Hasil Pencarian - Thorsten Laser

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  1. 1
    Metabolomics and random forests in patients with complex congenital heart disease

    Metabolomics and random forests in patients with complex congenital heart disease oleh Miriam Michel, Kai Thorsten Laser, Karl-Otto Dubowy, Sabine Scholl-Bürgi, Erik Michel

    Diterbitkan 2022-10-01
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  2. 2
    Left-Ventricular Reference Myocardial Strain Assessed by Cardiovascular Magnetic Resonance Feature Tracking and fSENC—Impact of Temporal Resolution and Cardiac Muscle Mass

    Left-Ventricular Reference Myocardial Strain Assessed by Cardiovascular Magnetic Resonance Feature Tracking and fSENC—Impact of Temporal Resolution and Cardiac Muscle Mass oleh Elena Weise Valdés, Peter Barth, Misagh Piran, Kai Thorsten Laser, Wolfgang Burchert, Hermann Körperich

    Diterbitkan 2021-11-01
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  3. 3
    The transverse four-chamber view for the assessment of atrial tissue deformation in the fetus.

    The transverse four-chamber view for the assessment of atrial tissue deformation in the fetus. oleh Johannes Steinhard, Andreas Entenmann, Elise van der Valk, Ralf Schmitz, Jörg Heinig, Kai Thorsten Laser, Miriam Michel

    Diterbitkan 2018-01-01
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  4. 4
    Substantial radiation reduction in pediatric and adult congenital heart disease interventions with a novel X-ray imaging technology

    Substantial radiation reduction in pediatric and adult congenital heart disease interventions with a novel X-ray imaging technology oleh Nikolaus A. Haas, Christoph M. Happel, Maria Mauti, Cherif Sahyoun, Lea Z. Tebart, Deniz Kececioglu, Kai Thorsten Laser

    Diterbitkan 2015-03-01
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  5. 5
    Assessment of pulmonary artery stiffness by multiparametric cardiac magnetic resonance-surrogate for right heart catheterization

    Assessment of pulmonary artery stiffness by multiparametric cardiac magnetic resonance-surrogate for right heart catheterization oleh Hermann Körperich, Jan Eckstein, Medhat Atito, Peter Barth, Kai Thorsten Laser, Wolfgang Burchert, Oliver M. Weber, Christian Stehning, Misagh Piran

    Diterbitkan 2023-08-01
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  6. 6
    Cardiac Muscle Training—A New Way of Recognizing and Supporting Recovery for LVAD Patients in the Pediatric Population

    Cardiac Muscle Training—A New Way of Recognizing and Supporting Recovery for LVAD Patients in the Pediatric Population oleh Anca Racolta, Jae-Hyun Johannes Ahn, Marinos Kantzis, Hendrik Milting, Volker Lauenroth, Hermann Körperich, Eugen Sandica, Stephan Schubert, Kai Thorsten Laser

    Diterbitkan 2022-10-01
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  7. 7
    Altered Serum Proteins Suggest Inflammation, Fibrogenesis and Angiogenesis in Adult Patients with a Fontan Circulation

    Altered Serum Proteins Suggest Inflammation, Fibrogenesis and Angiogenesis in Adult Patients with a Fontan Circulation oleh Miriam Michel, David Renaud, Ronny Schmidt, Matthias Einkemmer, Lea Valesca Laser, Erik Michel, Karl Otto Dubowy, Daniela Karall, Kai Thorsten Laser, Sabine Scholl-Bürgi

    Diterbitkan 2024-05-01
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  8. 8
    Compound Heterozygous <i>FKTN</i> Variants in a Patient with Dilated Cardiomyopathy Led to an Aberrant α-Dystroglycan Pattern

    Compound Heterozygous <i>FKTN</i> Variants in a Patient with Dilated Cardiomyopathy Led to an Aberrant α-Dystroglycan Pattern oleh Anna Gaertner, Lidia Burr, Baerbel Klauke, Andreas Brodehl, Kai Thorsten Laser, Karin Klingel, Jens Tiesmeier, Uwe Schulz, Edzard zu Knyphausen, Jan Gummert, Hendrik Milting

    Diterbitkan 2022-06-01
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  9. 9
    Pathogenic Variants in Cardiomyopathy Disorder Genes Underlie Pediatric Myocarditis—Further Impact of Heterozygous Immune Disorder Gene Variants?

