Current and future diagnosis of cystic fibrosis: Performance and limitations-Reference-Cited by-同舟云学术

Current and future diagnosis of cystic fibrosis: Performance and limitations

Published:2020-02 Issue: Volume:27 Page:eS19-eS24
ISSN:0929-693X
Container-title:Archives de Pédiatrie
language:en
Short-container-title:Archives de Pédiatrie

Author:

Bienvenu T.,Nguyen-Khoa T.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference41 articles.

1. ECFS best practice guidelines: the 2018 revision;Castellani;J Cyst Fibros,2018

2. Diagnosis of Cystic Fibrosis: Consensus Guidelines from the Cystic Fibrosis Foundation;Farrell;J Pediatr,2017

3. Haute Autorité de Santé. Protocole National De Soins-Mucoviscidose, Juillet 2017. [online] www.has-sante.fr/portail/jcms/c_2792719/fr/mucoviscidose

4. Diagnosis of Cystic Fibrosis in Nonscreened Populations;Sosnay;J Pediatr,2017

5. Guidelines for the clinical management and follow-up of infants with inconclusive cystic fibrosis diagnosis through newborn screening;Sermet-Gaudelus;Arch Pediatr,2017

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1. Mucoviscidose : explorations biologiques et nouvelles thérapies;Option/Bio;2023-07

2. Reclassifying inconclusive diagnosis for cystic fibrosis with new generation sweat test;European Respiratory Journal;2022-07-01

3. CFTR protein quantification as a cystic fibrosis diagnostic biomarker in dried blood spots using multiple reaction monitoring tandem mass spectrometry;Journal of Pharmaceutical and Biomedical Analysis;2022-07

4. International Approaches to Management of CFTR-Related Metabolic Syndrome/Cystic Fibrosis Screen Positive, Inconclusive Diagnosis;International Journal of Neonatal Screening;2022-01-11

5. Sweat Testing and Recent Advances;Frontiers in Pediatrics;2021-05-04