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.
Comparison of Continuous Glucose Monitoring in Cystic Fibrosis Patients With or Without Pancreatic Exocrine Insufficiency.
Horm Metab Res
; 54(6): 407-412, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35272389
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.
Toward the Standardization of Mycological Examination of Sputum Samples in Cystic Fibrosis: Results from a French Multicenter Prospective Study.
Mycopathologia
; 183(1): 101-117, 2018 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-28748285
5.
Long-Term Rasamsonia argillacea Complex Species Colonization Revealed by PCR Amplification of Repetitive DNA Sequences in Cystic Fibrosis Patients.
J Clin Microbiol
; 54(11): 2804-2812, 2016 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-27605712
6.
Lessons from a French collaborative case-control study in cystic fibrosis patients during the 2009 A/H1N1 influenza pandemy.
BMC Infect Dis
; 16: 55, 2016 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26830335
7.
Early glucose abnormalities revealed by continuous glucose monitoring associate with lung function decline in cystic fibrosis: A five-year prospective study.
J Diabetes Complications
; 38(4): 108703, 2024 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-38430625
8.
Severe bronchiolitis in infants born very preterm and neurodevelopmental outcome at 2 years.
Eur J Pediatr
; 172(5): 639-44, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23338967
9.
Breastfeeding and respiratory, ear and gastro-intestinal infections, in children, under the age of one year, admitted through the paediatric emergency departments of five hospitals.
Front Pediatr
; 10: 1053473, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36874253
10.
Sputum versus nasopharyngeal samples for the molecular diagnosis of respiratory viral infection in cystic fibrosis: A pilot study.
J Cyst Fibros
; 20(3): 432-435, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32943334
11.
Effect of one-year lumacaftor-ivacaftor treatment on glucose tolerance abnormalities in cystic fibrosis patients.
J Cyst Fibros
; 19(5): 712-716, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32201160
12.
Health-related quality of life in infants and children with interstitial lung disease.
Pediatr Pulmonol
; 54(6): 828-836, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30868755
13.
Pulmonary hemosiderosis in children with Down syndrome: a national experience.
Orphanet J Rare Dis
; 13(1): 60, 2018 04 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-29678139
14.
Infectious disease. Life-threatening influenza and impaired interferon amplification in human IRF7 deficiency.
Science
; 348(6233): 448-53, 2015 Apr 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-25814066
15.
New insights into pediatric idiopathic pulmonary hemosiderosis: the French RespiRare(®) cohort.
Orphanet J Rare Dis
; 8: 161, 2013 Oct 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-24125570
16.
A national internet-linked based database for pediatric interstitial lung diseases: the French network.
Orphanet J Rare Dis
; 7: 40, 2012 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22704798