Hakutulokset - Ludwig Thierfelder

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  1. 1
    Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations.

    Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations. Tekijä Hugh Watkins, Ludwig Thierfelder, D.S. Hwang, William J. McKenna, J G Seidman, Christine E. Seidman

    Julkaistu 1992
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  2. 2
    Novel Gene Locus for Autosomal Dominant Left Ventricular Noncompaction Maps to Chromosome 11p15

    Novel Gene Locus for Autosomal Dominant Left Ventricular Noncompaction Maps to Chromosome 11p15 Tekijä Sabine Klaassen, Susanne Probst, Brenda Gerull, Erwin Oechslin, Peter Nürnberg, Arnd Heuser, Rolf Jenni, Hans Christian Hennies, Ludwig Thierfelder

    Julkaistu 2004
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  3. 3
    Molecular Insights into Arrhythmogenic Right Ventricular Cardiomyopathy Caused by Plakophilin-2 Missense Mutations

    Molecular Insights into Arrhythmogenic Right Ventricular Cardiomyopathy Caused by Plakophilin-2 Missense Mutations Tekijä Florian Kirchner, A. Schuetz, Leif‐Hendrik Boldt, Kristina Martens, Gunnar Dittmar, Wilhelm Haverkamp, Ludwig Thierfelder, Udo Heinemann, Brenda Gerull

    Julkaistu 2012
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  4. 4
    Sarcomere Gene Mutations in Isolated Left Ventricular Noncompaction Cardiomyopathy Do Not Predict Clinical Phenotype

    Sarcomere Gene Mutations in Isolated Left Ventricular Noncompaction Cardiomyopathy Do Not Predict Clinical Phenotype Tekijä Susanne Probst, Erwin Oechslin, Pia Schuler, Matthias Greutmann, Philipp Boyé, Walter Knirsch, Felix Berger, Ludwig Thierfelder, Rolf Jenni, Sabine Klaassen

    Julkaistu 2011
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  5. 5
    Familial Hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3.

    Familial Hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3. Tekijä Calum A. MacRae, Nitin Ghaisas, Susan Kass, S. L. Donnelly, Craig T. Basson, Hugh Watkins, Ryuchiro Anan, Ludwig Thierfelder, K McGarry, Edward Rowland

    Julkaistu 1995
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  6. 6
    Prognostic implications of novel beta cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy.

    Prognostic implications of novel beta cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy. Tekijä Ryuichiro Anan, Gottfried Greve, Ludwig Thierfelder, Hugh Watkins, William J. McKenna, Scott D. Solomon, C Vecchio, H. Shono, Shoichiro Nakao, Hiromitsu Tanaka

    Julkaistu 1994
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  7. 7
    A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2.

    A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2. Tekijä Ludwig Thierfelder, Calum A. MacRae, Hugh Watkins, James Tomfohrde, Maggie Williams, William J. McKenna, Kati Böhm, G Noeske, M Schlepper, A. Bowcock

    Julkaistu 1993
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  8. 8
    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) Tekijä 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

    Julkaistu 2005
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  9. 9
    Mutant Desmocollin-2 Causes Arrhythmogenic Right Ventricular Cardiomyopathy

    Mutant Desmocollin-2 Causes Arrhythmogenic Right Ventricular Cardiomyopathy Tekijä Arnd Heuser, Eva Plovie, Patrick T. Ellinor, Katja S. Grossmann, Jordan T. Shin, Thomas Wichter, Craig T. Basson, Bruce B. Lerman, Sabine Klaassen, Ludwig Thierfelder, Calum A. MacRae, Brenda Gerull

    Julkaistu 2006
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  10. 10
    Mutations in the Genes for Cardiac Troponin T and α-Tropomyosin in Hypertrophic Cardiomyopathy

    Mutations in the Genes for Cardiac Troponin T and α-Tropomyosin in Hypertrophic Cardiomyopathy Tekijä Hugh Watkins, William J. McKenna, Ludwig Thierfelder, Ho‐Jun Suk, Ryuichiro Anan, Annie O'Donoghue, Paolo Spirito, Akira Matsumori, Christine S. Moravec, Jonathan G. Seidman, Christine E. Seidman

    Julkaistu 1995
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  11. 11
    Stress-induced dilated cardiomyopathy in a knock-in mouse model mimicking human titin-based disease

