Role of Immunofluorescence and Molecular Diagnosis in the Characterization of Primary Ciliary Dyskinesia-Reference-Cited by-同舟云学术

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Role of Immunofluorescence and Molecular Diagnosis in the Characterization of Primary Ciliary Dyskinesia

Published:2019-08 Issue:8 Volume:55 Page:439-441
ISSN:1579-2129
Container-title:Archivos de Bronconeumología (English Edition)
language:en
Short-container-title:Archivos de Bronconeumología (English Edition)

Author:

Baz-Redón Noelia,Rovira-Amigo Sandra,Camats-Tarruella Núria,Fernández-Cancio Mónica,Garrido-Pontnou Marta,Antolín María,Reula Ana,Armengot-Carceller Miguel,Carrascosa Antonio,Moreno-Galdó Antonio

Funder

Instituto de Salud Carlos III

Spanish Society of Pediatric Pulmonology

Catalan Foundation of Pulmonology (FUCAP)

Publisher

Elsevier BV

Reference15 articles.

1. Diagnosis and management of primary ciliary dyskinesia;Lucas;Arch Dis Child,2014

2. New insights in primary ciliary dyskinesia;Reula;Expert Opin Orphan Drugs,2017

3. Advances in the genetics of primary ciliary dyskinesia: clinical implications;Horani;Chest,2018

4. European Respiratory Society guidelines for the diagnosis of primary ciliary dyskinesia;Lucas;Eur Respir J,2017

5. [Value of nasal nitric oxide in the diagnosis of primary ciliary dyskinesia];Moreno Galdó;An Pediatr (Barc),2010

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