Myotonic Dystrophy
Present management, future therapy
Peter Harper editor Baziel van Engelen editor Bruno Eymard editor Douglas Wilcox editor
Format:Hardback
Publisher:Oxford University Press
Published:15th Jan '04
Currently unavailable, and unfortunately no date known when it will be back
This book provides a full and practical account of management of myotonic dystrophy, the commonest muscular dystrophy of adult life and a condition of exceptional variability. Written for neurologists, clinical geneticists and other clinical specialities involved with the disorder, it deals with both the neurological aspects and also the wide range of systemic complications that may occur. In addition it provides details of information and support available to patients and families and gives a summary of the present state of clinical trials of therapeutic agents. These sections are preceded by general introductory chapters describing both the clinical features and also the current state of research into understanding the underlying mechanisms.
The book is academically very good and written in a practical way that both patients and doctors will find useful...I can recommend the book, not only for patients but also for such doctors in general practice. * The Journal of the Norwegian Medical Association *
This book written by the main world experts in the field is a practical outline for both the clinicians and families. I strongly recommend it. * European Journal of Paediatric Neurology, Vol 10 *
. . . illustrates all the various clinical aspects of this complex disease and gives insight into the pathogenesis and possibilities of the management of each complication at the different stages of myotonic dystrophy. The completeness of the data presented in each chapter is imporessive. The chapters are well structured and the illustrations are clear and informative. The flow charts are adequately structured and easy to understand. The references are well-selected and up-to-date. All chapters are written by renowned experts in the field of the myotonic dystrophies and neuromuscular diseases. It is a most educative book for clinicians working in the field of the neuromuscular diseases and for geneticists responsible for the genetic counselling of patients with myotonic dystrophy. * Human Genetics *
. . . a book that offers a wealth of up-to-date, practical and relevant information. Reflecting the central role of neuromuscular assessment and clinical management issues, this book is to be recommended as an essential reference for every neurologist involved in the care of patients with myotonic dystrophy. * Neuromuscular Disorders, 14 *
ISBN: 9780198527824
Dimensions: 241mm x 161mm x 19mm
Weight: 536g
264 pages