The French proposal for a health identification number.
01/2006; DOI:10.3233/978-1-58603-647-8-201 In proceeding of: Ubiquity: Technologies for Better Health in Aging Societies - Proceedings of MIE2006, The XXst International Congress of the European Federation for Medical Informatics, Maastricht, The Netherlands, August 27-30, 2006
- [show abstract] [hide abstract]
ABSTRACT: The main objective of INFORARE project is to organize the gathering, assessment and sharing of medical information between sickle-cell anaemia patient and the health workforce. The method is based on the: evaluation of the sickle-cell anaemia patients’ acceptability of the familial data collection; centralised management of medical files which have been rendered anonymous; proposition of an identification model for sickle-cell anaemia patients and the evaluation of first the feasibility of the identification data collection, second the data linkage quality.Irbm. 01/2010; 31(2):127-130.
Data provided are for informational purposes only. Although carefully collected, accuracy cannot be guaranteed. The impact factor represents a rough estimation of the journal's impact factor and does not reflect the actual current impact factor. Publisher conditions are provided by RoMEO. Differing provisions from the publisher's actual policy or licence agreement may be applicable.