المؤلفون: Norma B. Romero, Gillian Butler-Browne, Herbert Budka, Julia Wanschitz, Bruno Eymard, Michael B. Fischer, Odile Dubourg, Romana Höftberger, Olivier Benveniste, E. Lacène, Thomas Voit, Serge Herson

المساهمون: University of Zurich, Wanschitz, Julia V

المصدر: Neuromuscular Disorders
Neuromuscular Disorders; Vol 23

مصطلحات موضوعية: Male, Cellular differentiation, MyoD, Polymyositis, Muscular Dystrophies, 0302 clinical medicine, Satellite cells, Myocyte, Genetics(clinical), Genetics (clinical), Aged, 80 and over, Sporadic inclusion body myositis, 0303 health sciences, Myogenesis, PAX7 Transcription Factor, Cell Differentiation, Middle Aged, Cell biology, 2728 Neurology (clinical), Myogenic Regulatory Factors, Neurology, Female, Myogenin, Adult, musculoskeletal diseases, 2716 Genetics (clinical), Adolescent, education, 10208 Institute of Neuropathology, Clinical Neurology, 610 Medicine & health, Biology, Article, Dermatomyositis, Myositis, Inclusion Body, Young Adult, 03 medical and health sciences, MyoD Protein, parasitic diseases, medicine, Humans, Regeneration, Endothelium, 2735 Pediatrics, Perinatology and Child Health, Pediatrics, Perinatology, and Child Health, Muscle, Skeletal, Aged, Cell Proliferation, 030304 developmental biology, medicine.disease, Microvascularization, Case-Control Studies, 2808 Neurology, Microvessels, Pediatrics, Perinatology and Child Health, Myogenic regulatory factors, Immunology, 570 Life sciences, biology, Neurology (clinical), 030217 neurology & neurosurgery

وصف الملف: Wanschitz_NeurMuscDis_2012.pdf - application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::362cc3781842469b7e421487afc539eaTest

المؤلفون: Ans T. van der Ploeg, Linda E.M. van den Berg, Pieter A. van Doorn, Robert M. Verdijk, Juna M. de Vries, Arnold J. J. Reuser

المصدر: Neuromuscular Disorders; Vol 21

مصطلحات موضوعية: myalgia, Adult, Pathology, medicine.medical_specialty, Biopsy, Clinical Neurology, Lysosomal storage disease, Glycogenosis type II, Disease, Gene mutation, Biology, 03 medical and health sciences, 0302 clinical medicine, medicine, Myocyte, Muscle pathology, Humans, Genetics(clinical), Pediatrics, Perinatology, and Child Health, Genetics (clinical), Fatigue, 030304 developmental biology, 0303 health sciences, Muscle biopsy, medicine.diagnostic_test, Glycogen Storage Disease Type II, Enzyme replacement therapy, medicine.disease, Muscle fiber type, 3. Good health, Muscle Fibers, Slow-Twitch, Neurology, Pediatrics, Perinatology and Child Health, Physical therapy, Female, Neurology (clinical), medicine.symptom, 030217 neurology & neurosurgery, Limb-girdle muscular dystrophy

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a79be9f4b89f7b086cf585a93d36d03Test

المصدر: Neuromuscular Disorders.

مصطلحات موضوعية: 0303 health sciences, education.field_of_study, medicine.medical_specialty, Neuromuscular disease, Population, Emerin, Cardiomyopathy, Biology, medicine.disease, 03 medical and health sciences, 0302 clinical medicine, Endocrinology, Neurology, Internal medicine, Pediatrics, Perinatology and Child Health, medicine, Myocyte, Neurology (clinical), Emery–Dreifuss muscular dystrophy, Muscular dystrophy, education, 030217 neurology & neurosurgery, Genetics (clinical), 030304 developmental biology, Muscle contracture

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::0c879fb6a33807b3da2d3dc506cf57b6Test