Chronic pancreatitis

Current Opinion in Gastroenterology

Volumn 16, Issue 5, 2000, Pages 414-418

  Chari, Suresh T ^a   DiMagno, Eugene P ^a  

^a MAYO CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

TRYPSINOGEN;

ALCOHOLISM; ARTICLE; CHRONIC PANCREATITIS; COLON DISEASE; CYSTIC FIBROSIS; EARLY DIAGNOSIS; ENDOSCOPIC ECHOGRAPHY; ENDOSCOPIC THERAPY; EXTRACORPOREAL LITHOTRIPSY; GENE MUTATION; HUMAN; PANCREAS CALCIFICATION; PANCREAS FUNCTION TEST; STEATORRHEA;

EID: 0034456394     PISSN: 02671379     EISSN: None     Source Type: Journal    
DOI: 10.1097/00001574-200009000-00004     Document Type: Article

References (33)

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4. The different courses of early- and late-onset idiopathic and alcoholic chronic pancreatitis
5. Hereditary pancreatitis is caused by a mutation in the cationic trypsinogen gene
6. Mutations in the cationic trypsinogen gene are associated with recurrent acute and chronic panreatitis
7. Mustations in exons 2 and 3 of the cationic trypsinogen gene in Japanese families with hereditary pancreatitis
8. Identification of a hereditary pancreatitis mutation in four West Virginia families
9. Mutations in the cationic trypsinogen gene and evidence for genetic hetergeneity in hereditary pancreatitis
10. Mutations of the cationic trypsinogen in hereditary pancreatitis
11. Strong evidence that the N211 substitution in the cationic trypinsogen gene causes disease in hereditary pancreatitis
12. Hetergeneity in hereditary pancreatitis
13. A signal peptide cleavage site mutation in the cationic trypsinogen gene is strongly associated with chronic pancreatitis
14. Trysinogen mutations in chronic pancreatitis
15. The A16V signal peptide cleavage site mutation in the cationic trysinogen gene and chronic pancreatitis
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17. Hereditary pancreatitis is caused by a mutation in the cationic trypsinogen gene
18. Hereditary pancreatitis: New insights into acute and chronic pancreatitis
19. Hereditary pancreatitis-associated mutation asn(21) → ile stabilizes rat trypsinogen in vitro
20. Mutational analysis of the human pancreatic secretory trypsin inhibitor (PSTI) gene in hereditary and sporadic chronic pancreatitis
21. Exclusion of anionic trypsinogen and mesotrypsinogen involvement in hereditary pancreatitis without cationic trypsinogen gene mutations
22. Evidence that hereditary pancreatitis is genetically heterogeneous disorder
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24. Diagnosis of lipid malabsorption in patients with chronic pancreatitis: A new indirect test using postprandial plasma apoplipoprotein B-48 [see comments]
25. Fate of orally ingested enzymes in pancreatic insufficiency: Comparison of two dosage schedules
26. Post-prandial intragastric and duodenal acidity are increased in patients with chronic pancreatitis
27. Mismatch of duodenal deliveries of dietary fat and pancreatin from enterally coated microspheres
28. A double-blind, randomized, multicentre, crossover study to prove equivalence of pancreatin minimicrospheres versus microspheres in exocrine pancreatic insufficiency
29. First adult patient with fibrosing colonopathy
30. Fibrosing colonopathy in an adult owing to overuse of pancreatic enzyme supplements
31. Colonic toxicity from pancreatins: A contemporary safety issue
32. A prospective study of pancreatic disease in patients with alcoholic cirrhosis: Comparative diagnostic value of ERCP and EUS and long-term significance of isolated parenchymal abnomalities
33. Long term follow up of patients with chronic pancreatitis and pancreatic stones treated with extracorporeal shock wave lithotripsy