Zobrazeno 1 - 10
of 62
pro vyhledávání: '"Regis A, Campos"'
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
Autor:
Pedro Giavina-Bianchi, Luisa Karla Arruda, Marcelo V. Aun, Regis A. Campos, Herberto J. Chong-Neto, Rosemeire N. Constantino-Silva, Fátima R. Fernandes, Maria F. Ferraro, Mariana P.L. Ferriani, Alfeu T. França, Gustavo Fusaro, Juliana F.B. Garcia, Shirley Komninakis, Luana S.M. Maia, Eli Mansour, Adriana S. Moreno, Antonio A. Motta, João B. Pesquero, Nathalia Portilho, Nelson A. Rosário, Faradiba S. Serpa, Dirceu Solé, Priscila Takejima, Eliana Toledo, Solange O.R. Valle, Camila L. Veronez, Anete S. Grumach
Publikováno v:
Clinics, Vol 73, Iss 0 (2018)
Hereditary angioedema is an autosomal dominant disease characterized by recurrent angioedema attacks with the involvement of multiple organs. The disease is unknown to many health professionals and is therefore underdiagnosed. Patients who are not ad
Externí odkaz:
https://doaj.org/article/5d806db294424e8384232d19198cdd13
Akademický článek
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Autor:
Solange Oliveira Rodrigues Valle, Alfeu Tavares França, Regis A. Campos, Anete Sevciovic Grumach
Publikováno v:
Clinical Medicine Insights: Blood Disorders, Vol 2011, Iss 4, Pp 21-30 (2011)
Externí odkaz:
https://doaj.org/article/36bcbda536a04d529414a9228c6c27a8
Autor:
Pedro Giavina-Bianchi, Alfeu T. França, Anete S. Grumach, Abílio A Motta, Fátima R Fernandes, Regis A. Campos, Solange O Valle, Nelson A Rosário, Dirceu Sole
Publikováno v:
Clinics, Vol 66, Iss 9, Pp 1627-1636 (2011)
Hereditary angioedema is an autosomal dominant disease characterized by edema attacks with multiple organ involvement. It is caused by a quantitative or functional deficiency of the C1 inhibitor, which is a member of the serine protease inhibitor fam
Externí odkaz:
https://doaj.org/article/382cb3dcbba248609023e0c34b7a170d
Autor:
Olavo de Godoy Mion, Regis A. Campos, Martti Antila, Priscila Bogar Rapoport, Nelson Rosario, João Ferreira de Mello Junior, Roberto Eustáquio Santos Guimarães, Marcos Mocellin, Giovanni Di Gesu, Dirceu Solé, Luc Wexler, João Ferreira de Mello, Fábio Morato Castro, Maria Letícia Chavarria
Publikováno v:
Brazilian Journal of Otorhinolaryngology, Vol 75, Iss 5, Pp 673-679 (2009)
Allergic rhinitis affects 10-30% of the population, negatively impacting one's quality of life and productivity. It has been associated with sinusitis, otitis media, sleep disorders, and asthma. Rupatadine is a second generation antihistamine with in
Externí odkaz:
https://doaj.org/article/b631515d024946e8a7b09b42ce6619df
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Autor:
Maria Abadia Consuelo M. S. Gomide, Eliana Toledo, Solange Oliveira Rodrigues Valle, Regis A. Campos, Alfeu T. França, Nieves Prior Gomez, Heitor Franco Andrade Jr., Teresa Caballero, Anete S. Grumach
Publikováno v:
Clinics, Vol 68, Iss 1, Pp 81-83 (2013)
OBJECTIVE: Hereditary angioedema is a serious medical condition caused by a rare autosomal dominant genetic disorder and it is associated with deficient production or dysfunction of the C1 esterase inhibitor. In most cases, affected patients experien
Externí odkaz:
https://doaj.org/article/6b364684388745cd8de95773f816b0d8
Publikováno v:
Jornal de Pediatria, Volume: 97 Supplement 1, Pages: 10-16, Published: 26 APR 2021
Jornal de Pediatria, Vol 97, Iss, Pp S10-S16 (2021)
Jornal de Pediatria v.97 suppl.1 2021
Jornal de Pediatria
Sociedade Brasileira de Pediatria (SBP)
instacron:SBPE
Jornal de Pediatria, Vol 97, Iss, Pp S10-S16 (2021)
Jornal de Pediatria v.97 suppl.1 2021
Jornal de Pediatria
Sociedade Brasileira de Pediatria (SBP)
instacron:SBPE
Objectives To describe the hereditary angioedema to improve awareness of this condition and reduce diagnostic delay. Data sources Relevant articles in the MEDLINE database through PubMed. Data synthesis Hereditary angioedema is rare and has an autoso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63e1f04de558dcecf582d8eaec31e260
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0021-75572021000700010&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0021-75572021000700010&lng=en&tlng=en
Autor:
Solange Oliveira Rodrigues Valle, Marcelo Vivolo Aun, Antonio Abilio Motta, Faradiba Sarquis Serpa, Herberto José Chong Neto, Pedro Giavina-Bianchi, Eliana de Toledo, Luisa Karla de Paula Arruda, Eli Mansour, Regis A. Campos, Anete Sevciovic Grumach
Publikováno v:
Einstein
Einstein (São Paulo)
einstein (São Paulo) v.19 2021
Instituto Israelita de Ensino e Pesquisa Albert Einstein (IIEPAE)
instacron:IIEPAE
Einstein (São Paulo)
einstein (São Paulo) v.19 2021
Instituto Israelita de Ensino e Pesquisa Albert Einstein (IIEPAE)
instacron:IIEPAE
Angioedema attacks are common causes of emergency care, and due to the potential for severity, it is important that professionals who work in these services know their causes and management. The mechanisms involved in angioedema without urticaria may
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb1636bace62269607bd1d5b077b0f0d
http://europepmc.org/articles/PMC8020838
http://europepmc.org/articles/PMC8020838