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Patient‐physician interactions in hereditary angioedema—Key learnings from the coronavirus disease 2019 pandemic [PDF]

open access: greenClinical and Translational Allergy, 2023
Background The coronavirus disease pandemic and its containing measures have caused concerns for patients with hereditary angioedema (HAE) and their treating physicians.
Marcus Maurer   +5 more
doaj   +2 more sources

Management of hereditary angioedema with normal C1Inh: a series of 163 French patients [PDF]

open access: yesOrphanet Journal of Rare Diseases
Background The diagnosis of hereditary angioedema with a normal C1Inh was genetic. The two most frequent pathogenic variants are found in the FXII and PLG genes.
Alexis Bocquet   +15 more
doaj   +2 more sources

Angioedema

open access: yesAllergy, Asthma & Clinical Immunology
Angioedema can occur in the absence of urticaria and can be broadly divided into three main categories: mast cell-mediated (e.g., histamine), non-mast-cell-mediated (bradykinin-induced) and idiopathic angioedema.
Gina Lacuesta   +3 more
doaj   +3 more sources

Urticaria and angioedema

open access: yesAllergy, Asthma & Clinical Immunology, 2011
Urticaria (hives) is a common disorder that often presents with angioedema (swelling that occurs beneath the skin). It is generally classified as acute, chronic or physical.
Kanani Amin   +2 more
doaj   +3 more sources

Angioedema [PDF]

open access: yesDeutsches Ärzteblatt international, 2017
Acute angioedema of the upper airways can be life-threatening. An important distinction is drawn between mast-cell-mediated angioedema and bradykinin-mediated angioedema; the treatment of these two entities is fundamentally different.This review is based on pertinent articles retrieved by a selective search in PubMed and on guidelines concerning the ...
Janina, Hahn   +5 more
openaire   +4 more sources

Acquired Angioedema Due to C1 inhibitor Deficiency Caused by Non-Hodgkin Lymphoma in a Patient with Myasthenia Gravis

open access: yesRomanian Journal of Laboratory Medicine, 2021
Acquired angioedema due to C1-inhibitor deficiency is a very rare disorder that usually appears in patients with lymphoproliferative and/or autoimmune diseases.
Bara Noémi   +3 more
doaj   +1 more source

A clinical pathway for the diagnosis of sesame allergy in children

open access: yesWorld Allergy Organization Journal, 2022
Background: Sesame allergy (SA) is a common cause of life-threatening, persistent food allergy, not only in the Middle East and Asia, but increasingly worldwide. Commercially available tests such as extracts for skin testing or specific IgE for sesame or
Diti Machnes-Maayan, MD   +7 more
doaj   +1 more source

The analysis of the effect of the COVID-19 pandemic on patients with hereditary angioedema type I and type II

open access: yesScientific Reports, 2023
Due to the similarity between the pathomechanism of SARS-CoV-2 infections and hereditary angioedema due to C1-inhibitor deficiency (C1-INH-HAE), a possibility emerged that C1-INH-HAE may worsen the course of the infection, or that the infection may ...
Dávid Szilágyi   +5 more
doaj   +1 more source

Hereditary angioedema [PDF]

open access: yesInternational Journal of Emergency Medicine, 2021
AbstractA 14-year-old African American female presented to the emergency department with spontaneous, sudden-onset lip swelling for 1 h. On examination, there was significant water-bag edema of the upper lip extending to the philtrum and premaxilla. Nasopharyngeal laryngoscopy revealed a patent airway without edema.
Helen Lesser, Jason E. Cohn
openaire   +3 more sources

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