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1
Screening in infancy.婴儿期筛查。
Arch Dis Child. 1995 Jan;72(1):93-6. doi: 10.1136/adc.72.1.93.
2
Earlier identification of biliary atresia and hepatobiliary disease: selective screening in the third week of life.早期识别胆道闭锁和肝胆疾病:出生后第三周的选择性筛查。
Arch Dis Child. 1995 Jan;72(1):90-2. doi: 10.1136/adc.72.1.90.
3
Screening for biliary atresia.胆道闭锁的筛查
Arch Dis Child. 1995 Aug;73(2):182-3. doi: 10.1136/adc.73.2.182-b.
4
Newborn Screening for Biliary Atresia.胆道闭锁的新生儿筛查
Pediatrics. 2015 Dec;136(6):e1663-9. doi: 10.1542/peds.2015-3570.
5
Neonatal screening for biliary atresia.新生儿胆道闭锁筛查
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Newborn Screening for Biliary Atresia: Bilirubin or Bust?新生儿胆道闭锁筛查:胆红素检测还是其他方法?
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Newborn Bilirubin Screening for Biliary Atresia.新生儿胆道闭锁的胆红素筛查
N Engl J Med. 2016 Aug 11;375(6):605-6. doi: 10.1056/NEJMc1601230.
8
Screening for biliary atresia.胆道闭锁的筛查
Lancet. 1993 Jul 31;342(8866):256. doi: 10.1016/0140-6736(93)91814-3.
9
Newborn Screening for Biliary Atresia.胆道闭锁的新生儿筛查
JAMA. 2020 Mar 24;323(12):1137-1138. doi: 10.1001/jama.2020.2727.
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Biliary Atresia: Clinical Lessons Learned.胆道闭锁:汲取的临床经验
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引用本文的文献

1
International perspectives on newborn screening.新生儿筛查的国际视角。
J Inherit Metab Dis. 2006 Apr-Jun;29(2-3):390-6. doi: 10.1007/s10545-006-0259-2.
2
Newborn screening: new developments, new dilemmas.新生儿筛查:新进展,新困境。
J Med Ethics. 2005 Jul;31(7):393-8. doi: 10.1136/jme.2004.008219.
3
Population newborn screening for inherited metabolic disease: current UK perspectives.英国当前关于遗传性代谢疾病的新生儿群体筛查观点。
J Inherit Metab Dis. 1999 Jun;22(4):572-9. doi: 10.1023/a:1005572710844.
4
Examination for cardiac malformations at six weeks of age.六周龄时心脏畸形检查。
Arch Dis Child Fetal Neonatal Ed. 1999 Jan;80(1):F46-8. doi: 10.1136/fn.80.1.f46.
5
Prospective surveillance study of medium chain acyl-CoA dehydrogenase deficiency in the UK.英国中链酰基辅酶A脱氢酶缺乏症的前瞻性监测研究。
Arch Dis Child. 1998 Aug;79(2):116-9. doi: 10.1136/adc.79.2.116.
6
Neonatal screening for cystic fibrosis. Cystic fibrosis should be added to diseases sought in all newborn babies.新生儿囊性纤维化筛查。应将囊性纤维化纳入所有新生儿疾病筛查范围。
BMJ. 1998 Aug 8;317(7155):411.
7
Hypoglycaemia of the newborn: a review.新生儿低血糖症:综述
Bull World Health Organ. 1997;75(3):261-90.

本文引用的文献

1
The development of a neonatal stool colour comparator.一种新生儿粪便颜色比对器的研发。
Midwifery. 1993 Mar;9(1):35-40. doi: 10.1016/0266-6138(93)90040-y.
2
Costs and cost-minimisation analysis.成本与成本最小化分析。
BMJ. 1993 Sep 18;307(6906):726-8. doi: 10.1136/bmj.307.6906.726.
3
Resources and strategies: how parents cope with the care of a disabled child.资源与策略:父母如何应对残疾儿童的照料问题。
J Child Psychol Psychiatry. 1994 Jan;35(1):171-209. doi: 10.1111/j.1469-7610.1994.tb01136.x.
4
Feasibility of otoacoustic emission detection followed by ABR as a universal neonatal screening test for hearing impairment.以耳声发射检测随后进行听性脑干反应作为听力障碍通用新生儿筛查测试的可行性。
Br J Audiol. 1994 Feb;28(1):47-51. doi: 10.3109/03005369409077912.
5
Earlier identification of biliary atresia and hepatobiliary disease: selective screening in the third week of life.早期识别胆道闭锁和肝胆疾病:出生后第三周的选择性筛查。
Arch Dis Child. 1995 Jan;72(1):90-2. doi: 10.1136/adc.72.1.90.
6
Late referral for biliary atresia--missed opportunities for effective surgery.胆管闭锁的延迟转诊——有效手术的错失良机。
Lancet. 1989 Feb 25;1(8635):421-3. doi: 10.1016/s0140-6736(89)90012-3.
7
Persistent perceptions of vulnerability following neonatal jaundice.新生儿黄疸后持续存在的易感性认知。
Am J Dis Child. 1990 Feb;144(2):238-41. doi: 10.1001/archpedi.1990.02150260118043.
8
Breast mild jaundice: natural history, familial incidence and late neurodevelopmental outcome of the infant.母乳性轻度黄疸:婴儿的自然病史、家族发病率及远期神经发育结局
Eur J Pediatr. 1991 Feb;150(4):267-70. doi: 10.1007/BF01955528.
9
Screening infants for hearing loss--an economic evaluation.对婴儿进行听力损失筛查——一项经济学评估。
J Epidemiol Community Health. 1992 Aug;46(4):350-6. doi: 10.1136/jech.46.4.350.
10
Screening, ethics, and the law.筛查、伦理与法律。
BMJ. 1992 Aug 1;305(6848):267-8. doi: 10.1136/bmj.305.6848.267.

Screening in infancy.

作者信息

Hall D M, Michel J M

机构信息

Department of Paediatrics, Children's Hospital, Western Bank, Sheffield.

出版信息

Arch Dis Child. 1995 Jan;72(1):93-6. doi: 10.1136/adc.72.1.93.

DOI:10.1136/adc.72.1.93
PMID:7717751
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1510957/
Abstract
摘要