Muscular Dystrophy And Other Neuromuscular Diseases
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Muscular Dystrophy And Other Neuromuscular Diseases
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Author : Leon I. Charash
language : en
Publisher: Routledge
Release Date : 2014-09-19
Muscular Dystrophy And Other Neuromuscular Diseases written by Leon I. Charash and has been published by Routledge this book supported file pdf, txt, epub, kindle and other format this book has been release on 2014-09-19 with Medical categories.
Here is a thoughtful new book for professionals who assist persons afflicted with neuromuscular disorders to help them and their families adapt to lifestyle changes accompanying the onset of these disorders. Health care professionals provide strategies to maintain the psychosocial well-being of children and adults with neuromuscular disorders which, in addition to physical damage, also assault the sense of self and challenge the individual’s ability to move and communicate. Chapters describe the psychosocial aspects of a variety of neuromuscular diseases such as Duchenne and myotonic muscular dystrophy, multiple sclerosis, amyotrophic lateral sclerosis, Friedeich’s ataxia, and Charcot-Marie-Tooth disease. The distinctive characteristics of each disease are examined with special attention given to the natural history, treatment, management, and psychosocial issues of the specific disorder. Beyond the clinical and research importance of Muscular Dystrophy and Other Neuromuscular Diseases, it also addresses the anxiety, doubts, and questions felt by patients with chronic progressive disabilities and their families. This helpful guide is unique in the way it features the interaction of professionals in the social services, psychology, religion, and various medical specialties in the care and treatment of these patients. Professionals in all of these disciplines, as well as the patients and families afflicted by these disorders, will benefit from this valuable resource.
Muscular Dystrophy And Other Neuromuscular Disorders
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Author : Molly Jones
language : en
Publisher: Mason Crest Publishers
Release Date : 2018
Muscular Dystrophy And Other Neuromuscular Disorders written by Molly Jones and has been published by Mason Crest Publishers this book supported file pdf, txt, epub, kindle and other format this book has been release on 2018 with Young Adult Nonfiction categories.
Every physical action you takewhether you want to walk or run, type on your phone, or raise your hand in classdepends on clear lines of communication between your brain and your muscles. If that communication breaks down, a condition known as a neuromuscular disorder may be to blame. This book explains the many different kinds of neuromuscular disorders that may occur, including many types of muscular dystrophy, ALS, and Parkinsons disease.Diseases and disorders transform the experience of childhood, forcing kids to confront adult concerns that we wish they could avoid. The set Living with Diseases and Disorders provides reliable facts about some of the most significant chronic illnesses, while also offering reassuring tips and advice about how to manage the disorders and have the best life possible.
Neuromuscular Disorders Of Infancy Childhood And Adolescence
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Author : Basil T. Darras
language : en
Publisher: Elsevier
Release Date : 2014-12-03
Neuromuscular Disorders Of Infancy Childhood And Adolescence written by Basil T. Darras and has been published by Elsevier this book supported file pdf, txt, epub, kindle and other format this book has been release on 2014-12-03 with Medical categories.
Neuromuscular disorders are diagnosed across the lifespan and create many challenges especially with infants, children and adolescents. This new edition of the definitive reference, edited by the established world renowned authorities on the science, diagnosis and treatment of neuromuscular disorders in childhood is a timely and needed resource for all clinicians and researchers studying neuromuscular disorders, especially in childhood. The Second Edition is completely revised to remain current with advances in the field and to insure this remains the standard reference for clinical neurologists and clinical research neurologists. The Second Edition retains comprehensive coverage while shortening the total chapter count to be an even more manageable and effective reference. Carefully revised new edition of the classic reference on neuromuscular disorders in infancy, childhood and adolescence. Definitive coverage of the basic science of neuromuscular disease and the latest diagnosis and treatment best practices. Includes coverage of clinical phenomenology, electrophysiology, histopathology, molecular genetics and protein chemistry
The Nincds Muscular Dystrophy And The Neuromuscular Disorders Research Program
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Author : National Institute of Neurological and Communicative Disorders and Stroke
language : en
Publisher:
Release Date : 1976
The Nincds Muscular Dystrophy And The Neuromuscular Disorders Research Program written by National Institute of Neurological and Communicative Disorders and Stroke and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 1976 with Medicine categories.
Neuromuscular Disorders In Clinical Practice
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Author : Bashar Katirji
language : en
Publisher: Springer Science & Business Media
Release Date : 2013-10-11
Neuromuscular Disorders In Clinical Practice written by Bashar Katirji and has been published by Springer Science & Business Media this book supported file pdf, txt, epub, kindle and other format this book has been release on 2013-10-11 with Medical categories.
Comprehensive, thoroughly updated, and expanded, Neuromuscular Disorders in Clinical Practice, Second Edition encompasses all disorders of the peripheral nervous system, covering all aspects of neuromuscular diseases from diagnosis to treatment. Mirroring the first book, this two-volume edition is divided into two parts. Part one discusses the approach to neuromuscular disorders, covering principles and basics, neuromuscular investigations, and assessment and treatment of neurological disorders. Part two then addresses the complete range of specific neuromuscular diseases: neuronopathies, peripheral neuropathies, neuromuscular junction disorders, muscle ion channel disorders, myopathies, and miscellaneous neuromuscular disorders and syndromes. Neuromuscular Disorders in Clinical Practice, Second Edition is intended to serve as a comprehensive text for both novice and experienced practitioners. General neurologists as well as specialists in neuromuscular medicine and trainees in neuromuscular medicine, clinical neurophysiology and electromyography should find this book inclusive, comprehensive, practical and highly clinically focused. Additionally, specialists in physical medicine and rehabilitation, rheumatology, neurosurgery, and orthopedics will find the book of great value in their practice.
