Hasil Pencarian - Monica Patten

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  1. 1
    Serum Biomarkers of Endothelial Dysfunction in Fabry Associated Cardiomyopathy

    Serum Biomarkers of Endothelial Dysfunction in Fabry Associated Cardiomyopathy oleh Jefferson Loso, Natalie Lund, Maxim Avanesov, Nicole Muschol, Susanne Lezius, Kathrin Cordts, Kathrin Cordts, Edzard Schwedhelm, Edzard Schwedhelm, Monica Patten, Monica Patten

    Diterbitkan 2018-08-01
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  2. 2
    A Novel miRNA Screen Identifies miRNA-4454 as a Candidate Biomarker for Ventricular Fibrosis in Patients with Hypertrophic Cardiomyopathy

    A Novel miRNA Screen Identifies miRNA-4454 as a Candidate Biomarker for Ventricular Fibrosis in Patients with Hypertrophic Cardiomyopathy oleh Tilo Thottakara, Natalie Lund, Elisabeth Krämer, Paulus Kirchhof, Lucie Carrier, Monica Patten

    Diterbitkan 2021-11-01
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  3. 3
    Orthostatic blood pressure test for risk stratification in patients with hypertrophic cardiomyopathy.

    Orthostatic blood pressure test for risk stratification in patients with hypertrophic cardiomyopathy. oleh Julia Münch, Ali Aydin, Anna Suling, Christian Voigt, Stefan Blankenberg, Monica Patten

    Diterbitkan 2015-01-01
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  4. 4
    Association of NT-proBNP and hs-cTnT with Imaging Markers of Diastolic Dysfunction and Focal Myocardial Fibrosis in Hypertrophic Cardiomyopathy

    Association of NT-proBNP and hs-cTnT with Imaging Markers of Diastolic Dysfunction and Focal Myocardial Fibrosis in Hypertrophic Cardiomyopathy oleh Céleste Chevalier, Miriam Wendner, Anna Suling, Ersin Cavus, Kai Muellerleile, Gunnar Lund, Paulus Kirchhof, Monica Patten

    Diterbitkan 2022-08-01
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  5. 5
    Association of Asymmetric Dimethylarginine and Diastolic Dysfunction in Patients with Hypertrophic Cardiomyopathy

    Association of Asymmetric Dimethylarginine and Diastolic Dysfunction in Patients with Hypertrophic Cardiomyopathy oleh Kathrin Cordts, Doreen Seelig, Natalie Lund, Lucie Carrier, Rainer H. Böger, Maxim Avanesov, Enver Tahir, Edzard Schwedhelm, Monica Patten

    Diterbitkan 2019-07-01
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  6. 6
    Comparison of classical Fabry and its p.D313Y and p.A143T variants by cardiac T1 mapping, LGE and feature tracking myocardial strain

    Comparison of classical Fabry and its p.D313Y and p.A143T variants by cardiac T1 mapping, LGE and feature tracking myocardial strain oleh Maxim Avanesov, Anahid Asgari, Nicole Muschol, Anja Friederike Köhn, Enver Tahir, Gerhard Adam, Paulus Kirchhof, Gunnar Lund, Ersin Cavus, Monica Patten

    Diterbitkan 2023-04-01
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  7. 7
    Ablation of Atrial Fibrillation in Patients With Hypertrophic Cardiomyopathy: Treatment Strategy, Characteristics of Consecutive Atrial Tachycardia and Long‐Term Outcome

    Ablation of Atrial Fibrillation in Patients With Hypertrophic Cardiomyopathy: Treatment Strategy, Characteristics of Consecutive Atrial Tachycardia and Long‐Term Outcome oleh Leon Dinshaw, Paula Münkler, Benjamin Schäffer, Niklas Klatt, Christiane Jungen, Jannis Dickow, Annika Tamenang, Ruben Schleberger, Simon Pecha, Hans Pinnschmidt, Monica Patten, Hermann Reichenspurner, Stephan Willems, Christian Meyer

    Diterbitkan 2021-02-01
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  8. 8
    Evaluation of MYBPC3 trans-Splicing and Gene Replacement as Therapeutic Options in Human iPSC-Derived Cardiomyocytes

