ライフサイエンスコーパス: neonatal screening

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1 a diagnostic criterion and can be applied to neonatal screening.

2 trategies for sickle cell disease, including neonatal screening.

3 ls to assess the effectiveness and safety of neonatal screening and early treatment.

4 blood spot samples obtained from the Danish Neonatal Screening Biobank and genotyped using the Illum

5 d individuals were retrieved from the Danish Neonatal Screening Biobank.

6 zation, and DNA was obtained from the Danish Neonatal Screening Biobank.

7 DNA was obtained from the Danish Neonatal Screening Biobank.

8 Neonatal screening for CAH and gene-specific prenatal di

9 We assessed neonatal screening for CAH from January 1, 1986, through

10 As a result of such screening efforts, neonatal screening for CAH has proven to be highly relia

11 nt reports have questioned the rationale for neonatal screening for congenital adrenal hyperplasia (C

12 Consideration must be given to universal neonatal screening for cytomegalovirus to facilitate ear

13 We reviewed the results of neonatal screening for homocystinuria over a period of 3

14 Neonatal screening for SCID would significantly improve

15 These include neonatal screening of immunodeficiencies and asthma biom

16 patients with cystic fibrosis identified by neonatal screening or by standard diagnostic methods.

17 In CF patients diagnosed through neonatal screening, P aeruginosa pulmonary infections oc

18 e facilitated the introduction of nationwide neonatal screening programmes for a large number of meta

19 ren necessitates implementation of universal neonatal screening programmes for hearing impairment.

20 Neonatal screening programmes, based on clinical screeni

21 s, stem cell transplantation facilities, and neonatal screening programs.

22 a detected in tandem mass spectrometry-based neonatal screening programs.

23 The Wisconsin CF Neonatal Screening Project is a longitudinal investigati

24 n and treatment protocol of the Wisconsin CF Neonatal Screening Project.

25 Although CF neonatal screening provides a potential opportunity for

26 Neonatal screening provides the opportunity to prevent m

27 ic categories: meconium ileus (MI), prenatal/neonatal screening (SCREEN), positive family history (FH

28 or blood methionine of 1 mg per deciliter in neonatal screening tests for homocystinuria should ident

29 infection as well as the lack of large-scale neonatal screening tools.

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