Results 271 to 280 of about 63,522 (282)

Hereditary angioedema: do patients have a specific “digital fingerprint” in Danish registries?

Jakob Lillemoen Drivenes
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Elevated level of circulating VEGF in Chinese patients with hereditary angioedema and its correlation with disease status. [PDF]

Orphanet J Rare Dis
Ji R, Xu Y, Zhi Y.
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Pediatric angioedema without urticaria: A rare presentation of autoimmune thyroid disease with complete remission on levothyroxine therapy.

J Postgrad Med
Archana MH, Shivane V, Yamichannaiah C, Memon SS.   +3 more
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Hereditary angioedema: Epidemiology and burden of disease.

Allergy and Asthma Proceedings, 2020
Hereditary angioedema (HAE) is a rare autosomal dominant genetic disorder characterized by swelling of subcutaneous, mucosal, and submucosal tissue without associated pruritus or wheals caused by a temporary localized increase in vascular permeability ...
W. Lumry, R. Settipane
semanticscholar   +1 more source

CRISPR-Cas9 In Vivo Gene Editing of KLKB1 for Hereditary Angioedema.

New England Journal of Medicine
BACKGROUND Hereditary angioedema is a rare genetic disease that leads to severe and unpredictable swelling attacks. NTLA-2002 is an in vivo gene-editing therapy based on clustered regularly interspaced short palindromic repeats (CRISPR)-CRISPR-associated
Hilary Longhurst, Karen Lindsay, Remy S. Petersen, Lauré M. Fijen, P. Gurugama, David Maag, James S Butler, Mrinal Y Shah, Adele Golden, Yuanxin Xu, Carri Boiselle, Joseph D Vogel, Ahmed M Abdelhady, Michael L Maitland, Mark D McKee, Jessica Seitzer, Bo W Han, Samantha Soukamneuth, John Leonard, Laura Sepp-Lorenzino, Eliana D Clark, David Lebwohl, D. M. Cohn   +22 more
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A myoferlin gain‐of‐function variant associates with a new type of hereditary angioedema

Allergy. European Journal of Allergy and Clinical Immunology, 2020
2Allergy and Immune Disorders, Murdoch Children’s Research Institute, Royal Children’s Hospital, Melbourne, Vic., Australia 3Department of Pediatrics, University of Melbourne, Melbourne, Vic., Australia 4School of Clinical Sciences, Monash University ...
A. Ariano, M. d’Apolito, M. Bova, F. Bellanti, S. Loffredo, G. D’Andrea, M. Intrieri, A. Petraroli, A. B. Maffione, G. Spadaro, R. Santacroce, M. Margaglione   +11 more
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Hereditary and acquired angioedema.

Allergy and Asthma Proceedings, 2019
Hereditary angioedema (HAE) is an autosomal dominant disorder defined by a deficiency of functional C1 esterase inhibitor (C1-INH). Acquired angioedema is due to either consumption (type 1) or inactivation (type 2) of CI-INH.
G. Patel, J. Pongracic
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Pathophysiology of Hereditary Angioedema (HAE) Beyond the SERPING1 Gene

Clinical reviews in allergy and immunology, 2021
Jyoti Sharma, A. Jindal, A. Banday, Anit Kaur, A. Rawat, Surjit Singh, H. Longhurst   +6 more
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The Expanding Spectrum of Mutations in Hereditary Angioedema.

Journal of Allergy and Clinical Immunology: In Practice, 2021
C. L. Veronez, D. Csuka, Farrukh R Sheik, B. Zuraw, H. Farkas, K. Bork   +5 more
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