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With five exceptions this text represents the contributions of the Guy's Hospital group. The majority of the chapters are written by Professor Adams. The text is difficult reading, to say the least. The insertion by name of all references destroys continuity of thought. The editor assumes his reader is knowledgeable concerning the metabolic abnormalities found in the various neurologic entities such as "Krabbe's" disease and arylsulfatase deficiencies (although he does not note the three types) in metachromatic leukodystrophies. Ganglioside accumulations in the various lipidoses are but casually noted, and the six types are not discussed. Unverricht's disease is not noted.
Neurohistochemistry.. Ann Intern Med. ;64:967–968. doi: 10.7326/0003-4819-64-4-967_2
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Published: Ann Intern Med. 1966;64(4):967-968.
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