Myotonic Dystrophy: Present Management, Future Therapy. Cet article n’est pas disponible.
Langue : anglais
Edité par Oxford Univ Pr, 2004
- Livre relié
- Neuf

Vendeur : Revaluation Books, Exeter, Royaume-UniRevaluation Books
Vendeur avec une évaluation de 5 étoiles
Vendeur AbeBooks depuis 6 janvier 2003
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Livre relié
Etat: Neuf
EUR 589,30
A propos de cet article
1st edition. 264 pages. 9.25x6.25x0.60 inches. In Stock.
N° de réf. du vendeur zk0198527829
- Titre
- Myotonic Dystrophy: Present Management, Future Therapy
- Auteur
- Harper, Pepter (Editor)/ Van Engelen, Baziel G. M. (Editor)/ Eymard, Bruno (Editor)/ Wilcox, Douglas E. (Editor)/ Harper, Peter S. (Editor)
- Éditeur
- Oxford Univ Pr
- Année de publication
- 2004
- État de l'article
- Brand New
- Reliure
- Hardcover
- Langue
- anglais
- ISBN à 10 chiffres
- 0198527829
- ISBN à 13 chiffres
- 9780198527824
- Poids de l'article
- 0,48 kilogramme
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.
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.
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Revue de presse
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)
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)
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