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

Palliation

Myasthenia Gravis and Other Myasthenic Syndromes,mber of congenital myasthenic syndromes discrete abnormalities in various components of the post-synaptic ACh receptor have been found, and in the Lambert—Eaton myasthenic syndrome release of ACh vesicles is abnormal (Table 12.1).

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Inherited Metabolic Myopathies,any of these disorders there are features of involvement of other systems. The severity of the clinical syndrome often varies according to the age of onset, reflecting the severity and distribution of the enzyme deficiency, so that infantile and adult-onset types of a disorder may present with strikingly different clinical features.

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Banquet

Classification of Neuromuscular Diseases,muscular Diseases modified its classification of Neuromuscular Diseases in 1994 in response to the changes necessary since its previous classifications of 1968 and 1988, and this internationally accepted classification of the neuromuscular diseases forms the basis of the organisation of chapters in

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Book 1997Latest editions, 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

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Michael Swash MD, FRCP, FRCPath,Martin S. Schwartz MD, FRCPcture, - Source, name of the genus, species, authors, family of the biological source from which the glycoside has been isolated, - Melting point, - Specific rotation, - Molecule weight, - Molecular formula, - UV spectral data : maxima, e or log e , solvent, - IR peaks in cm.-1. with medium in which

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