Care of the Child with Hemophilia

Ljung, Rolf LU (2010) In Textbook of Hemophilia, 2nd Edition p.127-132
Please use this url to cite or link to this publication:
  author       = {Ljung, Rolf},
  editor       = {Lee, Christine and Berntorp, Erik E. and Hoots, W. Keith},
  isbn         = {9781405169141},
  keyword      = {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},
  series       = {Textbook of Hemophilia, 2nd Edition},
  title        = {Care of the Child with Hemophilia},
  url          = {},
  year         = {2010},