Early and late outcome of cystic fibrosis screening.
作者信息
Green M R, Weaver L T
机构信息
Department of Paediatrics, St James's Hospital, Leeds.
出版信息
J R Soc Med. 1994;87 Suppl 21(Suppl 21):5-10.
Abstract
摘要
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本文引用的文献
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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
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.
3
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.
4
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.
5
6
Diagnostic delay in cystic fibrosis: lessons from newborn screening.囊性纤维化的诊断延迟：新生儿筛查的经验教训。
Arch Dis Child. 1983 Nov;58(11):863-6. doi: 10.1136/adc.58.11.863.
7
Improved sweat test method for the diagnosis of cystic fibrosis.用于诊断囊性纤维化的改良汗液测试方法。
Arch Dis Child. 1984 Oct;59(10):919-22. doi: 10.1136/adc.59.10.919.
8
Screening for cystic fibrosis: a four year regional experience.囊性纤维化的筛查：四年的区域经验。
Arch Dis Child. 1988 Dec;63(12):1438-43. doi: 10.1136/adc.63.12.1438.
9
Survival and clinical outcome in patients with cystic fibrosis, with or without neonatal screening.接受或未接受新生儿筛查的囊性纤维化患者的生存情况及临床结局
J Pediatr. 1989 Mar;114(3):362-7. doi: 10.1016/s0022-3476(89)80552-9.
10
Reduced morbidity in patients with cystic fibrosis detected by neonatal screening.通过新生儿筛查发现的囊性纤维化患者发病率降低。
Lancet. 1985 Dec 14;2(8468):1319-21. doi: 10.1016/s0140-6736(85)92623-6.
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