Resultados da busca - Andreas Entenmann

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  1. 1
    The dilemma to diagnose Wilson disease by genetic testing alone

    The dilemma to diagnose Wilson disease by genetic testing alone por Albert Friedrich Stättermayer, Andreas Entenmann, Michael Gschwantler, Heinz Zoller, Harald Hofer, Péter Ferenci

    Publicado em 2019
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  2. 2
    Vedolizumab use after failure of TNF-α antagonists in children and adolescents with inflammatory bowel disease

    Vedolizumab use after failure of TNF-α antagonists in children and adolescents with inflammatory bowel disease por Anna-Maria Schneider, Daniel Weghuber, Benjamin Hetzer, Andreas Entenmann, Andreas Th. Müller, Georg Zimmermann, Sebastian Schütz, Wolf‐Dietrich Huber, Judith Pichler

    Publicado em 2018
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  3. 3
    Adverse results of a decellularized tissue-engineered pulmonary valve in humans assessed with magnetic resonance imaging

    Adverse results of a decellularized tissue-engineered pulmonary valve in humans assessed with magnetic resonance imaging por Inga Voges, Jan Hinrich Bräsen, Andreas Entenmann, Michael Scheid, Jens Scheewe, Günther Fischer, Christopher Hart, Ana Andrade, Hoang Minh Pham, Hans‐Heiner Kramer, Carsten Rickers

    Publicado em 2013
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  4. 4
    Determination of volume-time curves for the right ventricle and its outflow tract for functional analyses

    Determination of volume-time curves for the right ventricle and its outflow tract for functional analyses por Dominik Daniel Gabbert, Andreas Entenmann, Michael Jerosch‐Herold, Felicitas Frettlöh, Christopher Hart, Inga Voges, Minh H. Pham, Ana Andrade, Eileen Pardun, Philip Wegner, Traudel Hansen, Hans‐Heiner Kramer, Carsten Rickers

    Publicado em 2013
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  5. 5
    Deficiency of the sphingosine-1-phosphate lyase SGPL1 is associated with congenital nephrotic syndrome and congenital adrenal calcifications

    Deficiency of the sphingosine-1-phosphate lyase SGPL1 is associated with congenital nephrotic syndrome and congenital adrenal calcifications por Andreas Janecke, Ruijuan Xu, Elisabeth Steichen‐Gersdorf, Siegfried Waldegger, Andreas Entenmann, Thomas Giner, Iris M. Krainer, Lukas A. Huber, Michael W. Hess, Yaacov Frishberg, Hila Barash, Shay Tzur, Nira Schreyer‐Shafir, Rivka Sukenik‐Halevy, Tania Zehavi, Annick Raas‐Rothschild, Cungui Mao, Thomas Müller

    Publicado em 2017
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  6. 6
    Biallelic IARS Mutations Cause Growth Retardation with Prenatal Onset, Intellectual Disability, Muscular Hypotonia, and Infantile Hepatopathy

    Biallelic IARS Mutations Cause Growth Retardation with Prenatal Onset, Intellectual Disability, Muscular Hypotonia, and Infantile Hepatopathy por Robert Kopajtich, Kei Murayama, Andreas Janecke, Tobias B. Haack, Maximilian Breuer, A. S. Knisely, Inga Harting, Toya Ohashi, Yasushi Okazaki, Daisaku WATANABE, Yoshimi Tokuzawa, Urania Kotzaeridou, Stefan Kölker, Sven W. Sauer, Michael Carl, Simon Straub, Andreas Entenmann, Elke R. Gizewski, René G. Feichtinger, Johannes A. Mayr, K. Lackner, Tim M. Strom, Thomas Meitinger, Thomas Müller, Akira Ohtake, Georg F. Hoffmann, Holger Prokisch, Christian Staufner

    Publicado em 2016
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