Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Rosemeire Navickas Constantino-Silva"'
Autor:
Camila Lopes Veronez, Régis Albuquerque Campos, Rosemeire Navickas Constantino-Silva, Priscila Nicolicht, João Bosco Pesquero, Anete Sevciovic Grumach
Publikováno v:
Frontiers in Medicine, Vol 6 (2019)
Abdominal pain due to intestinal swellings is one of the most common manifestations in hereditary angioedema (HAE). Bowel swellings can cause severe abdominal pain, nausea, vomiting, and diarrhea, which may lead to misdiagnosis of gastrointestinal di
Externí odkaz:
https://doaj.org/article/f15f112d33b245b584b2bae9abd391f7
Autor:
Régis A. Campos, Faradiba Sarquis Serpa, Eli Mansour, Maria Luiza Oliva Alonso, Luisa Karla Arruda, Marcelo Vivolo Aun, Maine Luellah Demaret Bardou, Ana Flávia Bernardes, Fernanda Lugão Campinhos, Herberto Jose Chong-Neto, Rosemeire Navickas Constantino-Silva, Jane da Silva, Sérgio Duarte Dortas-Junior, Mariana Paes Leme Ferriani, Joanemile Pacheco de Figueiredo, Pedro Giavina-Bianchi, Lais Souza Gomes, Ekaterini Goudouris, Anete Sevciovic Grumach, Marina Teixeira Henriques, Antônio Abilio Motta, Therezinha Ribeiro Moyses, Fernanda Leonel Nunes, Jorge A. Pinto, Nelson Augusto Rosario-Filho, Norma de Paula M. Rubini, Almerinda Maria do Rêgo Silva, Dirceu Solé, Ana Julia Ribeiro Teixeira, Eliana Toledo, Camila Lopes Veronez, Solange Oliveira Rodrigues Valle
Publikováno v:
Arquivos de Asmas Alergia e Imunologia. 6:170-196
Autor:
Régis A. Campos, Faradiba Sarquis Serpa, Eli Mansour, Maria Luiza Oliva Alonso, Luisa Karla Arruda, Marcelo Vivolo Aun, Maine Luellah Demaret Bardou, Ana Flávia Bernardes, Fernanda Lugão Campinhos, Herberto Jose Chong-Neto, Rosemeire Navickas Constantino-Silva, Jane da Silva, Sérgio Duarte Dortas-Junior, Mariana Paes Leme Ferriani, Joanemile Pacheco de Figueiredo, Pedro Giavina-Bianchi, Lais Souza Gomes, Ekaterini Goudouris, Anete Sevciovic Grumach, Marina Teixeira Henriques, Antônio Abilio Motta, Therezinha Ribeiro Moyses, Fernanda Leonel Nunes, Jorge A. Pinto, Nelson Augusto Rosario-Filho, Norma de Paula M. Rubini, Almerinda Maria do Rêgo Silva, Dirceu Solé, Ana Julia Ribeiro Teixeira, Eliana Toledo, Camila Lopes Veronez, Solange Oliveira Rodrigues Valle
Publikováno v:
Arquivos de Asmas Alergia e Imunologia. 6:151-169
Autor:
Toine Mercier, P F Herkert, Rik Schrijvers, Anne Puel, Ferry Hagen, Rosemeire Navickas Constantino-Silva, Caroline Sola, Carmem Bonfim, N.A. Rosário Filho, J B França, J.F. Meis, Anete Sevciovic Grumach, Johan Maertens, Jean-Laurent Casanova, Olivier Lortholary, Giovanni Luis Breda, Flavio Queiroz-Telles, Fanny Lanternier
Publikováno v:
Journal of Clinical Immunology, 39(5), 462-469. Springer Science+Business Media
Autosomal recessive (AR) CARD9 (caspase recruitment domain-containing protein 9) deficiency underlies invasive infections by fungi of the ascomycete phylum in previously healthy individuals at almost any age. Although CARD9 is expressed mostly by mye
Autor:
Luis Felipe Ensina, Herberto José Chong-Neto, Rozana Fátima Gonçalves, Adriana S. Moreno, Almerinda Maria Rêgo-Silva, Pedro Giavina-Bianchi, João Bosco Pesquero, Janaíra Fernandes Ferreira, Jane da Silva, Sandra Mitie Ueda Palma, Faradiba Sarquis Serpa, Solange Rodrigues Valle, Eli Mansour, Sérgio Duarte Dortas, Camila Lopes Veronez, Eliana de Toledo, Ekaterine S. Goudouris, Anete Sevciovic Grumach, Regis A. Campos, Rosario Filho Nelson, Joanna Araújo-Simões, Maria Luiza Oliva Alonso, Priscila Takejima, Mayara Madruga Marques, Fernanda Gontijo Minafra, Mariana Paes Leme Ferriani, Pérsio Roxo Júnior, Jorge Pinto, Luisa Karla de Paula Arruda, Rosemeire Navickas Constantino-Silva, I. Moreira, Aline Gisele Pena Boanova, Nyla Thyara Melo Lobão Fragnan
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Introduction: Hereditary angioedema (HAE) with C1 inhibitor (C1-INH) deficiency is a rare autosomal dominant disease. Although the first symptoms can appear in childhood, the diagnosis’s delay has a strong impact on the patient’s quality of life.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66b1e24c0be300026717eb06fa285fcc
