Improvement of fractional flow reserve and collateral flow by treatment with external counterpulsation (Art.Net.-2 Trial) von Buschmann, E. E., Utz, W., Pagonas, N., Schulz-Menger, J., Busjahn, A., Monti, J., Maerz, W., Le Noble, F., Thierfelder, L., Dietz, R., Klauss, V., Gross, M., Buschmann, I.R.

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Preserved heart function after left ventricular pressure overload in adult mice subjected to neonatal cardiac hypoplasia von Heinecke, K., Heuser, A., Blaschke, F., Jux, C., Thierfelder, L., Drenckhahn, J.-D.

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

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P448Dietary protein restriction throughout intrauterine development and postnatal life alters myocardial tissue composition but not left ventricular function in the adult mouse hea... von Drenckhahn, J D, Hennig, M, Shimoyama, S, Ewering, L, Ewald, D, Thierfelder, L, Jux, C

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

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Mutations of TTN , encoding the giant muscle filament titin, cause familial dilated cardiomyopathy von Granzier, Henk, Frenneaux, Michael, Labeit, Siegfried, Gerull, Brenda, Sasse-Klaassen, Sabine, Thierfelder, Ludwig, Trombitás, Karoly, McNabb, Mark, Seidman, J.G, Gramlich, Michael, Atherton, John, Seidman, Christine

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Cardiac magnetic field map topology quantified by Kullback-Leibler entropy identifies patients with hypertrophic cardiomyopathy von Schirdewan, A., Gapelyuk, A., Fischer, R., Koch, L., Schütt, H., Zacharzowsky, U., Dietz, R., Thierfelder, L., Wessel, N.

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

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A Familial Hypertrophic Cardiomyopathy Locus Maps to Chromosome 15q2 von Thierfelder, Ludwig, MacRae, Calum, Watkins, Hugh, Tomfohrde, James, Williams, Michele, McKenna, William, Bohm, Katarina, Noeske, Gerhard, Schlepper, Martin, Bowcock, Anne, Vosberg, Hans-Peter, Seidman, J. G., Seidman, Christine

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Familial Hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3 von MacRae, C A, Ghaisas, N, Kass, S, Donnelly, S, Basson, C T, Watkins, H C, Anan, R, Thierfelder, L H, McGarry, K, Rowland, E

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P313Embryonic cardiomyocytes can orchestrate various cell protective mechanisms to survive metabolic stress von Drenckhahn, JD, Magarin, M, Pohl, T, Lill, A, Donath, S, Thierfelder, L

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Isolated noncompaction of the left ventricular myocardium in the adult is an autosomal dominant disorder in the majority of patients von Sasse-Klaassen, Sabine, Gerull, Brenda, Oechslin, Erwin, Jenni, Rolf, Thierfelder, Ludwig

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Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations von WATKINS, H, THIERFELDER, L, HWANG, D.-S, MCKENNA, W, SEIDMAN, J. G, SEIDMAN, C. E

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Mutation detection by cycle sequencing von Thierfelder, L

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Novel gene locus for autosomal dominant left ventricular noncompaction maps to chromosome 11p15 von SASSE-KLAASSEN, Sabine, PROBST, Susanne, GERULL, Brenda, OECHSLIN, Erwin, NÜRNBERG, Peter, HEUSER, Arnd, JENNI, Rolf, HENNIES, Hans Christian, THIERFELDER, Ludwig

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Genetische Aspekte der Arrhythmieentstehung von Thierfelder, L

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Identification of a novel frameshift mutation in the giant muscle filament titin in a large Australian family with dilated cardiomyopathy von GERULL, Brenda, ATHERTON, John, GEUPEL, Anke, SASSE-KLAASSEN, Sabine, HEUSER, Arnd, FRENNEAUX, Michael, MCNABB, Mark, GRANZIER, Henk, LABEIT, Siegfried, THIERFELDER, Ludwig

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Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy von Jarcho, John A, Thierfelder, Ludwig, MacRae, Calum, McKenna, William J, Maron, Barry J, Seidman, J.G, Watkins, Hugh, Seidman, Christine E, Conner, David

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α-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: A disease of the sarcomere von Thierfelder, Ludwig, Watkins, Hugh, MacRae, Calum, Lamas, Roger, McKenna, William, Vosberg, Hans-Peter, Seldman, J.G., Seidman, Christine E.

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

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