Klassifikation, genetische Prädisposition und Risikofaktoren für die Entwicklung einer Kardiomyopathie-Reference-Cited by-同舟云学术

Klassifikation, genetische Prädisposition und Risikofaktoren für die Entwicklung einer Kardiomyopathie

Published:2008-02-16 Issue:4 Volume:49 Page:441-447
ISSN:0020-9554
Container-title:Der Internist
language:de
Short-container-title:Internist

Author:

Pankuweit S.,Richter A.,Ruppert V.,Funck R.,Maisch B.

Publisher

Springer Science and Business Media LLC

Subject

Internal Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00108-008-2050-y.pdf

Reference33 articles.

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3. Arad M, Seidman JG, Seidman CE (2002) Phenotypic diversity in hypertrophic cardiomyopathy. Hum Mol Genet 11: 2499–2506

4. Arbustini E, Morbini P, Pilotto A et al. (2001) Familial dilated cardiomyopathy: from clinical presentation to molecular genetics. Am J Hum Genet 69: 249–260

5. Ashrafian H, Watkins H (2007) Reviews of translational medicine and genomics in cardiovascular disease: new disease taxonomy and therapeutic implications cardiomyopathies: therapeutics based on molecular phenotype. J Am Coll Cardiol 49: 1251–1264

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1. Influence of different aetiologies on clinical course and outcome in patients with dilated cardiomyopathy;European Journal of Clinical Investigation;2015-08-06

2. A 56-year-old man with co-prevalence of Leriche syndrome and dilated cardiomyopathy: case report and review;Wiener klinische Wochenschrift;2013-12-17

3. Kardiale Magnetresonanztomographie in der Diagnostik der restriktiven und unklassifizierten Kardiomyopathien;Der Radiologe;2012-11-17