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Logo of procrsmedFormerly medchtJournal of the Royal Society of MedicineProceedings of the Royal Society of Medicine
 
Proc R Soc Med. 1967 November; 60(11 Pt 1): 1149–1152.
PMCID: PMC1902126

Recent Developments in the Management and Prognosis of some Inborn Errors of Metabolism

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.
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  • 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]
  • BUCHANAN EU, KOMROWER GM. The prognosis of idiopathic renal acidosis in infancy with observations on urine acidification and ammonia production in children. Arch Dis Child. 1958 Dec;33(172):532–535. [PMC free article] [PubMed]
  • CLAYTON BE, PATRICK AD. Use of dimercaprol or pencillamine in the treatment of cystinosis. Lancet. 1961 Oct 21;2(7208):909–910. [PubMed]
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  • COLLISS JE, LEVI AJ, MILNE MD. Stature and nutrition in cystinuria and Hartnup disease. Br Med J. 1963 Mar 2;1(5330):590–592. [PMC free article] [PubMed]
  • CRAWHALL JC, SCOWEN EF, WATTS RW. Effect of penicillamine on cystinuria. Br Med J. 1963 Mar 2;1(5330):588–590. [PMC free article] [PubMed]
  • CUSWORTH DC, DENT CE, FLYNN FV. The amino-aciduria in galactosaemia. Arch Dis Child. 1955 Apr;30(150):150–154. [PMC free article] [PubMed]
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  • DE VRIES A, KOCHWA S, LAZEBNIK J, FRANK M, DJALDETTI M. Glycinuria, a hereditary disorder associated with nephrolithiasis. Am J Med. 1957 Sep;23(3):408–415. [PubMed]
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  • KOPELMAN H, ASATOOR AM, MILNE MD. HYPERPROLINAEMIA AND HEREDITARY NEPHRITIS. Lancet. 1964 Nov 21;2(7369):1075–1079. [PubMed]
  • KAZANTZIS G, FLYNN FV, SPOWAGE JS, TROTT DG. Renal tubular malfunction and pulmonary emphysema in cadmium pigment workers. Q J Med. 1963 Apr;32:165–192. [PubMed]
  • MILNE MD. DISORDERS OF AMINO-ACID TRANSPORT. Br Med J. 1964 Feb 8;1(5379):327–336. [PMC free article] [PubMed]
  • Milne MD, Asatoor AM, Edwards KD, Loughridge LW. The intestinal absorption defect in cystinuria. Gut. 1961 Dec;2(4):323–337. [PMC free article] [PubMed]
  • MILNE MD, CRAWFORD MA, GIRAO CB, LOUGHRIDGE LW. The metabolic disorder in Hartnup disease. Q J Med. 1960 Jul;29:407–421. [PubMed]
  • SCRIVER CR, SCHAFER IA, EFRON ML. New renal tubular amino-acid transport system and a new hereditary disorder of amino-acid metabolism. Nature. 1961 Nov 18;192:672–673. [PubMed]
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  • SHERLOCK S. Pathogenesis and management of hepatic coma. Am J Med. 1958 May;24(5):805–813. [PubMed]

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