Skip to main content
NCBI home page
Thorax logoLink to Thorax
. 1991 Apr;46(4):261–267. doi: 10.1136/thx.46.4.261

Cystic fibrosis. 6. Gastrointestinal and nutritional aspects.

H Kopelman 1
PMCID: PMC463094  PMID: 2038735

Full text

PDF
261

Images in this article

262Image
on p.262
263Image
on p.263
264Image
on p.264
266Image
on p.266

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Baxter P. S., Wilson A. J., Read N. W., Hardcastle J., Hardcastle P. T., Taylor C. J. Abnormal jejunal potential difference in cystic fibrosis. Lancet. 1989 Mar 4;1(8636):464–466. doi: 10.1016/s0140-6736(89)91366-4. [DOI] [PubMed] [Google Scholar]
  2. Berschneider H. M., Knowles M. R., Azizkhan R. G., Boucher R. C., Tobey N. A., Orlando R. C., Powell D. W. Altered intestinal chloride transport in cystic fibrosis. FASEB J. 1988 Jul;2(10):2625–2629. doi: 10.1096/fasebj.2.10.2838365. [DOI] [PubMed] [Google Scholar]
  3. Boland M. P., Stoski D. S., MacDonald N. E., Soucy P., Patrick J. Chronic jejunostomy feeding with a non-elemental formula in undernourished patients with cystic fibrosis. Lancet. 1986 Feb 1;1(8475):232–234. doi: 10.1016/s0140-6736(86)90772-5. [DOI] [PubMed] [Google Scholar]
  4. Cleghorn G. J., Shepherd R. W., Holt T. L. The use of a synthetic prostaglandin E1 analogue (misoprostol) as an adjunct to pancreatic enzyme replacement in cystic fibrosis. Scand J Gastroenterol Suppl. 1988;143:142–147. doi: 10.3109/00365528809090235. [DOI] [PubMed] [Google Scholar]
  5. Cleghorn G. J., Stringer D. A., Forstner G. G., Durie P. R. Treatment of distal intestinal obstruction syndrome in cystic fibrosis with a balanced intestinal lavage solution. Lancet. 1986 Jan 4;1(8471):8–11. doi: 10.1016/s0140-6736(86)91894-5. [DOI] [PubMed] [Google Scholar]
  6. Corey M., McLaughlin F. J., Williams M., Levison H. A comparison of survival, growth, and pulmonary function in patients with cystic fibrosis in Boston and Toronto. J Clin Epidemiol. 1988;41(6):583–591. doi: 10.1016/0895-4356(88)90063-7. [DOI] [PubMed] [Google Scholar]
  7. Durie P. R., Gaskin K. J., Corey M., Kopelman H., Weizman Z., Forstner G. G. Pancreatic function testing in cystic fibrosis. J Pediatr Gastroenterol Nutr. 1984;3 (Suppl 1):S89–S98. doi: 10.1097/00005176-198400031-00015. [DOI] [PubMed] [Google Scholar]
  8. Gaskin K. J., Durie P. R., Lee L., Hill R., Forstner G. G. Colipase and lipase secretion in childhood-onset pancreatic insufficiency. Delineation of patients with steatorrhea secondary to relative colipase deficiency. Gastroenterology. 1984 Jan;86(1):1–7. [PubMed] [Google Scholar]
  9. Gaskin K. J., Waters D. L., Howman-Giles R., de Silva M., Earl J. W., Martin H. C., Kan A. E., Brown J. M., Dorney S. F. Liver disease and common-bile-duct stenosis in cystic fibrosis. N Engl J Med. 1988 Feb 11;318(6):340–346. doi: 10.1056/NEJM198802113180602. [DOI] [PubMed] [Google Scholar]
  10. Gaskin K., Gurwitz D., Durie P., Corey M., Levison H., Forstner G. Improved respiratory prognosis in patients with cystic fibrosis with normal fat absorption. J Pediatr. 1982 Jun;100(6):857–862. doi: 10.1016/s0022-3476(82)80501-5. [DOI] [PubMed] [Google Scholar]
  11. Kerem B., Rommens J. M., Buchanan J. A., Markiewicz D., Cox T. K., Chakravarti A., Buchwald M., Tsui L. C. Identification of the cystic fibrosis gene: genetic analysis. Science. 1989 Sep 8;245(4922):1073–1080. doi: 10.1126/science.2570460. [DOI] [PubMed] [Google Scholar]
