Zobrazeno 1 - 10
of 102
pro vyhledávání: '"Solange Oliveira Rodrigues, Valle"'
Autor:
Bibiana Mello de Oliveira, Filipe Andrade Bernardi, João Francisco Baiochi, Mariane Barros Neiva, Milena Artifon, Alberto Andrade Vergara, Ana Maria Martins, Anete Sevciovic Grumach, Angelina Xavier Acosta, Antonette Souto El Husny, Bethania de Freitas Rodrigues Ribeiro, Camila Ferreira Ramos, Carlos Eduardo Steiner, Chong Ae Kim, Denise Maria Christofolini, Diego Bettiol Yamada, Ellaine Doris Fernandes Carvalho, Erlane Marques Ribeiro, Fabíola de Arruda Bastos, Faradiba Sarquis Serpa, Flávia Reseda Brandão, Giselle Maria Araujo Felix Adjuto, Isabelle Carvalho, Jonas Alex Morales Saute, Juan Clinton Llerena Junior, Larissa Souza Mario Bueno, Luiz Carlos Santana da Silva, Mara Lucia Schmitz Ferreira Santos, Marcela Câmara Machado Costa, Marcia Maria Costa Giacon Giusti, Marcial Francis Galera, Márcio Eloi Colombo Filho, Maria Denise Fernandes Carvalho de Andrade, Maria Teresinha De Oliveira Cardoso, Marilaine Matos de Menezes Ferreira, Michelle Zeny, Milena Coelho Fernandes Caldato, Ney Boa Sorte, Nina Rosa de Castro Musolino, Paula Frassinetti Vasconcelos de Medeiros, Paulo Ricardo Gazzola Zen, Raquel Tavares Boy Da Silva, Rayana Elias Maia, Rodrigo Fock, Rosemarie Elizabeth Schimidt Almeida, Solange Oliveira Rodrigues Valle, Tatiana Amorim, Thaís Bomfim Teixeira, Vania Mesquita Gadelha Prazeres, Victor Evangelista de Faria Ferraz, Vinicius Costa Lima, Wagner José Martins Paiva, Ida Vanessa Doederlein Schwartz, Domingos Alves, Têmis Maria Félix, Raras Network Group
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-13 (2024)
Abstract Background The Brazilian Policy for Comprehensive Care for People with Rare Diseases was implemented in 2014; however, national epidemiological data on rare diseases (RDs) are scarce and mainly focused on specific disorders. To address this
Externí odkaz:
https://doaj.org/article/5b03fce23cb148d88e2d9b95dbec7a0d
Autor:
Alessandra Mileni Versuti Ritter, Suelen Silva, Robson de Paula, Juliana Senra, Fabio Carvalho, Tatiane Ribeiro, Solange Oliveira Rodrigues Valle
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
IntroductionHereditary angioedema (HAE) due to C1 inhibitor (C1-INH) deficiency is an ultra-rare autosomal dominant inherited disease that affects 1 in 67,000 people in the world. The attacks are based on subcutaneous and submucosal edema that can le
Externí odkaz:
https://doaj.org/article/e566de9673024487a29edf5e33dfae8f
Autor:
Herberto José Chong-Neto, M.D., Ph.D, Bárbara Padilha Aroni, M.D, Eli Mansour, M.D, Ph.D, Eliana Toledo, M.D., Ph.D, Faradiba Sarquis Serpa, M.D., Ph.D, Luisa Karla Arruda, M.D, Ph.D, Pedro Giavina-Bianchi, M.D., Ph.D, Solange Oliveira Rodrigues Valle, M.D., Ph.D, Caroline Guth de Freitas Batista de Moraes, M.T., MSc, Tatielly Kruk, M.T., MSc, Débora Carla Chong-Silva, MD, PhD, Dirceu Solé, M.D., Ph.D, Luciana Rodrigues Silva, M.D., Ph.D, Anete S. Grumach, M.D., Ph.D, Nelson Augusto Rosário Filho, M.D., Ph.D, Régis de Albuquerque Campos, M.D., Ph.D
Publikováno v:
World Allergy Organization Journal, Vol 16, Iss 6, Pp 100783- (2023)
Background: Hereditary angioedema (HAE) is an autosomal dominant disease characterized by recurrent episodes of subcutaneous or mucosal edema caused by excess bradykinin. The aim of the present study was to assess the knowledge of pediatricians about
Externí odkaz:
https://doaj.org/article/c6a8a53d1b3e4401aad27152faa079db
Autor:
Ivan Cherrez‐Ojeda, Emanuel Vanegas, Annia Cherrez, Miguel Felix, Karsten Weller, Markus Magerl, Rasmus Robin Maurer, Valeria L. Mata, Alicja Kasperska‐Zajac, Agnieszka Sikora, Daria Fomina, Elena Kovalkova, Kiran Godse, Nimmagadda Dheeraj Rao, Maryam Khoshkhui, Sahar Rastgoo, Roberta F. J. Criado, Mohamed Abuzakouk, Deepa Grandon, Martijn B. A. Van Doorn, Solange Oliveira Rodrigues Valle, Eduardo Magalhães De Souza Lima, Simon Francis Thomsen, German D. Ramón, Edgar E. Matos Benavides, Andrea Bauer, Ana M. Giménez‐Arnau, Emek Kocatürk, Carole Guillet, Jose Ignacio Larco, Zuo‐Tao Zhao, Michael Makris, Carla Ritchie, Paraskevi Xepapadaki, Luis Felipe Ensina, Sofia Cherrez, Marcus Maurer
Publikováno v:
Clinical and Translational Allergy, Vol 11, Iss 10, Pp n/a-n/a (2021)
