Shaping and managing the course of a child's disease: Parental experiences with osteogenesis imperfecta-Reference-Cited by-同舟云学术

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Shaping and managing the course of a child's disease: Parental experiences with osteogenesis imperfecta

Published:2014-07 Issue:3 Volume:7 Page:343-349
ISSN:1936-6574
Container-title:Disability and Health Journal
language:en
Short-container-title:Disability and Health Journal

Author:

Dogba Maman Joyce,Rauch Frank,Tre Ghislaine,Glorieux Francis H.,Bedos Christophe

Publisher

Elsevier BV

Subject

Public Health, Environmental and Occupational Health,General Medicine

Reference32 articles.

1. The Corbin and Strauss chronic illness trajectory model: an update;Corbin;Sch Inq Nurs Pract,1998

2. Revisiting how the Chronic Illness Trajectory Framework can be applied for persons living with HIV/AIDS;Nokes;Sch Inq Nurs Pract,1998

3. Processes of metastudy: a study of psychosocial adaptation to childhood chronic health conditions;Nicholas;Int J Qual Methods,2006

4. An update of childhood genetic disorders;Prows;J Nurs Scholarsh,2013

5. Family resources and parental health in families of children with Duchenne muscular dystrophy;Chen;J Nurs Res,2010

Cited by 27 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. Risk perception for fractures and its related factors among family caregivers of underage patients with osteogenesis imperfecta in China: A cross-sectional study;Journal of Pediatric Nursing;2024-07

2. Caregiver Burden, Parenting Stress and Coping Strategies: The Experience of Parents of Children and Adolescents with Osteogenesis Imperfecta;Healthcare;2024-05-14

3. A patient-centred and multi-stakeholder co-designed observational prospective study protocol: Example of the adolescent experience of treatment for X-linked hypophosphataemia (XLH);PLOS ONE;2024-01-19

4. The patient clinical journey and socioeconomic impact of osteogenesis imperfecta: a systematic scoping review;Orphanet Journal of Rare Diseases;2023-02-22

5. Carer burden in rare inherited diseases: a literature review and conceptual model;Orphanet Journal of Rare Diseases;2022-12-09

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