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Nutritional deficits exist before 2 months of age in some infants with cystic fibrosis identified by screening test.

作者信息

Reardon M C, Hammond K B, Accurso F J, Fisher C D, McCabe E R, Cotton E K, Bowman C M

出版信息

J Pediatr. 1984 Aug;105(2):271-4. doi: 10.1016/s0022-3476(84)80128-6.

DOI:10.1016/s0022-3476(84)80128-6
PMID:6747761
Abstract
摘要

相似文献

1
Nutritional deficits exist before 2 months of age in some infants with cystic fibrosis identified by screening test.
J Pediatr. 1984 Aug;105(2):271-4. doi: 10.1016/s0022-3476(84)80128-6.
2
The role of the laboratory in the diagnosis of cystic fibrosis.实验室在囊性纤维化诊断中的作用。
Clin Biochem. 1984 Oct;17(5):284-7. doi: 10.1016/s0009-9120(84)90553-8.
3
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.
4
Nutritional benefits of neonatal screening for cystic fibrosis. Wisconsin Cystic Fibrosis Neonatal Screening Study Group.囊性纤维化新生儿筛查的营养益处。威斯康星州囊性纤维化新生儿筛查研究组。
N Engl J Med. 1997 Oct 2;337(14):963-9. doi: 10.1056/NEJM199710023371403.
5
Dried-blood spot screening for cystic fibrosis in the newborn.新生儿囊性纤维化的干血斑筛查。
Lancet. 1979 Mar 3;1(8114):472-4. doi: 10.1016/s0140-6736(79)90825-0.
6
Sensitive trypsin assay for dried-blood specimens as a screening procedure for early detection of cystic fibrosis.用于干血标本的敏感胰蛋白酶检测作为早期检测囊性纤维化的筛查程序。
Lancet. 1979 Dec 8;2(8154):1217-9. doi: 10.1016/s0140-6736(79)92336-5.
7
Dried blood spot screening for cystic fibrosis.囊性纤维化的干血斑筛查
Lancet. 1979 Dec 8;2(8154):1236-7. doi: 10.1016/s0140-6736(79)92350-x.
8
The neonatal detection of cystic fibrosis by measurement of immunoreactive trypsin in blood.通过检测血液中的免疫反应性胰蛋白酶对新生儿进行囊性纤维化的检测。
Ann Clin Biochem. 1992 Jul;29 ( Pt 4):361-76. doi: 10.1177/000456329202900401.
9
Use of a dried blood spot in immunoreactive-trypsin assay for detection of cystic fibrosis in infants.利用干血斑进行免疫反应性胰蛋白酶检测以诊断婴儿囊性纤维化
Clin Chem. 1981 May;27(5):678-8.
10
[Diagnosis and treatment of the syndromes of disturbed absorption in children].[儿童吸收障碍综合征的诊断与治疗]
Pediatriia. 1974 Mar;3:3-8.

引用本文的文献

1
India: The Last and Best Frontier for Cystic Fibrosis Newborn Screening with Perspectives on Special Challenges.印度：囊性纤维化新生儿筛查的最后也是最佳前沿阵地及特殊挑战透视
Int J Neonatal Screen. 2025 Apr 17;11(2):27. doi: 10.3390/ijns11020027.
2
Newborn Screening for CF across the Globe-?全球范围内的囊性纤维化新生儿筛查 -？
Int J Neonatal Screen. 2020 Mar 4;6(1):18. doi: 10.3390/ijns6010018. eCollection 2020 Mar.
3
The Impact of the CFTR Gene Discovery on Cystic Fibrosis Diagnosis, Counseling, and Preventive Therapy.CFTR 基因发现对囊性纤维化的诊断、咨询和预防治疗的影响。
Genes (Basel). 2020 Apr 8;11(4):401. doi: 10.3390/genes11040401.
4
Newborn screening for cystic fibrosis.新生儿囊性纤维化筛查。
Clin Rev Allergy Immunol. 2008 Dec;35(3):107-15. doi: 10.1007/s12016-008-8082-1.
5
Clinical outcomes of newborn screening for cystic fibrosis.囊性纤维化新生儿筛查的临床结果。
Arch Dis Child Fetal Neonatal Ed. 1999 Jan;80(1):F1-7. doi: 10.1136/fn.80.1.f1.
6
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.
7
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.
8
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.
9
Cystic fibrosis. 7. Management of cystic fibrosis in different countries. Cystic fibrosis in Leeds.囊性纤维化。7. 不同国家的囊性纤维化管理。利兹的囊性纤维化情况。
Thorax. 1991 May;46(5):387-9; discussion 389-90. doi: 10.1136/thx.46.5.387.
10
Neonatal screening for cystic fibrosis in Wales and the West Midlands: clinical assessment after five years of screening.威尔士和西米德兰兹地区的新生儿囊性纤维化筛查：筛查五年后的临床评估。
Arch Dis Child. 1991 Jan;66(1 Spec No):29-33. doi: 10.1136/adc.66.1_spec_no.29.