Abstract Background Information/communication technologies such as mobile phone applications (apps) would enable chronic urticaria (CU) patients to self‐evaluate their disease activity and control. Yet, recently Antó et al (2021) reported a global
Externí odkaz:
https://doaj.org/article/76ba83ee17de440ea2e36c1c6e500157
Autor:
Ivan Cherrez-Ojeda, Emanuel Vanegas, Annia Cherrez, Miguel Felix, Karsten Weller, Markus Magerl, Rasmus Robin Maurer, Valeria L. Mata, Alicja Kasperska-Zajac, Agnieszka Sikora, Daria Fomina, Elena Kovalkova, Kiran Godse, Nimmagadda Dheeraj Rao, Maryam Khoshkhui, Sahar Rastgoo, Roberta FJ. Criado, Mohamed Abuzakouk, Deepa Grandon, Martijn B.A. Van Doorn, Solange Oliveira Rodrigues Valle, Eduardo Magalhães De Souza Lima, Simon Francis Thomsen, German D. Ramón, Edgar E. Matos Benavides, Andrea Bauer, Ana M. Giménez-Arnau, Emek Kocatürk, Carole Guillet, Jose Ignacio Larco, Zuo-Tao Zhao, Michael Makris, Carla Ritchie, Paraskevi Xepapadaki, Luis Felipe Ensina, Sofia Cherrez, Marcus Maurer
Publikováno v:
World Allergy Organization Journal, Vol 14, Iss 6, Pp 100542- (2021)
Background: Patients with chronic urticaria (CU) are increasingly using information and communication technologies (ICTs) to manage their health. What CU patients expect from ICTs and which ICTs they prefer remains unknown. We assessed why CU patient
Externí odkaz:
https://doaj.org/article/37a907e6851b448797cb8e5cc5de537c
Publikováno v:
Jornal de Pediatria, Vol 97, Iss , Pp S10-S16 (2021)
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 aut
Externí odkaz:
https://doaj.org/article/6ba5f412ad894078adc35788b04e6433
Autor:
María Margarita Olivares, Ricardo Dario Zwiener, Lina Maria Leiva Panqueva, Francisco Alberto Contreras Verduzco, Eli Mansour, Jairo Antonio Rodriguez, Solange Oliveira Rodrigues Valle, Sandra Nieto-Martínez, Jane da Silva, Daniel O. Vazquez, Oscar Calderon Llosa, Fernanda Casares Marcelino, Manuel Ratti Sisa, Ileana María Madrigal Beas, Rafael Zaragoza Urdaz, Eliana Toledo, Natalia Lorena Fili, Olga M. Barrera, Juan Carlos Fernandez de Cordova Aguirre, Sergio Castro Mora, Mauricio Sarrazola, Rodolfo Jaller Raad, Edison Morales Cardenas, Dario Oscar Josviack, Claudio Fantini, Monica Marocco, Elma I. Nievas, Faradiba Sarquis Serpa, Herberto J. Chong-Neto, Maria Luiza Oliva Alonso, Sergio Dortas Junior, Raisa Gusso Ulaf, Nelson Rosário, Rodolfo Ramón Leyva Barrero, Anete Sevciovic Grumach
Publikováno v:
The Journal of Allergy and Clinical Immunology. in Practice
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::167eba41cf3a466f5cd455eb4d4b025e
https://doi.org/10.1016/j.jaip.2021.12.008
https://doi.org/10.1016/j.jaip.2021.12.008
Autor:
Larissa Silva Brandão, Janaina Michelle Lima Melo, Gabriela Andrade Dias, Eli Mansour, Rozana de Fátima Gonçalves, Carolina Tavares De-Alcântara, Fernanda Lugao Campinhos, Daniela Farah Teixeira Raeder, Leila Vieira Borges Trancoso-Neves, Régis de Albuquerque Campos, Solange Oliveira Rodrigues Valle, Rosana Câmara Agondi, Alfeu Tavares Franca, Luis Felipe Chiaverini Ensina
Publikováno v:
Arquivos de Asmas Alergia e Imunologia. 6:197-213
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::778da1282b837a8a64ae3f6c683dad2b
https://doi.org/10.5935/2526-5393.20220021
https://doi.org/10.5935/2526-5393.20220021
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8a4fd4913225322dadb8d414335b8e14
https://doi.org/10.5935/2526-5393.20220019
https://doi.org/10.5935/2526-5393.20220019
Autor:
Solange Oliveira Rodrigues Valle, Maria Luiza Oliva Alonso, Sérgio Duarte Dortas Junior, Ekaterini Simões Goudouris, Ana Luiza Ribeiro Bard de Carvalho, Albertina Varandas Capelo, Eli Mansour, Ana Flávia Bernardes, Luiz Fernando Bacarini Leite, Pedro Giavina-Bianchi, Marcelo Vivolo Aun, Mariana Paes Leme Ferriani, Luisa Karla Arruda, Anete Sevciovic Grumach
Publikováno v:
International Archives of Allergy and Immunology. 183:572-577
Background: Acquired deficiency of C1 inhibitor (AAE-C1-INH) is a very rare cause of recurrent angioedema, with few cases reported in the literature. We aimed to describe a series of patients with AAE-C1-INH who were diagnosed and received care at an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8c894397bfa12d5ba5b0eb71af00f9b
https://doi.org/10.1159/000521646
https://doi.org/10.1159/000521646