Neuromuscular Diseases
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Author : Michael Swash
language : en
Publisher: Springer Science & Business Media
Release Date : 2013-03-14
Neuromuscular Diseases written by Michael Swash and has been published by Springer Science & Business Media this book supported file pdf, txt, epub, kindle and other format this book has been release on 2013-03-14 with Medical categories.
Nine years have elapsed since the second edition of this book was published. In this time the principal advances in neuromuscular diseases have been in the application of molecular genetics to understanding the aetiology and pathogenesis of this group of disorders. As a result many previously unrecognised disorders have been charac terised. Some clinical syndromes, such as the limb girdle dystrophies, have become better defined. In many such instances the new genetic information has led to major advances in knowledge of the biology of cell structures, for example, the membrane structural and channel proteins. The clinical syndromes themselves, and their patho logical and electrophysiological characteristics, however, remain as important as ever, since they constitute the clinical problem itself and, indeed, the database from which all other concepts emerge. Knowledge of the pathogenesis, genetics, and molecular biology of neuromuscular disorders is essential both in developing and applying new therapies and preventive measures, and in formulating genetic and prognostic advice. However, this informa tion does not necessarily always define clinically useful syndromes. Myotonia, for example, is an electrophysiological finding in some syndromes in which it is un detectable by clinical examination, although the phenomenon itself was originally defined as a clinical entity. The limb girdle muscular dystrophy syndromes can be defined by severity, distribution of weakness, age of onset, sex distribution and other characteristics and many of these can be better understood by study of the under lying defect in cell structural proteins.
A Clinician S View Of Neuromuscular Diseases
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Author : Michael H. Brooke
language : en
Publisher:
Release Date : 1986
A Clinician S View Of Neuromuscular Diseases written by Michael H. Brooke and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 1986 with Medical categories.
Muscular Dystrophy
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Author : National Institute of Neurological Diseases and Stroke
language : en
Publisher:
Release Date : 1971
Muscular Dystrophy written by National Institute of Neurological Diseases and Stroke and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 1971 with Muscular dystrophy categories.
Muscular Dystrophies
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Author : Robert C. Griggs
language : en
Publisher: Elsevier
Release Date : 2011-05-24
Muscular Dystrophies written by Robert C. Griggs and has been published by Elsevier this book supported file pdf, txt, epub, kindle and other format this book has been release on 2011-05-24 with Medical categories.
The Handbook of Clinical Neurology Vol 101: Muscular Dystrophies discusses the pathogenesis and treatment prospects for muscular dystrophies. It summarizes the advances in molecular and cell biology, biochemistry, and other biological sciences, with an emphasis on their application to this group of muscle disorders and to their clinical implications. Starting with an overview of muscular dystrophies, the book’s 16 chapters discuss dystrophinopathies; sarcoglycanopathies; congenital muscular dystrophies; collagen VI-related myopathies; limb-girdle muscular dystrophy 2A; dysferlinopathies; limb-girdle muscular dystrophy 2H and the role of TRIM32; and caveolinopathies. The book also covers myofibrillar myopathies; Emery-Dreifuss muscular dystrophy; facioscapulohumeral dystrophy and scapuloperoneal syndromes; oculopharyngeal muscular dystrophy; myotonic dystrophy types 1 and 2; and distal muscular dystrophies. This book is useful to basic investigators, as it offers an increased understanding of muscular dystrophies; and to clinicians, with its emphasis on issues that are relevant to the care, diagnosis, and management of patients with these disorders. Valuable insights into the muscular dystrophies, including treatment, diagnosis, and care and patient management A comprehensive compilation of the combined wisdom of the most highly regarded physicians, experts, and scientists studying the muscular dystrophies An evaluation of the way advances in molecular and cell biology, biochemistry, and other biological sciences continue to advance the study of these disorders
Duchenne Muscular Dystrophy
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Author : Alan E. H. Emery
language : en
Publisher: OUP Oxford
Release Date : 2015-02-19
Duchenne Muscular Dystrophy written by Alan E. H. Emery and has been published by OUP Oxford this book supported file pdf, txt, epub, kindle and other format this book has been release on 2015-02-19 with Medical categories.
Duchenne Muscular Dystrophy, an inherited and progressive muscle wasting disease, is one of the most common single gene disorders found in the developed world. In this fourth edition of the classic monograph on the topic, Alan Emery and Francesco Muntoni are joined by Rosaline Quinlivan, Consultant in Neuromuscular Disorders, to provide a thorough update on all aspects of the disorder. Recent understanding of the nature of the genetic defect responsible for Duchenne Muscular Dystrophy and isolation of the protein dystrophin has led to the development of new theories for the disease's pathogenesis. This new edition incorporates these advances from the field of molecular biology, and describes the resultant opportunities for screening, prenatal diagnosis, genetic counselling and from recent pioneering work with anti-sense oligonucleotides, the possibility of effective RNA therapy. Although there is still no cure for the disorder, there have been significant developments concerning the gene basis, publication of standards of care guidelines, and improvements in management leading to significantly longer survival, particularly with cardio-pulmonary care. The authors also investigate other forms of pharmacological, cellular and gene therapies. Duchenne Muscular Dystrophy will be essential reading not only for scientists and clinicians, but will also appeal to therapists and other professionals involved in the care of patients with muscular dystrophy.