These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
3. Essential fatty acid status in cystic fibrosis and the effects of safflower oil supplementation. Lloyd-Still JD; Johnson SB; Holman RT Am J Clin Nutr; 1981 Jan; 34(1):1-7. PubMed ID: 7446449 [TBL] [Abstract][Full Text] [Related]
4. Dietary essential fatty acids in cystic fibrosis. Rosenlund ML; Selekman JA; Kim HK; Kritchevsky D Pediatrics; 1977 Mar; 59(3):428-32. PubMed ID: 840562 [TBL] [Abstract][Full Text] [Related]
5. Screening for cystic fibrosis with chloride electrode. An investigation of sweat chloride with chloride electrode orion 417 in normal persons and in patients with cystic fibrosis. Steinrud J; Winkel S; Flensborg EW Dan Med Bull; 1974 Oct; 21(6):251-5. PubMed ID: 4430191 [No Abstract] [Full Text] [Related]
6. [Results of the sweat test, carried out by 2 methods, for the diagnosis of cystic fibrosis]. Vázquez C; Azcárate MJ; Sojo A; Vitoria JC An Esp Pediatr; 1987 Jan; 26(1):33-6. PubMed ID: 3826941 [TBL] [Abstract][Full Text] [Related]
7. Fatty acids composition of plasma phospholipids and triglycerides in children with cystic fibrosis. The effect of dietary supplementation with an olive and soybean oils mixture. Caramia G; Cocchi M; Gagliardini R; Malavolta M; Mozzon M; Frega NG Pediatr Med Chir; 2003; 25(1):42-9. PubMed ID: 12920976 [TBL] [Abstract][Full Text] [Related]
8. A therapeutic trial of fatty acid supplementation in cystic fibrosis. Elliott RB Pediatrics; 1976 Apr; 57(4):474-9. PubMed ID: 1264542 [TBL] [Abstract][Full Text] [Related]
9. Oral DHA supplementation in DeltaF508 homozygous cystic fibrosis patients. Van Biervliet S; Devos M; Delhaye T; Van Biervliet JP; Robberecht E; Christophe A Prostaglandins Leukot Essent Fatty Acids; 2008 Feb; 78(2):109-15. PubMed ID: 18276127 [TBL] [Abstract][Full Text] [Related]
10. Relation of sweat chloride concentration to severity of lung disease in cystic fibrosis. Davis PB; Schluchter MD; Konstan MW Pediatr Pulmonol; 2004 Sep; 38(3):204-9. PubMed ID: 15274098 [TBL] [Abstract][Full Text] [Related]
18. Cooperative study comparing three methods of performing sweat tests to diagnose cystic fibrosis. Denning CR; Huang NN; Cuasay LR; Shwachman H; Tocci P; Warwick WJ; Gibson LE Pediatrics; 1980 Nov; 66(5):752-7. PubMed ID: 7432881 [TBL] [Abstract][Full Text] [Related]
19. Sweat chloride concentration in cystic fibrosis patients varies with KM.19 genotype but not with the presence of the common F508 deletion. Gasparini P; Pignatti PF; Borgo G; Mastella G Am J Med Genet; 1991 May; 39(2):230-1. PubMed ID: 2063932 [No Abstract] [Full Text] [Related]
20. The evaluation of a novel conductometric device for the diagnosis of cystic fibrosis. Losty HC; Wheatley H; Doull I Ann Clin Biochem; 2006 Sep; 43(Pt 5):375-81. PubMed ID: 17022880 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]