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; Duchenne and Becker muscular dystrophies; Distal myopathies; Limb-girdle muscular dystrophy; Fascioscapulomuneral muscular dystrophy; Myotonic;
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Duchenne Muscular Dystrophy, an inherited and progressive muscle wasting disease, is one of the most common single gene disorders found;
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Duchenne Muscular Dystrophy (DMD) is one of the most prevalent genetic disorders of childhood and currently stands as an incurable;
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The prognosis for individuals with Duchenne Muscular Dystrophy (DMD) is improving, with some men with DMD living into their 30s and 40s;
Vergelijkbare producten zoals A Guide to Duchenne Muscular Dystrophy
A child with Duchenne Muscular Dystrophy (DMD) faces a childhood and adolescence with a disability that develops gradually. This book;
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Duchenne Muscular Dystrophy is a disease that only affects males, with an incidence of around 1 in 3500 new-born baby boys. Its relentless;
Vergelijkbare producten zoals The History of a Genetic Disease
muscles which control movement. There are many forms of muscular dystrophy, some noticeable at birth (congenital muscular dystrophy), others;
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This book compiles and explores cutting-edge research in degenerative skeletal disorders, such as Duchenne muscular dystrophy and;
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Muscular Dystrophies include a heterogeneous series of diseases that range from childhood to adult onset cases, of difficult diagnosis and;
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Muscular dystrophy: the facts is about living with muscular dystrophy and coping with its physical and psychological effects. Written;
Vergelijkbare producten zoals Muscular Dystrophy
Muscular dystrophy: the facts is about living with muscular dystrophy and coping with its physical and psychological effects. Written;
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muscular dystrophy 2A; dysferlinopathies; limb-girdle muscular dystrophy 2H and the role of TRIM32; and caveolinopathies. The book also covers;
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as Duchenne and myotonic muscular dystrophy, multiple sclerosis, amyotrophic lateral sclerosis, Friedeich's ataxia, and Charcot-Marie-Tooth;
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Facioscapulohumeral muscular dystrophy (FSHD) is a genetic disorder involving slowly progressive muscle degeneration in which the muscles;
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muscular dystrophy spinal muscular atrophy, hereditary neuropathies, congenital and metabolic neuropathies and myasthenic syndromes. Best practice;
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DMD is the most common muscular dystrophy in childhood and incurable to date. It is caused by the absence of dystrophin, what influences;
Vergelijkbare producten zoals Muscular Dystrophy Duchenne Modifying Genes and Pathways
This practical and concise guide offers an overview of muscular dystrophy's complicated features, treatment options and general resources;
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Duchenne Muscular Dystrophy, a debilitating and fatal disorder. Their collective goal was to support Harrison's Fund, set up in 2012 to support;
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, rather than a comprehensive treatise on every muscular dystrophy so far characterized.;
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of cytoskeletal components of uPAR expression and cellular distribution are examined as well. In addition, Duchenne Muscular Dystrophy (DMD) is an;
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Care of Duchenne Muscular Dystrophy; Management of Chronic Respiratory Failure in COPD - High and Low Intensity Ventilation; Management of Rare;
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, Huntington's chorea and muscular dystrophy.;
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A new edition of the beloved poetry collection includes sixteen pages of new poems and illustrations, written by eleven-year-old muscular;
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This issue will cover: sinle muscle fiber electrophysiology, skinned muscle fibers, magnetic resonance imaging in muscular dystrophy;
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Dystrophy, Spinal Muscular Atrophy, Advances in Clinical Genetics, FSHD New Diagnosis and Therapies, Congenital Myasthenic Syndrome, Diabetic;
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