A prospective study of treatment of acquired (autoimmune) factor VIII inhibitors with high-dose intravenous gammaglobulin.

No abstract is available for this paper.

• Publication year

  1995

• Venue

  Blood

• Publication date

  1995-07-15

• Fields of study

  Medicine

• Identifiers
  DOI 10.1182/BLOOD.V86.2.797.BLOODJOURNAL862797PMID 7606010
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Immunosuppression of factor VIII inhibitors in nonhemophilic patients.

  1993cited by this paper
• Origin of anti-idiotypic activity against anti-factor VIII autoantibodies in pools of normal human immunoglobulin G (IVIg).

  1992cited by this paper
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  1991cited by this paper
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  1991cited by this paper
• Acquired inhibitors in malignant and nonmalignant disease states.

  1991cited by this paper
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  1991cited by this paper
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  1991cited by this paper
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  1991cited by this paper
• Failure of high‐dose I.V. Gammaglobulin in the treatment of spontaneously acquired factor VIII inhibitors

  1988cited by this paper
• High-dose intravenous immunoglobulin for myasthenia gravis.

  1988cited by this paper
• Anti-idiotypes against autoantibodies and alloantibodies to VIII:C (anti-haemophilic factor) are present in therapeutic polyspecific normal immunoglobulins.

  1988cited by this paper
• Autoimmune Factor VIII Inhibitor Responsive to Gammaglobulin without In Vitro Neutralisation

  1988cited by this paper
• Effect of intravenous immunoglobulin on a spontaneous inhibitor to factor VIII.

  1988cited by this paper
• An Acquired Factor VIII Inhibitor Responsive to High-Dose Gamma Globulin

  1987cited by this paper
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  1987cited by this paper
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  1987cited by this paper
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  1986cited by this paper
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  1986cited by this paper
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  1985cited by this paper
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  1984cited by this paper
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  1983cited by this paper
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  1982cited by this paper
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