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Nutritional management of the infant with cystic fibrosis.

作者信息

Green M R, Buchanan E, Weaver L T

机构信息

Children's Hospital, Leicester Royal Infirmary.

出版信息

Arch Dis Child. 1995 May;72(5):452-6. doi: 10.1136/adc.72.5.452.

DOI:10.1136/adc.72.5.452
PMID:7618919
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1511098/
Abstract
摘要

相似文献

1
Nutritional management of the infant with cystic fibrosis.患有囊性纤维化婴儿的营养管理
Arch Dis Child. 1995 May;72(5):452-6. doi: 10.1136/adc.72.5.452.
2
Pancreatic insufficiency in cystic fibrosis: result of defect in ontogenesis of the exocrine pancreas.囊性纤维化中的胰腺功能不全:外分泌胰腺个体发生缺陷的结果。
J Pediatr Gastroenterol Nutr. 1984;3 Suppl 1:S51-4.
3
Growth of human milk-fed and formula-fed infants with cystic fibrosis.患有囊性纤维化的母乳喂养和配方奶喂养婴儿的生长情况。
J Pediatr. 1991 Jan;118(1):77-9. doi: 10.1016/s0022-3476(05)81850-5.
4
[Digestive and nutritional management of adults with cystic fibrosis].[成年囊性纤维化患者的消化与营养管理]
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5
Colonic strictures in cystic fibrosis.囊性纤维化中的结肠狭窄
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[Low weight at birth in cystic fibrosis and its relationship to insufficiency of the exocrine pancreas].[囊性纤维化患者出生时体重过低及其与外分泌胰腺功能不全的关系]
Minerva Pediatr. 1983 May 15;35(9):437-9.
7
Nutritional challenges of infants with cystic fibrosis.患有囊性纤维化的婴儿的营养挑战。
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Nutritional management of cystic fibrosis.囊性纤维化的营养管理。
Arch Dis Child. 1996 Jan;74(1):81-7. doi: 10.1136/adc.74.1.81.
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Nutrition Management of Cystic Fibrosis in the 21st Century.21世纪囊性纤维化的营养管理
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Letter: Essential fatty acid deficiency due to artificial diet in cystic fibrosis.信函:囊性纤维化患者因人工饮食导致必需脂肪酸缺乏
Br Med J. 1975 Apr 26;2(5964):192-3. doi: 10.1136/bmj.2.5964.192-b.

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The data and characteristics of the human milk banks in mainland China.中国大陆母乳库的数据和特点。
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2
The role of vitamins in cystic fibrosis.维生素在囊性纤维化中的作用。
J R Soc Med. 2000;93 Suppl 38(Suppl 38):14-9.
3
Cystic fibrosis--an Indian perspective on recent advances in diagnosis and management.囊性纤维化——印度对诊断与管理最新进展的观点
Indian J Pediatr. 1996 Mar-Apr;63(2):189-98. doi: 10.1007/BF02845243.
4
Annual review or continuous assessment?年度评审还是持续评估?
J R Soc Med. 1996;89 Suppl 27(Suppl 27):3-7.

本文引用的文献

1
Cystic fibrosis identified by neonatal screening: incidence, genotype, and early natural history.通过新生儿筛查确诊的囊性纤维化:发病率、基因型及早期自然病史
Arch Dis Child. 1993 Apr;68(4):464-7. doi: 10.1136/adc.68.4.464.
2
Population screening in cystic fibrosis.囊性纤维化的群体筛查
J R Soc Med. 1993;86 Suppl 20(Suppl 20):2-6.
3
Prospects for virus-based gene therapy for cystic fibrosis.基于病毒的囊性纤维化基因治疗前景。
J Bioenerg Biomembr. 1993 Feb;25(1):37-42. doi: 10.1007/BF00768066.
4
Early and late outcome of cystic fibrosis screening.囊性纤维化筛查的早期和晚期结果。
J R Soc Med. 1994;87 Suppl 21(Suppl 21):5-10.
5
Prognosis in cystic fibrosis treated with continuous flucloxacillin from the neonatal period.从新生儿期开始用氟氯西林持续治疗囊性纤维化的预后。
Arch Dis Child. 1994 Feb;70(2):84-9. doi: 10.1136/adc.70.2.84.
6
Resting energy expenditure in infants with cystic fibrosis.
J Pediatr Gastroenterol Nutr. 1994 Feb;18(2):214-9. doi: 10.1097/00005176-199402000-00015.
7
Correction of the ion transport defect in cystic fibrosis transgenic mice by gene therapy.通过基因疗法纠正囊性纤维化转基因小鼠的离子转运缺陷。
Nature. 1993 Mar 18;362(6417):250-5. doi: 10.1038/362250a0.
8
Fat digestion in very low-birth-weight infants: effect of addition of human milk to low-birth-weight formula.极低出生体重儿的脂肪消化:在低出生体重儿配方奶中添加母乳的效果
Pediatrics. 1981 Oct;68(4):484-9.
9
Changing feeding trends as a cause of electrolyte depletion in infants with cystic fibrosis.喂养方式的改变作为囊性纤维化婴儿电解质耗竭的一个原因
Pediatrics. 1981 Aug;68(2):203-7.
10
Screening for cystic fibrosis by died blood spot trypsin assay.通过干血斑胰蛋白酶测定法筛查囊性纤维化。
Arch Dis Child. 1982 Jan;57(1):18-21.