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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Primary Immune Deficiency Diseases
Last data update: May 24, 2024
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Increased risk of venous thromboembolism in young and middle-aged individuals with hereditary angioedema: a family study.
Linda Sundler Björkman et al. Blood 2024
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Real-world changes in costs over time among patients in the United States with hereditary angioedema on long-term prophylaxis with lanadelumab.
Chintal H Shah et al. J Med Econ 2023 1-20
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Content validation and psychometric evaluation of the Angioedema Quality of Life Questionnaire for hereditary angioedema.
Magdalena Vanya et al. Journal of patient-reported outcomes 2023 7(1) 33
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Challenges in the Management of Hereditary Angioedema in Urban and Rural Settings: Results of a US Survey.
J Allen Meadows et al. Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology 2023
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Burden of illness seen in hereditary angioedema in Japanese patients: Results from a patient reported outcome survey.
Beverley Yamamoto et al. Intractable & rare diseases research 2023 12(1) 35-44
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Efficacy and safety of garadacimab, a factor XIIa inhibitor for hereditary angioedema prevention (VANGUARD): a global, multicentre, randomised, double-blind, placebo-controlled, phase 3 trial.
Timothy J Craig et al. Lancet (London, England) 2023
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Expert review and consensus on the t2t management of hereditary angioedema: from the scientific evidence to clinical practice.
T Caballero et al. Journal of investigational allergology & clinical immunology 2023 0
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Hereditary Angioedema with Normal C1 Inhibitor: US Survey of Prevalence and Provider Practice Patterns.
Marc A Riedl et al. The journal of allergy and clinical immunology. In practice 2023
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A multicriteria decision analysis (MCDA) applied to three long-term prophylactic treatments for hereditary angioedema in Spain.
Zozaya Néboa et al. Global & regional health technology assessment 2023 914-21
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Consensus on diagnosis and management of Hereditary Angioedema in the Middle East: A Delphi initiative.
Maurer Marcus et al. The World Allergy Organization journal 2023 16(1) 100729
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Hereditary Angioedema During Pregnancy: Considerations in Management.
Riedl Marc A et al. Immunology and allergy clinics of North America 2022 43(1) 145-157
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Effectiveness and safety of lanadelumab in ethnic and racial minority subgroups of patients with hereditary angioedema: results from phase 3 studies.
Craig Timothy J et al. Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology 2022 18(1) 85
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Prevalence and impact of misdiagnosed drug allergy labels among patients with hereditary angioedema.
Wong Jane Chi Yan et al. Frontiers in allergy 2022 3953117
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Prospective study on the efficacy and impact of Cascade Screening and Evaluation of HAE (CaSE-HAE).
Wong Jane C Y et al. The journal of allergy and clinical immunology. In practice 2022
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Characteristics of Patients Who Underwent a Diagnostic Test for Hereditary Angioedema Admitted Due to Angioedema.
Sengül Emeksiz Zeynep et al. Journal of tropical pediatrics 2022 68(4)
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Risk Factors for Severe COVID-19 and Hospital Admission in Patients With Inborn Errors of Immunity - Results From a Multicenter Nationwide Study.
Milota Tomas et al. Frontiers in immunology 2022 13835770
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How do patients and physicians communicate about hereditary angioedema in the United States?
Jain Gagan et al. PloS one 2021 16(12) e0260805
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Measurement of C1-Inhibitor function alone is sufficient for diagnosis of hereditary angioedema.
Kiani-Alikhan Sorena et al. Journal of clinical pathology 2021
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Mitigating Disparity in Health-care Resources Between Countries for Management of Hereditary Angioedema.
Jindal Ankur Kumar et al. Clinical reviews in allergy & immunology 2021
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Physician and patient perspectives on the management of hereditary angioedema: a survey on treatment burden and needs.
Riedl Marc A et al. Allergy and asthma proceedings 2021 42(3) S17-S25
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Assessment and management of disease burden and quality of life in patients with hereditary angioedema: a consensus report.
Bork Konrad et al. Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology 2021 17(1) 40
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Leveraging unstructured data to identify hereditary angioedema patients in electronic medical records.
Brouwer Emily S et al. Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology 2021 17(1) 41
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Clinical characteristics and burden of illness in patients with hereditary angioedema: findings from a multinational patient survey.
Mendivil Joan et al. Orphanet journal of rare diseases 2021 Feb 16(1) 94
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Optimal Management of Hereditary Angioedema: Shared Decision-Making.
Banerji Aleena et al. Journal of asthma and allergy 2021 14119-125
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The practice of active patient involvement in rare disease research using ICT: experiences and lessons from the RUDY JAPAN project.
Hamakawa Nao et al. Research involvement and engagement 2021 Feb 7(1) 9
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The Challenges in the Follow-Up and Treatment of Brazilian Children with Hereditary Angioedema.
Araújo-Simões Joanna et al. International archives of allergy and immunology 2021 Jan 1-7
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Informed decision-making in hereditary angioedema prophylaxis.
Burnette Autumn Ford et al. International forum of allergy & rhinology 2021 Jan
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Quality of Life in Patients with Hereditary Angioedema in Canada.
Lee Erika Yue et al. Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology 2021 Jan
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Androgen use in hereditary angioedema: A critical appraisal and approaches to transitioning from androgens to other therapies.
Johnston Douglas T et al. Allergy and asthma proceedings 2020 Dec
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Impact of lanadelumab on health-related quality of life in patients with hereditary angioedema in the HELP Study.
Lumry William R et al. Allergy 2020 Nov
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Page last reviewed:
Feb 1, 2024
Page last updated:
May 24, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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