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Duchenne Muscular Dystrophy 4 E

Duchenne Muscular Dystrophy, an inherited and progressive muscle wasting disease, is one of the most common single gene disorders found;

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Myopathies, An Issue of Neurologic Clinics

; Duchenne and Becker muscular dystrophies; Distal myopathies; Limb-girdle muscular dystrophy; Fascioscapulomuneral muscular dystrophy; Myotonic;

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Duchenne Muscular Dystrophy

Duchenne Muscular Dystrophy (DMD) is one of the most prevalent genetic disorders of childhood and currently stands as an incurable;

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A Guide to Duchenne Muscular Dystrophy

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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The History of a Genetic Disease

Duchenne Muscular Dystrophy is a disease that only affects males, with an incidence of around 1 in 3500 new-born baby boys. Its relentless;

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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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Trends in Muscular Dystrophy Research

muscles which control movement. There are many forms of muscular dystrophy, some noticeable at birth (congenital muscular dystrophy), others;

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Regenerative Medicine for Degenerative Muscle Diseases

This book compiles and explores cutting-edge research in degenerative skeletal disorders, such as Duchenne muscular dystrophy and;

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Muscular Dystrophy

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

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

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

muscular dystrophy 2A; dysferlinopathies; limb-girdle muscular dystrophy 2H and the role of TRIM32; and caveolinopathies. The book also covers;

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Muscular Dystrophy and Other Neuromuscular Diseases

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)

Facioscapulohumeral muscular dystrophy (FSHD) is a genetic disorder involving slowly progressive muscle degeneration in which the muscles;

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Management of Neuromuscular Disorders in Children

muscular dystrophy spinal muscular atrophy, hereditary neuropathies, congenital and metabolic neuropathies and myasthenic syndromes. Best practice;

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Muscular Dystrophy Duchenne Modifying Genes and Pathways

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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Muscular Dystrophy

This practical and concise guide offers an overview of muscular dystrophy's complicated features, treatment options and general resources;

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Triathlon - It HURTS

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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Molecular Mechanisms of Muscular Dystrophies

, rather than a comprehensive treatise on every muscular dystrophy so far characterized.;

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Cytoskeleton

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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Noninvasive Ventilation, An Issue of Sleep Medicine Clinics

Care of Duchenne Muscular Dystrophy; Management of Chronic Respiratory Failure in COPD - High and Low Intensity Ventilation; Management of Rare;

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Human Genetics

, Huntington's chorea and muscular dystrophy.;

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Heartsongs

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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Enigmajik

Written specifically for people with muscular dystrophy and their families, this guide answers many of the questions asked about how and;

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Recent Advancements in Neuromuscular Medicine, An Issue of Physical Medicine and Rehabilitation Clinics

This issue will cover: sinle muscle fiber electrophysiology, skinned muscle fibers, magnetic resonance imaging in muscular dystrophy;

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Case Studies in Neuromuscular Disorders, An Issue of Neurologic Clinics

Dystrophy, Spinal Muscular Atrophy, Advances in Clinical Genetics, FSHD New Diagnosis and Therapies, Congenital Myasthenic Syndrome, Diabetic;

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