Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Camila Lopes Veronez"'
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:
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:
Camila Lopes Veronez, Fabio D Nascimento, Katia R B Melo, Helena B Nader, Ivarne L S Tersariol, Guacyara Motta
Publikováno v:
PLoS ONE, Vol 9, Iss 3, p e91280 (2014)
INTRODUCTION: The aim of this work was to evaluate the role of human plasma prekallikrein assembly and processing in cells and to determine whether proteoglycans, along with high molecular weight kininogen (H-kininogen), influence this interaction. M
Externí odkaz:
https://doaj.org/article/2b08a626812f4c0298dd19912d991caa
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:
João Bosco Pesquero, Adriana S. Moreno, Marcelo Vivolo Aun, Anete Sevciovic Grumach, Marcel Gutierrez, Pedro Giavina-Bianchi, Camila Lopes Veronez, L. Karla Arruda, Solange Oliveira Rodrigues Valle, Rozana Fátima Gonçalves, Maria Luiza Oliva Alonso, Mariana Paes Leme Ferriani
Publikováno v:
Clinical Reviews in Allergy & Immunology. 61:60-65
Hereditary angioedema (HAE) is an autosomal dominant disease mostly due to the deficiency of C1 inhibitor (C1-INH). HAE with normal C1-INH was first described in 2000 and associated with mutations in the coagulation factor XII in 2006. Both diseases
Publikováno v:
Current Opinion in Allergy & Clinical Immunology. 20:253-260
Purpose of review Angioedema without urticaria is composed of an increasing subtype's variety and presents a challenging diagnosis. This review summarizes the subtypes recently described and subsequent new findings helpful within their classification
Autor:
Jose Fabiani, Emel Aygören-Pürsün, Sladjana Andrejevic, Christian Drouet, Nóra Veszeli, Matija Rijavec, Georg Dewald, Markus Magerl, Michael Kirschfink, Marco Cicardi, Camila Lopes Veronez, Imola Beatrix Nagy, Massimo Triggiani, Maria Zamanakou, Henrik Halle Boysen, Matthaios Speletas, Maria Bova, Maria Staevska, Maurizio Margaglione, Sandra C. Christiansen, Teresa Caballero, Milos Jesenak, Vesna Grivcheva-Panovska, Allen P. Kaplan, Kinga Viktoria Köhalmi, Anthony J. Castaldo, Roman Hakl, Gaëlle Hardy, Walter A. Wuillemin, Inmaculada Martinez Saguer, Margarita López Trascasa, João Bosco Pesquero, Sven Cichon, Jonathan A. Bernstein, Grzegorz Porebski, Patrik Nordenfelt, C. Katelaris, Anette Bygum, Maria Teresa Gonzalez-Quevedo, Stephen Jolles, Henriette Farkas, Sandra A. Nieto, William R. Lumry, Hilary Longhurst, Spath Peter, Iris Leibovich, Nihal M. Gökmen, Christina Weber, Noemi-Anna Bara, Konrad Bork, Alberto López Lera, Dorottya Csuka, Fotis Psarros, Laurence Bouillet, Marc A. Riedl, Bruce L. Zuraw, Anete Sevciovic Grumach, Farrukh R. Sheikh, Marcin Stobiecki, Anastasios E. Germenis, Ágnes Szilágyi, Avner Reshef, Susan Waserman, J. Gooi
Publikováno v:
Germenis, A E, Margaglione, M, Pesquero, J B, Farkas, H, Cichon, S, Csuka, D, Lera, A L, Rijavec, M, Jolles, S, Szilagyi, A, Trascasa, M L, Veronez, C L, Drouet, C, Zamanakou, M & Hereditary Angioedema International Working Group 2020, ' International Consensus on the Use of Genetics in the Management of Hereditary Angioedema ', The Journal of Allergy and Clinical Immunology: In Practice, vol. 8, no. 3, pp. 901-911 . https://doi.org/10.1016/j.jaip.2019.10.004
Hereditary angioedema (HAE) is becoming much more genetically complex than was initially considered. Thus, the role of HAE genetics is expanding beyond research laboratories, and the genotyping of subjects suffering from HAE has become diagnostically
Publikováno v:
Clinical reviews in allergyimmunology. 60(3)
Biochemical studies performed during the last decades resulted in the development of various innovative medicinal products for hereditary angioedema (HAE). These therapeutic agents target the production or the function of bradykinin-the main mediator
Autor:
Pedro Giavina-Bianchi, Herberto José Chong-Neto, Faradiba Sarquis Serpa, Camila Lopes Veronez, Adriana S. Moreno, João Bosco Pesquero, Eliana C. Toledo, Solange Oliveira Rodrigues Valle, Anete Sevciovic Grumach, Luisa Karla de Paula Arruda, Regis A. Campos, Eli Mansour
Publikováno v:
Arquivos de Asmas Alergia e Imunologia. 5