Хайлтын үр дүнгүүд - Jörg‐Detlef Drenckhahn

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  1. 1
    The impact of implantable cardioverter-defibrillator therapy on survival in autosomal-dominant arrhythmogenic right ventricular cardiomyopathy (ARVD5)

    The impact of implantable cardioverter-defibrillator therapy on survival in autosomal-dominant arrhythmogenic right ventricular cardiomyopathy (ARVD5) -н Kathy Hodgkinson, Patrick S. Parfrey, Anne S. Bassett, Christine Kupprion, Jörg‐Detlef Drenckhahn, Mark Norman, Ludwig Thierfelder, Susan Stuckless, Elizabeth Dicks, William J. McKenna, Sean P. Connors

    Хэвлэсэн 2005
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    Artigo
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  2. 2
    Compensatory Growth of Healthy Cardiac Cells in the Presence of Diseased Cells Restores Tissue Homeostasis during Heart Development

    Compensatory Growth of Healthy Cardiac Cells in the Presence of Diseased Cells Restores Tissue Homeostasis during Heart Development -н Jörg‐Detlef Drenckhahn, Quenten Schwarz, Stephen P. Gray, Adrienne Laskowski, Helen Kiriazis, Ziqiu Ming, Richard P. Harvey, Xiao‐Jun Du, David R. Thorburn, Timothy C. Cox

    Хэвлэсэн 2008
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    Artigo
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  3. 3
    Mutations in Sarcomere Protein Genes in Left Ventricular Noncompaction

    Mutations in Sarcomere Protein Genes in Left Ventricular Noncompaction -н Sabine Klaassen, Susanne Probst, Erwin Oechslin, Brenda Gerull, Gregor Krings, Pia Schuler, Matthias Greutmann, David Hürlimann, M. Yegitbasi, Lucía Pons, Michael Gramlich, Jörg‐Detlef Drenckhahn, Arnd Heuser, Felix Berger, Rolf Jenni, Ludwig Thierfelder

    Хэвлэсэн 2008
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    Artigo
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  4. 4
    Arrhythmogenic Right Ventricular Cardiomyopathy Type 5 Is a Fully Penetrant, Lethal Arrhythmic Disorder Caused by a Missense Mutation in the TMEM43 Gene

    Arrhythmogenic Right Ventricular Cardiomyopathy Type 5 Is a Fully Penetrant, Lethal Arrhythmic Disorder Caused by a Missense Mutation in the TMEM43 Gene -н Nancy D. Merner, Kathy Hodgkinson, Annika Haywood, Sean P. Connors, Vanessa French, Jörg‐Detlef Drenckhahn, Christine Kupprion, Kalina Ramadanova, Ludwig Thierfelder, William J. McKenna, Barry Gallagher, Lynn Morris-Larkin, Anne S. Bassett, Patrick S. Parfrey, Terry‐Lynn Young

    Хэвлэсэн 2008
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    Artigo
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  5. 5
    Fine Mapping of the 1p36 Deletion Syndrome Identifies Mutation of PRDM16 as a Cause of Cardiomyopathy

    Fine Mapping of the 1p36 Deletion Syndrome Identifies Mutation of PRDM16 as a Cause of Cardiomyopathy -н Anne-Karin Arndt, Sebastian Schäfer, Jörg‐Detlef Drenckhahn, M. Khaled Sabeh, Eva Plovie, Almuth Caliebe, Eva Klopocki, Gabriel Musso, Andreas A. Werdich, Hermann Kalwa, Matthias Heinig, Robert F. Padera, Katharina Wassilew, Julia Bluhm, Christine Harnack, Janine Martitz, Paul J.R. Barton, Matthias Greutmann, Felix Berger, Norbert Hübner, Reiner Siebert, Hans‐Heiner Kramer, Stuart A. Cook, Calum A. MacRae, Sabine Klaassen

    Хэвлэсэн 2013
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    Artigo
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