Search Results - Ludwig Thierfelder

  • Showing 1 - 18 results of 18
Refine Results
  1. 1
    Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations.

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

    Published 1992
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  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 by Sabine Klaassen, Susanne Probst, Brenda Gerull, Erwin Oechslin, Peter Nürnberg, Arnd Heuser, Rolf Jenni, Hans Christian Hennies, Ludwig Thierfelder

    Published 2004
    Get full text
    Artigo
    Save to List
    Saved in:
  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 by Florian Kirchner, A. Schuetz, Leif‐Hendrik Boldt, Kristina Martens, Gunnar Dittmar, Wilhelm Haverkamp, Ludwig Thierfelder, Udo Heinemann, Brenda Gerull

    Published 2012
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  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 by Susanne Probst, Erwin Oechslin, Pia Schuler, Matthias Greutmann, Philipp Boyé, Walter Knirsch, Felix Berger, Ludwig Thierfelder, Rolf Jenni, Sabine Klaassen

    Published 2011
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  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. by Calum A. MacRae, Nitin Ghaisas, Susan Kass, S. L. Donnelly, Craig T. Basson, Hugh Watkins, Ryuchiro Anan, Ludwig Thierfelder, K McGarry, Edward Rowland

    Published 1995
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  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. by Ryuichiro Anan, Gottfried Greve, Ludwig Thierfelder, Hugh Watkins, William J. McKenna, Scott D. Solomon, C Vecchio, H. Shono, Shoichiro Nakao, Hiromitsu Tanaka

    Published 1994
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  7. 7
    A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2.

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

    Published 1993
    Get full text
    Artigo
    Save to List
    Saved in:
  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) by 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

    Published 2005
    Get full text
    Artigo
    Save to List
    Saved in:
  9. 9
    Mutant Desmocollin-2 Causes Arrhythmogenic Right Ventricular Cardiomyopathy

    Mutant Desmocollin-2 Causes Arrhythmogenic Right Ventricular Cardiomyopathy by 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

    Published 2006
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  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 by 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

    Published 1995
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  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 by 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

    Published 2009
    Get full text
    Artigo
    Save to List
    Saved in:
  12. 12
    Mutations in Sarcomere Protein Genes in Left Ventricular Noncompaction

    Mutations in Sarcomere Protein Genes in Left Ventricular Noncompaction by 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

    Published 2008
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  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 by 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

    Published 2008
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  14. 14
    Mutations in the Sarcomere Gene <i>MYH7</i> in Ebstein Anomaly

    Mutations in the Sarcomere Gene <i>MYH7</i> in Ebstein Anomaly by 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

    Published 2010
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  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 by 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

    Published 2004
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  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 by 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

    Published 2015
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  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 by 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

    Published 1998
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  18. 18
    RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing

    RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing by 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

    Published 2012
    Get full text
    Artigo
    Save to List
    Saved in:

Search Tools: