Search Results - "Post, M.C"

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    Long-term real world clinical outcomes of macitentan therapy in chronic thromboembolic pulmonary hypertension by van Thor, M.C.J., ten Klooster, L., Snijder, R.J., Mager, J.J., Post, M.C.

    Published in Respiratory medicine (01-06-2020)
    “…Macitentan treatment for chronic thromboembolic pulmonary hypertension (CTEPH) in the routine clinical setting is increasing. However, ‘real world’ macitentan…”
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    Journal Article
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    Long-term clinical value and outcome of riociguat in chronic thromboembolic pulmonary hypertension by van Thor, M.C.J., ten Klooster, L., Snijder, R.J., Post, M.C., Mager, J.J.

    “…To improve clinical outcome, patients with inoperable and residual chronic thromboembolic pulmonary hypertension (CTEPH) can be treated with riociguat. The aim…”
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    Echocardiographic pulmonary hypertension probability is associated with clinical outcomes after transcatheter aortic valve implantation by Nijenhuis, V.J, Huitema, M.P, Vorselaars, V.M.M, Swaans, M.J, de Kroon, T, van der Heyden, J.A.S, Rensing, B.J.W.M, Heijmen, R, ten Berg, J.M, Post, M.C

    Published in International journal of cardiology (15-12-2016)
    “…Abstract Aims Pulmonary hypertension (PH) is associated with mortality after transcatheter aortic valve implantation (TAVI). However, diagnosis based on…”
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    Journal Article
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    Does combination therapy work in chronic thromboembolic pulmonary hypertension? by van Thor, M.C.J., Snijder, R.J., Kelder, J.C., Mager, J.J., Post, M.C.

    “…•Long-term overall survival of CTEPH patients receiving PH-specific medial therapy is very reasonable.•Despite worse baseline characteristics at baseline,…”
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    Quality of life in pulmonary arterial hypertension by Post, M.C., Mager, J.J.

    Published in Netherlands heart journal (01-05-2015)
    “…The majority of the studies on QoL in PAH patients used different standard generic questionnaires or tools specific for heart or lung diseases, not reflecting…”
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    Echocardiographic findings associated with mortality or transplant in patients with pulmonary arterial hypertension: A systematic review and meta-analysis by Baggen, V.J.M., Driessen, M.M.P., Post, M.C., van Dijk, A.P., Roos-Hesselink, J.W., van den Bosch, A.E., Takkenberg, J.J.M., Sieswerda, G.T

    Published in Netherlands heart journal (01-06-2016)
    “…Background Identification of patients at risk of deterioration is essential to guide clinical management in pulmonary arterial hypertension (PAH). This study…”
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    Evolution of Pulmonary Arteriovenous Malformations by Hessels, J., Kroon, S., Vorselaars, V.V.M., Boerman, S., Mager, J.J., Post, M.C.

    Published in Chest (01-03-2023)
    “…Pulmonary arteriovenous malformations (PAVMs) are direct connections between the pulmonary artery and the pulmonary vein, mostly associated with hereditary…”
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    Value of echocardiography using knowledge-based reconstruction in determining right ventricular volumes in pulmonary sarcoidosis: comparison with cardiac magnetic resonance imaging by Mathijssen, H, Huitema, M.P, Bakker, A.L.M, Akdim, F, Van Es, H.W, Grutters, J.C, Post, M.C

    Published in European heart journal (12-10-2021)
    “…Abstract Background Right ventricular (RV) dysfunction in sarcoidosis is associated with adverse outcomes. Assessment of RV function by conventional…”
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    Journal Article
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    Mortality in a well-defined group of predominantly Caucasian pulmonary sarcoidosis patients by Huitema, M.P, Mathijssen, H, Bakker, A.L.M, Mager, J.J, Grutters, J.C, Post, M.C

    Published in European heart journal (01-11-2020)
    “…Abstract Background Sarcoidosis is an inflammatory systemic disease. Mortality has often been described in patients with more advanced disease, especially in…”
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    Aetiology of sarcoidosis-associated pulmonary hypertension by Mathijssen, H, Huitema, M.P, Bakker, A.L.M, Smits, F, Snijder, R.J, Mager, H.J, Grutters, J.C, Post, M.C

    Published in European heart journal (01-11-2020)
    “…Abstract Background Pulmonary hypertension (PH) is a known complication of pulmonary sarcoidosis and its aetiology is unclear. The severity of PH may not…”
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    CMR markers for early right ventricular dysfunction in precapillary pulmonary hypertension by Vos, J, Leiner, T, Van Dijk, A.P.J, Meijboom, F.J, Sieswerda, G.T, Snijder, R.J, Post, M.C, Nijveldt, R, Driessen, M.M.P

    Published in European heart journal (01-11-2020)
    “…Abstract Introduction Precapillary pulmonary hypertension (pPH) causes right ventricular (RV) pressure overload inducing RV remodeling, often resulting in…”
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    Long-term monitoring of arrhythmias in cardiac sarcoidosis by Bakker, A, Mathijssen, H, Balt, J, Van Dijk, V.F, Veltkamp, M, Swaans, M, Akdim, F, Grutters, J.C, Post, M.C

    Published in European heart journal (01-11-2020)
    “…Abstract Introduction Screening for cardiac sarcoidosis (CS) is recommended since it can manifest with ventricular arrhythmias (VA), atrioventricular…”
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    Effectiveness and safety of infliximab in cardiac Sarcoidosis by Bakker, A.L.M., Mathijssen, H., Azzahhafi, J., Swaans, M.J., Veltkamp, M., Keijsers, R.G.M., Akdim, F., Post, M.C., Grutters, J.C.

    Published in International journal of cardiology (01-05-2021)
    “…Immunosuppressive therapy in active cardiac sarcoidosis (CS) might prevent potential life-threatening complications. Infliximab (IFX) is a tumor necrosis…”
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