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Acquired angioedema

 
National Institutes of Health

Papers overview

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2017
2017
BACKGROUND Acquired angioedema due to C1-inhibitor deficiency (C1-INH-AAE) is a rare disease with no prevalence data or approved… Expand
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2016
2016
Abstract Acquired angioedema (AAE) due to C1-inhibitor (C1INH) deficiency is rare. Treatment options for acute attacks are… Expand
Highly Cited
2014
Highly Cited
2014
Hereditary angioedema (HAE) and acquired angioedema (AAE) are rare life‐threatening conditions caused by deficiency of C1… Expand
Review
2013
Review
2013
Angioedema due to the acquired deficiency of C1-inhibitor is a rare disease known as acquired angioedema (AAE), which was first… Expand
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2010
2010
Acquired angioedema (AAE) is characterized by acquired deficiency of C1 inhibitor (C1-INH), hyperactivation of the classical… Expand
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Review
2008
Review
2008
Angioedema due to an acquired deficiency in the inhibitor of the first component of human complement (CI-INH) is a rare syndrome… Expand
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2007
2007
  • M. Lahiri, A. Lim
  • Annals of the Academy of Medicine, Singapore
  • 2007
  • Corpus ID: 10050126
INTRODUCTION We report angioedema as a rare presentation leading to a diagnosis of systemic lupus erythematosus (SLE). CLINICAL… Expand
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Review
2006
Review
2006
Patients with hereditary angioedema (HAE) present with recurrent, circumscribed, and self-limiting episodes of tissue or mucous… Expand
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Highly Cited
1997
Highly Cited
1997
Activation of the contact and complement systems in C1-inhibitor deficiencies is thought to contribute to the pathogenesis of… Expand
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1989
1989
To the Editor .—Two types of acquired angioedema (AAE) are recognized today; type I with low levels of functional C1-inhibitor… Expand