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(V1172) |
Therapeutic consequences after a combined diagnostic work-up including endomyocardial Biopsy in an all-comer population of patients with heart failure. |
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E. Sotiriou, S. Wagner, K.-H. Schmidt, K.-F. Kreitner, T. Münzel, E. Schulz, P. Wenzel (Mainz) |
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Diskussion |
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(V1173) |
Characterization of novel FLNC (Filamin C) mutations associated with familial restrictive cardiomyopathy |
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A. Brodehl, R. A. Ferrier, S. J. Hamilton, S. C. Greenway, M.-A. Brundler, K. Martens, M. L. McKinnon, N. Alvarez, J. Schwartzentruber, B. Gerull (Calgary, Vancouver, Montréal, CA) |
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Diskussion |
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(V1174) |
cTnI-R170G/W, -D127Y, novel mutations in TNNI3 associated with severe infant restrictive cardiomyopathy |
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D. Cimiotti, M. Majchrzak, N. Smolina, A. Kostareva, K. T. Laser, D. Kececioglu, H. Milting, R. Stehle, G. Pfitzer, A. Mügge, K. Jaquet (Bochum, Bad Oeynhausen, Köln; Stockholm, SE) |
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Diskussion |
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(V1175) |
Variable expression of cardiac high sensitive troponin T in different forms of muscular dystrophy |
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R. Bauer, N. Ade, E. Giannitsis, H. A. Katus, O. J. Müller (Heidelberg) |
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Diskussion |
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(V1176) |
The novel DES mutation p.L136P is associated with dilated cardiomyopathy and inhibits the desmin filament assembly |
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A. Brodehl, M. Dieding, N. Biere, A. Unger, B. Klauke, V. Walhorn, J. Gummert, U. Schulz, W. A. Linke, B. Gerull, M. Vorgert, D. Anselmetti, H. Milting (Calgary, CA; Bielefeld, Bochum, Bad Oeynhausen) |
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Diskussion |
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(V1177) |
Proteinbiochemical analyses of new fukutin-variants in a patient with dilated cardiomyopathy and elevated creatin kinase levels |
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A. Gärtner-Rommel, J. Chudzenski, B. Klauke, M. Morshuis, J. Gummert, H. Milting (Bad Oeynhausen) |
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Diskussion |