Cardiomyopathies-Reference-Cited by-同舟云学术

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Cardiomyopathies

Published:2019 Issue: Volume: Page:205-225
ISSN:
Container-title:Cardiac Pathology
language:
Short-container-title:

Author:

Bunning Clare R.,Suvarna S. Kim

Publisher

Springer International Publishing

Link

http://link.springer.com/content/pdf/10.1007/978-3-030-24560-3_11

Reference82 articles.

1. Arbustini E, Narula N, Dec WG, et al. The MOGE(S) Classification for a phenotype–genotype nomenclature of cardiomyopathy. Endorsed by the World Heart Federation. J Am Col Cardiol. 2013;62:2046–72.

2. McNally E, Golbus J, Puckelwatz M. Genetic mutations and mechanisms in dilated cardiomyopathy. J Clin Invest. 2013;123(1):19–26.

3. Vikhorev PG, Smoktunowicz N, Munster AB, et al. Abnormal contractility in human heart myofibrils from patients with dilated cardiomyopathy due to mutations in TTN and contractile protein genes. Sci Rep. 2017;7(1):14829.

4. Ware JS, Li J, Mazaika E, et al. Shared genetic predisposition in peripartum and dilated cardiomyopathies. N Engl J Med. 2016;374(3):233–41.

5. Marian AJ, van Rooij E, Roberts R. Genetics and genomics of single-gene cardiovascular diseases: common hereditary cardiomyopathies as prototypes of single-gene disorders. J Am Coll Cardiol. 2016;68(25):2831–49.

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1. Post Mortem Computed Tomography of the Heart;Post Mortem CT for Non-Suspicious Adult Deaths;2021

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