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1
A rational approach to the nutritional care of patients with cystic fibrosis.一种针对囊性纤维化患者营养护理的合理方法。
J R Soc Med. 1989;82 Suppl 16(Suppl 16):11-20.
2
3.19 Nutrition in cystic fibrosis.
World Rev Nutr Diet. 2015;113:244-9. doi: 10.1159/000367876. Epub 2015 Apr 13.
3
Consensus report on nutrition for pediatric patients with cystic fibrosis.囊性纤维化儿科患者营养共识报告。
J Pediatr Gastroenterol Nutr. 2002 Sep;35(3):246-59. doi: 10.1097/00005176-200209000-00004.
4
[Mucoviscidosis. Nutritional management].
Presse Med. 1997;26(15):721-6.
5
Nutritional assessment and management in cystic fibrosis: a consensus report. The Consensus Committee.囊性纤维化的营养评估与管理：共识报告。共识委员会。
Am J Clin Nutr. 1992 Jan;55(1):108-16. doi: 10.1093/ajcn/55.1.108.
6
[Malnutrition and nutrition in patients with cystic fibrosis].
Med Klin (Munich). 1995 Jan 15;90(1):40-4.
7
[Question 2. What strategy for maintaining optimal nutritional state? Influence of nutritional state on the progression of cystic fibrosis: physiopathologic, epidemiologic and clinical aspects of nutrition disorders].
Arch Pediatr. 2003 Aug;10 Suppl 3:449s-452s. doi: 10.1016/s0929-693x(03)90009-1.
8
Malnutrition and age-specific nutritional management in cystic fibrosis.囊性纤维化中的营养不良与特定年龄的营养管理
Neth J Med. 1992 Oct;41(3-4):127-9.
9
Cystic fibrosis: nutrition.
Br Med Bull. 1992 Oct;48(4):823-46. doi: 10.1093/oxfordjournals.bmb.a072580.
10
Nutrition in the management of cystic fibrosis.
Nutr Rev. 1996 Jan;54(1 Pt 1):31-3. doi: 10.1111/j.1753-4887.1996.tb03771.x.

引用本文的文献

1
Can Existing Knowledge on Eating Behaviors and Obesity Support People with Cystic Fibrosis Who Are Nutritionally Compromised?关于饮食行为和肥胖的现有知识能否帮助营养状况不佳的囊性纤维化患者？
Front Psychol. 2016 Sep 27;7:1477. doi: 10.3389/fpsyg.2016.01477. eCollection 2016.
2
Vitamin B12-mediated restoration of defective anaerobic growth leads to reduced biofilm formation in Pseudomonas aeruginosa.维生素 B12 介导的缺陷厌氧生长的恢复导致铜绿假单胞菌生物膜形成减少。
Infect Immun. 2012 May;80(5):1639-49. doi: 10.1128/IAI.06161-11. Epub 2012 Feb 27.
3
A CFTR potentiator in patients with cystic fibrosis and the G551D mutation.囊性纤维化跨膜电导调节因子增效剂治疗囊性纤维化跨膜电导调节因子 G551D 突变患者。
N Engl J Med. 2011 Nov 3;365(18):1663-72. doi: 10.1056/NEJMoa1105185.
4
Growth hormone and exercise tolerance in patients with cystic fibrosis.囊性纤维化患者的生长激素与运动耐量
Sports Med. 2004;34(2):81-90. doi: 10.2165/00007256-200434020-00002.
5
Perceived body image and eating behavior in young adults with cystic fibrosis and their healthy peers.患有囊性纤维化的年轻人及其健康同龄人对身体形象的认知和饮食行为。
J Behav Med. 2000 Dec;23(6):501-17. doi: 10.1023/a:1005532602084.
6
Increasing calorie consumption in children with cystic fibrosis: replication with 2-year follow-up.增加囊性纤维化患儿的热量摄入：两年随访的重复研究
J Appl Behav Anal. 1993 Winter;26(4):435-50. doi: 10.1901/jaba.1993.26-435.
7
Clinical management of children and adults with cystic fibrosis.患有囊性纤维化的儿童和成人的临床管理。
BMJ. 1994 Feb 12;308(6926):459-62. doi: 10.1136/bmj.308.6926.459.
8
Monitoring steatorrhoea in cystic fibrosis.
Eur J Pediatr. 1994 Jun;153(6):416-8. doi: 10.1007/BF01983404.
9
Fluoroscopically guided percutaneous gastrostomy in patients with cystic fibrosis.荧光镜引导下的囊性纤维化患者经皮胃造口术
Thorax. 1994 May;49(5):519-20. doi: 10.1136/thx.49.5.519.
10
Cystic fibrosis.囊性纤维化
Arch Dis Child. 1990 Jan;65(1):152-7. doi: 10.1136/adc.65.1.152.

本文引用的文献

1
Therapy of cystic fibrosis of the pancreas.胰腺囊性纤维化的治疗。
Pediatrics. 1960 Jan;25:155-63.
2
GROWTH PATTERNS IN CHILDREN WITH CYSTIC FIBROSIS.囊性纤维化患儿的生长模式
J Pediatr. 1964 Nov;65:664-76. doi: 10.1016/s0022-3476(64)80151-7.
3
NEUROAXONAL DYSTROPHY IN MUCOVISCIDOSIS.黏多糖贮积症中的神经轴索性营养不良
J Neuropathol Exp Neurol. 1964 Oct;23:567-83. doi: 10.1097/00005072-196410000-00001.
4
Long chain non-esterified fatty acid pattern in plasma of cystic fibrosis patients and their parents.囊性纤维化患者及其父母血浆中的长链非酯化脂肪酸模式。
Pediatr Res. 1980 Sep;14(9):1088-91. doi: 10.1203/00006450-198009000-00015.
5
Vitamin status in treated patients with cystic fibrosis.接受治疗的囊性纤维化患者的维生素状况。
Arch Dis Child. 1981 Sep;56(9):708-14. doi: 10.1136/adc.56.9.708.
6
Selenium and vitamin E status in cystic fibrosis.
J Pediatr. 1981 Oct;99(4):583-5. doi: 10.1016/s0022-3476(81)80262-4.
7
Some biochemical indices of nutrition in treated cystic fibrosis patients.接受治疗的囊性纤维化患者的一些营养生化指标。
Am J Clin Nutr. 1981 Apr;34(4):462-74. doi: 10.1093/ajcn/34.4.462.
8
Evidence for a primary defect of pancreatic HCO3-secretion in cystic fibrosis.
Pediatr Res. 1982 Jul;16(7):554-7. doi: 10.1203/00006450-198207000-00012.
9
[Remarks suggested by a case of anencephaly with a different Pi type in fetal and maternal blood (author's transl)].
Clin Chim Acta. 1980 Mar 14;102(1):105-10. doi: 10.1016/0009-8981(80)90439-8.
10
Effect of hyperventilation and starvation on rat lung mechanics and surfactant.过度通气和饥饿对大鼠肺力学及表面活性剂的影响。
Am Rev Respir Dis. 1982 Aug;126(2):286-90. doi: 10.1164/arrd.1982.126.2.286.

A rational approach to the nutritional care of patients with cystic fibrosis.

作者信息

Durie P R, Pencharz P B

机构信息

Department of Pediatrics, Hospital for Sick Children, Toronto, Ontario, Canada.

出版信息

J R Soc Med. 1989;82 Suppl 16(Suppl 16):11-20.

PMID:2657050
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1291914/
Abstract
摘要