Zobrazeno 1 - 10 of 41 pro vyhledávání: '"Danny M Cohn"'
1
Akademický článek
Daratumumab-based treatment of monoclonal gammopathy–associated angioedema due to acquired C1-inhibitor deficiency
Autor: Remy S. Petersen, MD, Lauré M. Fijen, MD, PhD, Laurens E. Franssen, MD, PhD, Josephine M.I. Vos, MD, PhD, Danny M. Cohn, MD, PhD
Publikováno v: Journal of Allergy and Clinical Immunology: Global, Vol 3, Iss 4, Pp 100322- (2024)
Daratumumab-based treatment could control severe, treatment-refractory, life-threatening angioedema due to acquired C1-inhibitor deficiency associated with monoclonal gammopathy.
Externí odkaz: https://doaj.org/article/6c20e97b8c52416c88335adfdabeabe4
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2
Akademický článek
Evaluation of patient‐reported outcome measures for on‐demand treatment of hereditary angioedema attacks and design of KONFIDENT, a phase 3 trial of sebetralstat
Autor: Danny M. Cohn, Emel Aygören‐Pürsün, Jonathan A. Bernstein, Henriette Farkas, William R. Lumry, Marcus Maurer, Andrea Zanichelli, Matthew Iverson, James Hao, Michael D. Smith, Christopher M. Yea, Paul K. Audhya, Marc A. Riedl
Publikováno v: Clinical and Translational Allergy, Vol 13, Iss 9, Pp n/a-n/a (2023)
Abstract Background Hereditary angioedema (HAE) with C1‐inhibitor deficiency (HAE‐C1‐INH) is characterized by recurrent, debilitating episodes of swelling. Sebetralstat, an investigational oral plasma kallikrein inhibitor, demonstrated promisin
Externí odkaz: https://doaj.org/article/fa5357d5066e444bb5ad301768e9507f
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3
Akademický článek
Inhalation of Low Molecular Weight Heparins as Prophylaxis against SARS-CoV-2
Autor: Julia Eder, Marta Bermejo-Jambrina, Killian E. Vlaming, Tanja M. Kaptein, Viktoria Zaderer, E. Marleen Kemper, Doris Wilflingseder, Sietze Reitsma, Godelieve J. de Bree, Danny M. Cohn, Teunis B. H. Geijtenbeek
Publikováno v: mBio, Vol 13, Iss 6 (2022)
ABSTRACT New SARS-CoV-2 variants of concern and waning immunity demonstrate the need for a quick and simple prophylactic agent to prevent infection. Low molecular weight heparins (LMWH) are potent inhibitors of SARS-CoV-2 binding and infection in vit
Externí odkaz: https://doaj.org/article/be136ae2d1a34d2388548dd0bfd91721
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4
Akademický článek
The international WAO/EAACI guideline for the management of hereditary angioedema – The 2021 revision and update
Autor: Marcus Maurer, MD, Markus Magerl, MD, Stephen Betschel, MD, Werner Aberer, MD, Ignacio J. Ansotegui, MD, PhD, Emel Aygören-Pürsün, MD, Aleena Banerji, MD, Noémi-Anna Bara, MD, Isabelle Boccon-Gibod, MD, Konrad Bork, MD, Laurence Bouillet, Pr, MD, PhD, Henrik Balle Boysen, Nicholas Brodszki, MD, PhD, Paula J. Busse, MD, Anette Bygum, MD, DMSci, Teresa Caballero, MD, PhD, Mauro Cancian, MD, PhD, Anthony J. Castaldo, Danny M. Cohn, MD, PhD, Dorottya Csuka, MD, Henriette Farkas, MD, PhD, DSc, Mark Gompels, MBBS, BSc, MD, Richard Gower, MD, Anete S. Grumach, MD, PhD, Guillermo Guidos-Fogelbach, MD, PhD, Michihiro Hide, MD, PhD, Hye-Ryun Kang, MD, PhD, Allen P. Kaplan, MD, Constance H. Katelaris, MBBS, PhD, Sorena Kiani-Alikhan, PhD, Wei-Te Lei, MD, Richard F. Lockey, MD, Hilary Longhurst, PhD, William Lumry, MD, Andrew MacGinnitie, MD, PhD, Alejandro Malbran, MD, PhD, Inmaculada Martinez Saguer, MD, Juan José Matta Campos, MD, Alexander Nast, MD, Dinh Nguyen, MD, PhD, Sandra A. Nieto-Martinez, MD, Ruby Pawankar, MD, PhD, Jonathan Peter, MB ChB, MMed, FCP (SA), PhD, Grzegorz Porebski, MD, Nieves Prior, MD, PhD, Avner Reshef, MD, Marc Riedl, MD, Bruce Ritchie, MD, Farrukh Rafique Sheikh, MBBS, William B. Smith, MBBS, PhD, Peter J. Spaeth, PhD, Marcin Stobiecki, MD, Elias Toubi, MD, Lilian Agnes Varga, PhD, Karsten Weller, MD, Andrea Zanichelli, MD, Yuxiang Zhi, MD, Bruce Zuraw, MD, Timothy Craig, MD
Publikováno v: World Allergy Organization Journal, Vol 15, Iss 3, Pp 100627- (2022)
Hereditary Angioedema (HAE) is a rare and disabling disease for which early diagnosis and effective therapy are critical. This revision and update of the global WAO/EAACI guideline on the diagnosis and management of HAE provides up-to-date guidance f
Externí odkaz: https://doaj.org/article/8b9e359b6d224c3ca799a778ade61235
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5
The Influence of Plasma Prekallikrein Oligonucleotide Antisense Therapy on Coagulation and Fibrinolysis Assays: A Post-hoc Analysis
Autor: Lauré M. Fijen, Remy S. Petersen, Joost C. M. Meijers, Laura Bordone, Marcel Levi, Danny M. Cohn
Publikováno v: Thrombosis and haemostasis, 122(12), 2045-2049. Schattauer GmbH
Background Congenital prekallikrein deficiency has been associated with increased risk of thrombosis in a few uncontrolled studies. Prekallikrein levels were reduced by 36-94% (median 75%) in a phase 2 study with the prekallikrein specific antisense
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06b780fddd766cb4befa85cd88496e39
https://doi.org/10.1055/a-1926-2367
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8
The Disease Burden and Societal Costs of Hereditary Angioedema
Autor: Lauré M. Fijen, Philip C.G. Klein, Danny M. Cohn, Tim A. Kanters
Publikováno v: Journal of Allergy and Clinical Immunology: In Practice. Elsevier Inc.
Journal of Allergy and Clinical Immunology: In Practice
Background: According to the current treatment guidelines, the goals of treatment of patients with hereditary angioedema (HAE) are to achieve total control of the disease and to normalize patients’ lives. Objective: This study aims to establish the
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::065916ce8ecc2f7129e8b0bbd86ae01b
https://doi.org/10.1016/j.jaip.2023.03.032
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10
Hereditary Angioedema: The Clinical Picture of Excessive Contact Activation
Autor: Remy S. Petersen, Lauré M. Fijen, Marcel Levi, Danny M. Cohn
Publikováno v: Seminars in thrombosis and hemostasis. Thieme Medical Publishers
Hereditary angioedema is a rare, genetic disorder characterized by painful, debilitating and potentially life-threatening angioedema attacks in subcutaneous and submucosal tissue. While usually unpredictable, attacks can be provoked by a variety of t
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d9a7aae9060f1da0f658e2b58278306
https://pubmed.ncbi.nlm.nih.gov/36417927
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