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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
; Duchenne and Becker muscular dystrophies; Distal myopathies; Limb-girdle muscular dystrophy; Fascioscapulomuneral muscular dystrophy; Myotonic;
Vergelijkbare producten zoals Myopathies, An Issue of Neurologic Clinics
of the genetic defect responsible for Duchenne Muscular Dystrophy and isolation of the protein dystrophin has led to the development of new;
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of muscular dystrophy. It also shows some profiles of excellent clinicians and scientists that have contributed to this book with a description;
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of Duchenne Muscular Dystrophy is traced in detail, and is interwoven with a commentary of Meryon's research which has led to our current;
Vergelijkbare producten zoals The History of a Genetic Disease
The muscular dystrophies (MD) are a group of genetic diseases characterised by progressive weakness and degeneration of the skeletal;
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This book compiles and explores cutting-edge research in degenerative skeletal disorders, such as Duchenne muscular dystrophy and;
Vergelijkbare producten zoals Regenerative Medicine for Degenerative Muscle Diseases
Muscular Dystrophies include a heterogeneous series of diseases that range from childhood to adult onset cases, of difficult diagnosis and;
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Here is a thoughtful new book for professionals who assist persons afflicted with neuromuscular disorders to help them and their families;
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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: the facts is about living with muscular dystrophy and coping with its physical and psychological effects. Written;
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dystrophy; myotonic dystrophy types 1 and 2; and distal muscular dystrophies. This book is useful to basic investigators, as it offers an;
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Dystrophy offers clinicians, researchers, pharmaceutical executives and patient advocacy groups an easy-to-read reference that provides the;
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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;
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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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parts of the muscular system and how they work together to help us move from place to place and to maintain many internal processes, such as a;
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This issue will cover: sinle muscle fiber electrophysiology, skinned muscle fibers, magnetic resonance imaging in muscular dystrophy;
Vergelijkbare producten zoals Recent Advancements in Neuromuscular Medicine, An Issue of Physical Medicine and Rehabilitation Clinics
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