By J. F. Goodwin (auth.), Fulvio Camerini, Antonello Gavazzi, Renata De Maria (eds.)

ISBN-10: 8847021553

ISBN-13: 9788847021556

ISBN-10: 8847021812

ISBN-13: 9788847021815

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Read Online or Download Advances in Cardiomyopathies: Proceedings of the II Florence Meeting on Advances on Cardiomyopathies April 24–26, 1997 PDF

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Extra info for Advances in Cardiomyopathies: Proceedings of the II Florence Meeting on Advances on Cardiomyopathies April 24–26, 1997

Sample text

Shapiro LM, Zezulka A (1983) Hypertrophic cardiomyopathy: a common disease with a good prognosis: five year experience of a district general hospital. Br Heart J 50:530-533 22. Kofftard MJ, Waldstein DJ, Vos J, ten Cate FJ (1993) Prognosis in hypertrophic cardiomyopathy observed in a large clinic population. Am J Cardiol 72:939-943 23 Maron BJ, Spirito P (1993) Impact of patient selection biases on the perception of hypertrophic cardiomyopathy and its natural history. Am J Cardiol 72:970-972 24.

Cecchi F, Maron BJ, Epstein SE (1989) Long-term outcome of patients with hypertrophic cardiomyopathy successfully resuscitated after arrest. J Am ColI Cardiol 13: 1283-1288 19. McKenna WJ, Carnm AJ (1989) Sudden death in hypertrophic cardiomyopathy: assessment of patients at high risk. Circulation 80:1489-1494 20. Maron BJ, Henry WL, Clark CE, Redwood DR, Roberts WC, Epstein SE (1976) Asymmetric septal hypertrophy in childhood. Circulation 53:9-14 21. Shapiro LM, Zezulka A (1983) Hypertrophic cardiomyopathy: a common disease with a good prognosis: five year experience of a district general hospital.

Hypertrophy can be localized to one segment of the left ventricle or involve all segments of both ventricles, and the clinical spectrum may vary, in patients with the same morphologic appearance, from the absence of symptoms to severe functional limitation [13,5,6]. The majority of the studies on prognosis published in the major cardiology journals have come from only two tertiary referral centers [23,27] and their reported annual mortality varies from 2% to 6%. Patients in these studies were characterized by young age at diagnosis, malignant family history, severe symptoms, high prevalence of obstructive forms, and sudden death [1,9-20].

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Advances in Cardiomyopathies: Proceedings of the II Florence Meeting on Advances on Cardiomyopathies April 24–26, 1997 by J. F. Goodwin (auth.), Fulvio Camerini, Antonello Gavazzi, Renata De Maria (eds.)


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