    Evaluation of MYBPC3 trans-Splicing and Gene Replacement as Therapeutic Options in Human iPSC-Derived Cardiomyocytes oleh Maksymilian Prondzynski, Elisabeth Krämer, Sandra D. Laufer, Aya Shibamiya, Ole Pless, Frederik Flenner, Oliver J. Müller, Julia Münch, Charles Redwood, Arne Hansen, Monica Patten, Thomas Eschenhagen, Giulia Mearini, Lucie Carrier

    Diterbitkan 2017-06-01
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  9. 9
    Generation of bi-allelic MYBPC3 truncating mutant and isogenic control from an iPSC line of a patient with hypertrophic cardiomyopathy

    Generation of bi-allelic MYBPC3 truncating mutant and isogenic control from an iPSC line of a patient with hypertrophic cardiomyopathy oleh Nele Warnecke, Bärbel M. Ulmer, Sandra D. Laufer, Aya Shibamiya, Elisabeth Krämer, Christiane Neuber, Sophia Hanke, Charlotta Behrens, Malte Loos, Julia Münch, Jirko Kühnisch, Sabine Klaassen, Thomas Eschenhagen, Monica Patten-Hamel, Lucie Carrier, Giulia Mearini

    Diterbitkan 2021-08-01
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  10. 10
    Analysis of Contractile Function of Permeabilized Human Hypertrophic Cardiomyopathy Multicellular Heart Tissue

    Analysis of Contractile Function of Permeabilized Human Hypertrophic Cardiomyopathy Multicellular Heart Tissue oleh Nico Kresin, Nico Kresin, Sabrina Stücker, Sabrina Stücker, Elisabeth Krämer, Elisabeth Krämer, Frederik Flenner, Frederik Flenner, Giulia Mearini, Giulia Mearini, Julia Münch, Monica Patten, Charles Redwood, Lucie Carrier, Lucie Carrier, Felix W. Friedrich, Felix W. Friedrich

    Diterbitkan 2019-03-01
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  11. 11
    Hereditary transthyretin-related amyloidosis is frequent in polyneuropathy and cardiomyopathy of no obvious aetiology

    Hereditary transthyretin-related amyloidosis is frequent in polyneuropathy and cardiomyopathy of no obvious aetiology oleh Volha Skrahina, Ulrike Grittner, Christian Beetz, Thomas Skripuletz, Martin Juenemann, Heidrun H. Krämer, Katrin Hahn, Andreas Rieth, Volker Schaechinger, Monica Patten, Christian Tanislav, Stephan Achenbach, Birgit Assmus, Fabian Knebel, Stefan Gingele, Aliaksandr Skrahin, Jörg Hartkamp, Toni M. Förster, Sabine Roesner, Catarina Pereira, Arndt Rolfs

    Diterbitkan 2021-01-01
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  12. 12
    Disease modeling of a mutation in α‐actinin 2 guides clinical therapy in hypertrophic cardiomyopathy

    Disease modeling of a mutation in α‐actinin 2 guides clinical therapy in hypertrophic cardiomyopathy oleh Maksymilian Prondzynski, Marc D Lemoine, Antonia TL Zech, András Horváth, Vittoria Di Mauro, Jussi T Koivumäki, Nico Kresin, Josefine Busch, Tobias Krause, Elisabeth Krämer, Saskia Schlossarek, Michael Spohn, Felix W Friedrich, Julia Münch, Sandra D Laufer, Charles Redwood, Alexander E Volk, Arne Hansen, Giulia Mearini, Daniele Catalucci, Christian Meyer, Torsten Christ, Monica Patten, Thomas Eschenhagen, Lucie Carrier

    Diterbitkan 2022-08-01
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  13. 13
    Disease modeling of a mutation in α‐actinin 2 guides clinical therapy in hypertrophic cardiomyopathy

    Disease modeling of a mutation in α‐actinin 2 guides clinical therapy in hypertrophic cardiomyopathy oleh Maksymilian Prondzynski, Marc D Lemoine, Antonia TL Zech, András Horváth, Vittoria Di Mauro, Jussi T Koivumäki, Nico Kresin, Josefine Busch, Tobias Krause, Elisabeth Krämer, Saskia Schlossarek, Michael Spohn, Felix W Friedrich, Julia Münch, Sandra D Laufer, Charles Redwood, Alexander E Volk, Arne Hansen, Giulia Mearini, Daniele Catalucci, Christian Meyer, Torsten Christ, Monica Patten, Thomas Eschenhagen, Lucie Carrier

    Diterbitkan 2019-12-01
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