Titlebook: Handbook of Neurochemistry; Volume VII Pathologi Abel Lajtha Book 1972 Plenum Press, New York 1972 Alzheimer‘s disease.Alzheimer′s disease.

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mucous-membrane

Neurochemical Aspects of Mucopolysaccharidoses,teins in the body. This definition, somewhat broader than conventional, is adopted because the line between mucopolysaccharides and glycoprotein is becoming more and more obscure, and because there are disorders of glycoprotein metabolism which will not otherwise be covered in the Handbook. Several

本能

Lipidoses,tations in infants afflicted with conditions such as Gaucher’s disease, Fabry’s disease, globoid leukodystrophy (Krabbe’s disease), metachromatic leukodystrophy, generalized gangliosidosis, Tay-Sachs disease, and Niemann-Pick disease. Recent discoveries have led to the elucidation of the metabolic d

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Biochemical Aspects of Multiple Sclerosis,line all the important reactions and pathological events taking place in the CNS, as well as in the whole organism, in the different phases of this disease. Regarding the very heterogeneous biochemical systems of the CNS, and the many correlations with the organism, the neurochemist who plans to ana

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sulcus

Basic Protein of Myelin and Its Role in Experimental Allergic Encephalomyelitis and Multiple Scleron emulsion into monkeys.. Some 14 years later, Kabat, Wolf, and Bezer. produced EAE with one injection of whole brain with Freund’s adjuvant. This and subsequent reports provided a detailed description of the pathological and some of the immunological aspects of the disease. Soon, however, it was re

cutlery

植物學(xué)

Brain Damage in the Aminoacidurias,conditions, notably phenylketonuria and maple syrup disease, the enzyme implicated is normally absent from brain; neurologic symptoms are therefore produced indirectly, most likely the result of postnatal brain development taking place in an environment having a markedly distorted amino acid content

細(xì)節(jié)

Abnormal Metabolism of Sulfur-Containing Amino Acids Associated with Brain Dysfunction,ed with disorders of the central nervous system. The reader is referred to Vol. III, Chapter 8, of the . for fuller discussion of the normal metabolism of these compounds in brain. However, attention will be called to gaps in our knowledge of normal metabolism which the study of these metabolic . ha

Coterminous

Amino Acid and Protein Metabolism in Wallerian Degeneration,ructure is specifically affected, whereas in the latter the whole neuron together with its myelin sheath undergoes degeneration. The major distinction between primary and secondary degeneration depends therefore on the initial integrity of the axon in the former group.