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2006, Immunology and allergy clinics of North America, ISBN 9781416038092, Volume 26, no. 4., xv, 387-601
Book
ALLERGOLOGIE, ISSN 0344-5062, 03/2013, Volume 36, Issue 3, pp. 83 - 84
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2013, Volume 131, Issue 6, pp. 1491 - 1493.e25
Journal Article
Journal Article
Postepy Dermatologii i Alergologii, ISSN 1642-395X, 2013, Volume 30, Issue 3, pp. 152 - 158
Introduction: Administration of human Cl esterase inhibitor (Berinert (R) P) from target import is the most widespread treatment strategy for patients with... 
Human C1 esterase inhibitor | Conestat alfa | Hereditary angioedema | Cost-utility analysis | Acute angioedema attacks | TRIALS | MANAGEMENT | cost-utility analysis | human C1 esterase inhibitor | POLAND | DEFICIENCY | DERMATOLOGY | hereditary angioedema | CONCENTRATE | THERAPY | ALLERGY | conestat alfa | QUALITY-OF-LIFE | acute angioedema attacks | Original Paper
Journal Article
Deutsches Arzteblatt International, ISSN 1866-0452, 07/2017, Volume 114, Issue 29-30, pp. 489 - 496
Background: Acute angioedema of the upper airways can be life-threatening. An important distinction is drawn between mast-cell-mediated angioedema and... 
INDIVIDUALS | MEDICINE, GENERAL & INTERNAL | METAANALYSIS | HEREDITARY ANGIOEDEMA | EDEMA | INHIBITOR-INDUCED ANGIOEDEMA | MEDIATED ANGIOEDEMA | HISTAMINE H-1 RECEPTOR | ANAPHYLAXIS | BRADYKININ | EPIDEMIOLOGY | Review
Journal Article
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, ISSN 0091-6749, 02/2008, Volume 121, Issue 2, pp. S398 - S401
Hereditary angioedema is an episodic swelling disorder with autosomal dominant inheritance. Attacks are characterized by brawny, self-limited, nonpruritic... 
MANAGEMENT | androgens | bradykinin | C1 inhibitor | C1-INHIBITOR | IMMUNOLOGY | C1 esterase inhibitor | hereditary angioedema | CONCENTRATE | INHIBITOR DEFICIENCY | ANGIONEUROTIC EDEMA | THERAPY | ALLERGY | antifibrinolytics | danazol | complement
Journal Article
The Journal of Allergy and Clinical Immunology: In Practice, ISSN 2213-2198, 07/2018, Volume 6, Issue 4, pp. 1427 - 1429
In addition to mutations in Factor XII of the clotting cascade (Hageman factor), there are reports of plasminogen abnormalities being associated with AE.2 Of... 
IDIOPATHIC NONHISTAMINERGIC ANGIOEDEMA | ICATIBANT | IMMUNOLOGY | HEREDITARY ANGIOEDEMA | ALLERGY | Laboratories | Angioedema | Gastrointestinal surgery | Family medical history | Mutation | Patients | Abdomen
Journal Article
CLINICAL REVIEWS IN ALLERGY & IMMUNOLOGY, ISSN 1080-0549, 10/2002, Volume 23, Issue 2, pp. 217 - 231
Angioedema is a constellation of syndromes that present a great challenge to the clinician. The term "angioedema" describes the localized, transient, episodic... 
ACTIVATION | gastrointestinal tract | HEREDITARY ANGIONEUROTIC-EDEMA | skin | ACQUIRED C1-INHIBITOR DEFICIENCY | SYMPTOMS | CONVERTING ENZYME-INHIBITORS | IMMUNOLOGY | C1 INHIBITOR | abdominal pain | THERAPY | PLASMA | ALLERGY | urticaria | DANAZOL | angiodema | BRADYKININ
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2010, Volume 126, Issue 4, pp. 821 - 827.e14
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 02/2017, Volume 376, Issue 8, pp. 717 - 728
Journal Article
World Allergy Organization Journal, ISSN 1939-4551, 2012, Volume 5, Issue 12, pp. 182 - 199
: Hereditary Angioedema (HAE) is a rare disease and for this reason proper diagnosis and appropriate therapy are often unknown or not available for physicians... 
Therapy | Hereditary Angioedema | Medications | Diagnosis | Management | HAE | Guidelines | International | Angioneurotic edema | Care and treatment | Health care industry | Evidence-based medicine
Journal Article
Journal Article