Data on cardiac defects, morbidity and mortality in patients affected by RASopathies. CARNET study results-Reference-Cited by-同舟云学术

Data on cardiac defects, morbidity and mortality in patients affected by RASopathies. CARNET study results

Published:2018-02 Issue: Volume:16 Page:649-654
ISSN:2352-3409
Container-title:Data in Brief
language:en
Short-container-title:Data in Brief

Author:

Calcagni Giulio,Limongelli Giuseppe,D'Ambrosio Angelo,Gesualdo Francesco,Digilio Maria Cristina,Baban Anwar,Albanese Sonia B.,Versacci Paolo,De Luca Enrica,Ferrero Giovanni B.,Baldassarre Giuseppina,Agnoletti Gabriella,Banaudi Elena,Marek Jan,Kaski Juan P.,Tuo Giulia,Russo Maria Giovanna,Pacileo Giuseppe,Milanesi Ornella,Messina Daniela,Marasini Maurizio,Cairello Francesca,Formigari Roberto,Brighenti Maurizio,Dallapiccola Bruno,Tartaglia Marco,Marino Bruno

Publisher

Elsevier BV

Subject

Multidisciplinary

Reference6 articles.

1. Cardiac defects, morbidity and mortality in patients affected by RASopathies. CARNET study results;Calcagni;Int. J. Cardiol.,2017

2. A weakly informative default prior distribution for logistic and other regression models;Gelman;Ann. Appl. Stat.,2008

3. Bootstrap methods for standard errors, confidence intervals, and other measures of statistical accuracy;Efron;Stat. Sci.,1986

4. Bootstrap confidence intervals;DiCiccio;Stat. Sci.,1996

5. Low P-values or narrow confidence intervals: which are more durable?;Poole;Epidemiology,2001

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Natural history and outcomes in paediatric RASopathy‐associated hypertrophic cardiomyopathy;ESC Heart Failure;2024-01-13

2. Multidisciplinary Management of Costello Syndrome: Current Perspectives;Journal of Multidisciplinary Healthcare;2022-06

3. Atypical cardiac defects in patients with RASopathies: Updated data on CARNET study;Birth Defects Research;2020-06

4. Pediatric patients with RASopathy-associated hypertrophic cardiomyopathy: the multifaceted consequences of PTPN11 mutations;Orphanet Journal of Rare Diseases;2019-07-05

5. Clinical and functional characterization of a novel RASopathy‐causing SHOC2 mutation associated with prenatal‐onset hypertrophic cardiomyopathy;Human Mutation;2019-05-06