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2015, Fourth edition., Oxford monographs on medical genetics, ISBN 9780199681488, Volume no. 67., ix, 308 pages
Book
2003, 3rd ed., ISBN 9780198515319, x, 270 p., [2] p. of plates
Book
1987, Oxford medical publications., ISBN 0192615564, Volume no. 15., xv, 315
Book
1993, 2nd ed., Oxford medical publications., ISBN 0192623702, Volume no. 24, xv, 392
Book
JOURNAL OF PAEDIATRICS AND CHILD HEALTH, ISSN 1034-4810, 08/2015, Volume 51, Issue 8, pp. 759 - 764
Journal Article
07/2010
Duchenne muscular dystrophy (DMD), an X-linked disorder, is the most common muscular dystrophy in children, presenting in early childhood and characterized by... 
corticosteroids | Continuous positive airway pressure | Duchenne muscular dystrophy | gene therapy | creatine kinase | muscle disease | pediatric
Web Resource
2006, Neurological disease and therapy, ISBN 0824723252, Volume 79., xxii, 461
Duchenne Muscular Dystrophy (DMD) is one of the most prevalent genetic disorders of childhood and currently stands as an incurable condition. This... 
Treatment | Muscular Dystrophy, Duchenne | Duchenne muscular dystrophy | therapy | Medical Genetics | Neurology | Neuroscience | Muscular Dystrophy, Duchenne - therapy
Book
The New England Journal of Medicine, ISSN 0028-4793, 04/2011, Volume 364, Issue 16, pp. 1513 - 1522
Journal Article
2018, Methods in Molecular Biology, ISBN 1493973738, Volume 1687
eBook
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 12/2012, Volume 109, Issue 50, pp. 20614 - 20619
Duchenne muscular dystrophy (DMD) is a devastating genetic muscular disorder of childhood marked by progressive debilitating muscle weakness and wasting, and... 
Artificial satellites | Plasmids | Duchenne muscular dystrophy | Stem cells | Muscles | Electroporation | Muscle fibers | Skeletal muscle | Hypertrophy | Myoblasts | Noncanonical Wnt signaling | REGENERATION | MULTIDISCIPLINARY SCIENCES | MOUSE | SUSCEPTIBILITY | INJURY | SATELLITE STEM-CELLS | MDX MICE | DAMAGE | noncanonical Wnt signaling | SKELETAL-MUSCLE | CONTRACTION | PATHWAY | skeletal muscle | Genetic Therapy | Muscular Dystrophy, Animal - genetics | Muscular Dystrophy, Animal - drug therapy | Muscular Dystrophy, Animal - physiopathology | Humans | Male | RNA, Messenger - metabolism | Muscular Dystrophy, Animal - pathology | Gene Knockdown Techniques | Wnt Proteins - genetics | Mice, Inbred mdx | Plasmids - genetics | Electrochemotherapy | MEF2 Transcription Factors | Myogenic Regulatory Factors - genetics | Signal Transduction | Mice, Inbred C57BL | RNA, Messenger - genetics | Myogenic Regulatory Factors - metabolism | Wnt Proteins - therapeutic use | Regeneration - physiology | Animals | Muscle Contraction - physiology | Muscle, Skeletal - physiopathology | Mice | Wnt Proteins - physiology | Muscle, Skeletal - pathology | Plasmids - administration & dosage | Physiological aspects | Care and treatment | Rapamycin | Health aspects | Muscular dystrophy | Signal transduction | Genetic disorders | Rodents | Cells | Index Medicus | Biological Sciences
Journal Article
Science Signaling, ISSN 1945-0877, 08/2012, Volume 5, Issue 236, pp. ra56 - ra56
Journal Article
1996, Don't turn away, ISBN 0836815971, 48
Describes the life, including medical attention and various daily activities, of a nine-year-old boy with Duchenne muscular dystrophy. 
Duchenne muscular dystrophy | Diseases
Book
2007, Protein epidemiology : understanding human diseases at the level of protein structure and function
Web Resource