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31 - Peripartum Cardiomyopathy

from Scenario Section 9 - Cardiac

Published online by Cambridge University Press:  25 March 2019

Kirsty MacLennan
Affiliation:
Manchester University Hospitals NHS Trust
Catherine Robinson
Affiliation:
Manchester University Hospitals NHS Trust
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Publisher: Cambridge University Press
Print publication year: 2019

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References

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Sliwa, K., Hilfiker-Kleiner, D., Petrie, M. C., et al. (2014). Current state of knowledge on aetiology, diagnosis, management, and therapy of peripartum cardiomyopathy: a position statement from the Heart Failure Association of the European Society of Cardiology Working Group on peripartum cardiomyopathy. European Journal of Heart Failure, 12(8), 767778.CrossRefGoogle Scholar
Stapel, B., Kohlhaus, M., Ricke-Hoch, M., et al. (2017). Low STAT3 expression sensitizes to toxic effects of β-adrenergic receptor stimulation in peripartum cardiomyopathy. European Heart Journal, 35(5), 349361.Google Scholar
Ware, J. S., Li, J., Mazaika, E., et al. (2016). Shared genetic predisposition in peripartum and dilated cardiomyopathies. The New England Journal of Medicine, 374(3), 233241.CrossRefGoogle ScholarPubMed

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