Literature DB >> 1524272

Angioedema and C1 inhibitor deficiency.

N A Orfan1, G B Kolski.   

Abstract

Deficiency of C1 inhibitor resulting in episodes of angioedema causes significant morbidity and mortality in affected patients, yet often goes undiagnosed for years. As biochemical understanding of the disorder has improved, competing theories for the pathophysiologic mechanism of angioedema have emerged. Further, existing therapeutic interventions have been refined by experience and newer modalities currently available in Europe may soon become available in the United States.

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Year:  1992        PMID: 1524272

Source DB:  PubMed          Journal:  Ann Allergy        ISSN: 0003-4738


  4 in total

1.  Hereditary angioedema presenting with recurrent ascites.

Authors:  Rada Jesic; Djordje Culafic; Branka Bonaci-Nikolic
Journal:  Dig Dis Sci       Date:  2005-01       Impact factor: 3.199

2.  Combined treatment with C1 esterase inhibitor and antithrombin III improves survival in severe acute experimental pancreatitis.

Authors:  H Yamaguchi; H Weidenbach; H Lührs; M M Lerch; G Dickneite; G Adler
Journal:  Gut       Date:  1997-04       Impact factor: 23.059

3.  [Hereditary angioedema. Diagnostic and treatment errors as systemic lupus erythematosus].

Authors:  P Harten; D Körbächer; C Renk; H H Euler; H Löffler
Journal:  Med Klin (Munich)       Date:  1999-06-15

4.  Retro-orbital oedema and transient blindness following endoscopic oesophagogastroduodenoscopy: a case report.

Authors:  Tahrina Salam; Tamara Nissner; Afshin Kahin; Andrew C Coombes; Daniel G Ezra
Journal:  Cases J       Date:  2009-09-02
  4 in total

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