    Pathogenic Variants in Cardiomyopathy Disorder Genes Underlie Pediatric Myocarditis—Further Impact of Heterozygous Immune Disorder Gene Variants? oleh Franziska Seidel, Kai Thorsten Laser, Karin Klingel, Josephine Dartsch, Simon Theisen, Thomas Pickardt, Manuel Holtgrewe, Anna Gärtner, Felix Berger, Dieter Beule, Hendrik Milting, Stephan Schubert, Sabine Klaassen, Jirko Kühnisch

    Diterbitkan 2022-07-01
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  10. 10
    High proportion of genetic cases in patients with advanced cardiomyopathy including a novel homozygous Plakophilin 2-gene mutation.

    High proportion of genetic cases in patients with advanced cardiomyopathy including a novel homozygous Plakophilin 2-gene mutation. oleh Baerbel Klauke, Anna Gaertner-Rommel, Uwe Schulz, Astrid Kassner, Edzard Zu Knyphausen, Thorsten Laser, Deniz Kececioglu, Lech Paluszkiewicz, Ute Blanz, Eugen Sandica, Antoon J van den Bogaerdt, J Peter van Tintelen, Jan Gummert, Hendrik Milting

    Diterbitkan 2017-01-01
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  11. 11
    Targeted metabolomic analysis of serum phospholipid and acylcarnitine in the adult Fontan patient with a dominant left ventricle

    Targeted metabolomic analysis of serum phospholipid and acylcarnitine in the adult Fontan patient with a dominant left ventricle oleh Miriam Michel, Karl-Otto Dubowy, Manuela Zlamy, Daniela Karall, Mark Gordian Adam, Andreas Entenmann, Markus Andreas Keller, Jakob Koch, Irena Odri Komazec, Ralf Geiger, Christina Salvador, Christian Niederwanger, Udo Müller, Sabine Scholl-Bürgi, Kai Thorsten Laser

    Diterbitkan 2020-04-01
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  12. 12
    De Novo Missense Mutations in <i>TNNC1</i> and <i>TNNI3</i> Causing Severe Infantile Cardiomyopathy Affect Myofilament Structure and Function and Are Modulated by Troponin Targeting Agents

    De Novo Missense Mutations in <i>TNNC1</i> and <i>TNNI3</i> Causing Severe Infantile Cardiomyopathy Affect Myofilament Structure and Function and Are Modulated by Troponin Targetin... oleh Roua Hassoun, Heidi Budde, Hans Georg Mannherz, Mária Lódi, Setsuko Fujita-Becker, Kai Thorsten Laser, Anna Gärtner, Karin Klingel, Desirée Möhner, Robert Stehle, Innas Sultana, Thomas Schaaf, Mario Majchrzak, Verena Krause, Christian Herrmann, Marc M. Nowaczyk, Andreas Mügge, Gabriele Pfitzer, Rasmus R. Schröder, Nazha Hamdani, Hendrik Milting, Kornelia Jaquet, Diana Cimiotti

    Diterbitkan 2021-09-01
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  13. 13
    Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset

    Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset oleh Andreas Brodehl, Alexey Meshkov, Roman Myasnikov, Anna Kiseleva, Olga Kulikova, Bärbel Klauke, Evgeniia Sotnikova, Caroline Stanasiuk, Mikhail Divashuk, Greta Marie Pohl, Maria Kudryavtseva, Karin Klingel, Brenda Gerull, Anastasia Zharikova, Jan Gummert, Sergey Koretskiy, Stephan Schubert, Elena Mershina, Anna Gärtner, Polina Pilus, Kai Thorsten Laser, Valentin Sinitsyn, Sergey Boytsov, Oxana Drapkina, Hendrik Milting

    Diterbitkan 2021-04-01
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