Martin K Johnson
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Explore the profile of Martin K Johnson including associated specialties, affiliations and a list of published articles.
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27
Citations
557
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Recent Articles
1.
Stubbs H, Cannon J, Knightbridge E, Durrington C, Roddis C, Gin-Sing W, et al.
BMJ Open Respir Res
. 2024 Mar;
11(1).
PMID: 38519115
Background: N-terminal pro-B-type natriuretic peptide (NT-proBNP) is a biomarker of cardiac ventricular wall stress that is incorporated into pulmonary hypertension (PH) risk stratification models. Sendaway sampling may enable patients to...
2.
McGettrick M, Dormand H, Brewis M, Johnson M, Lang N, Church A
Front Cardiovasc Med
. 2022 Dec;
9:1004169.
PMID: 36582741
Background: Ventricular septal flattening reflects RV pressure overload in pulmonary arterial hypertension. Eccentricity index (EI) and pulmonary artery distensibility (PAD) correlate with pulmonary artery pressure. We assessed the utility of...
3.
Jones R, De Bie E, Groves E, Zalewska K, Swietlik E, Treacy C, et al.
Am J Respir Crit Care Med
. 2022 Mar;
206(1):81-93.
PMID: 35316153
Autoimmunity is believed to play a role in idiopathic pulmonary arterial hypertension (IPAH). It is not clear whether this is causative or a bystander of disease and if it carries...
4.
McGettrick M, McCaughey P, MacLellan A, Brewis M, Church A, Johnson M
ERJ Open Res
. 2020 Dec;
6(4).
PMID: 33263038
Socioeconomic factors have been shown to have an adverse impact on survival in some respiratory diseases. Studies from the USA and China have suggested worse survival in idiopathic pulmonary arterial...
5.
Lewis R, Armstrong I, Bergbaum C, Brewis M, Cannon J, Charalampopoulos A, et al.
Eur Respir J
. 2020 Jul;
57(2).
PMID: 32631835
Health-related quality of life (HRQoL) scores assess symptom burden in pulmonary arterial hypertension (PAH) but data regarding their role in prognostication and risk stratification are limited. We assessed these relationships...
6.
Peacock A, Ling Y, Johnson M, Kiely D, Condliffe R, Elliot C, et al.
Pulm Circ
. 2020 Apr;
10(1):2045894020914851.
PMID: 32284847
Patients classified as idiopathic pulmonary arterial hypertension (defined as Group 1 on European Respiratory Society (ERS)/European Cardiac Society (ESC) criteria) may have evidence of minor co-existing lung disease on thoracic...
7.
Jayasekera G, Wilson K, Buist H, Woodward R, Uckan A, Hughes C, et al.
Pulm Circ
. 2020 Feb;
10(1):2045894019897513.
PMID: 32095230
Cardiac magnetic resonance-derived ventricular variables are predictive of mortality in pulmonary arterial hypertension. Rodent models which emphasize ventricular function, allowing serial monitoring, are needed to identify pathophysiological features and novel...
8.
Brash L, Barnes G, Brewis M, Church A, Gibbs S, Howard L, et al.
JACC Basic Transl Sci
. 2018 Jun;
3(2):176-186.
PMID: 29876530
Apelin agonism causes systemic vasodilatation and increased cardiac contractility in humans, and improves pulmonary arterial hypertension (PAH) in animal models. Here, the authors examined the short-term pulmonary hemodynamic effects of...
9.
Pellino K, Kerridge S, Church C, Peacock A, Crowe T, Jayasekera G, et al.
Eur Respir J
. 2018 Feb;
51(2).
PMID: 29386345
Several demographic and clinical factors have prognostic significance in idiopathic pulmonary arterial hypertension (IPAH). Studies in China and the USA have suggested an association between low socioeconomic status and reduced...
10.
Panagiotou M, Johnson M, Louvaris Z, Baker J, Church A, Peacock A, et al.
J Appl Physiol (1985)
. 2017 Jul;
123(4):851-859.
PMID: 28663381
Daily physical activity is reduced in precapillary pulmonary hypertension (PH), but the underlying mechanisms are inadequately explored. We sought to investigate clinical and physiological relations of daily physical activity and...