Phosphatidylcholine and lysophosphatidylcholine excretion is increased in children with cystic fibrosis and is associated with plasma homocysteine, S-adenosylhomocysteine, and S-adenosylmethionine-Reference-Cited by-同舟云学术

Phosphatidylcholine and lysophosphatidylcholine excretion is increased in children with cystic fibrosis and is associated with plasma homocysteine, S-adenosylhomocysteine, and S-adenosylmethionine

Published:2005-03-01 Issue:3 Volume:81 Page:686-691
ISSN:0002-9165
Container-title:The American Journal of Clinical Nutrition
language:en
Short-container-title:

Author:

Chen Alice H,Innis Sheila M,Davidson A George F,James S Jill

Publisher

Oxford University Press (OUP)

Subject

Nutrition and Dietetics,Medicine (miscellaneous)

Link

http://academic.oup.com/ajcn/article-pdf/81/3/686/23875298/686.pdf

Reference44 articles.

1. Intracellular CFTR. Localization and function;Bradbury;Physiol Rev,1999

2. Pancreatic function in infants identified as having cystic fibrosis in a neonatal screening program;Waters;N Engl J Med,1990

3. Decline of exocrine pancreatic function in cystic fibrosis patients with pancreatic sufficiency;Couper;Pediatr Res,1992

4. Introduodenal events in cystic fibrosis;Weber;J Pediatr Gastroenterol Nutr,1984

5. Twenty-four hour ambulatory gastric and duodenal pH profiles in cystic fibrosis: effect of duodenal hyperacidity on pancreatic enzyme function and fat absorption;Barraclough;J Pediatr Gastroenterol Nutr,1996

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