Abstract
Our laboratory as part of the Beaumont-May Institute of Neurology has long been interested in hereditary neurological diseases in humans and in the study of the normal development of the nervous system. These latter studies have been employing small animals primarily the rat and, in a few instances, the rhesus monkey and minipig. Recently, some of our results on the metabolism of glycolipids have been summarized in a review entitled “Factors affecting Incorporation of Precursors into body constituents — A review of common sense considerations with glycolipids or examples” (2). In an effort to translate the information gained from laboratory animal experiments to the human and to gain further insight into human cerebral lipidosis, we have entered a long term collaborative study with a number of departments at Washington University Medical School and St. Louis Children’s Hospital. Our objectives are to make and correlate studies of the clinical, pathological, electron microscopic and biochemical aspects of hereditary neurological diseases.
Supported by USPHS grants N501575-14 and FR37
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Burton, R.M., Handa, S., Howard, R.E., Vietti, T. (1972). Radioactive Precursor Incorporation into Lipids of Humans with Cerebral Lipidoses:1-14C-Glucosamine, U3H-Serine, and 3H-Acetate. In: Volk, B.W., Aronson, S.M. (eds) Sphingolipids, Sphingolipidoses and Allied Disorders. Advances in Experimental Medicine and Biology, vol 19. Springer, Boston, MA. https://doi.org/10.1007/978-1-4757-6570-0_19
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DOI: https://doi.org/10.1007/978-1-4757-6570-0_19
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