• [Translated article] Acquired Nonfamilial Vibratory Angioedema
• A case of acquired angioedema
• A Case of Acquired Angioedema Leading to the Diagnosis of Systemic Lupus Erythematosus
• A follow-up survey of patients with acquired angioedema due to C1-inhibitor deficiency
• A National Survey of Hereditary Angioedema and Acquired C1 Inhibitor Deficiency in the United Kingdom
• A Retrospective Analysis of Long-Term Prophylaxis with Berotralstat in Patients with Hereditary Angioedema and Acquired C1-Inhibitor Deficiency-Real-World Data
• A safety review of prophylaxis drugs for adolescent patients with hereditary angioedema
• A Systematic Review of Aquagenic Urticaria-Subgroups and Treatment Options
• Acquired Angioedema
• Acquired Angioedema
• Acquired Angioedema Acute Attack After Administration of the Moderna COVID-19 (mRNA-1273) Vaccine
• Acquired Angioedema and Chronic Lymphocytic Leukemia: Unraveling the Complex Interplay and Addressing Refractory Cases
• Acquired angioedema as a late-onset complication after cord blood transplantation: a subtype of chronic graft-versus-host disease
• Acquired Angioedema Associated with Lymphoproliferative Disorders
• Acquired Angioedema due to C1 Inhibitor Deficiency Preceding Splenic Marginal Zone Lymphoma: Further Insights from Clinical Practice
• Acquired Angioedema Due to C1-Inhibitor Deficiency (AAE-C1-INH)-A Bicenter Retrospective Study on Diagnosis, Course, and Therapy
• Acquired Angioedema due to C1-Inhibitor Deficiency: A Challenging Condition
• Acquired angioedema due to C1-inhibitor-deficiency (AAE-C1-INH) - a bi-center retrospective study on diagnosis, course and therapy
• Acquired angioedema in B cell lymphoproliferative disease: A retrospective case series
• Acquired Angioedema in Selected Neoplastic Diseases
• Acquired angioedema late in the course of nivolumab treatment
• Acquired Angioedema with C1 Inhibitor Deficiency: Occurrence, Clinical Features, and Management: A Nationwide Retrospective Study in the Czech Republic Patients
• Acquired angioedema: an unusual presentation of haematological malignancy
• Acquired Non-histaminergic Angioedema With C1q Autoantibody and Urticaria: A Case Report
• Acquired vibratory angioedema with a severe impact on work performance
• Acute Abdominal Pain as the Initial Presentation of an Acquired C1 Inhibitor Deficiency
• AIDS-Related Kaposi Sarcoma Associated with Steroid-Unresponsive Periorbital Lymphedema that Responded to Chemotherapy
• Altered levels of phospholipases C, diacylglycerols, endocannabinoids, and N-acylethanolamines in patients with hereditary angioedema due to FXII mutation
• An unusual case of acquired angioedema associated with monoclonal gammopathies of uncertain significance
• Anesthetic management of a patient with acquired angioedema submitted to broncofibroscopy: a case report
• Angioedema
• Angioedema as a Rare Presentation of Systemic Lupus Erythematosus
• Angioedema Due to Acquired Deficiency of C1-Inhibitor: A Cohort Study in Spain and a Comparison With Other Series
• Angioedema in the Absence of C1 Esterase Inhibitor Deficiency in a Young Patient With Anti-dsDNA Negative Lupus Nephritis
• Angioedema in the emergency department: an evidence-based update
• Angioedema without Urticaria: Medical History and Findings
• Angioedema without wheals: a clinical update
• Angioedema Without Wheals: Challenges in Laboratorial Diagnosis
• Angioedema-like presentation as the presenting finding of juvenile myositis and juvenile dermatomyositis in 2 patients
• Angioedema. Interdisciplinary diagnostic and therapeutic recommendations of the Polish Dermatological Society (PTD) and Polish Society of Allergology (PTA)
• Attenuated androgen discontinuation in patients with hereditary angioedema: a commented case series
• C1-inhibitor/C1-inhibitor antibody complexes in acquired angioedema due to C1-inhibitor deficiency
• Clinical features and potential markers of disease in idiopathic non-histaminergic angioedema, a real-life study
• Clinical practice of hereditary angioedema in Belgium: opportunities for optimized care
• Cold Urticaria Syndromes: Diagnosis and Management
• Consecutive Severe Orofacial Complications in Intensive Care Unit Patients: Quincke's Disease and Macroglossia due to Prolonged Prone Positioning for Management of Acute Respiratory Distress Syndrome
• Cross-sectional study of cholinergic urticaria subtypes and bronchial hyperresponsiveness
• Current and Future Approaches in Management of Chronic Spontaneous Urticaria Using Anti-IgE Antibodies
• Deciphering the Genetics of Primary Angioedema with Normal Levels of C1 Inhibitor
• Deucrictibant for angioedema due to acquired C1-inhibitor deficiency: A randomized-controlled trial
• Diagnosis of hereditary angioedema after thirty years of clinical manifestations
• Effectiveness of C1-INH therapy in angiotensin converting enzyme inhibitor induced angioedema
• Efficacy and safety of rituximab-based treatments in angioedema with acquired C1 inhibitor deficiency
• Efficacy and Safety of Rituximab-Based Treatments in Angioedema With Acquired C1-Inhibitor Deficiency
• Efficacy of lanadelumab in acquired angioedema with C1-inhibitor deficiency
• Efficacy of lanadelumab in angioedema due to acquired C1 inhibitor deficiency
• Episodic Angioedema with Hypereosinophilia (Gleich's Syndrome): A Case Report and Extensive Review of the Literature
• Extremely Late Diagnosis of Hereditary Angioedema Type I in an Elderly Female
• Genetic Variants Leading to Urticaria and Angioedema and Associated Biomarkers
• Hereditary Angioedema Post-liver Transplant
• Hereditary Angioedema: Diagnostic Algorithm and Current Treatment Concepts
• Hereditary angioedema: how to approach it at the emergency department?
