Paolo Rusconi
University of Miami
59 Papers
351 Citations
Paolo Rusconi is an academic researcher from University of Miami. The author has contributed to research in topics: Cardiomyopathy & Heart failure. The author has an hindex of 18, co-authored 54 publications. Previous affiliations of Paolo Rusconi include National Institutes of Health.
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Papers
International Society for Heart and Lung Transplantation: Practice guidelines for management of heart failure in children.
David N. Rosenthal,Maryanne R.K. Chrisant,Erik Edens,Lynn Mahony,Charles E. Canter,Steven D. Colan,Anne M. Dubin,Jacque M. Lamour,Robert D. Ross,Robert E. Shaddy,Linda J. Addonizio,Lee B. Beerman,Stuart Berger,Daniel Bernstein,Elizabeth D. Blume,Mark M. Boucek,Paul A. Checchia,Anne I. Dipchand,Jonathan J. Drummond-Webb,Jay Fricker,Richard A. Friedman,Sara Hallowell,Robert D.B. Jaquiss,Seema Mital,Elfriede Pahl,Bennett Pearce,Larry A. Rhodes,Kathy Rotondo,Paolo Rusconi,Janet Scheel,Tajinder P. Singh,Jeffrey A. Towbin +31 more
TL;DR: This document has attempted to summarize the relevant literature and synthesize management guidelines for children with HF and has been prepared in a consensus fashion, with input from pediatric cardiologists at multiple sites throughout the United States and Canada.
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Outcomes of restrictive cardiomyopathy in childhood and the influence of phenotype: A report from the pediatric cardiomyopathy registry
Steven A. Webber,Steven E. Lipshultz,Lynn A. Sleeper,Minmin Lu,James D. Wilkinson,Linda J. Addonizio,Charles E. Canter,Steven D. Colan,Melanie D. Everitt,John L. Jefferies,Paul F. Kantor,Jacqueline M. Lamour,Renee Margossian,Elfriede Pahl,Paolo Rusconi,Jeffrey A. Towbin +15 more
TL;DR: In this article, the authors used the Pediatric Cardiomyopathy Registry (PCR) database to analyze outcomes of childhood restrictionive cardiopathy (RCM) with a focus on the impact of phenotype comparing pure RCM with cases that have additional features of hypertrophic cardioma (HCM).
211
Ventricular remodeling and survival are more favorable for myocarditis than for idiopathic dilated cardiomyopathy in childhood: An outcomes study from the pediatric cardiomyopathy registry
Susan R. Foerster,Charles E. Canter,Amy Cinar,Lynn A. Sleeper,Steven A. Webber,Elfriede Pahl,Paul F. Kantor,Jorge A. Alvarez,Steven D. Colan,John L. Jefferies,Jacqueline M. Lamour,Renee Margossian,Jane Messere,Paolo Rusconi,Robert E. Shaddy,Jeffrey A. Towbin,James D. Wilkinson,Steven E. Lipshultz +17 more
TL;DR: Children with biopsy-confirmed or probable myocarditis had similar proportions of death, transplantation, and echocardiographic normalization 3 years after presentation and better outcomes than those of children with idiopathic dilated cardiomyopathy.
149
Recurrent Third-Trimester Fetal Loss and Maternal Mosaicism for Long-QT Syndrome
Todd Miller,Elicia Estrella,Robert J. Myerburg,Jocelyn Garcia de Viera,Niberto A. Moreno,Paolo Rusconi,Mary Ellen Ahearn,Lisa Baumbach,Paul Kurlansky,Grace S. Wolff,Nanette H. Bishopric +10 more
TL;DR: A case of repeated germ-line transmission of a severe form of long-QT syndrome from an asymptomatic mother with mosaicism for a mutation in the cardiac sodium channel, SCN5A, with important implications for genetic counseling.
81
Usefulness of tissue Doppler echocardiography for evaluating ventricular function in children without heart disease.
TL;DR: Tissue Doppler echocardiographic imaging is a valuable tool for assessing ventricular function, particularly diastolic function, and establishment of normative data for TDI in the pediatric age group should broaden the clinical applicability of this useful modality.
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