Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Anete S, Grumach"'
Autor:
Herberto José Chong-Neto, M.D., Ph.D, Bárbara Padilha Aroni, M.D, Eli Mansour, M.D, Ph.D, Eliana Toledo, M.D., Ph.D, Faradiba Sarquis Serpa, M.D., Ph.D, Luisa Karla Arruda, M.D, Ph.D, Pedro Giavina-Bianchi, M.D., Ph.D, Solange Oliveira Rodrigues Valle, M.D., Ph.D, Caroline Guth de Freitas Batista de Moraes, M.T., MSc, Tatielly Kruk, M.T., MSc, Débora Carla Chong-Silva, MD, PhD, Dirceu Solé, M.D., Ph.D, Luciana Rodrigues Silva, M.D., Ph.D, Anete S. Grumach, M.D., Ph.D, Nelson Augusto Rosário Filho, M.D., Ph.D, Régis de Albuquerque Campos, M.D., Ph.D
Publikováno v:
World Allergy Organization Journal, Vol 16, Iss 6, Pp 100783- (2023)
Background: Hereditary angioedema (HAE) is an autosomal dominant disease characterized by recurrent episodes of subcutaneous or mucosal edema caused by excess bradykinin. The aim of the present study was to assess the knowledge of pediatricians about
Externí odkaz:
https://doaj.org/article/c6a8a53d1b3e4401aad27152faa079db
Autor:
Anete S. Grumach, Noga Gadir, Aharon Kessel, Ashley Yegin, Inmaculada Martinez‐Saguer, Jonathan A. Bernstein
Publikováno v:
Clinical and Translational Allergy, Vol 13, Iss 5, Pp n/a-n/a (2023)
Abstract Patients with hereditary angioedema (HAE) experience a high burden of disease due to unpredictable, painful, disfiguring, and potentially life‐threatening HAE attacks. Multiple HAE‐specific medications for the on‐demand treatment, shor
Externí odkaz:
https://doaj.org/article/abb44bfb4d1b41ffae0d18e1bf99b195
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
Externí odkaz:
https://doaj.org/article/0c70b679e186458b8ead8df1c6b64270
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:
Natalia Gabriel, Fernanda Marcelino, Mariana P. L. Ferriani, L. Karla Arruda, Regis A. Campos, Rozana F. Gonçalves, Herberto Chong-Neto, Nelson Rosario Filho, Solange O. R. Valle, Joao B. Pesquero, Anete S. Grumach
Publikováno v:
Frontiers in Allergy, Vol 3 (2022)
BackgroundHAE with normal C1 inhibitor (HAE-nC1-INH) has been identified as a bradykinin mediated angioedema. Estrogens are one of the main trigger factors. Pregnancy in HAE with C1 inhibitor deficiency showed variable course, however, few reports ar
Externí odkaz:
https://doaj.org/article/a8eae9143bbe4f0481a7e26768b6d309
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
Angioedema is a prevailing symptom in different diseases, frequently occurring in the presence of urticaria. Recurrent angioedema without urticaria (AE) can be hereditary (HAE) and acquired (AAE), and several subtypes can be distinguished, although c
Externí odkaz:
https://doaj.org/article/1e462d2fe21742c39a5079a6af224f95
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:
Francisco A. Araújo, Luiz C. Abreu, Gabriel Z. Laporta, Vinicius S. Santos, Jose G.V. Moreira, Anete S. Grumach
Publikováno v:
Brazilian Journal of Infectious Diseases, Vol 25, Iss 1, Pp 101042- (2021)
Background: Hanseniasis is a public health concern in developing countries. Although a decrease in the number of new cases in Brazil has been reported, there is a prevalence above that recommended in some regions. Aims: Considering the goal of the Wo
Externí odkaz:
https://doaj.org/article/c5b0b0966bee44aeaa0e84d809162a39
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:
Avner Reshef, Anete S Grumach
Publikováno v:
The Lancet. 401:413-415
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::345794ec797b617ad0db0d9373d8b8c5
https://doi.org/10.1016/s0140-6736(23)00267-2
https://doi.org/10.1016/s0140-6736(23)00267-2