    Stress-induced dilated cardiomyopathy in a knock-in mouse model mimicking human titin-based disease Tekijä Michael Gramlich, Beate Michely, Christian Krohne, Arnd Heuser, Bettina Erdmann, Sabine Klaassen, Bryan D. Hudson, Manuela Magarin, Florian Kirchner, Mihail Todiraş, Henk Granzier, Siegfried Labeit, Ludwig Thierfelder, Brenda Gerull

    Julkaistu 2009
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  12. 12
    Mutations in Sarcomere Protein Genes in Left Ventricular Noncompaction

    Mutations in Sarcomere Protein Genes in Left Ventricular Noncompaction Tekijä 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

    Julkaistu 2008
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  13. 13
    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 Tekijä 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

    Julkaistu 2008
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  14. 14
    Mutations in the Sarcomere Gene <i>MYH7</i> in Ebstein Anomaly

    Mutations in the Sarcomere Gene <i>MYH7</i> in Ebstein Anomaly Tekijä Alex V. Postma, Klaartje van Engelen, Judith van de Meerakker, Thahira Rahman, Susanne Probst, Marieke J.H. Baars, Ulrike Bauer, Thomas Pickardt, Silke Sperling, Felix Berger, Antoon F.M. Moorman, Barbara J.M. Mulder, Ludwig Thierfelder, Bernard Keavney, Judith Goodship, Sabine Klaassen

    Julkaistu 2010
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  15. 15
    Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy

    Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy Tekijä Brenda Gerull, Arnd Heuser, Thomas Wichter, Matthias Paul, Craig T. Basson, Deborah A. McDermott, Bruce B. Lerman, Steve Markowitz, Patrick T. Ellinor, Calum A. MacRae, Stefan Peters, Katja S. Grossmann, Beate Michely, Sabine Klaassen, Walter Birchmeier, Rainer Dietz, Günter Breithardt, Eric Schulze‐Bahr, Ludwig Thierfelder

    Julkaistu 2004
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  16. 16
    Antisense‐mediated exon skipping: a therapeutic strategy for titin‐based dilated cardiomyopathy

    Antisense‐mediated exon skipping: a therapeutic strategy for titin‐based dilated cardiomyopathy Tekijä Michael Gramlich, Luna Simona Pane, Qifeng Zhou, Zhifen Chen, Marta Murgia, Sonja Schötterl, Alexander Goedel, Katja Metzger, Thomas Brade, Elvira Immacolata Parrotta, Martin Schaller, Brenda Gerull, Ludwig Thierfelder, Annemieke Aartsma‐Rus, Siegfried Labeit, J. Atherton, Julie McGaughran, Richard P. Harvey, Daniel Sinnecker, Matthias Mann, Karl‐Ludwig Laugwitz, Meinrad Gawaz, Alessandra Moretti

    Julkaistu 2015
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  17. 17
    Mutations in the Gene for Cardiac Myosin-Binding Protein C and Late-Onset Familial Hypertrophic Cardiomyopathy

    Mutations in the Gene for Cardiac Myosin-Binding Protein C and Late-Onset Familial Hypertrophic Cardiomyopathy Tekijä Hideshi Niimura, Linda L. Bachinski, Somkiat Sangwatanaroj, Hugh Watkins, Albert E. Chudley, William J. McKenna, Arni Kristinsson, Robert J. Roberts, Michael J. Sole, Barry J. Maron, Jonathan G. Seidman, Christine E. Seidman, Ludwig Thierfelder, John A. Jarcho, Aris Anastasakis, Pavlos Toutouzas, Eleanor Elstein, Choong‐Chin Liew, Jack Liew, John D. Mably, Harry Rakowski, E.Douglas Wigle, Minshun Zhao, Rosemarie Salerni, Halldóra Björnsdóttir

    Julkaistu 1998
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  18. 18
    RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing

    RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing Tekijä Wei Guo, Sebastian Schäfer, Marion L. Greaser, Michaël Radkë, Martin Liss, Thirupugal Govindarajan, Henrike Maatz, Herbert Schulz, Shijun Li, Amanda M. Parrish, Vita Dauksaite, Padmanabhan Vakeel, Sabine Klaassen, Brenda Gerull, Ludwig Thierfelder, Vera Regitz‐Zagrosek, Timothy A. Hacker, Kurt W. Saupe, G. William Dec, Patrick T. Ellinor, Calum A. MacRae, Bastian Spallek, Robert Fischer, Andreas Perrot, Cemil Özcelik, Kathrin Saar, Norbert Hübner, Michael Gotthardt

    Julkaistu 2012
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