Research LettersEradication of Helicobacter pylori and improvement of hereditary angioneurotic oedema
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Cited by (63)
Angioedema Due to Acquired Deficiency of C1-Inhibitor: A Cohort Study in Spain and a Comparison With Other Series
2022, Journal of Allergy and Clinical Immunology: In PracticeCitation Excerpt :Of note, many of the patients with autoimmune disease had associated hematologic disorders, as reported in the Italian series.3 Infection and neoplasm have been reported elsewhere,32-34 as in the case of a young patient with AIDS who developed transient C1-INH deficiency and angioedema. However, most infections and neoplasms are uncommon in this type of angioedema and are probably coincidental.
Triggers of Exacerbation in Chronic Urticaria and Recurrent Angioedema—Prevalence and Relevance
2021, Journal of Allergy and Clinical Immunology: In PracticeActivation of the ficolin-lectin pathway during attacks of hereditary angioedema
2014, Journal of Allergy and Clinical ImmunologyAngio-oedema due to hereditary C1 inhibitor deficiency in children
2013, Allergologia et ImmunopathologiaWAO guideline for the management of hereditary angioedema
2012, World Allergy Organization JournalParameters of the classical complement pathway predict disease severity in hereditary angioedema
2011, Clinical ImmunologyCitation Excerpt :The severity of the disease may change over time and relatively event-free periods may alternate with clustered attacks. This diversity of attack properties is attributed to genetic [6–10] and environmental influences [11,12]. Evaluation of disease severity is important when initiating therapy or appraising its efficacy — it may also lead to a better understanding of the pathomechanism.