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National Hemophilia Registry - Source of Information about the Quality of Hemophilia Medical Care in a Developing Country

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36th Hemophilia Symposium Hamburg 2005

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References

  1. Skinner MW. Increasing The Worldwide Supply Of Safe, Affordable Factor Replacement Therapy. 26 September 2005-Fourth WFH Global Forum-Montreal, Canada

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  2. Evatt B. Guide to Developing a National Patient Registry. WFH 2005

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  3. Evatt BL, Black C, Batorova A, Street A, Srivastava A. Comprehensive care for hemophilia around the world. Hemophilia 2004;10 (Suppl 4):9–13.

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  4. Krebs H, Domsch C, Adelhard K, Brackmann HH, Graw J, Oldenburg J, Schwaab R, Schramm W. The national GTH hemophilia registry as database within the scope of the German human genome project. Hämostaseologie. 2003; 23(1):18–23

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Authors
  1. D. Lighezan
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  2. F. Vladareanu
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  3. V. Uscatescu
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  4. C. Petrescu
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  5. C. Jinca
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  6. D. Mihailov
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  7. M. Bătăneant
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  8. L. Pop
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  9. W. Schramm
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  10. M. Serban
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Editor information

Editors and Affiliations

  1. III. Med. Clinic, University Hospital, Langenbeckstr. 1, D-55131, Mainz, Germany

    Inge Scharrer

  2. Dept. of Hemostaseology, University Hospital, Ziemssenstr. 1a, D-80336, München, Germany

    Wolfgang Schramm

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© 2007 Springer Verlag Berlin Heidelberg

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Lighezan, D. et al. (2007). National Hemophilia Registry - Source of Information about the Quality of Hemophilia Medical Care in a Developing Country. In: Scharrer, I., Schramm, W. (eds) 36th Hemophilia Symposium Hamburg 2005. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-36715-4_3

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  • DOI: https://doi.org/10.1007/978-3-540-36715-4_3

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-540-36714-7

  • Online ISBN: 978-3-540-36715-4

  • eBook Packages: MedicineMedicine (R0)

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