Copper and Neurological Function
- 1 January 1980
- book chapter
- Published by Wiley
- Vol. 79, 247-266
- https://doi.org/10.1002/9780470720622.ch13
Abstract
This chapter contains section titled: References Discussion ReferencesKeywords
This publication has 34 references indexed in Scilit:
- Degeneration of the cerebellar system in X‐chromosome—linked copper malabsorptionAnnals of Neurology, 1979
- Trace element binding in the copper deficient mottled mutants in the mouseLife Sciences, 1979
- A study of copper treatment and tissue copper levels in the murine congenital copper deficiency, mottledLife Sciences, 1976
- COPPER DEFICIENCY IN THE DEVELOPING RAT BRAIN: EVIDENCE FOR ABNORMAL MITOCHONDRIA1Journal of Neurochemistry, 1975
- Primary defect in copper transport underlies mottled mutants in the mouseNature, 1974
- Lesions produced by copper deficiency in neonate and older ratsBritish Journal of Nutrition, 1973
- AN INHERITED DEFICIENCY IN NORADRENALINE BIOSYNTHESIS IN THE BRINDLED MOUSEJournal of Neurochemistry, 1972
- OCCURRENCE AND PROPERTIES OF CATECHOL‐O‐METHYL TRANSFERASE IN ADRENERGIC NEURONSJournal of Neurochemistry, 1971
- Demyelination in Lambs Born of Ewes Maintained on High Intakes of Sulphate and MolybdateNature, 1960
- The biochemistry of copper deficiency I. Enzymological disturbances, blood chemistry and excretion of amino-acidsProceedings of the Royal Society of London. B. Biological Sciences, 1956