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Logo of procrsmedFormerly medchtJournal of the Royal Society of MedicineProceedings of the Royal Society of Medicine
Proc R Soc Med. 1958 October; 51(10): 859–863.
PMCID: PMC1889852

Discussion on Some Clinical, Genetic and Biochemical Aspects of Metabolic Disorders of the Nervous System

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Selected References

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  • ALLAN JD, CUSWORTH DC, DENT CE, WILSON VK. A disease, probably hereditary characterised by severe mental deficiency and a constant gross abnormality of aminoacid metabolism. Lancet. 1958 Jan 25;1(7013):182–187. [PubMed]
  • BARON DN, DENT CE, HARRIS H, HART EW, JEPSON JB. Hereditary pellagra-like skin rash with temporary cerebellar ataxia, constant renal amino-aciduria, and other bizarre biochemical features. Lancet. 1956 Sep 1;271(6940):421–428. [PubMed]
  • BERGREN WR, DONNELL G, KALCKAR HM. Congenital galactosaemia and mental health. Lancet. 1958 Feb 1;1(7014):267–268. [PubMed]
  • BICKEL H, GOLLNER I, GRUTER W, SCHULTZE HE. Versuche zur Coeruloplasminsubstitution bei der hepatocerebralen Degeneration (Wilsonsche Krankheit). Klin Wochenschr. 1956 Sep 15;34(35-36):961–968. [PubMed]
  • COATES S, NORMAN AP, WOOLF LI. Phenylketonuria with normal intelligence and Gowers' muscular dystrophy. Arch Dis Child. 1957 Aug;32(164):313–317. [PMC free article] [PubMed]
  • CONN JW, FAJANS SS, LOUIS LH, STREETEN DH, JOHNSON RD. Intermittent aldosteronism in periodic paralysis; dependence of attacks on retention of sodium, and failure to induce attacks by restriction of dietary sodium. Lancet. 1957 Apr 20;272(6973):802–805. [PubMed]
  • DAVIS BD. Genetic and environmental control of enzyme formation. Res Publ Assoc Res Nerv Ment Dis. 1954;33:23–38. [PubMed]
  • DEAN G, BARNES HD. Porphyria; a South African screening experiment. Br Med J. 1958 Feb 8;1(5066):298–301. [PMC free article] [PubMed]
  • DINE MS. Congenital methemoglobinemia in the newborn period. AMA J Dis Child. 1956 Jul;92(1):15–19. [PubMed]
  • GARCIN R, LAPRESLE J. Manifestations nerveuses des porphyries. Sem Hop. 1950 Sep 2;26(65):3404–3423. [PubMed]
  • GARLAND H. Diabetic amyotrophy. Br Med J. 1955 Nov 26;2(4951):1287–1290. [PMC free article] [PubMed]
  • GREENFIELD JG. Is hepatolenticular degeneration a clinico-pathological entity. Proc R Soc Med. 1954 Feb;47(2):150–152. [PMC free article] [PubMed]
  • DRISCOLL KW, HSIA DY, KNOX WE, TROLL W. Detection by phenylalanine tolerance tests of heterozygous carriers of phenylketonuria. Nature. 1956 Dec 1;178(4544):1239–1240. [PubMed]
  • MARSTON HR. Cobalt, copper and molybdenum in the nutrition of animals and plants. Physiol Rev. 1952 Jan;32(1):66–121. [PubMed]
  • PETERS HA, WOODS S, EICHMAN PL, REESE HH. The treatment of acute porphyria with chelating agents: a report of 21 cases. Ann Intern Med. 1957 Nov;47(5):889–899. [PubMed]
  • SCHWARZ V, HOLZEL A, KOMROWER GM. Laboratory diagnosis of congenital galactosaemia at birth. Lancet. 1958 Jan 4;1(7010):24–25. [PubMed]
  • WALSHE JM. Penicillamine, a new oral therapy for Wilson's disease. Am J Med. 1956 Oct;21(4):487–495. [PubMed]
  • WORSTER-DROUGHT C, WHITE JC, SARGENT F. Familial idiopathic methaemoglobinaemia, associated with mental deficiency and neurological abnormalities. Br Med J. 1953 Jul 18;2(4828):114–118. [PMC free article] [PubMed]

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