• How Angioedema Quality of Life Questionnaire Can Help Physicians in Treating C1-Inhibitor Deficiency Patients?
• Immunodeficiency
• Isolated angioedema: A review of classification and update on management
• Leveraging Genetics for Hereditary Angioedema: A Road Map to Precision Medicine
• Life-threatening Idiopathic Nonhistaminergic Acquired Angioedema With Response to Lanadelumab
• Long term follow-up of complement parameters to improve the management of acquired angioedema due to C1-inhibitor deficiency
• Longitudinal experience with treatment of acquired angioedema using tranexamic acid
• Malignancy and immune disorders in patients with hereditary angioedema
• Multicentric Observational Study on Safety and Tolerability of COVID-19 Vaccines in Patients with Angioedema with C1 Inhibitor Deficiency: Data from Italian Network on Hereditary and Acquired Angioedema (ITACA)
• Nasal Septal Mucocele Causing Saddle Nose Deformity
• National audit of a hereditary and acquired angioedema cohort in New Zealand
• Over diagnosis of bradykinin angioedema in patients treated with angiotensin-converting enzyme inhibitors or angiotensin II receptor blockers
• Pathophysiology of bradykinin and histamine mediated angioedema
• Patterns of Recurrent Thrombosis in Primary Antiphospholipid Syndrome-Multicenter, Real-Life Long-Term Follow-Up
• Pediatric Angioedema without Wheals: How to Guide the Diagnosis
• Physicochemical and Biological Characterization of rhC1INH Expressed in CHO Cells
• Practical Management of New-Onset Urticaria and Angioedema Presenting in Primary Care, Urgent Care, and the Emergency Department
• Predictive model to differentiate chronic histaminergic angioedema and chronic spontaneous urticaria with angioedema
• Pregnancy in women with Hereditary Angioedema due to C1-inhibitor deficiency: Results from the ITACA cohort study on outcome of mothers and children with <em>in utero</em> exposure to plasma-derived C1-inhibitor
• Presentation of an extraordinary colic: abdominal pain as the first and only utterance of an acquired C1-inhibitor deficiency
• Profile of serious angioedema requiring an urgent advice from a national reference call center
• Pseudo-Allergies in the Emergency Department: A Common Misdiagnosis of Hypersensitivity Type 1 Allergic Reaction
• Rare manifestations of monoclonal gammopathies: About two clinical cases and literature review
• Refractory acquired angioedema in chronic lymphocytic leukemia
• Resolution of Laryngeal Oedema in a Patient with Acquired C1-Inhibitor Deficiency. a Case Report
• Rituximab in the Treatment of Acquired Angioedema Secondary to Marginal Zone Lymphoma of the Spleen
• Splenectomy allows remission of angioedema with acquired C1-INH deficiency associated with splenic marginal zone lymphoma
• Taming the Tongue: The Surgical Approach to Macroglossia
• The characteristics of upper airway edema in hereditary and acquired angioedema with C1-inhibitor deficiency
• The impact of puberty on the onset, frequency, location, and severity of attacks in hereditary angioedema due to C1-inhibitor deficiency: A survey from the Italian Network for Hereditary and Acquired Angioedema (ITACA)
• The Importance of Complement Testing in Acquired Angioedema Related to Angiotensin-Converting Enzyme Inhibitors
• The Panorama of Primary Angioedema in the Brazilian Population
• The validity and reliability of a Thai version of the Angioedema Control Test: Which recall period is preferable?
• Tolerance of bradykinin-releasing drugs in patients with acquired C1 inhibitor deficiency: a case series and review of the literature
• Urticaria and Angioedema: Understanding Complex Pathomechanisms to Facilitate Patient Communication, Disease Management, and Future Treatment
• Vision loss due to atypical bilateral edema of the optic nerve in a patient with hereditary angioedema: A case report
• WHAT LESSONS ARE LEARNED? OUR CHANGING PRACTICE DURING THIRTY YEARS OF HEREDITARY ANGIOEDEMA TREATMENT
• Where we are with acquired angioedema due to C1 inhibitor deficiency: A systematic literature review