  12. Kopelman H., Corey M., Gaskin K., Durie P., Weizman Z., Forstner G. Impaired chloride secretion, as well as bicarbonate secretion, underlies the fluid secretory defect in the cystic fibrosis pancreas. Gastroenterology. 1988 Aug;95(2):349–355. doi: 10.1016/0016-5085(88)90490-8. [DOI] [PubMed] [Google Scholar]
  13. Kopelman H., Durie P., Gaskin K., Weizman Z., Forstner G. Pancreatic fluid secretion and protein hyperconcentration in cystic fibrosis. N Engl J Med. 1985 Feb 7;312(6):329–334. doi: 10.1056/NEJM198502073120601. [DOI] [PubMed] [Google Scholar]
  14. Levy L. D., Durie P. R., Pencharz P. B., Corey M. L. Effects of long-term nutritional rehabilitation on body composition and clinical status in malnourished children and adolescents with cystic fibrosis. J Pediatr. 1985 Aug;107(2):225–230. doi: 10.1016/s0022-3476(85)80130-x. [DOI] [PubMed] [Google Scholar]
  15. Mansell A. L., Andersen J. C., Muttart C. R., Ores C. N., Loeff D. S., Levy J. S., Heird W. C. Short-term pulmonary effects of total parenteral nutrition in children with cystic fibrosis. J Pediatr. 1984 May;104(5):700–705. doi: 10.1016/s0022-3476(84)80947-6. [DOI] [PubMed] [Google Scholar]
  16. Moore D. J., Forstner G. G., Largman C., Cleghorn G. J., Wong S. S., Durie P. R. Serum immunoreactive cationic trypsinogen: a useful indicator of severe exocrine dysfunction in the paediatric patient without cystic fibrosis. Gut. 1986 Nov;27(11):1362–1368. doi: 10.1136/gut.27.11.1362. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Quinton P. M. Cystic fibrosis: a disease in electrolyte transport. FASEB J. 1990 Jul;4(10):2709–2717. doi: 10.1096/fasebj.4.10.2197151. [DOI] [PubMed] [Google Scholar]
  18. Scott R. B., O'Loughlin E. V., Gall D. G. Gastroesophageal reflux in patients with cystic fibrosis. J Pediatr. 1985 Feb;106(2):223–227. doi: 10.1016/s0022-3476(85)80291-2. [DOI] [PubMed] [Google Scholar]
  19. Shepherd R. W., Holt T. L., Vasques-Velasquez L., Coward W. A., Prentice A., Lucas A. Increased energy expenditure in young children with cystic fibrosis. Lancet. 1988 Jun 11;1(8598):1300–1303. doi: 10.1016/s0140-6736(88)92119-8. [DOI] [PubMed] [Google Scholar]
  20. Shepherd R., Cooksley W. G., Cooke W. D. Improved growth and clinical, nutritional, and respiratory changes in response to nutritional therapy in cystic fibrosis. J Pediatr. 1980 Sep;97(3):351–357. doi: 10.1016/s0022-3476(80)80180-6. [DOI] [PubMed] [Google Scholar]
  21. Strandvik B., Hjelte L., Gabrielsson N., Glaumann H. Sclerosing cholangitis in cystic fibrosis. Scand J Gastroenterol Suppl. 1988;143:121–124. doi: 10.3109/00365528809090231. [DOI] [PubMed] [Google Scholar]
  22. Taylor C. J., Baxter P. S., Hardcastle J., Hardcastle P. T. Failure to induce secretion in jejunal biopsies from children with cystic fibrosis. Gut. 1988 Jul;29(7):957–962. doi: 10.1136/gut.29.7.957. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Welsh M. J. Abnormal regulation of ion channels in cystic fibrosis epithelia. FASEB J. 1990 Jul;4(10):2718–2725. doi: 10.1096/fasebj.4.10.1695593. [DOI] [PubMed] [Google Scholar]

Articles from Thorax are provided here courtesy of BMJ Publishing Group

RESOURCES