Lung Function Longitudinal Study by Phenotype and Genotype in Primary Ciliary Dyskinesia-Reference-Cited by-同舟云学术

Lung Function Longitudinal Study by Phenotype and Genotype in Primary Ciliary Dyskinesia

Published:2020-07 Issue:1 Volume:158 Page:117-120
ISSN:0012-3692
Container-title:Chest
language:en
Short-container-title:Chest

Author:

Pifferi Massimo,Bush Andrew,Mariani Francesca,Piras Martina,Michelucci Angela,Cangiotti Angela,Di Cicco Maria,Caligo Maria Adelaide,Miccoli Mario,Boner Attilio L.,Peroni Diego

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine,Critical Care and Intensive Care Medicine,Pulmonary and Respiratory Medicine

Reference10 articles.

1. Lung function in patients with primary ciliary dyskinesia: a cross-sectional and 3-decade longitudinal study;Marthin;Am J Respir Crit Care Med,2010

2. Clinical characteristics, functional respiratory decline and follow-up in adult patients with primary ciliary dyskinesia;Frija-Masson;Thorax,2017

3. Clinical features of childhood primary ciliary dyskinesia by genotype and ultrastructural phenotype;Davis;Am J Respir Crit Care Med,2015

4. A longitudinal study characterising a large adult primary ciliary dyskinesia population;Shah;Eur Respir J,2016

5. Primary ciliary dyskinesia: longitudinal study of lung disease by ultrastructure defect and genotype;Davis;Am J Respir Crit Care Med,2019

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. Impact of TAS2R38 polymorphisms on nasal nitric oxide andPseudomonasinfections in primary ciliary dyskinesia: relation to genotype;Thorax;2024-08-24

2. Analyses of 1236 genotyped primary ciliary dyskinesia individuals identify regional clusters of distinct DNA variants and significant genotype–phenotype correlations;European Respiratory Journal;2024-06-13

3. Primary Ciliary Dyskinesia: A Clinical Review;Cells;2024-06-04

4. Genetic Spectrum and Clinical Characteristics of Patients with Primary Ciliary Dyskinesia: a Belgian Single Center Study;Lung;2024-04-11

5. Loss of an extensive ciliary connectome induces proteostasis and cell fate switching in a severe motile ciliopathy;2024-03-21