Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Sabine Sasse-Klaassen"'
Autor:
Craig T. Basson, Patrick T. Ellinor, Jordan T. Shin, Eva Plovie, Sabine Sasse-Klaassen, Brenda Gerull, Calum A. MacRae, Arnd Heuser, Thomas Wichter, Ludwig Thierfelder, Bruce B. Lerman, Katja S. Grossmann
Publikováno v:
The American Journal of Human Genetics. 79(6):1081-1088
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a genetically heterogeneous heart-muscle disorder characterized by progressive fibrofatty replacement of right ventricular myocardium and an increased risk of sudden cardiac death. Mutations i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e4aeaca438d5dc0cfd12ff9abd4129e
Autor:
Sabine Sasse-Klaassen, Henk Granzier, Anke Geupel, Arnd Heuser, Mark McNabb, Michael P. Frenneaux, Ludwig Thierfelder, Brenda Gerull, Siegfried Labeit, John Atherton
Publikováno v:
Journal of Molecular Medicine. 84:478-483
Dilated cardiomyopathy (DCM) is an etiologically heterogeneous cardiac disease characterized by left ventricular dilation and systolic dysfunction. Approximately 25-30% of DCM patients show a family history of mainly autosomal dominant inheritance. W
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c39d65b029028cbc57213f0a25ce286a
https://doi.org/10.1007/s00109-006-0060-6
https://doi.org/10.1007/s00109-006-0060-6
Autor:
Jonathan G. Seidman, Henk Granzier, Christine E. Seidman, Brenda Gerull, John Atherton, Mark McNabb, Siegfried Labeit, Ludwig Thierfelder, Sabine Sasse-Klaassen, Michael Gramlich, Michael P. Frenneaux, Karoly Trombitás
Publikováno v:
Nature Genetics. 30:201-204
Congestive heart failure (CHF) can result from various disease states with inadequate cardiac output. CHF due to dilated cardiomyopathy (DCM) is a familial disease in 20-30% of cases and is associated with mutations in genes encoding cytoskeletal, co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec131cc36593625e7db55c19bf992678
https://doi.org/10.1038/ng815
https://doi.org/10.1038/ng815
Autor:
Patrick T. Ellinor, Jordan T. Shin, Bernhard Pilz, Arnd Heuser, Gregor Krings, Beate Michely, Sabine Sasse-Klaassen, Brenda Gerull, G. William Dec, Bruce Coplin, Bong Seok Song, Ludwig Thierfelder, Andrea Toeppel, Hans Christian Hennies, Danita M. Yoerger, Calum A. MacRae, Peter Lange, Susanne Probst
Publikováno v:
Journal of the American College of Cardiology. 48(1)
OBJECTIVES We sought to identify the genetic locus for an inherited form of dilated cardiomyopathy (DCM) that is characterized by diffuse myocardial fibrosis and sudden death. BACKGROUND Genetic studies have mapped multiple loci for DCM, which is a m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b7c90d96a34b36cb9bdedf2a4a30651
https://pubmed.ncbi.nlm.nih.gov/16814656
https://pubmed.ncbi.nlm.nih.gov/16814656
Autor:
Calum A. MacRae, Beate Michely, Katja S. Grossmann, Thomas Wichter, Craig T. Basson, Matthias Paul, Deborah A. McDermott, Walter Birchmeier, Günter Breithardt, Stefan Peters, Rainer Dietz, Bruce B. Lerman, Patrick T. Ellinor, Ludwig Thierfelder, Eric Schulze-Bahr, Sabine Sasse-Klaassen, Arnd Heuser, Brenda Gerull, Steve M Markowitz
Publikováno v:
Nature genetics. 36(11)
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is associated with fibrofatty replacement of cardiac myocytes, ventricular tachyarrhythmias and sudden cardiac death. In 32 of 120 unrelated individuals with ARVC, we identified heterozygous muta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3997dfdb3c4e2ee77b5387e9db096785
https://pubmed.ncbi.nlm.nih.gov/15489853
https://pubmed.ncbi.nlm.nih.gov/15489853
Publikováno v:
American journal of medical genetics. Part A. (2)
Isolated noncompaction of the ventricular myocardium (INVM, MIM 300183 and 604169) is a congenital unclassified cardiomyopathy with numerous prominent trabeculations and deep intertrabecular recesses in a hypertrophied and hypokinetic myocardium. Mut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9979c9aadfe07a87034f39883688b94e
https://pubmed.ncbi.nlm.nih.gov/15389715
https://pubmed.ncbi.nlm.nih.gov/15389715
Publikováno v:
American Journal of Medical Genetics Part A. :222-223
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a8fdf6f9990d52f04ca57f1549a7aef2
https://doi.org/10.1002/ajmg.a.30211
https://doi.org/10.1002/ajmg.a.30211