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, and psychosocial issues of the specific disorder. Beyond the clinical and research importance of Muscular Dystrophy and Other Neuromuscular;
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Congential myopathies, Muscular dystropies, Glycogen storage diseases of muscle, and Idiopathic and Inflammatory myopathies are presented;
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cardio-pulmonary care. The authors also investigate other forms of pharmacological, cellular and gene therapies. Duchenne Muscular Dystrophy;
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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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muscular dystrophy 2A; dysferlinopathies; limb-girdle muscular dystrophy 2H and the role of TRIM32; and caveolinopathies. The book also covers;
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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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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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Muscular Dystrophies include a heterogeneous series of diseases that range from childhood to adult onset cases, of difficult diagnosis and;
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patients with autism, epilepsy, Multiple Sclerosis, Parkinson's disease, Muscular Dystrophy, and other diseases. This work reveals the science;
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muscular dystrophy spinal muscular atrophy, hereditary neuropathies, congenital and metabolic neuropathies and myasthenic syndromes. Best practice;
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While most spine deformities such as scoliosis, kyphosis, and lordosis are idiopathic, muscular dystrophy, cerebral palsy, spinal cord;
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of the face, shoulder blades and upper arms are among the most severely affected. It is the third most common inherited muscular dystrophy;
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This practical and concise guide offers an overview of muscular dystrophy's complicated features, treatment options and general resources;
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The muscular dystrophies (MD) are a group of genetic diseases characterised by progressive weakness and degeneration of the skeletal;
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is of high importance in the diagnosis and monitoring of diseases and thus is examined with relation to DM1 (myotonic dystrophy type 1) patients;
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A child with Duchenne Muscular Dystrophy (DMD) faces a childhood and adolescence with a disability that develops gradually. This book;
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-mediated neuromuscular diseases, including Guillain-Barre syndrome and other autoimmune neuropathies, the Lambert-Eaton myasthenic syndrome;
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. Muscular system diseases and disorders, symptoms and treatments are explored, including muscular dystrophy and hypertrophy. This reference;
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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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Huntington's diseases, amyotrophic sclerosis, multiple sclerosis, muscular dystrophy and retinal degeneration, in which stem cells could potentially be;
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/Thalessemia; Muscle dystrophy; Spinal muscular atrophy; Wilson Disease; Hemophilia; National and International Accreditation; Blood Banking;
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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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There is no doubt that the study of the muscular dystrophies in recent years has been exciting and rewarding. It has attracted the;
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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;
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, Huntington's chorea and muscular dystrophy.;
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