Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Nathália Cagini"'
Autor:
Gustavo Pafume de Sá, Leda das Neves Almeida Sandrin, Caio Perez Gomes, Regis A. Campos, Eliana de Toledo, Ana Paula Beltran Moschione Castro, Camila Lopes Veronez, Nelson Augusto Rosário Filho, Elke C. Ferreira Mascarenhas, Camila A. Campos Teixeira, Laila Sabino Garro, Solange Rodrigues Valle, Caroliny Souza Leite, Agatha Ribeiro Mendes, Fernanda Casares Marcelino, Leandro Augusto Vilela Rabelo, Ana Julia R. M. Teixeira, Anete Sevciovic Grumach, Fernanda Gontijo Minafra, Luiz Fernando Bacarini Leite, Carolina Sanchez Aranda, Nathália Cagini, Eli Mansour, Joanemile P. Figueiredo, Luis Felipe Ensina, Herberto José Chong-Neto, Clarissa Soares Tavares, Gabriela Andrade Coelho Dias, Pedro Rocha Rolins Neto, Raphael Coelho Figueredo, Pedro Giavina-Bianchi, Ronney Corrêa Mendes, Carolina Guth, Jackeline Motta Franco, Helena F. Velasco, Cristiane Alves Boll, Ekaterini Goudouris, Therezinha Ribeiro Moyses, Ellaine Dóris Fernandes Carvalho, Jane da Silva, Fernanda Lugão Campinhos, Faradiba Sarquis Serpa, Miguel Alberto Piccirillo, Rizzo Mc, M. Bernardes, Maria Denise Fernandes Carvalho de Andrade, Ana Carolina Martins Pinto Swensson, João Bosco Pesquero, Janaíra Fernandes Ferreira, Rozana Fátima Gonçalves, Valéria Soraya de Farias Sales, Ludmilla Luzia Pires Amaral Resende, Natasha Rebouças Ferraroni, Thais Bomfim Teixeira, Adriana Pereira de Lira Marques, Ana Carolina da Matta Ain
Publikováno v:
The journal of allergy and clinical immunology. In practice. 9(6)
Background Primary angioedema (PA) is a complex disorder, presenting multiple hereditary (hereditary angioedema) and acquired subtypes (acquired angioedema). Despite a very similar clinical presentation among subtypes, the differential diagnosis is l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24055811da2aa85479fcc0cc1b12463a
https://pubmed.ncbi.nlm.nih.gov/33276216
https://pubmed.ncbi.nlm.nih.gov/33276216
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d657700d90b31c877fca72fe6d1ec1a7
https://doi.org/10.1515/hsz-2015-0222
https://doi.org/10.1515/hsz-2015-0222
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4deb0681a292836ac032c94e79c16aff
https://doi.org/10.1515/hsz-2015-0212
https://doi.org/10.1515/hsz-2015-0212
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:
Anete Sevciovic Grumach, Markus M. Nöthen, Elisabete Cordeiro, Christiane Stieber, João Bosco Pesquero, Sven Cichon, Camila Lopes Veronez, Nathália Cagini, Rosemeire Navickas Constantino-Silva
Publikováno v:
Allergy. 71(1)
Hereditary angio-oedema (HAE) with normal C1 inhibitor is associated with heterozygous mutations in the factor XII gene (FXII-HAE). We report two Brazilian FXII-HAE families segregating the mutation c.983 C>A (p.Thr328Lys). In each family, one patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4bab353403756f2bdab5bb57281b309
https://pubmed.ncbi.nlm.nih.gov/26392288
https://pubmed.ncbi.nlm.nih.gov/26392288
Autor:
Jane da Silva, Edelton Flávio Morato, Nathália Cagini, Maria Madalena Luz, Camila Lopes Veronez, João Bosco Pesquero, Jéssica Goedert Pereira
Publikováno v:
The World Allergy Organization Journal
Background Hereditary angioedema (HAE) types I and II (due to quantitative and qualitative C1-INH deficiency, respectively) is a rare autosomal dominant condition in which more than 300 different mutations in the entire C1-INH gene (SERPING1) have be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d358ebfef727ca288ea1ff3ebd19d570
http://europepmc.org/articles/PMC4406207
http://europepmc.org/articles/PMC4406207
Autor:
Elisabete Cordeiro, João Bosco Pesquero, Neusa Falbo Wandalsen, Nathália Cagini, Camila Lopes Veronez, Rozana Fátima Gonçalves, Gustavo Fusaro, Sven Cichon, Christiane Stieber, Rosemeire Navickas Constantino-Silva, Anete Sevciovic Grumach
Publikováno v:
Journal of Allergy and Clinical Immunology. 133:AB32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1975996338f32a8bacb501438c1d158d
https://doi.org/10.1016/j.jaci.2013.12.140
https://doi.org/10.1016/j.jaci.2013.12.140