G.M. van Engelen, Nicol C. Voermans, Corinne G.C. Horlings

المساهمون: Neurology, Amsterdam Neuroscience - Neurodegeneration

المصدر: Neuromuscular Disorders, 29, 758-765
Neuromuscular disorders, 29(10). Elsevier Limited
Neuromuscular Disorders, 29, 10, pp. 758-765

مصطلحات موضوعية: Adult, Male, musculoskeletal diseases, 0301 basic medicine, congenital, hereditary, and neonatal diseases and abnormalities, Pediatrics, medicine.medical_specialty, Myotonic dystrophy, Head trauma, 03 medical and health sciences, All institutes and research themes of the Radboud University Medical Center, 0302 clinical medicine, medicine, Humans, Myotonic Dystrophy, Clinical significance, Prospective Studies, Prospective cohort study, Genetics (clinical), Balance (ability), Muscle Weakness, business.industry, Incidence (epidemiology), Age Factors, Muscle weakness, Middle Aged, Disorders of movement Donders Center for Medical Neuroscience [Radboudumc 3], medicine.disease, 030104 developmental biology, Neurology, Pediatrics, Perinatology and Child Health, Accidental Falls, Female, Neurology (clinical), medicine.symptom, business, 030217 neurology & neurosurgery, Fall prevention

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2cb2fd0c47cacebd58209292dda3a297Test
https://doi.org/10.1016/j.nmd.2019.08.012Test

المؤلفون: William Howlett, H.A. van Duyvenvoorde, A.A. Tieleman, O.J. Igogo, Marieke C. J. Dekker, Ben C.J. Hamel

المصدر: Neuromuscular Disorders, 29, 317-320
Neuromuscular Disorders, 29, 4, pp. 317-320
Neuromuscular Disorders, 29(4), 317-320. PERGAMON-ELSEVIER SCIENCE LTD

مصطلحات موضوعية: 0301 basic medicine, Male, Pediatrics, medicine.medical_specialty, Weakness, Other Research Donders Center for Medical Neuroscience [Radboudumc 0], Global neurology, Muscle disorder, Medical care, Tanzania, 03 medical and health sciences, 0302 clinical medicine, Genotype, parasitic diseases, Medicine, Humans, Muscular dystrophy, Genetics (clinical), biology, business.industry, Middle Aged, Disorders of movement Donders Center for Medical Neuroscience [Radboudumc 3], biology.organism_classification, medicine.disease, Pedigree, Muscular Dystrophy, Duchenne, 030104 developmental biology, Neurology, Becker muscular dystrophy, Pediatrics, Perinatology and Child Health, Africa, Neurology (clinical), medicine.symptom, business, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0752a7384cf77838f3b6b66d836efc0Test
http://hdl.handle.net/2066/207145Test

المؤلفون: R.J.H. Ensink, B.J.M. de Swart, S. Knuijt, B.G.M. van Engelen, J.A. van der Vliet, A.A. Tieleman

المصدر: Neuromuscular Disorders, 19, 196-8
Neuromuscular Disorders, 19, 3, pp. 196-8
Neuromuscular Disorders, 19, 196-198

مصطلحات موضوعية: Adult, Male, musculoskeletal diseases, Pediatrics, medicine.medical_specialty, Quality of nursing and allied health care [NCEBP 6], Myotonic dystrophy type 2, Aspiration pneumonia, Severity of Illness Index, Myotonic dystrophy, Endoscopy, Gastrointestinal, Disability Evaluation, Age Distribution, Esophagus, Swallowing, Weight loss, Surveys and Questionnaires, medicine, Perception and Action [DCN 1], otorhinolaryngologic diseases, Humans, Myotonic Dystrophy, Genetic Predisposition to Disease, Muscle, Skeletal, Genetics (clinical), Aged, Human Movement & Fatigue [NCEBP 10], business.industry, Data Collection, digestive, oral, and skin physiology, Middle Aged, Speech Therapist, medicine.disease, Dysphagia, Deglutition, Surgery, Neurology, Pediatrics, Perinatology and Child Health, Pharynx, Female, Neurology (clinical), medicine.symptom, Underweight, Deglutition Disorders, business

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14692239c72066e6a751dfc5d9d5731dTest
https://hdl.handle.net/20.500.12470/577Test

المؤلفون: A.A. Tieleman, Pieter E. Vos, Ton M. van der Vliet

المصدر: Neurology, 67, 3, pp. 535-6
Neurology, 67, 535-6

مصطلحات موضوعية: Male, Pediatrics, medicine.medical_specialty, Subarachnoid hemorrhage, Hemorrhage, Neuroinformatics [DCN 3], Aneurysm, Cognitive neurosciences [UMCN 3.2], Prepontine Cistern, Familial predisposition, medicine, Genetic predisposition, Perception and Action [DCN 1], Humans, Genetic Predisposition to Disease, cardiovascular diseases, First-degree relatives, Family history, Family Health, business.industry, Subarachnoid Hemorrhage, medicine.disease, nervous system diseases, Surgery, Etiology, Female, Neurology (clinical), Functional Imaging [UMCN 1.1], business, Functional Neurogenomics [DCN 2]

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::faa1bbafbaa7ab055656bbfe8eb42ddcTest
https://pubmed.ncbi.nlm.nih.gov/16894127Test