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Published in 2017 at "Clinical biochemistry"
DOI: 10.1016/j.clinbiochem.2017.04.007
Abstract: OBJECTIVES Low complement factor C4 is usually considered a valuable screening tool for patients with the potentially life-threatening hereditary angioedema with C1-inhibitor (C1-INH) deficiency (C1-INH-HAE). However, there are patients with C1-INH-HAE presenting with normal C4…
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Keywords:
total antigenic;
hae patients;
non functional;
hae ... See more keywords
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Published in 2019 at "International immunopharmacology"
DOI: 10.1016/j.intimp.2019.106079
Abstract: Hereditary angioedema is a disabling, life-threatening condition caused by deficiency (type I) or dysfunction (type II) of the C1 inhibitor protein (C1-INH-HAE) leading to bradykinin accumulation and recurrent episodes of edema attack. Vascular leakage is…
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Keywords:
attack;
remission;
vasoactive mediators;
patients inh ... See more keywords
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Published in 2022 at "Orphanet Journal of Rare Diseases"
DOI: 10.1186/s13023-022-02202-2
Abstract: Background The generic 36-item Short-Form Health Survey (SF-36v2) has been used to assess health related quality of life in adult patients with hereditary angioedema due to C1-inhibitor deficiency (C1-INH-HAE) even though it has not yet…
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Keywords:
inhibitor deficiency;
due inhibitor;
inh hae;
hereditary angioedema ... See more keywords
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Published in 2018 at "Frontiers in Immunology"
DOI: 10.3389/fimmu.2018.01721
Abstract: Background Hereditary angioedema (HAE) caused by deficiency (type I) or dysfunction (type II) of the C1 inhibitor protein (C1-INH-HAE) is a disabling, potentially fatal condition characterized by recurrent episodes of swelling. We have recently found…
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Keywords:
hgiia;
inhibitor;
permeability;
inh hae ... See more keywords