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32nd Hemophilia Symposium Hamburg 2001

  • Conference proceedings
  • © 2003

Overview

Editors:
  1. Inge Scharrer

    1. Hemophilia Center, Dept. of Internal Medicine, University Hospital, Frankfurt am Main, Germany

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  2. Wolfgang Schramm

    1. Dept. of Hemostasiology, University Hospital, München, Germany

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Table of contents (50 papers)

  1. Front Matter

    Pages II-XXIX
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  3. Genetic Diagnosis of Clotting Disorders

    1. Front Matter

      Pages 23-23
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    2. Human Genome Project

      1. 11 novel Mutations in the Factor VIII encoding Gene lead to severe or moderate Hemophilia A
        • C. Uen, N. Klopp, J. Oldenburg, H.-H. Brackmann, W. Schramm, R. Schwaab et al.
        Pages 25-31

    3. Register and Genetic Diagnosis

      1. Molecular Analysis of Hemophilia B: »Greifswald Registry FIX Deficiency (Hemophilia B)«
        • K. Wulff, W. Schröder, F. H. Herrmann, study group
        Pages 35-48
      2. Gly222Asp and Ser379Lys — Novel Factor X Gene Mutations in severe FX Deficiency — Greifswald Registry of Factor X congenital Deficiency
        • F. H. Herrmann, K. Wulff, S. Lopaciuk, H. Pollmann
        Pages 49-57

    4. Gene Therapy

      1. Hematopoietic Stem Cells as Targets for Gene Therapy of Hemophilia A
        • T. Tonn, S. Becker, C. Herder, M. Grez, E. Seifried
        Pages 61-71
      2. Adenovirus-mediated regulatable Expression of human Factor IX <i>in vitro</i> and <i>in vivo</i>
        • M. A. Srour, H. Fechner, X. Wang, U. Siemetzki, T. Albert, J. Oldenburg et al.
        Pages 72-80

  4. Hemophilia

    1. Front Matter

      Pages 81-81
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    2. Orthopedics

      1. Experiences with MRI Examination of the Joints of hemophilic Children
        • K. Kurnik, N. Nohe, K. Stehr, M. Praun, A. Lieb, Th. Pfluger
        Pages 83-86
      2. Rhenium-186 Hydroxyethylidenediphosphonate (186Re HEDP) — A novel Treatment for hemophilic Arthropathies?
        • T. A. Wallny, L. Hess, H.-H. Brackmann, A. Seuser, H. Palmedo, C. Kraft
        Pages 87-91

    3. Monitoring of Substitution Therapy

      1. Monitoring of Anticoagulant Therapy with the endogenous Thrombin Potential
        • A. Siegemund, T. Siegemund, U. Scholz, S. Petros, L. Engelmann
        Pages 95-100

  5. Pediatric Hemostaseology

    1. Front Matter

      Pages 101-101
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    2. First thromboembolic Onset in Children carrying either the heterozygeous Factor V G1691A Mutation or the Prothrombin G20210A Variant

      • A. Kosch, S. Becker, K. Kurnik, K. Sudbrak, R. Schobess, R. Junker et al.
      Pages 103-110

    3. UFH Bolus Administration in Comparison to subcutaneous Low Molecular Weight Heparin in pediatric cardiac Catheterization

      • B. Roschitz, A. Beitzke, A. Gamillscheg, K. Sudi, B. Leschnik, M. Köstenberger et al.
      Pages 111-114

    4. Incidence of Inhibitor Development in consecutively recruited severe Hemophilia A and B Patients — a retrospective Single Centre Study

      • S. Halimeh, A. Kosch, N. Bogdanova, K. Abshagen, H. Jürgens
      Pages 115-119
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Keywords

Editors and Affiliations

  • Hemophilia Center, Dept. of Internal Medicine, University Hospital, Frankfurt am Main, Germany

    Inge Scharrer

  • Dept. of Hemostasiology, University Hospital, München, Germany

    Wolfgang Schramm

Bibliographic Information

  • Book Title: 32nd Hemophilia Symposium Hamburg 2001

  • Editors: Inge Scharrer, Wolfgang Schramm

  • DOI: https://doi.org/10.1007/978-3-642-18150-4

  • Publisher: Springer Berlin, Heidelberg

  • eBook Packages: Springer Book Archive

  • Copyright Information: Springer-Verlag Berlin Heidelberg 2003

  • Softcover ISBN: 978-3-540-43884-7Published: 23 October 2002

  • eBook ISBN: 978-3-642-18150-4Published: 28 September 2012

  • Edition Number: 1

  • Number of Pages: XXIX, 318

  • Number of Illustrations: 112 b/w illustrations

  • Topics: Hematology, Pediatrics, Anesthesiology, Blood Transfusion Medicine, Intensive / Critical Care Medicine

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