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Anästhesie bei seltenen Erkrankungen pp 38–57Cite as

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Zusammenfassung

Peroneale Muskelatrophie, Charcot-Marie-Amyotrophie (Muskeldystrophie), heredodegenerative neurale Muskelatrophie, Atrophia musculorum progressiva neurotica sive neuralis, engl. »peroneal muscular atrophy«, hereditäre motorisch-sensible Neuropathie (HMSN) Typ I und II.

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Authors and Affiliations

  1. Institut für Anästhesiologie, Universitätsspital Zürich, Rämistr. 100, 8091, Zürich

    PD Dr. med. Peter Biro DEAA

  2. Klinik für Anästhesiologie und Intensivmedizin Notfallmedizin, Schmerztherapie, Palliativmedizin, Krankenhaus Hetzelstift, Stiftstr. 10, 67434, Neustadt/Weinstraße

    Prof. Dr. med. habil. Dierk A. Vagts MSc., DEAA, EDIC

  3. Ospedale Castelli, Via Fiume 18, 28922, Verbania

    Dr. med. Uta Emmig

  4. Sennhofstr. 92, 8125, Zollikerberg

    Prof. Dr. med. Thomas Pasch FRCA

Authors
  1. PD Dr. med. Peter Biro DEAA
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  2. Prof. Dr. med. habil. Dierk A. Vagts MSc., DEAA, EDIC
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  3. Dr. med. Uta Emmig
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  4. Prof. Dr. med. Thomas Pasch FRCA
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© 2011 Springer-Verlag Berlin Heidelberg

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Biro, P., Vagts, D.A., Emmig, U., Pasch, T. (2011). C. In: Anästhesie bei seltenen Erkrankungen. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-01047-7_3

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  • DOI: https://doi.org/10.1007/978-3-642-01047-7_3

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-01046-0

  • Online ISBN: 978-3-642-01047-7

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