Detalhe da pesquisa
1.
Long-term evolution of neuroendocrine cell hyperplasia of infancy: the FRENCHI findings.
Eur J Pediatr;
182(2): 949-956, 2023 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36449078
2.
Exposure to inorganic particles in paediatric sarcoidosis: the PEDIASARC study.
Thorax;
77(4): 404-407, 2022 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34675126
3.
French national cohort of neuroendocrine cell hyperplasia of infancy (FRENCHI) study: diagnosis and initial management.
Eur J Pediatr;
181(8): 3067-3073, 2022 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35678871
4.
Impact of Gender on the Characteristics of Patients with Idiopathic Pulmonary Fibrosis Included in the RaDiCo-ILD Cohort.
Respiration;
101(1): 34-45, 2022.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34515219
5.
Genotype-Phenotype Relationships in Inheritable Idiopathic Pulmonary Fibrosis: A Greek National Cohort Study.
Respiration;
101(6): 531-543, 2022.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35078193
6.
MUC5B Promoter Variant and Rheumatoid Arthritis with Interstitial Lung Disease.
N Engl J Med;
379(23): 2209-2219, 2018 12 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30345907
7.
Deep phenotyping, including quantitative ciliary beating parameters, and extensive genotyping in primary ciliary dyskinesia.
J Med Genet;
57(4): 237-244, 2020 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31772028
8.
Use of ruxolitinib in COPA syndrome manifesting as life-threatening alveolar haemorrhage.
Thorax;
75(1): 92-95, 2020 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31666386
9.
One-year outcomes in a multicentre cohort study of incident rare diffuse parenchymal lung disease in children (ChILD).
Thorax;
75(2): 172-175, 2020 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31748256
10.
Functional assessment and phenotypic heterogeneity of SFTPA1 and SFTPA2 mutations in interstitial lung diseases and lung cancer.
Eur Respir J;
56(6)2020 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32855221
11.
Cystic Fibrosis Liver Disease: Outcomes and Risk Factors in a Large Cohort of French Patients.
Hepatology;
69(4): 1648-1656, 2019 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30058245
12.
Paediatric sarcoidosis.
Paediatr Respir Rev;
29: 53-59, 2019 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30917882
13.
Germline SFTPA1 mutation in familial idiopathic interstitial pneumonia and lung cancer.
Hum Mol Genet;
25(8): 1457-67, 2016 Apr 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26792177
14.
RSPH3 Mutations Cause Primary Ciliary Dyskinesia with Central-Complex Defects and a Near Absence of Radial Spokes.
Am J Hum Genet;
97(1): 153-62, 2015 Jul 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26073779
15.
International management platform for children's interstitial lung disease (chILD-EU).
Thorax;
73(3): 231-239, 2018 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29056600
16.
Genetic causes and clinical management of pediatric interstitial lung diseases.
Curr Opin Pulm Med;
24(3): 253-259, 2018 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29517585
17.
Growth and nutritional status, and their association with lung function: a study from the international Primary Ciliary Dyskinesia Cohort.
Eur Respir J;
50(6)2017 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29269581
18.
The international primary ciliary dyskinesia cohort (iPCD Cohort): methods and first results.
Eur Respir J;
49(1)2017 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28052956
19.
Shared genetic predisposition in rheumatoid arthritis-interstitial lung disease and familial pulmonary fibrosis.
Eur Respir J;
49(5)2017 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28495692
20.
Mutations in GAS8, a Gene Encoding a Nexin-Dynein Regulatory Complex Subunit, Cause Primary Ciliary Dyskinesia with Axonemal Disorganization.
Hum Mutat;
37(8): 776-85, 2016 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27120127