Margarete Olivier
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Explore the profile of Margarete Olivier including associated specialties, affiliations and a list of published articles.
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24
Citations
98
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Recent Articles
1.
Welsner M, Gruber W, Blosch C, Koerner-Rettberg C, Brinkmann F, Dillenhoefer S, et al.
Res Q Exerc Sport
. 2024 Mar;
95(4):804-812.
PMID: 38478996
Maintaining physical fitness plays an important role in the management of people with cystic fibrosis (pwCF). Longitudinal data on the course of physical fitness and the potential impact of the...
2.
Gruber W, Stehling F, Blosch C, Dillenhoefer S, Olivier M, Brinkmann F, et al.
Front Sports Act Living
. 2024 Mar;
6:1284878.
PMID: 38463712
Background: Habitual physical activity (PA) and exercise training are accepted as important aspects of care for people with cystic fibrosis (pwCF) to improve health-related measures of physical fitness, which in...
3.
Welsner M, Gruber W, Blosch C, Olivier M, Mellies U, Dillenhoefer S, et al.
Pediatr Pulmonol
. 2024 Jan;
59(4):949-963.
PMID: 38214406
Background: The influence of habitual physical activity and exercise capacity on health-related quality of life (HRQoL) in people with cystic fibrosis (pwCF) is poorly characterized. This study investigated the influence...
4.
Gruber W, Welsner M, Blosch C, Dillenhoefer S, Olivier M, Brinkmann F, et al.
Healthcare (Basel)
. 2023 Nov;
11(21).
PMID: 37958017
Background: Longitudinal data on changes in health-related quality of life (HRQoL) in adult people with cystic fibrosis (pwCF) and the longitudinal effects of Elexacaftor/Tezacaftor/Ivacaftor therapy (ETI) on HRQoL or HRQoL...
5.
Olivier M, Kavvalou A, Welsner M, Hirtz R, Strassburg S, Sutharsan S, et al.
Front Pharmacol
. 2023 May;
14:1176815.
PMID: 37229253
Recently, cystic fibrosis transmembrane regulator modulator therapy with elexacaftor/tezacaftor/ivacaftor has become available for children with cystic fibrosis (CF) carrying at least one mutation. To assess the intermediate term effects of...
6.
Kavvalou A, Stehling F, Tschiedel E, Kehrmann J, Walkenfort B, Hasenberg M, et al.
BMC Infect Dis
. 2022 Dec;
22(1):921.
PMID: 36494632
Background: Mycobacterium (M.) chimaera is a non-tuberculous mycobacterium (NTM) that belongs to M. avium complex (MAC). In patients with cystic fibrosis (CF), MAC can cause bronchopulmonary infections that can be...
7.
Dillenhoefer S, Stehling F, Welsner M, Schlegtendal A, Sutharsan S, Olivier M, et al.
Int J Environ Res Public Health
. 2022 Oct;
19(20).
PMID: 36293733
Background: Nowadays physical activity (PA)/exercise is an important component of cystic fibrosis (CF) therapy. The aim of the study was to assess the barriers to PA and the barrier management...
8.
Gruber W, Stehling F, Blosch C, Dillenhoefer S, Olivier M, Koerner-Rettberg C, et al.
Int J Environ Res Public Health
. 2022 Jul;
19(13).
PMID: 35805585
Background: The aim of this study was to investigate the effects of a monitored exercise program on aerobic fitness in children with cystic fibrosis (CF). Methods: Six children (2f/4m) with...
9.
Steindor M, Wagner C, Kavvalou A, Bock C, Olivier M, Stehling F
Pediatr Pulmonol
. 2022 May;
57(9):2048-2052.
PMID: 35574827
High-flow nasal therapy (HFNT) is a safe and simple way to deliver humidified air and oxygen for respiratory support in infants and children. HFNT is well established in an inpatient...
10.
Gruber W, Welsner M, Dillenhofer S, Olivier M, Koerner-Rettberg C, Sutharsan S, et al.
Percept Mot Skills
. 2021 Aug;
128(5):2097-2116.
PMID: 34338055
Little is known about motor competence and the longitudinal development of motor performance among youth with cystic fibrosis (CF). In this study, we assessed aspects of motor performance in different...