Detalhe da pesquisa
1.
High risk of lung cancer in surfactant-related gene variant carriers.
Eur Respir J
; 63(5)2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38575158
2.
Similarities and differences of interstitial lung disease associated with pathogenic variants in SFTPC and ABCA3 in adults.
Respirology
; 29(4): 312-323, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38345107
3.
Children's views on artificial intelligence and digital twins for the daily management of their asthma: a mixed-method study.
Eur J Pediatr
; 182(2): 877-888, 2023 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-36512148
4.
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
5.
Exposure to inorganic particles in paediatric sarcoidosis: the PEDIASARC study.
Thorax
; 77(4): 404-407, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34675126
6.
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
7.
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
8.
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
9.
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
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.
Paediatric sarcoidosis.
Paediatr Respir Rev
; 29: 53-59, 2019 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-30917882
12.
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
13.
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
14.
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
15.
Severe Acute Respiratory Syndrome Coronavirus 2 Variant Delta Infects All 6 Siblings but Spares Comirnaty (BNT162b2, BioNTech/Pfizer)-Vaccinated Parents.
J Infect Dis
; 224(11): 1984-1986, 2021 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34409999
16.
Loss-of-function mutations in RSPH1 cause primary ciliary dyskinesia with central-complex and radial-spoke defects.
Am J Hum Genet
; 93(3): 561-70, 2013 Sep 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-23993197
17.
Atypical presentation of COVID-19 in young infants.
Lancet
; 395(10235): 1481, 2020 05 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32353326
18.
Ultrasonography and Computed Tomographic Manifestations of Abdominal Sarcoidosis in Children.
J Pediatr Gastroenterol Nutr
; 63(2): 195-9, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-26913758
19.
Lung sarcoidosis in children: update on disease expression and management.
Thorax
; 70(6): 537-42, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25855608
20.
Dramatic improvement after tocilizumab of severe COVID-19 in a child with sickle cell disease and acute chest syndrome.
Am J Hematol
; 95(8): E192-E194, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32358817