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.
Abstract
摘要
相似文献
1
Nutritional management of the infant with cystic fibrosis.
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.
J Pediatr Gastroenterol Nutr. 1984;3 Suppl 1:S51-4.
3
Growth of human milk-fed and formula-fed infants with cystic fibrosis.
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].
Rev Mal Respir. 2000 Aug;17(3 Pt 2):785-97.
5
Colonic strictures in cystic fibrosis.
J R Soc Med. 1995;88 Suppl 25(Suppl 25):3-8.
6
[Low weight at birth in cystic fibrosis and its relationship to insufficiency of the exocrine pancreas].
Minerva Pediatr. 1983 May 15;35(9):437-9.
7
Nutritional challenges of infants with cystic fibrosis.
Early Hum Dev. 2001 Nov;65 Suppl:S53-61. doi: 10.1016/s0378-3782(01)00206-7.
8
Nutritional management of cystic fibrosis.
Arch Dis Child. 1996 Jan;74(1):81-7. doi: 10.1136/adc.74.1.81.
9
Nutrition Management of Cystic Fibrosis in the 21st Century.
Nutr Clin Pract. 2015 Aug;30(4):488-500. doi: 10.1177/0884533615591604. Epub 2015 Jun 25.
10
Letter: Essential fatty acid deficiency due to artificial diet in cystic fibrosis.
Br Med J. 1975 Apr 26;2(5964):192-3. doi: 10.1136/bmj.2.5964.192-b.
引用本文的文献
1
The data and characteristics of the human milk banks in mainland China.
World J Pediatr. 2019 Apr;15(2):190-197. doi: 10.1007/s12519-019-00226-6. Epub 2019 Feb 22.
2
The role of vitamins in cystic fibrosis.
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.
Indian J Pediatr. 1996 Mar-Apr;63(2):189-98. doi: 10.1007/BF02845243.
4
Annual review or continuous assessment?
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.
Arch Dis Child. 1993 Apr;68(4):464-7. doi: 10.1136/adc.68.4.464.
2
Population screening in cystic fibrosis.
J R Soc Med. 1993;86 Suppl 20(Suppl 20):2-6.
3
Prospects for virus-based gene therapy for cystic fibrosis.
J Bioenerg Biomembr. 1993 Feb;25(1):37-42. doi: 10.1007/BF00768066.
4
Early and late outcome of cystic fibrosis screening.
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.
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.
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.
Pediatrics. 1981 Oct;68(4):484-9.
9
Changing feeding trends as a cause of electrolyte depletion in infants with cystic fibrosis.
Pediatrics. 1981 Aug;68(2):203-7.
10
Screening for cystic fibrosis by died blood spot trypsin assay.
Arch Dis Child. 1982 Jan;57(1):18-21.
Zotero 插件