Zobrazeno 1 - 10
of 401
pro vyhledávání: '"Werner Aberer"'
Autor:
Lukas Koch, Karin Laipold, Lisa Arzt‐Gradwohl, Eva Maria Sturm, Werner Aberer, Martina Aumayr, Wolfgang Hemmer, Urban Čerpes, Gunter J. Sturm
Publikováno v:
Clinical and Translational Allergy, Vol 13, Iss 3, Pp n/a-n/a (2023)
Abstract Background The specificity of extract‐based pollen allergy diagnosis is decreased due to cross‐reactivity via cross‐reactive carbohydrate determinants (CCDs) or panallergens such as profilins or polcalcins. This study aimed to explore
Externí odkaz:
https://doaj.org/article/16caadccc9164167a57860b38b06f33a
Publikováno v:
The Korean Journal of Internal Medicine, Vol 37, Iss 5, Pp 1094-1095 (2022)
Externí odkaz:
https://doaj.org/article/dff680478b974446b798a6be627552ed
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
Autor:
Anette Bygum, Teresa Caballero, Anete S. Grumach, Hilary J. Longhurst, Laurence Bouillet, Werner Aberer, Andrea Zanichelli, Jaco Botha, Irmgard Andresen, Marcus Maurer, for the IOS Study Group
Publikováno v:
Clinical and Translational Allergy, Vol 9, Iss 1, Pp 1-8 (2019)
Abstract Background Hereditary angioedema with C1 inhibitor deficiency (C1-INH-HAE) is characterized by recurrent swelling in subcutaneous or submucosal tissues. Symptoms often begin by age 5–11 years and worsen during puberty, but attacks can occu
Externí odkaz:
https://doaj.org/article/72f62a8e376a440c91f20ca5f1c41d12
Autor:
Andrea Zanichelli, Markus Magerl, Hilary J. Longhurst, Werner Aberer, Teresa Caballero, Laurence Bouillet, Anette Bygum, Anete S. Grumach, Jaco Botha, Irmgard Andresen, Marcus Maurer, the IOS Study Group
Publikováno v:
Clinical and Translational Allergy, Vol 8, Iss 1, Pp 1-5 (2018)
Abstract The objective of this analysis was to evaluate the change over time in age at first symptoms, age at diagnosis, and delay in diagnosis using data from the Icatibant Outcome Survey (IOS). Patients with a diagnosis of C1-INH-HAE who were born
Externí odkaz:
https://doaj.org/article/3c9276941ce64034a53aca00eb6720c0
Autor:
Annick Barbaud, Marie Weinborn, Lene Heise Garvey, Sergio Testi, Violeta Kvedariene, Sevim Bavbek, Holger Mosbech, Eva Gomes, Werner Aberer, Hanneke N. G. Oude Elberink, Maria Jose Torres, Claude Ponvert, C. Ayav, Jimmy Gooi, Knut Brockow
Publikováno v:
Frontiers in Medicine, Vol 7 (2020)
Background: Intradermal tests (IDTs) are performed and interpreted differently in drug allergy centers making valid comparison of results difficult.Objective: To reduce method-related and intercenter variability of IDTs by the introduction of a stand
Externí odkaz:
https://doaj.org/article/3772a04025d24181bbfdcb013df0ef1a
Autor:
Teresa Caballero, Andrea Zanichelli, Werner Aberer, Marcus Maurer, Hilary J. Longhurst, Laurence Bouillet, Irmgard Andresen, the IOS Study Group
Publikováno v:
Clinical and Translational Allergy, Vol 8, Iss 1, Pp 1-10 (2018)
Abstract Background Icatibant is a bradykinin B2-receptor antagonist used for the treatment of hereditary angioedema attacks resulting from C1-inhibitor deficiency. Treatment is not adjusted by body weight however the impact of body mass index (BMI)
Externí odkaz:
https://doaj.org/article/8353b2779ad441c2b831554a2b29079a
Publikováno v:
Acta Dermato-Venereologica, Vol 98, Iss 5, Pp 501-505 (2018)
Treatment recommendations for pityriasis rubra pilaris (PRP) are based solely on case reports and small case series, as to-date no randomized controlled trials are available. We present here a case series of 3 patients and a literature review of 28 s
Externí odkaz:
https://doaj.org/article/b9e98bacbfa84f38a3e5be60ec541cc8
Autor:
Maja A. Hofmann, Ana Giménez-Arnau, Werner Aberer, Carsten Bindslev-Jensen, Torsten Zuberbier
Publikováno v:
Clinical and Translational Allergy, Vol 8, Iss 1, Pp 1-6 (2018)
Abstract Background European legislation has banned the preservative methylisothiazolinone (MI) from inclusion in leave-on cosmetics. However, the risk for allergic reactions depends on exposure. The aim of this study was to determine the risk of MI
Externí odkaz:
https://doaj.org/article/000b224fb895412b8ba38106a1f77ba0
Autor:
Werner Aberer, Marcus Maurer, Laurence Bouillet, Andrea Zanichelli, Teresa Caballero, Hilary J. Longhurst, Amandine Perrin, Irmgard Andresen, for the IOS Study Group
Publikováno v:
Allergy, Asthma & Clinical Immunology, Vol 13, Iss 1, Pp 1-9 (2017)
Abstract Background Patients with hereditary angioedema (HAE) due to C1-inhibitor deficiency (C1-INH-HAE) experience recurrent attacks of cutaneous or submucosal edema that may be frequent and severe; prophylactic treatments can be prescribed to prev
Externí odkaz:
https://doaj.org/article/b0a93622203441dead517aa57b6f57f9