Inconclusive Cystic Fibrosis neonatal screening results: long-term psychosocial effects on parents-Reference-Cited by-同舟云学术

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Inconclusive Cystic Fibrosis neonatal screening results: long-term psychosocial effects on parents

Published:2009-12 Issue:12 Volume:98 Page:1927-1934
ISSN:0803-5253
Container-title:Acta Paediatrica
language:en
Short-container-title:

Author:

Perobelli Sandra,Zanolla Luisa,Tamanini Anna,Rizzotti Paolo,Maurice Assael Baroukh,Castellani Carlo

Publisher

Wiley

Subject

General Medicine,Pediatrics, Perinatology and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.2009.01485.x/fullpdf

Reference29 articles.

1. Newborn screening for cystic fibrosis: techniques and strategies;Wilcken;J Inherit Metab Dis,2007

2. Guidelines for implementation of cystic fibrosis newborn screening programs: Cystic Fibrosis Foundation workshop report;Comeau;Pediatrics,2007

3. On behalf of the ECFS CF Neonatal Screening Working Group. A survey of newborn screening for cystic fibrosis in Europe;Southern;J Cyst Fibros,2007

4. Sweat chloride concentrations in infants homozygous or heterozygous for ΔF508 cystic fibrosis;Farrell;Pediatrics,1996

5. Guidelines for diagnosis of cystic fibrosis in newborns through older adults: Cystic Fibrosis Foundation consensus report;Farrell;J Pediatr,2008

Cited by 25 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Parents' and childrens’ views of wider genomic testing when used as part of newborn screening to identify cystic fibrosis;SSM - Qualitative Research in Health;2024-12

2. Literary evidence of the impact of nonbiological risk factors on CRMS/CFSPID: A scoping review;Pediatric Pulmonology;2024-08-21

3. ECFS standards of care on CFTR-related disorders: Towards a comprehensive program for affected individuals;Journal of Cystic Fibrosis;2024-05

4. International Perspectives of Extended Genetic Sequencing When Used as Part of Newborn Screening to Identify Cystic Fibrosis;International Journal of Neonatal Screening;2024-04-08

5. Patient preferences in genetic newborn screening for rare diseases: study protocol;BMJ Open;2024-04

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