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. 1986;79(Suppl 12):32–35.

Practical management of nutrition and gastrointestinal tract in cystic fibrosis.

M C Goodchild
PMCID: PMC1290124  PMID: 3723545

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Selected References

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

  1. Allan J. D., Mason A., Moss A. D. Nutritional supplementation in treatment of cystic fibrosis of the pancreas. Am J Dis Child. 1973 Jul;126(1):22–26. doi: 10.1001/archpedi.1973.02110190018004. [DOI] [PubMed] [Google Scholar]
  2. Chase H. P., Long M. A., Lavin M. H. Cystic fibrosis and malnutrition. J Pediatr. 1979 Sep;95(3):337–347. doi: 10.1016/s0022-3476(79)80504-1. [DOI] [PubMed] [Google Scholar]
  3. Congden P. J., Bruce G., Rothburn M. M., Clarke P. C., Littlewood J. M., Kelleher J., Losowsky M. S. Vitamin status in treated patients with cystic fibrosis. Arch Dis Child. 1981 Sep;56(9):708–714. doi: 10.1136/adc.56.9.708. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Davidson G. P., Hassel F. M., Crozier D., Corey M., Forstner G. G. Iatrogenic hyperuricemia in children with cystic fibrosis. J Pediatr. 1978 Dec;93(6):976–978. doi: 10.1016/s0022-3476(78)81225-6. [DOI] [PubMed] [Google Scholar]
  5. Durie P. R., Bell L., Linton W., Corey M. L., Forstner G. G. Effect of cimetidine and sodium bicarbonate on pancreatic replacement therapy in cystic fibrosis. Gut. 1980 Sep;21(9):778–786. doi: 10.1136/gut.21.9.778. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Durie P. R., Newth C. J., Forstner G. G., Gall D. G. Malabsorption of medium-chain triglycerides in infants with cystic fibrosis: correction with pancreatic enzyme supplement. J Pediatr. 1980 May;96(5):862–864. doi: 10.1016/s0022-3476(80)80559-2. [DOI] [PubMed] [Google Scholar]
  7. 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]
  8. Gow R., Bradbear R., Francis P., Shepherd R. Comparative study of varying regimens to improve steatorrhoea and creatorrhoea in cystic fibrosis: Effectiveness of an enteric-coated preparation with and without antacids and cimetidine. Lancet. 1981 Nov 14;2(8255):1071–1074. doi: 10.1016/s0140-6736(81)91276-9. [DOI] [PubMed] [Google Scholar]
  9. Hubbard V. S., Mangrum P. J. Energy intake and nutrition counseling in cystic fibrosis. J Am Diet Assoc. 1982 Feb;80(2):127–131. [PubMed] [Google Scholar]
  10. 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]
  11. 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]
  12. Park R. W., Grand R. J. Gastrointestinal manifestations of cystic fibrosis: a review. Gastroenterology. 1981 Dec;81(6):1143–1161. [PubMed] [Google Scholar]
  13. Parsons H. G., Beaudry P., Dumas A., Pencharz P. B. Energy needs and growth in children with cystic fibrosis. J Pediatr Gastroenterol Nutr. 1983;2(1):44–49. doi: 10.1097/00005176-198302010-00005. [DOI] [PubMed] [Google Scholar]
  14. Primosch R. E. Tetracycline discoloration, enamel defects, and dental caries in patients with cystic fibrosis. Oral Surg Oral Med Oral Pathol. 1980 Oct;50(4):301–308. doi: 10.1016/0030-4220(80)90411-9. [DOI] [PubMed] [Google Scholar]
  15. Shepherd R. W., Thomas B. J., Bennett D., Cooksley W. G., Ward L. C. Changes in body composition and muscle protein degradation during nutritional supplementation in nutritionally growth-retarded children with cystic fibrosis. J Pediatr Gastroenterol Nutr. 1983;2(3):439–446. doi: 10.1097/00005176-198302030-00008. [DOI] [PubMed] [Google Scholar]
  16. 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]
  17. Stead R. J., Redington A. N., Hinks L. J., Clayton B. E., Hodson M. E., Batten J. C. Selenium deficiency and possible increased risk of carcinoma in adults with cystic fibrosis. Lancet. 1985 Oct 19;2(8460):862–863. doi: 10.1016/s0140-6736(85)90127-8. [DOI] [PubMed] [Google Scholar]
  18. Stern R. C., Izant R. J., Jr, Boat T. F., Wood R. E., Matthews L. W., Doershuk C. F. Treatment and prognosis of rectal prolapse in cystic fibrosis. Gastroenterology. 1982 Apr;82(4):707–710. [PubMed] [Google Scholar]
  19. Yassa J. G., Prosser R., Dodge J. A. Effects of an artificial diet on growth of patients with cystic fibrosis. Arch Dis Child. 1978 Oct;53(10):777–783. doi: 10.1136/adc.53.10.777. [DOI] [PMC free article] [PubMed] [Google Scholar]

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