Titlebook: Biochemical Aspects of Nervous Diseases; J. N. Cumings (Professor of Chemical Pathology) Book 1972 Plenum Publishing Company Ltd. 1972 bio

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https://doi.org/10.1007/978-3-658-01144-4nowledge of the underlying mechanisms is still scanty, and this new knowledge may prove to be very important in the understanding of some muscle diseases. It is pertinent, therefore, first of all to review briefly the existing knowledge and hypotheses in this field.

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Book 1972d muscles has increased in a remarkable manner. As a consequence some very important books have been published both in America and in Europe in which some, at least, of this information has become available in an easily readable form to an ever increasing group of laboratory and scientific workers.

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Biochemistry of Muscle Diseases,e made to several reviews and to the published proceedings of a number of meetings concerned with the subject [1–5]. In this chapter an attempt is made to deal concisely with some aspects and, since this book is concerned primarily with the nervous system, to pay particular attention to the possible

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The Biochemistry of Demyelination and Demyelinating Diseases, After severing a peripheral nerve there is increasing loss of cerebrosides, sphingomyelin, cholesterol and phospholipids, that of the cephalins starting earlier and exceeding that of lecithin [1]. During the first 14 days after neurotomy the decrease of fatty aldehydes exceeds that of phosphatides

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,The Biochemistry of Copper in Man and Its Role in the Pathogenesis of Wilson’s Disease (Hepatolentiby abnormalities of renal function and by visible deposits of copper in the cornea, the Kayser Fleischer rings. The biochemical lesion consists of excessive deposition of copper in most tissues but principally the brain, liver and kidneys; in the plasma the concentration of both copper and the coppe

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Biochemical Neurological Disease in Children,m. Some biochemical diseases are almost entirely environmental in origin, e.g. lead encephalopathy, but at present attention is largely directed to genetically determined conditions-the inborn errors of metabolism and other molecular diseases. In some cases it is the interaction between genotype and

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Book 2022 provides an overview of the history of evidence-based practices and their importance as applied to the law, school settings, and factors that influence the use for treatment of ASD. Additional areas of coverage include evidence-based and non-evidence-based ABA interventions for autism as well as de