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Methodisches und klinisches Spektrum von Lupusantikoagulanzien

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Book cover 24. Hämophilie-Symposion

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Zusammenfassung

Das Auftreten von Lupusantikoagulanzien (LA) gewinnt eine zunehmende klinische und diagnostische Bedeutung, v.a. im Zusammenhang mit thromboembolischen Erkrankungen, Autoimmunerkrankungen (Kollagenosen, SLE u.a.), rezidivierenden Spontanaborten und Totgeburten, Thrombozytopenien, dermatologischen Erkrankungen (z.B. Livedo racemosa) und zerebralen Ischämien bei jungen Patienten [1].

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Literatur

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Authors
  1. S. Ehrenforth
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  2. S. Siegert
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  3. M. von Depka Prondzinski
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  4. C. Goldmann
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  5. S. Lüdtke
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  6. B. Zwinge
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  7. I. Scharrer
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Editor information

Editors and Affiliations

  1. Abteilung für Angiologie, Zentrum der Inneren Medizin, Klinikum der Johann-Wolfgang-Goethe-Universität, Theodor-Stern-Kai 7, D-60590, Frankfurt am Main, Germany

    Inge Scharrer

  2. Hämostaseologische Abteilung, Medizinische Klinik, Klinikum Innenstadt der Ludwig-Maximilians-Universität, Ziemssenstraße 1a, D-80336, München, Germany

    Wolfgang Schramm

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© 1994 Springer-Verlag Berlin Heidelberg

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Ehrenforth, S. et al. (1994). Methodisches und klinisches Spektrum von Lupusantikoagulanzien. In: Scharrer, I., Schramm, W. (eds) 24. Hämophilie-Symposion. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-79009-6_31

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  • DOI: https://doi.org/10.1007/978-3-642-79009-6_31

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-540-57999-1

  • Online ISBN: 978-3-642-79009-6

  • eBook Packages: Springer Book Archive

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