Detalhe da pesquisa
1.
Ex vivo adult stem cell characterization from multiple muscles in ambulatory children with cerebral palsy during early development of contractures.
Differentiation
; 133: 25-39, 2023.
Artigo
Inglês
| MEDLINE | ID: mdl-37451110
2.
In Vitro Susceptibility of Burkholderia cepacia Complex Isolated from Cystic Fibrosis Patients to Ceftazidime-Avibactam and Ceftolozane-Tazobactam.
Antimicrob Agents Chemother
; 62(9)2018 09.
Artigo
Inglês
| MEDLINE | ID: mdl-29914964
3.
ECFS standards of care on CFTR-related disorders: Identification and care of the disorders.
J Cyst Fibros
; 2024 Mar 19.
Artigo
Inglês
| MEDLINE | ID: mdl-38508949
4.
ECFS standards of care on CFTR-related disorders: Towards a comprehensive program for affected individuals.
J Cyst Fibros
; 2024 Feb 21.
Artigo
Inglês
| MEDLINE | ID: mdl-38388234
5.
CFTR biomarkers: time for promotion to surrogate end-point.
Eur Respir J
; 41(1): 203-16, 2013 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-22878883
6.
Malacia, inflammation and bronchoalveolar lavage culture in children with persistent respiratory symptoms.
Eur Respir J
; 39(2): 392-5, 2012 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-21778166
7.
Everything in excess is opposed to nature, even vitamin D: a case report.
Endocrinol Diabetes Metab Case Rep
; 20222022 Feb 01.
Artigo
Inglês
| MEDLINE | ID: mdl-35170432
8.
ECFS standards of care on CFTR-related disorders: Updated diagnostic criteria.
J Cyst Fibros
; 21(6): 908-921, 2022 11.
Artigo
Inglês
| MEDLINE | ID: mdl-36220763
9.
Standards of care guidance for sweat testing; phase two of the ECFS quality improvement programme.
J Cyst Fibros
; 21(3): 434-441, 2022 05.
Artigo
Inglês
| MEDLINE | ID: mdl-35063396
10.
Long-term use of tube feeding in children with cystic fibrosis: results from two Belgian CF centers.
Eur J Clin Nutr
; 75(4): 620-627, 2021 04.
Artigo
Inglês
| MEDLINE | ID: mdl-33077878
11.
Characteristics of gastroesophageal reflux and potential risk of gastric content aspiration in children with cystic fibrosis.
J Pediatr Gastroenterol Nutr
; 50(2): 161-6, 2010 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-19966579
12.
Well-nourished cystic fibrosis patients have normal mineral density, but reduced cortical thickness at the forearm.
Osteoporos Int
; 20(2): 309-14, 2009 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-18536951
13.
Letter to the editor: Risk of false newborn screening after intra-uterine exposure to ETI.
J Cyst Fibros
; 23(1): 176-177, 2024 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-37495469
14.
What can the CF registry tell us about rare CFTR-mutations? A Belgian study.
Orphanet J Rare Dis
; 12(1): 142, 2017 08 22.
Artigo
Inglês
| MEDLINE | ID: mdl-28830496
15.
A semi-blinded study comparing 2 methods of measuring nasal potential difference: Subcutaneous needle versus dermal abrasion.
J Cyst Fibros
; 15(1): 60-6, 2016 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-26190830
16.
Increase in ventilated air spaces after eradication of chronic methicillin-resistant Staphylococcus aureus infection in cystic fibrosis patients.
Acta Clin Belg
; 70(1): 30-3, 2015 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-25253536
17.
The relationship between gastroesophageal reflux and cough in children with chronic unexplained cough using combined impedance-pH-manometry recordings.
Pediatr Pulmonol
; 46(3): 286-94, 2011 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-20967945