Autor:
Nicolas de Albuquerque Weidebach, Anete Sevciovic Grumach, Rosemeire Navickas Constantino-Silva, Sandro Félix Perazzio
Publikováno v:
Journal of Fungi
Journal of Fungi, Vol 6, Iss 238, p 238 (2020)
Journal of Fungi, Vol 6, Iss 238, p 238 (2020)
Background: NADPH-oxidase and myeloperoxidase (MPO) play an important role on defense against pathogenic microorganisms. Defects on these mechanisms have been described in association with recurrent infections due to such as Staphylococcus aureus and
Autor:
Anete Sevciovic Grumach, Renan Paulo Martin, Camila Lopes Veronez, Eli Mansour, Marcia Buzolin, Nathália Cagini, João Bosco Pesquero, Rosemeire Navickas Constantino-Silva, Licio A. Velloso
Publikováno v:
Biological Chemistry. 397:337-344
Hereditary Angioedema is an autosomal dominant inherited disease leading to oedema attacks with variable severity and localization predominantly caused by C1-INH deficit. More than 400 mutations have been already identified, however no genetic analys
Autor:
Eli Mansour, João Bosco Pesquero, Camila Lopes Veronez, Anete Sevciovic Grumach, Elton Dias da Silva, Nathália Cagini, Rosemeire Navickas Constantino-Silva, Licio A. Velloso, Patricia Varela Lima Teixeira
Publikováno v:
Biological Chemistry. 397:315-322
Hereditary angioedema (HAE) is accompanied by an overproduction of bradykinin (BK) as the primary mediator of swelling. Although many proteins may be involved in regulating the wide spectrum of HAE symptoms, most studies have only focused on C1-INH a
Autor:
Christiane Stieber, Nathália Cagini, L. Karla Arruda, Sven Cichon, Victor Koji Nakamura, Eliana de Toledo, Fabio Fernandes Morato Castro, Solange Rodrigues Valle, Miguel Alberto Piccirillo, Faradiba Sarquis Serpa, Anete Sevciovic Grumach, João Bosco Pesquero, Gabriela Andrade Coelho Dias, Rosemeire Navickas Constantino-Silva, M. Bernardes, Mariana Paes Leme Ferriani, Camila Lopes Veronez, Eli Mansour, Rozana Fátima Gonçalves, Adriana S. Moreno, Luana S.M. Maia
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Background Hereditary angioedema (HAE) with normal C1 inhibitor (C1-INH) is a rare condition with clinical features similar to those of HAE with C1-INH deficiency. Mutations in the F12 gene have been identified in subsets of patients with HAE with no
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ad63368dc71480b2d6bf8ca058c0306
Autor:
Juliana F.B. Garcia, Herberto José Chong-Neto, Fátima Rodrigues Fernandes, Alfeu Tavares França, Dirceu Solé, Mariana Paes Leme Ferriani, Priscila Takejima, Pedro Giavina-Bianchi, Eliana de Toledo, Camila Lopes Veronez, Shirley Vasconcelos Komninakis, Adriana S. Moreno, Marcelo Vivolo Aun, Anete Sevciovic Grumach, Gustavo Fusaro, Solange Oliveira Rodrigues Valle, João Bosco Pesquero, Luana S.M. Maia, Maria Fernanda Ferraro, Regis A. Campos, Nathalia Coelho Portilho, Eli Mansour, Antonio Abilio Motta, Faradiba Sarquis Serpa, Rosemeire Navickas Constantino-Silva, Nelson Rosario, Luisa Karla de Paula Arruda
Publikováno v:
Clinics; v. 73 (2018); e310
Clinics; Vol. 73 (2018); e310
Clinics
Universidade de São Paulo (USP)
instacron:USP
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Clinics, Vol 73, Iss 0 (2018)
Clinics, Volume: 73, Article number: e310, Published: 03 MAY 2018
Clinics; Vol. 73 (2018); e310
Clinics
Universidade de São Paulo (USP)
instacron:USP
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Clinics, Vol 73, Iss 0 (2018)
Clinics, Volume: 73, Article number: e310, Published: 03 MAY 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://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f7377beb104a0bb7598e45ddbe381e9
https://www.revistas.usp.br/clinics/article/view/146277
https://www.revistas.usp.br/clinics/article/view/146277