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المؤلفون: Johanne M. Groothuismink, Manon Damen, Mascha M.V.A.P. Schijvenaars, Marlies Schimmel-Naber, A.A. Tieleman, Marieke J H Coenen
المصدر: Journal of Neuromuscular Diseases, 8, 715-722
Journal of Neuromuscular Diseases, 8, 4, pp. 715-722مصطلحات موضوعية: 0301 basic medicine, Adult, Male, India, Single-nucleotide polymorphism, 030105 genetics & heredity, Biology, 03 medical and health sciences, Young Adult, 0302 clinical medicine, All institutes and research themes of the Radboud University Medical Center, Genetic variation, SNP, Humans, Myotonic Dystrophy, Gene, Aged, Netherlands, Genetics, Suriname, Portugal, Haplotype, Intron, Middle Aged, Disorders of movement Donders Center for Medical Neuroscience [Radboudumc 3], Morocco, Neurology, Haplotypes, Inflammatory diseases Radboud Institute for Health Sciences [Radboudumc 5], Microsatellite, Female, Neurology (clinical), Trinucleotide repeat expansion, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6129650892a4acf407400b9ea40a10d8Test
https://hdl.handle.net/2066/236726Test -
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المؤلفون: Anneke J. van der Kooi, A.A. Tieleman, Judith van Vliet, George F. Borm, Baziel G.M. van Engelen, Jan B.M.J. Jansen
المساهمون: ANS - Amsterdam Neuroscience, Neurology
المصدر: Neuromuscular disorders, 18(8), 646-649. Elsevier Limited
Neuromuscular Disorders, 18, 8, pp. 646-9
Neuromuscular Disorders, 18, 646-9مصطلحات موضوعية: Adult, Male, Risk, musculoskeletal diseases, medicine.medical_specialty, Abdominal pain, Constipation, Gastrointestinal Diseases, Disease, Gastroenterology, Myotonic dystrophy, Proximal myotonic myopathy, Internal medicine, Surveys and Questionnaires, medicine, Perception and Action [DCN 1], Humans, Myotonic Dystrophy, Molecular gastro-enterology and hepatology [IGMD 2], Defecation, Gastrointestinal Transit, Genetics (clinical), Aged, Netherlands, Aged, 80 and over, Human Movement & Fatigue [NCEBP 10], Gastrointestinal tract, business.industry, Effective Hospital Care [EBP 2], Middle Aged, medicine.disease, Dysphagia, Health Surveys, Neuromuscular development and genetic disorders [UMCN 3.1], Surgery, Abdominal Pain, Neurology, Genetic defects of metabolism [UMCN 5.1], Evaluation of complex medical interventions [NCEBP 2], Pediatrics, Perinatology and Child Health, Female, Neurology (clinical), medicine.symptom, business, Deglutition Disorders, Functional Neurogenomics [DCN 2]
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41226f054e01e1586459a9814abc5ecfTest
https://doi.org/10.1016/j.nmd.2008.05.010Test -
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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, 567-70مصطلحات 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