Discussion on some clinical, genetic and biochemical aspects of metabolic disorders of the nervous system: metabolic disease of the nervous system: clinical aspects.
- 1 October 1958
- journal article
- Vol. 51 (10) , 859-63
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- A DISEASE, PROBABLY HEREDITARY, CHARACTERISED BY SEVERE MENTAL DEFICIENCY AND A CONSTANT GROSS ABNORMALITY OF AMINOACID METABOLISMThe Lancet, 1958
- LABORATORY DIAGNOSIS OF CONGENITAL GALACTOSqMIA AT BIRTHThe Lancet, 1958
- Phenylketonuria with Normal Intelligence and Gowers' Muscular DystrophyArchives of Disease in Childhood, 1957
- Penicillamine, a new oral therapy for Wilson's diseaseThe American Journal of Medicine, 1956
- Versuche zur Coeruloplasminsubstitution bei der hepatocerebralen Degeneration (Wilsonsche Krankheit)Klinische Wochenschrift, 1956
- Congenital Methemoglobinemia in the Newborn PeriodArchives of Pediatrics & Adolescent Medicine, 1956
- Diabetic AmyotrophyBMJ, 1955
- Genetic and environmental control of enzyme formation.1954
- Cobalt, Copper and Molybdenum in the Nutrition of Animals and PlantsPhysiological Reviews, 1952
- [Nervous manifestations of porphyria].1950