Newborn screening programmes in Europe; arguments and efforts regarding harmonization. Part 1 - From blood spot to screening result

Author:

Loeber J. Gerard,Burgard Peter,Cornel Martina C.,Rigter Tessel,Weinreich Stephanie S.,Rupp Kathrin,Hoffmann Georg F.,Vittozzi Luciano

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference15 articles.

1. Aymé S, Rodwell C, eds. “2011 Report on the state of the art of rare disease activities in Europe of the European Union Committee of Experts on Rare Diseases - Part I: overview of rare disease activities in Europe and key developments in 2010”, July 2011. http://www.eucerd.eu/upload/file/Reports/2011ReportStateofArtRDActivities.pdf (Accessed 28 Nov 2011)

2. Bodamer OA, Hoffmann GF, Lindner M (2007) Expanded newborn screening in Europe. J Inherit Metab Dis 30:439–444

3. Burgard P, Cornel M, Di Filippo F et al. (2011) Report on the practices of newborn screening for rare disorders implemented in Member States of the European Union, Candidate, Potential Candidate and EFTA Countries. http://www.iss.it/cnmr/prog/cont.php?id=1621&lang=1&tipo=64 Accessed 24 Feb 2012

4. Burgard P, Rupp K, Lindner M et al. (2012) Results of a survey for the evaluation of population newborn screening practices for rare disorders in Europe – From screening laboratory results to treatment, and follow-up, and quality assurance. J Inherit Metab Dis, (in press)

5. Communication from the Commission to the European Parliament, The Council, The European Economic and Social Committee and The Committee of the Regions on Rare Diseases: Europe’s Challenges (2008). Retrieved from http://ec.europa.eu/health/ph_threats/non_com/docs/rare_com_en.pdf Accessed 22 Nov 2011

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