Detalhe da pesquisa
1.
Mucus Release and Airway Constriction by TMEM16A May Worsen Pathology in Inflammatory Lung Disease.
Int J Mol Sci
; 22(15)2021 Jul 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-34360618
2.
Precision medicine in cystic fibrosis: predictive role of forskolin-induced swelling assay.
Eur Respir J
; 63(4)2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38485147
3.
Ivacaftor pharmacokinetics and lymphatic transport after enteral administration in rats.
Front Pharmacol
; 15: 1331637, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38444938
4.
Pulmonary tularaemia in a female adolescent with inflammatory bowel disease receiving infliximab: Do not miss the diagnosis.
Pediatr Pulmonol
; 58(3): 980-982, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36510661
5.
Response to elexacaftor/tezacaftor/ivacaftor in intestinal organoids derived from people with cystic fibrosis.
J Cyst Fibros
; 21(2): 243-245, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34348870
6.
Ventilation Inhomogeneity and Bronchial Basement Membrane Changes in Chronic Neutrophilic Airway Inflammation.
Chest
; 157(4): 779-789, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31711989
7.
Assessment of Distinct Electrophysiological Parameters in Rectal Biopsies for the Choice of the Best Diagnosis/Prognosis Biomarkers for Cystic Fibrosis.
Front Physiol
; 11: 604580, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33424627
8.
Mutant CFTR Drives TWIST1 mediated epithelial-mesenchymal transition.
Cell Death Dis
; 11(10): 920, 2020 10 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-33106471
9.
Organoids as a personalized medicine tool for ultra-rare mutations in cystic fibrosis: The case of S955P and 1717-2A>G.
Biochim Biophys Acta Mol Basis Dis
; 1866(11): 165905, 2020 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32730979
10.
TMEM16A in Cystic Fibrosis: Activating or Inhibiting?
Front Pharmacol
; 10: 3, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30761000
11.
Do linear logistic model analyses of volatile biomarkers in exhaled breath of cystic fibrosis patients reliably indicate Pseudomonas aeruginosa infection?
J Breath Res
; 10(3): 036013, 2016 08 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-27532768
12.
Breath concentration of acetic acid vapour is elevated in patients with cystic fibrosis.
J Breath Res
; 10(2): 021002, 2016 May 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-27184114
13.
Acetic acid is elevated in the exhaled breath of cystic fibrosis patients.
J Cyst Fibros
; 16(5): e17-e18, 2017 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-28215621