Care of the Child with Hemophilia
Ljung, Rolf LU
(2010)
p.127-132
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/bf66bfed-f380-4ace-ab87-2fee4ea8fa5c
- author
- Ljung, Rolf
LU
- organization
- publishing date
- 2010-08-13
- type
- Chapter in Book/Report/Conference proceeding
- publication status
- published
- subject
- keywords
- Care of children with hemophilia - and treatment regimen used, Day-care center attendance and school, Family and affected child - perceiving themselves healthy, despite hemophilia diagnosis, Healthcare professionals, aware of hemophilia being a hereditary disorder, Hemophilia child care, Hemophilia identification cards - in physician consultation and dental work, Implantable central venous line - for children with difficult venous access in peripheral veins, Knowledge of mutation type - carrier detection and prenatal diagnosis in family and risk of developing inhibitors, Venous access, prerequisite of administering blood factor concentrates to young children with hemophilia A or B, World Health Organization (WHO), health as a state of complete physical, psychological, and social well-being
- host publication
- Textbook of Hemophilia, 2nd Edition
- editor
- Lee, Christine ; Berntorp, Erik E. and Hoots, W. Keith
- article number
- 19
- pages
- 127 - 132
- publisher
- Wiley-Blackwell
- external identifiers
-
- scopus:84885814442
- ISBN
- 9781405169141
- DOI
- 10.1002/9781444318555.ch19
- language
- English
- LU publication?
- yes
- id
- bf66bfed-f380-4ace-ab87-2fee4ea8fa5c
- date added to LUP
- 2016-12-29 10:45:33
- date last changed
- 2022-01-30 08:54:00
@inbook{bf66bfed-f380-4ace-ab87-2fee4ea8fa5c,
author = {{Ljung, Rolf}},
booktitle = {{Textbook of Hemophilia, 2nd Edition}},
editor = {{Lee, Christine and Berntorp, Erik E. and Hoots, W. Keith}},
isbn = {{9781405169141}},
keywords = {{Care of children with hemophilia - and treatment regimen used; Day-care center attendance and school; Family and affected child - perceiving themselves healthy, despite hemophilia diagnosis; Healthcare professionals, aware of hemophilia being a hereditary disorder; Hemophilia child care; Hemophilia identification cards - in physician consultation and dental work; Implantable central venous line - for children with difficult venous access in peripheral veins; Knowledge of mutation type - carrier detection and prenatal diagnosis in family and risk of developing inhibitors; Venous access, prerequisite of administering blood factor concentrates to young children with hemophilia A or B; World Health Organization (WHO), health as a state of complete physical, psychological, and social well-being}},
language = {{eng}},
month = {{08}},
pages = {{127--132}},
publisher = {{Wiley-Blackwell}},
title = {{Care of the Child with Hemophilia}},
url = {{http://dx.doi.org/10.1002/9781444318555.ch19}},
doi = {{10.1002/9781444318555.ch19}},
year = {{2010}},
}