The Role of Congenital Heart Disease Patient Organizations in Advocacy, Resources, and Support Across the Lifespan-Reference-Cited by-同舟云学术

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The Role of Congenital Heart Disease Patient Organizations in Advocacy, Resources, and Support Across the Lifespan

Published:2023-12 Issue:6 Volume:2 Page:256-266
ISSN:2772-8129
Container-title:CJC Pediatric and Congenital Heart Disease
language:en
Short-container-title:CJC Pediatric and Congenital Heart Disease

Author:

Ross Shelagh,Verstappen Amy

Publisher

Elsevier BV

Reference27 articles.

1. Congenital heart disease: education and employment considerations and outcomes;Girouard;Int J Cardiol Congen Heart Dis,2020

2. Health care policy and congenital heart disease: 2020 focus on our 2030 future;Chowdhury;J Am Heart Assoc,2021

3. Current research status on the psychological situation of parents of children with congenital heart disease;Biber;Cardiovasc Diagn Ther,2019

4. Depression and anxiety in adult congenital heart disease: predictors and prevalence;Kovacs;Int J Cardiol,2009

5. Self-advocacy strategy instruction: enhancing student motivation, self-determination, and responsibility in the learning process;Van Reusen,1998

Cited by 1 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. Challenges and Opportunities for Patients With Tetralogy of Fallot Across the Lifespan;CJC Pediatric and Congenital Heart Disease;2023-12

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