A Malfroot
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Explore the profile of A Malfroot including associated specialties, affiliations and a list of published articles.
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56
Citations
647
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Recent Articles
11.
Vanderhelst E, De Meirleir L, Verbanck S, Pierard D, Vincken W, Malfroot A
J Cyst Fibros
. 2011 Sep;
11(1):2-7.
PMID: 21907637
Background: Risk factors for methicillin-resistant Staphylococcus aureus (MRSA) in Cystic Fibrosis (CF) and the impact on CF disease progression are still under debate. The objectives of this study were to...
12.
De Baets F, De Schutter I, Aarts C, Haerynck F, Van Daele S, De Wachter E, et al.
Eur Respir J
. 2011 Jul;
39(2):392-5.
PMID: 21778166
In children with persistent respiratory symptoms despite regular anti-asthma inhalation treatment, diagnostic investigations to exclude underlying disease are warranted. 124 children were prospectively enrolled, and 24-h oesophageal pH measurement and...
13.
Rumke H, Loch H, Hoppenbrouwers K, Vandermeulen C, Malfroot A, Helm K, et al.
Vaccine
. 2011 Mar;
29(22):3842-9.
PMID: 21382484
Background: The MMRV combination vaccine, Priorix-Tetra™, is currently licensed in several European countries using a two-dose schedule in infants aged ≥9 months, with a preferred 6-week to 3-month interval between...
14.
Havermans T, Wuytack L, Deboel J, Tijtgat A, Malfroot A, DE Boeck C, et al.
Child Care Health Dev
. 2010 Nov;
37(2):252-60.
PMID: 21083689
Objective: To asses self-reported quality of life (QoL) and perception of impact of illness on siblings of children with cystic fibrosis (CF). Methods: The Child Health Questionnaire was used to...
15.
Blondeau K, Mertens V, Dupont L, Pauwels A, Farre R, Malfroot A, et al.
Pediatr Pulmonol
. 2010 Oct;
46(3):286-94.
PMID: 20967945
Introduction: Assessment of the reflux-cough association in children is challenging. Esophageal (impedance) pH recording is sensitive to recognize reflux. However, cough recorded by an event marker, possibly lacks accuracy. We...
16.
Hirche T, Bradley J, dAlquen D, De Boeck K, Dembski B, Elborn J, et al.
J Cyst Fibros
. 2010 Sep;
9(6):385-99.
PMID: 20850392
There are no European Guidelines on issues specifically related to travel for people with cystic fibrosis (CF). The contributors to these recommendations included 30 members of the ECORN-CF project. The...
17.
Blondeau K, Pauwels A, Dupont L, Mertens V, Proesmans M, Orel R, et al.
J Pediatr Gastroenterol Nutr
. 2009 Dec;
50(2):161-6.
PMID: 19966579
Objectives: Increased gastroesophageal reflux (GER) is common in children with cystic fibrosis (CF). We studied the occurrence of acid, weakly acidic (WA), and weakly alkaline (WALK) reflux in children with...
18.
Lebecque P, Leonard A, De Boeck K, De Baets F, Malfroot A, Casimir G, et al.
J Cyst Fibros
. 2008 Oct;
8(1):26-30.
PMID: 18838309
Background: Published studies concerning the impact of specialist care on lung disease in cystic fibrosis remain limited and most are either biased due to comparison with historical controls and/or underpowered....
19.
Blondeau K, Dupont L, Mertens V, Verleden G, Malfroot A, Vandenplas Y, et al.
Gut
. 2008 Mar;
57(8):1049-55.
PMID: 18372497
Background: Gastro-oesophageal reflux (GOR) is increased in cystic fibrosis (CF), but its prevalence, characteristics, association with gastric aspiration and respiratory impact are not well characterised. We investigated acid and weakly...
20.
Schelstraete P, Van Daele S, De Boeck K, Proesmans M, Lebecque P, Leclercq-Foucart J, et al.
Eur Respir J
. 2007 Dec;
31(4):822-9.
PMID: 18094014
The source of acquisition of Pseudomonas aeruginosa in cystic fibrosis (CF) patients remains unknown. Patient-to-patient transmission has been well documented but the role of the environment as a source of...