Results 21 to 30 of about 144,374 (198)

Treatment of hereditary angioedema with plasma-derived C1 inhibitor

Therapeutics and Clinical Risk Management, 2008
Michael J Prematta, Tracy Prematta, Timothy J CraigSection of Allergy and Immunology, Penn State University, Milton S. Hershey Medical Center, PA, USABackground: Plasma-derived C1 inhibitor (C1-INH) concentrate is a treatment option for acute hereditary ...
Michael J Prematta, Tracy Prematta, Timothy J Craig   +2 more
doaj   +1 more source

Position statement of the hereditary angioedema Section of the Polish Society of Allergology on the management of hereditary angioedema due to C1 inhibitor deficiency: 2025 update. Part I: Classification, pathophysiology, clinical presentation, diagnosis, and differential diagnosis

Alergologia Polska
Hereditary angioedema due to a genetically determined deficiency of the C1 complement inhibitor (HAE-C1INH) is a rare disease that significantly impairs daily functioning and may be life-threatening in severe cases.
Grzegorz Porębski, Aleksandra Kucharczyk, Tomasz Matuszewski, Hanna Danielewicz, Jacek Gocki, Katarzyna Grzela, Aldona Juchacz, Marcin Kurowski, Krzysztof Kuziemski, Mateusz Łukaszyk, Małgorzata Sokołowska, Marcin Stobiecki, Ewa Trębas-Pietraś, Marta Tykwińska, Krystyna Obtułowicz   +14 more
doaj   +2 more sources

Unmet needs in hereditary angioedema: an international survey of physicians [PDF]

Orphanet Journal of Rare Diseases
Background Hereditary angioedema (HAE) is a rare and potentially life-threatening genetic disorder characterized by unpredictable attacks of angioedema.
Thomas Buttgereit, Felix Aulenbacher, Adil Adatia, Carolina Vera Ayala, Maryam Ali Al-Nesf, Sabine Altrichter, Mohamed Abuzakouk, Mona Al-Ahmad, Ramzy Mohammed Ali, Alejandro Berardi, Isabelle Boccon-Gibod, Laurence Bouillet, Luisa Brussino, Marko Barešić, Paula J. Busse, Stephen D. Betschel, Herberto Chong-Neto, Oscar Calderón Llosa, Timothy J. Craig, Anthony D. Dorr, Sérgio Duarte Dortas Junior, Daria Fomina, Henriette Farkas, Jie Shen Fok, Anete S. Grumach, Jens Greve, Mar Guilarte, Margarida Gonçalo, Vesna Grivcheva-Panovska, Michihiro Hide, Roman Hakl, Ankur Jindal, Constance H. Katelaris, Shailajah Kamaleswaran, Tamar Kinaciyan, Elena Latysheva, José Ignacio Larco Sousa, Ramón Lleonart Bellfill, Hassan Mobayed, Martin Metz, Iman Nasr, Natasa T. Mitrevska, Stefania Nicola, Claudio Alberto Salvador Parisi, Grzegorz Porebski, Jonny Peter, Mariana Paes Leme Ferriani, Nelson Rosario Filho, Bülent Enis Şekerel, Faradiba Sarquis Serpa, Marcin Stobiecki, Susanne Trainotti, Anna Valerieva, Chamard Wongsa, Jane C. Y. Wong, Esra Yucel, Yinglei Li, Chiara Nenci, Marcus Maurer, Markus Magerl, Philip H. Li   +60 more
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Diagnosis and screening of patients with hereditary angioedema in primary care

Therapeutics and Clinical Risk Management, 2016
Maria Paula Henao,1 Jennifer L Kraschnewski,1 Theodore Kelbel,2 Timothy J Craig3 1Department of Medicine, 2Division of Allergy and Immunology, 3Department of Medicine and Pediatrics, Pennsylvania State University College of Medicine at Hershey Medical ...
Henao MP, Kraschnewski JL, Kelbel T, Craig TJ   +3 more
doaj   +1 more source

A narrative review of recent literature of the quality of life in hereditary angioedema patients

World Allergy Organization Journal, 2023
Hereditary angioedema (HAE) is a rare disorder that causes unpredictable and debilitating cutaneous and submucosal edema and can lead to death. HAE can impair patients' ability to perform daily activities, proportional to pain severity, with patients ...
Herberto José Chong-Neto
doaj   +1 more source

Vascular endothelial growth factor (VEGF) emerging as a mediator of hereditary angioedema (HAE). [PDF]

World Allergy Organ J
Giavina-Bianchi P, Aun MV, Kalil J.
europepmc   +4 more sources

Mutant plasminogen in hereditary angioedema is bypassing FXII/kallikrein to generate bradykinin

Frontiers in Physiology, 2023
Hereditary angioedema (HAE) is characterized by recurrent localized edema in various organs, which can be potentially fatal. There are different types of hereditary angioedema, which include genetic deficiency of C1 inhibitor (C1-INH) and hereditary ...
Stefan Hintze, Stefan Hintze, Britta S. Möhl, Jessica Beyerl, Jessica Beyerl, Jessica Beyerl, Karin Wulff, Andreas Wieser, Andreas Wieser, Andreas Wieser, Andreas Wieser, Konrad Bork, Peter Meinke   +12 more
doaj   +1 more source

Prophylaxis in hereditary angioedema (HAE) with C1 inhibitor deficiency [PDF]

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, 2016
SummaryHereditary angioedema (HAE) is a rare congenital disorder characterized by recurrent episodes of subcutaneous or submucosal edema. Laryngeal manifestations can be life‐threatening. In the majority of cases, the disease can be adequately treated with an on‐demand approach – in some cases, however, short‐ or long‐term prophylaxis is indicated ...
Greve, J., Strassen, U., Gorczyza, M., Dominas, Nina, Frahm, U. M., Muhlberg, H., Wiednig, M., Zampeli, V., Magerl, M.   +8 more
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A Case Report of Hereditary Angioedema: Challenges in Diagnosis and Management

Acta Medica Indonesiana, 2023
Hereditary angioedema (HAE) is a rare autosomal dominant genetic disorder which causes bradykinin mediated angioedema. Although it can be life threatening, HAE may be underdiagnosed due to a lack of awareness of the disease and limited access to ...
Alvina Widhani, Suzy Maria, Rifky Yulian, Anshari Saifuddin Hasibuan, Sukamto Koesnoe   +4 more
doaj   +2 more sources

Correction to: Pathophysiology of Hereditary Angioedema (HAE) Beyond the SERPING1 Gene [PDF]

Clinical Reviews in Allergy & Immunology, 2021
The original version of this article unfortunately contained a mistake. The image of Fig. 1 should be corrected. In the previous figure, we had shown that the plasma kallikrein cleaves both high molecular weight kininogen (HMWK) and low molecular weight kininogen (LMWK) to produce bradykinin. However, the plasma kallikrein activates only high molecular
Jyoti Sharma, Ankur Kumar Jindal, Aaqib Zaffar Banday, Anit Kaur, Amit Rawat, Surjit Singh, Hilary Longhurst   +6 more
openaire   +1 more source