References
- Shapiro BL, Lam LF, Feigal RJ. Mitochondrial NADH dehydrogenase in cystic fibrosis: enzyme kinetics in cultured fibroblasts. Am J Hum Genet 1982: 34(6): 846–52
- Parsons HG, Beaudry P, Dumas A, et al. Energy needs and growth in children with cystic fibrosis. J Pediatr Gastroenterol Nutr 1983: 2(1): 44–9
- Reardon MC. Hammond KB, Accurso FJ, et al. Nutritional deficits exist before 2 months of age in some infants with cystic fibrosis identified by screening test. J Pediatr 1984: 105(2): 271–4
- Shepherd RW, Holt TL, Thomas BJ, et al. Nutritional rehabilitation in cystic fibrosis: controlled studies of effects on nutritional growth retardation, body protein turnover, and course of pulmonary disease. J Pediatr 1986: 109(5): 788–94
- Leroy C, Lepage G, Morin CL, et al. Effect of dietary fat and residues on fecal loss of sterols and on their microbial degradation in cystic fibrosis. Dig Dis Sci 1986: 31(9): 911–8
- O'Loughlin E, Forbes D, Parsons H, et al. Nutritional rehabilitation of malnourished patients with cystic fibrosis. Am J Clin Nutr 1986: 43(5): 732–7
- Holt TL, Ward LC, Francis PJ, et al. Whole body protein turnover in malnourished cystic fibrosis patients and its relationship to pulmonary disease. Am J Clin Nutr 1985: 41 (5): 1061–6
- Soutter VL, Kristidis P, Gruca MA, et al. Chronic undemutrition/growth retardation in cystic fibrosis. Clin Gastroenterol 1986: 15(1): 137–55
- Abman SH, Accurso F J, Bowman CM. Persistent morbidity and mortality or protein calorie malnutrition in young infants with CF. J Pediatr Gastroenterol Nutr 1986: 5(3): 393–6
- Moore MC, Greene HL, Donald WD, et al. Enteral-tube feeding as adjunct therapy in malnourished patients with cystic fibrosis: a clinical study and literature review. Am J Clin Nutr 1986: 44(1): 33–41