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Publikováno v:
The Lancet. 377:1600-1609
Primary biliary cirrhosis is a chronic liver disease characterised by intrahepatic bile-duct destruction, cholestasis, and, in some cases, cirrhosis. Evidence supporting the autoimmune nature of this disorder includes the appearance of highly specifi
Publikováno v:
The Lancet. 299:605-608
In an attempt to expedite diagnosis in jaundiced patients where a surgical cause has not been excluded, and in particular to reduce the period of delay in diagnosis where carcinoma of the head of the pancreas might be present, a triple test combining
Publikováno v:
The Lancet. 318:1319-1321
Neurological syndromes similar to those associated with abetalipoproteinaemia or Friedreich's ataxia developed in four patients with chronic steatorrhoea, two of whom had cystic fibrosis and two chronic cirrhosis of childhood. Serum concentrations of
Autor:
A.J. Scott, G.A. Khan
Publikováno v:
The Lancet. 290:790-792
In four groups of patients with chronic calculous biliary disease and jaundice due to choledocholithiasis (A) or postoperative biliary stricture (B) or no biliary disease but with jaundice due to tumours of the lower common bileduct (C) or hepatic du