Family Engagement in Pediatric Sickle Cell Disease Visits-Reference-Cited by-同舟云学术

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Family Engagement in Pediatric Sickle Cell Disease Visits

Published:2016-05-09 Issue:1 Volume:32 Page:51-59
ISSN:1041-0236
Container-title:Health Communication
language:en
Short-container-title:Health Communication

Author:

Cox Elizabeth D.,Swedlund Matthew P.,Young Henry N.,Moreno Megan A.,Schopp Jennifer M.,Rajamanickam Victoria,Panepinto Julie A.

Funder

National Center for Research Resources (NCRR)

National Center for Advancing Translational Sciences (NCATS)

Publisher

Informa UK Limited

Subject

Communication,Health (social science)

Link

https://www.tandfonline.com/doi/pdf/10.1080/10410236.2015.1099503

Reference60 articles.

1. Patients' Perceptions of Quality of Care for Colorectal Cancer by Race, Ethnicity, and Language

2. National Institutes of Health Consensus Development Conference Statement: Hydroxyurea Treatment for Sickle Cell Disease

3. Race, Gender, and Partnership in the Patient-Physician Relationship

4. Development and validation of PRISM: A survey tool to identify diabetes self-management barriers

5. Influence of race and socioeconomic status on engagement in pediatric primary care

Cited by 9 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. Adolescent, Parent, and Clinician Perspectives on Increasing Adolescent Involvement in Decision-Making During Clinic Visits;Journal of Pediatric Health Care;2023-09

2. A systematic review of social determinants of health in pediatric organ transplant outcomes;Pediatric Transplantation;2022-11

3. Family‐centered communication in pediatric sickle cell disease;Pediatric Blood & Cancer;2022-09-24

4. Der Alltag von Jugendlichen mit einer Sichelzellerkrankung – Eine qualitative, explorative und partizipative Photovoice-Studie;Pflege;2020-12

5. Pediatric Hematologists Report Infrequent Prognosis Discussions in the Routine Care of Children with Sickle Cell Disease;Journal of Health Care for the Poor and Underserved;2020

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