Burden on parents of children with haemophilia: The impact of sociodemographic and child's medical condition-Reference-Cited by-同舟云学术

Burden on parents of children with haemophilia: The impact of sociodemographic and child's medical condition

Published:2019-09-03 Issue:21-22 Volume:28 Page:4077-4086
ISSN:0962-1067
Container-title:Journal of Clinical Nursing
language:en
Short-container-title:J Clin Nurs

Author:

Myrin Westesson Linda¹²^ORCID,Sparud‐Lundin Carina²,Baghaei Fariba¹,Khair Kate³,Mackensen Sylvia⁴,Acuña Mora Mariela²⁵,Wallengren Catarina²⁶

Affiliation:

1. Sahlgrenska University Hospital Gothenburg Sweden

2. Institute of Health and Care Sciences The Sahlgrenska Academy, University of Gothenburg Gothenburg Sweden

3. Centre for Outcomes and Experience Research in Children’s Health, Illness and Disability (ORCHID) Great Ormond Street Hospital for Children NHS Trust London UK

4. Department of Medical Psychology University Medical Centre Hamburg‐Eppendorf Hamburg Germany

5. Department of Public Health and Primary Care KU Leuven Leuven Belgium

6. Centre for Person‐Centred Care (GPCC) University of Gothenburg Gothenburg Sweden

Publisher

Wiley

Subject

General Medicine,General Nursing

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/jocn.15003

Reference43 articles.

1. Insurance, Home Therapy, and Prophylaxis in U.S. Youth with Severe Hemophilia

2. Treatment of haemophilia A and B and von Willebrand’s disease: summary and conclusions of a systematic review as part of a Swedish health-technology assessment

3. European retrospective study of real-life haemophilia treatment

4. Modern haemophilia care

5. Hemophilia Care in the Pediatric Age

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