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Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2016, Volume 139, Issue 2, pp. AB233 - AB233
(4) National Reference Centre for Angioedema, Internal Medicine Department, Grenoble University Hospital, Grenoble, France 
Allergy and Immunology | Medical colleges | Angioneurotic edema
Journal Article
The Journal of Allergy and Clinical Immunology, ISSN 0091-6749, 02/2018, Volume 141, Issue 2, pp. AB46 - AB46
Angiopoietin 1 antagonizes the action of VEGF on vascular permeability, suggesting that an alteration of this gene could lead to the increase permeability and... 
Permeability | Mutation | Genes | Angioedema
Journal Article
ALLERGY AND ASTHMA PROCEEDINGS, ISSN 1088-5412, 05/2019, Volume 40, Issue 3, pp. 193 - 197
Background: Hereditary angioedema (HAE) is an autosomal dominant disorder that affects similar to 1 in 50,000 individuals. The disorder is characterized by... 
ALLERGY | NEED | ADHERENCE | Edema | Swelling | Angioedema | Mucosa | Asphyxia | Patients | Pharynx | Patient compliance | Hereditary diseases | Fear | Questionnaires | Diagnosis | Emergency medical services
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2014, Volume 133, Issue 2, pp. AB31 - AB31
Journal Article
World Allergy Organization Journal, ISSN 1939-4551, 04/2015, Volume 8, Issue Suppl 1, p. A77
Journal Article
World Allergy Organization Journal, ISSN 1939-4551, 04/2015, Volume 8, Issue 135
Journal Article
Clinical and Translational Allergy, ISSN 2045-7022, 10/2018, Volume 8, Issue 1, pp. 42 - 5
The objective of this analysis was to evaluate the change over time in age at first symptoms, age at diagnosis, and delay in diagnosis using data from the... 
C1-INH-HAE | Hereditary angioedema | Diagnosis | Delay in diagnosis | HAE | ALLERGY | BURDEN | Medicine, Experimental | Medical research | Angioneurotic edema | Patient outcomes | Immunology | Hospitals | Dermatology | Enrollments | Mortality | Family medical history | Regression analysis | Clinical medicine | Patients | Age
Journal Article
The Journal of Allergy and Clinical Immunology, ISSN 0091-6749, 02/2019, Volume 143, Issue 2, pp. AB43 - AB43
Journal Article
The Journal of Allergy and Clinical Immunology: In Practice, ISSN 2213-2198, 03/2019, Volume 7, Issue 3, pp. 1078 - 1080
[...]longer delays in diagnosis attributed to specialists may be because of referral later in the patient's diagnostic journey. [...]retrospective data on... 
ALLERGY | IMMUNOLOGY | Pediatrics | Dermatology | Physicians | Angioedema | Family medical history | Patients | Family physicians | Medical referrals | Immunology | Hospitals | Child development | Children | Age
Journal Article
The Journal of Allergy and Clinical Immunology, ISSN 0091-6749, 02/2018, Volume 141, Issue 2, pp. AB53 - AB53
Rationale Data from the Icatibant Outcome Survey (IOS; NCT01034969), an international registry monitoring the safety and effectiveness of icatibant for the... 
Reinjection | Angioedema
Journal Article
Allergy, ISSN 0105-4538, 08/2018, Volume 73, Issue 8, pp. 1575 - 1596
Hereditary Angioedema (HAE) is a rare and disabling disease. Early diagnosis and appropriate therapy are essential. This update and revision of the global... 
hereditary angioedema | C1‐inhibitor | management | recommendations | guideline | C1-inhibitor | Angioneurotic edema | Pregnancy | Inhibitors | Angioedema | Medical services | Management | Children | Patients
Journal Article
Revista do Instituto de Medicina Tropical de Sao Paulo, ISSN 0036-4665, 11/2016, Volume 58, p. 84
BCG adverse events (BCG-AE) are rare conditions with no well-established treatment. This study aims to describe clinical characteristics and outcome of... 
SEVERE COMBINED IMMUNODEFICIENCY | Mycobacterium bovis | Therapeutics | DISEASE | Adverse event | CALMETTE-GUERIN VACCINE | COMPLICATIONS | BCG vaccine | TROPICAL MEDICINE | BCG Vaccine - adverse effects | Humans | Child, Preschool | Female | Infant | Male | Child | Infant, Newborn | Lymphadenitis - etiology
Journal Article
FRONTIERS IN MEDICINE, ISSN 2296-858X, 02/2019, Volume 6, p. 28
Hereditary angioedema (HAE) is an autosomal dominant disease caused by C1-INH deficiency due to mutations in SERPING1 (C1-INH-HAE) in most of the cases, or by... 
C1 INHIBITOR | EXON-1 POLYMORPHISM | hereditary angioedema | MEDICINE, GENERAL & INTERNAL | Kallikrein-Kinin System | F12 mutation | genotype-phenotype correlation | genetic variation | C1 inhibitor deficiency | BRADYKININ RECEPTOR | DEFICIENCY | Angioneurotic edema | Usage | Genetic variation | Genetic aspects | Research | Nucleotide sequencing | DNA sequencing
Journal Article
FRONTIERS IN MEDICINE, ISSN 2296-858X, 04/2019, Volume 6, p. 80
Abdominal pain due to intestinal swellings is one of the most common manifestations in hereditary angioedema (HAE). Bowel swellings can cause severe abdominal... 
C1 INHIBITOR | hereditary angioedema | MEDICINE, GENERAL & INTERNAL | F12 mutation | acute pancreatitis | abdominal swelling | CLASSIFICATION | BRADYKININ | C1-inhibitor deficiency | ESTERASE INHIBITOR | Complications and side effects | Medical research | Angioneurotic edema | Pancreatitis | Medicine, Experimental | Research | Risk factors
Journal Article
Journal of Allergy and Clinical Immunology, ISSN 0091-6749, 05/2017, Volume 139, Issue 5, pp. 1720 - 1721
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2014, Volume 133, Issue 2, pp. AB32 - AB32
Journal Article
Journal of Allergy and Clinical Immunology, ISSN 0091-6749, 05/2017, Volume 139, Issue 5, pp. 1720 - 1721
Journal Article
The Journal of Allergy and Clinical Immunology, ISSN 0091-6749, 05/2017, Volume 139, Issue 5, pp. 1720 - 1721
Journal Article
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