Results 151 to 160 of about 144,374 (198)
Prevalence and Incidence of Hereditary Angioedema: A Systematic Literature Review.
Craig TJ +5 more
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Pathophysiology of Hereditary Angioedema (HAE) Beyond the SERPING1 Gene
Clinical Reviews in Allergy and Immunology, 2021Hereditary Angioedema (HAE) is an autosomal dominant disorder characterized clinically by recurrent episodes of swelling involving subcutaneous tissues, gastrointestinal tract, and oro-pharyngeal area. Gene mutations are the most common genetic cause of HAE and observed in more than 90% of patients.
Aaqib Zaffar Banday, Amit Rawat
exaly +3 more sources
Hereditary Angioedema with Normal C1-INH (HAE Type III)
Journal of Allergy and Clinical Immunology: in Practice, 2013Hereditary angioedema (HAE) with normal C1 inhibitor (C1-INH), also known as HAE type III, is a familial condition only clinically recognized within the past three decades. Similar to HAE from C1-INH deficiency (HAE types I and II), affected individuals experience unpredictable angioedema episodes of the skin, gastrointestinal tract, and airway. Unique
Marc A Riedl
exaly +3 more sources
HAE Update: Special considerations in the female patient with hereditary angioedema
Allergy and Asthma Proceedings, 2013This review on hereditary angioedema (HAE) focuses on special topics regarding HAE in female patients. HAE is a bradykinin-mediated disorder, and the role of hormonal regulation of disease expression will be discussed focusing on the effect of estrogen on disease mechanism.
Marc A Riedl
exaly +3 more sources
Hintergrund Hereditäres Angioödem (HAE) ist eine seltene genetische Krankheit, die einen erheblichen Einfluss auf die Gesundheit und Lebensqualität hat, da sie zu wiederkehrenden Schwellungsattacken führt, die Haut, Bauch und Kehlkopf betreffen. Viele Aspekte der Krankheit und ihrer Auswirkungen auf das Leben der Patienten bleiben jedoch unklar.
Aykanat, Seda
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Hereditary angioedema (HAE): a case report and literature overview [PDF]
Recognition of the unique clinical and immunological characteristics of the rare causes of Hereditary angioedema (HAE) is important in order to obtain proper and timely diagnosis and treatment of the patient. Hereditary angioedema is a rare disease with great heterogeneity of symptoms like edema of the skin, gastrointestinal mucosa and larynx or ...
Gjorgjievska Kamceva, Martina +3 more
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Journal of Allergy and Clinical Immunology
In the recent years, there was an important improvement in the understanding of the pathogenesis of hereditary angioedema (HAE). Notwithstanding, in a large portion of patients with unknown mutation (HAE-UNK) the genetic cause remains to be identified.To identify new genetic targets associated with HAE, a large Argentine family with HAE-UNK spanning 3 ...
Maurizio Margaglione +2 more
exaly +4 more sources
In the recent years, there was an important improvement in the understanding of the pathogenesis of hereditary angioedema (HAE). Notwithstanding, in a large portion of patients with unknown mutation (HAE-UNK) the genetic cause remains to be identified.To identify new genetic targets associated with HAE, a large Argentine family with HAE-UNK spanning 3 ...
Maurizio Margaglione +2 more
exaly +4 more sources
Risk of angioedema following invasive or surgical procedures in HAE type I and II – the natural history [PDF]
Background: Hereditary angioedema (HAE), caused by deficiency in C1-inhibitor (C1-INH), leads to unpredictable edema of subcutaneous tissues with potentially fatal complications.
Thomas Klingebiel, E Aygören-Pürsün
exaly +2 more sources
The Enigma of Prodromes in Hereditary Angioedema (HAE)
Clinical Reviews in Allergy & Immunology, 2021A prodrome is a premonitory set of signs and symptoms indicating the onset of a disease. Prodromes are frequently reported by hereditary angioedema (HAE) patients, antedating attacks by a few hours or even longer. In some studies, high incidence of prodromes was reported by patients, with considerable number being able to predict oncoming attacks ...
Iris Leibovich-Nassi, Avner Reshef
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