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Recommended Books on Muscular Dystrophy
Facioscapulohumeral Muscular Dystrophy (FSHD): Clinical Medicine and Molecular Cell Biology Facioscapulohumeral muscular dystrophy (FSHD) is a genetic disorder involving slowly progressive muscle degeneration in which the muscles of the face, shoulder blades and upper arms are among the most severely affected. It is the third most common inherited muscular dystrophy, affecting 1 in 20,000. The search for the molecular basis of the disease is of interest to all genetic researchers, involving a deletion outside a coding region resulting in over-expression of adjacent genes. This volume summarizes the current understanding of the disorder, including clinical, molecular and therapeutic aspects.
Muscular Dystrophy Medical Guide The Muscular Dystrophy Medical Guide is a publication which has been designed to better help readers understand Muscular Dystrophy. This Qontro Medical Guide has been designed with the reader in mind, and is a useful information source for readers at all levels looking to learn more about Muscular Dystrophy. The Muscular Dystrophy Medical Guide is highly recommended for those interested in understanding and learning more about Muscular Dystrophy.
2009 Conquering Muscular Dystrophy (MD) - The Empowered Patient's Complete Reference - Diagnosis, Treatment Options, Prognosis (Two CD-ROM Set) This up-to-date and comprehensive set of two CD-ROM discs provides a superb collection of authoritative documents on the subject of muscular dystrophy (MD). Muscular dystrophy (MD) refers to a group of more than 30 inherited diseases that cause muscle weakness and muscle loss. Some forms of MD appear in infancy or childhood, while others may not appear until middle age or later. The different muscular dystrophies vary in who they affect and the symptoms. All forms of MD grow worse as the person's muscles get weaker. Most people with MD eventually lose the ability to walk. There is no cure for muscular dystrophy. Treatments include physical and speech therapy, orthopedic devices, surgery and medications. Some people with muscular dystrophy have mild cases that worsen slowly. Others cases are disabling and severe. For patients, practical information is provided in clearly written patient education documents. For medical professionals, doctor reference tools and texts have detailed technical information and clinical background material. There is no other reference that is as fast, convenient, and portable - everything you need to know, from the federal sources you trust. This thoroughly researched collection presents vital information from many authoritative sources: Food and Drug Administration (FDA), Centers for Disease Control (CDC), National Institutes of Health (NIH) and the relevant institute for this disease, and others. In addition to the comprehensive disease-specific coverage, this disc set also includes our Medical Encyclopedia, a $19.95 value! The Encyclopedia presents a collection of official documents about a wide range of medical topics, diseases, illnesses, health and wellness. There is vital information from the National Institutes of Health (NIH), the Centers for Disease Control (CDC), National Cancer Institute, and more. Topics covered include: major diseases, including cancer, heart and vascular disease, stroke, blood diseases and disorders, lung diseases, and neurological disorders such as dementia and epilepsy * CDC Health Topics A to Z, Foodborne Illnesses, Infants and Children, Injuries, Occupational Health, Older Adults, Women * CDC Travelers' Health - Destinations, Vaccinations, Diseases, Mosquito, Tick, Food, Water, Clinics, Yellow Book, Children, Airplanes, Cruise Ships, Special Needs, Relief Workers * Dietary Guidelines * NIH A to Z from abnormalities to X-rays. Since navigating the Internet to find additional non-governmental medical information can be confusing, we've also provided our exclusive "Guide to Leading Medical Websites" with updated links to 67 of the best sites for medical information! Built-in weblinks let you quickly check for the latest clinical updates directly from the government and the best commercial portals, news sites, reference/textbook/non-commercial portals, and health organizations.
Duchenne Muscular Dystrophy: Advances in Therapeutics (Neurological Disease and Therapy) Duchenne Muscular Dystrophy (DMD) is one of the most prevalent genetic disorders of childhood and currently stands as an incurable condition. This authoritative guide provides a clear overview of the latest current and experimental approaches to the treatment of DMD and examines the clinical, genetic, and pathophysiological aspects of the disease in the context of emerging therapeutic modalities. The only available source on the subject, this reference emphasizes the importance of accurate diagnosis, carrier detection, and genetic counseling, and supplies state-of-the-art contributions on pharmacological interventions, regenerative medicine, and gene therapy.
Duchenne Muscular Dystrophy Univ. of Edinburgh, UK. Provides an update on research and new theories concerning Duchenne muscular dystrophy. Describes screening, prenatal diagnosis, genetic counseling, and management. Text provides new understanding of the progression of the disease and advances in management of respiratory and cardiac symptoms. Previous edition: c1993.
The Muscular Dystrophies The muscular dystrophies are an important group of inherited disorders. They are characterized by muscle wasting and weakness, but vary considerably in their clinical manifestations and severity. This text reviews our understanding of the most important of these disorders. In many instances, the genes and protein products responsible for the dystrophies have been identified and it is now possible to establish a precise diagnosis, detect preclinical cases, identify carriers and offer prenatal dianostic testing. The book goes on to describe the opportunities for management of the symptoms through respiratory care, physiotherapy and surgical correction of contracture, and examines the potential, in the future, for effective treatment utilizing the new techniques of gene and cell therapy. Professor Emery has invited chapters from the leading international experts in the field providing a unique insight into the current situation and the hopes for the future.
A Wing and a Prayer: An Artist's Journey with Muscular Dystrophy A Wing And A Prayer is a story about growing up with a disability, not only her own but her sisters too. Diagnosed at age five with Limb Girdle Muscular Dystrophy Barb shares her experiences from losing her ability to walk to regaining freedom to move about by using a wheelchair. Not knowing what the future held, she decided to pursue her interest in art. Barb speaks of the influence of a childhood friend and the decision to go away to college. Upon receiving a BFA, life took a turn for the worst. Within a period of seven months a machine was breathing for her and she lost two very important people in her life. She tells what life is like being ventilator dependent, about living life as an artist, having to depend on her nurses and caregivers and relying on her strong faith in God.
Muscular Dystrophy in Children: A Guide for Families Written for children with muscular dystrophy (MD) and their families, friends and teachers, this book is a guide through the often-frightening labyrinth of medical care that follows the diagnosis of MD. Forthright, clear, supportive and empowering, the book helps readers understand the significance of the signs and symptoms of the disease, treatment options, the disease's probable course and what may affect it, and choices in directing therapy. This incomparable guide covers:
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The diagnosis of childhood muscular dystrophy
* Early childhood
* Prepuberty
* Fractures
* Adolescence
* Late problems
* Caregiver's self-help guide
* New research
* Suggestions for further reading.
Filled with state-of-the-art information, it honestly addresses questions and concerns. Like having the finest doctor with a wonderful bedside manner at your side throughout, this book clearly defines medical options at every stage of the disease and offers hope and guidance-even when it may seem that little or nothing can be done.
Moonrise: One Family, Genetic Identity, and Muscular Dystrophy In this riveting and thought-provoking memoir about her family, her son Ansel, and his progressive disability, Penny Wolfson embarks on a quest that explores special education, giftedness, prenatal testing, and the genes she shares with her mother, sisters, and son. While Moonrise is an eloquent narrative of one family, it also asks profound questions about our genetic selves.
Muscular Dystrophy: theFacts European Neuromuscular Centre, Baarn, The Netherlands. Discusses living with muscular dystrophy and coping with its physical effects. Written for people with this illness and their families, it answers many questions asked by those diagnosed with muscular dystrophy. Previous edition: c1994. Softcover.
© 2005-2010 Muscular Dystrophy Research Today. All Rights Reserved.
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