Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Agatha Ribeiro Mendes"'
Autor:
Camila Lopes Veronez, Anne Aabom, Renan Paulo Martin, Rafael Filippelli-Silva, Rozana Fátima Gonçalves, Priscila Nicolicht, Agatha Ribeiro Mendes, Jane Da Silva, Mar Guilarte, Anete Sevciovic Grumach, Eli Mansour, Anette Bygum, João Bosco Pesquero
Publikováno v:
Frontiers in Medicine, Vol 6 (2019)
Hereditary angioedema (HAE) is an autosomal dominant disease caused by C1-INH deficiency due to mutations in SERPING1 (C1-INH-HAE) in most of the cases, or by specific mutations in factor XII gene, F12 (F12-HAE). Identification of polymorphisms in th
Externí odkaz:
https://doaj.org/article/11f2c8ef89a14a6c8e850219d5e9c290
Autor:
Sandra Aparecida Moreira Gomes Monteiro, Renan Paulo Martin, Rafael Filippelli-Silva, Maryana Mara Marins, Caio Perez Gomes, Patricia Varela, Agatha Ribeiro Mendes, Priscila Nicolicht de Amorim, Erica Assis, João Bosco Pesquero, Carolina Sanches Aranda, Allan Chiaratti de Oliveira, Thais das Neves Fraga Moreira, Lily Yin Weckx, Maria Isabel de Moraes-Pinto
Purpose: In Mycobacterium tuberculosis endemic regions, BCG vaccine is administered early after birth to confer protection against severe form of tuberculosis disease. Previous reports suggest that BCG adverse events, even localized ones (BCGitis), c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1cfd51989277e6847c441e5a70211f8d
https://doi.org/10.21203/rs.3.rs-1108372/v1
https://doi.org/10.21203/rs.3.rs-1108372/v1
Autor:
Beatriz Nogueira, Renan Paulo Martin, Maryana Mara Marins, Isabelle Hernandez Cantão, Agatha Ribeiro Mendes, Gabriella Campagnoli, João Bosco Pesquero, Taiza Stumpp
Environment is crucial for manifestation and development of schizophrenia, bringing to light epigenetic mechanisms involved, such as post-transcriptional control of gene expression by miRNA, in this disorder. MiRNAs participate in physiological proce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4e8e07a20abb9bf5531f029e1ec9a209
https://doi.org/10.21203/rs.3.rs-118724/v1
https://doi.org/10.21203/rs.3.rs-118724/v1
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
Autor:
Eli Mansour, Rozana Fátima Gonçalves, Anette Bygum, Agatha Ribeiro Mendes, Jane Da Silva, Mar Guilarte, Priscila Nicolicht, Camila Lopes Veronez, Rafael Filippelli-Silva, Anete Sevciovic Grumach, Renan Paulo Martin, Anne Aabom, João Bosco Pesquero
Publikováno v:
Frontiers in Medicine, Vol 6 (2019)
Frontiers in Medicine
Veronez, C L, Aabom, A, Martin, R P, Filippelli-Silva, R, Gonçalves, R F, Nicolicht, P, Mendes, A R, Da Silva, J, Guilarte, M, Grumach, A S, Mansour, E, Bygum, A & Pesquero, J B 2019, ' Genetic variation of Kallikrein-Kinin system and related genes in patients with hereditary angioedema ', Frontiers in Medicine, vol. 6, no. FEB, 28 . https://doi.org/10.3389/fmed.2019.00028
Scientia
Frontiers in Medicine
Veronez, C L, Aabom, A, Martin, R P, Filippelli-Silva, R, Gonçalves, R F, Nicolicht, P, Mendes, A R, Da Silva, J, Guilarte, M, Grumach, A S, Mansour, E, Bygum, A & Pesquero, J B 2019, ' Genetic variation of Kallikrein-Kinin system and related genes in patients with hereditary angioedema ', Frontiers in Medicine, vol. 6, no. FEB, 28 . https://doi.org/10.3389/fmed.2019.00028
Scientia
Kallikrein-Kinin System; Genetic variation; Hereditary angioedema Sistema calicreina-cinina; Variació genètica; Angioedema hereditari Sistema calicreina-cinina; Variación genética; Angioedema hereditario Hereditary angioedema (HAE) is an autosoma
Autor:
João Bosco Pesquero, Celso Arrais-Rodrigues, Maria Stella Figueiredo, Ana Rita Da Fonseca, Caio Perez Gomes, Vinicius Campos de Molla, Agatha Ribeiro Mendes, Martha Mariana de Almeida Santos Arruda, Patricia Eiko Yamakawa, Fabiana Bettoni
Publikováno v:
Blood. 134:944-944
Introduction: Paroxysmal nocturnal hemoglobinuria (PNH) is a disorder due to an acquired loss-of-function mutation in the phosphatidylinositol glycan class A (PIG-A) gene. A large spectrum of acquired PIG-A mutations has been described, like insertio