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Titlebook: Neuromuscular Diseases; A Practical Approach Michael Swash,Martin S. Schwartz Book 1997Latest edition Springer-Verlag London 1997 assessmen

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發(fā)表于 2025-3-21 18:48:33 | 只看該作者 |倒序瀏覽 |閱讀模式
書目名稱Neuromuscular Diseases
副標(biāo)題A Practical Approach
編輯Michael Swash,Martin S. Schwartz
視頻videohttp://file.papertrans.cn/665/664246/664246.mp4
概述theoretical information that will be useful to managing patients with neuromuscular problems..Both authors are recognised experts in the field of neuromuscular disorders and the book is based on their
圖書封面Titlebook: Neuromuscular Diseases; A Practical Approach Michael Swash,Martin S. Schwartz Book 1997Latest edition Springer-Verlag London 1997 assessmen
描述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, fo
出版日期Book 1997Latest edition
關(guān)鍵詞assessment; biopsie; biopsy; childhood; classification; diagnosis; diseases; inflammation; management; muscle
版次3
doihttps://doi.org/10.1007/978-1-4471-3834-1
isbn_softcover978-1-4471-3836-5
isbn_ebook978-1-4471-3834-1
copyrightSpringer-Verlag London 1997
The information of publication is updating

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沙發(fā)
發(fā)表于 2025-3-21 23:36:55 | 只看該作者
Clinical Assessment and Measurement, impulses, the function of the neuromuscular junction and the physical and biochemical processes of muscular contraction, has increased. Indeed, some neuromuscular disorders have themselves led to insights into these basic mechanisms. Huxley (1986) has reviewed the historical background of discoveries in relation to muscular contraction.
板凳
發(fā)表于 2025-3-22 02:40:56 | 只看該作者
Acquired Polyneuropathies,uent. About half of all insulin-dependent diabetics have symptomatic neuropathy, representing about 0.5% of the population of developed countries (Brown and Green 1984; Brown and Asbury 1984) (Table 11.1)
地板
發(fā)表于 2025-3-22 07:47:28 | 只看該作者
Inflammatory Myopathies and Related Disorders,l features suggestive of inflammation. The inflammatory myopathies, as a group of disorders, are the commonest of the acquired myopathies. Characteristically, muscular involvement is mainly proximal, although focal and distal presentations may occur. The syndrome may be acute, subacute or chronic.
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發(fā)表于 2025-3-23 03:59:10 | 只看該作者
ld of neuromuscular disorders and the book is based on theirNine 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
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發(fā)表于 2025-3-23 07:01:42 | 只看該作者
A Clinical Approach to the Neuropathies,heir axons, or both, may be affected. Although autonomic disturbances rarely form a major aspect of the clinical features of peripheral neuropathy, autonomic neuropathy, e.g. in diabetes mellitus, can be a major source of disability.
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