Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Ellaine Dóris Fernandes Carvalho"'
Autor:
Isabella Fernandes Carvalho, Louise Cristina Pereira Freitas, Phillipe Nogueira Barbosa Alencar, Maria Cláudia de Freitas Lima, Daniel de Sá Cavalcante, José Luciano Pimenta Couto, Paulo Tarcio Aded Silva, Dhaniel Anderson Olímpio Barbosa, Ellaine Dóris Fernandes Carvalho, Fabrício Bitu Sousa
Publikováno v:
Journal of Dental Research, Dental Clinics, Dental Prospects, Vol 16, Iss 1, Pp 76-80 (2022)
Zika virus congenital syndrome (ZVCS) is a congenital viral infection resulting from the transmission of the Zika virus (ZV) to the fetus during pregnancy. This report describes a clinical case involving a 20-month-old female child with ZVCS, who pre
Externí odkaz:
https://doaj.org/article/1e0e71fe56494dd9a92e031b6eec0899
Autor:
Isabella Fernandes Carvalho, Phillipe Nogueira Barbosa Alencar, Maria Denise Carvalho de Andrade, Paulo Goberlânio de Barros Silva, Ellaine Dóris Fernandes Carvalho, Lavina Sousa Araújo, Michelly Pedrosa Monteiro Cavalcante, Fabrício Bitú Sousa
Publikováno v:
Journal of Applied Oral Science, Vol 27, Iss 0 (2019)
Abstract Objective: The aim of this study was to investigate possible malformations in the soft, bone and/or dental tissues in patients with congenital Zika Virus (ZIKV) by clinical and x-ray evaluation. Methodology: Thirty children born with ZIKV an
Externí odkaz:
https://doaj.org/article/f8df3a2d52cf4b56800f34af0fd89271
Publikováno v:
Revista de Medicina da UFC, Vol 57, Iss 2, Pp 6-7 (2017)
The concept of rare disease (RD), according to the World Health Organization (WHO), is a disease that affects up to 65 people in every 100 thousand individuals, that means 1.3 for each 2 thousand people. In Brazil, it is estimated that 13 million peo
Externí odkaz:
https://doaj.org/article/8d270f4c50e84ab08c05b2fe10ef7895
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:
Arine Alcoforado Amorim, Maria Claudia de Freitas Lima, Paulo Goberlânio de Barros Silva, Samara Kelly da Silva Cavalcante, Ellaine Doris Fernandes Carvalho, Fernanda Araújo Sampaio, Maria Denise Fernandes Carvalho de Andrade, Phillipe Nogueira Barbosa Alencar, Maysa Luna de Souza, Letícia Tavares de Oliveira, Isabella Fernandes Carvalho
Publikováno v:
Pesquisa Brasileira em Odontopediatria e Clínica Integrada, Vol 25 (2024)
Objective: To determine the prevalence of possible sleep and awake bruxism and its related risk factors in children with Congenital Zika Virus Syndrome. Material and Methods: The case group consists of 20 children with congenital Zika, age range from
Externí odkaz:
https://doaj.org/article/7219590977c74e879520867848fa9e4c
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:
Norberto Guelbert, Oscar Mauricio Espitia Segura, Carolina Amoretti, Angélica Arteaga Arteaga, Nora Graciela Atanacio, Sabrina Bazan Natacha, Ellaine Doris Fernandes Carvalho, Maria Denise Fernandes Carvalho de Andrade, Inés María Denzler, Consuelo Durand, Erlane Ribeiro, Juan Carlos Giugni, Gabriel González, Dolores González Moron, Guillermo Guelbert, Zulma Janneth Hernández Rodriguez, Katiane Embiruçu Emilia, Marcelo Andrés Kauffman, Nury Isabel Mancilla, Laureano Marcon, Alessandra Marques Pereira, Carolina Fischinger Moura de Souza, Victor Adrián Muñoz, Ricardo Andrés Naranjo Flórez, André Luiz Pessoa, María Victoria Ruiz, Martha Luz Solano Villareal, Norma Spécola, Lina Marcela Tavera, Javiera Tello, Mónica Troncoso Schifferli, Sonia Ugrina, María Magdalena Vaccarezza, Diane Vergara, María Mercedes Villanueva
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 38, Iss , Pp 101060- (2024)
Introduction: Late infantile neuronal ceroid lipofuscinosis type 2 (CLN2), is a neurodegenerative autosomal recessive disease caused by TPP1 gene variants, with a spectrum of classic and atypical phenotypes. The aim of treatment is to slow functional
Externí odkaz:
https://doaj.org/article/d1f6513168dd43cd873e78c97646f8bf
Autor:
Fabrício Bitu Sousa, Ellaine Dóris Fernandes Carvalho, Paulo Goberlânio de Barros Silva, Michelly Pedrosa Monteiro Cavalcante, Maria Denise Carvalho de Andrade, Lavina Sousa Araújo, Isabella Fernandes Carvalho, Phillipe Nogueira Barbosa Alencar
Publikováno v:
Journal of Applied Oral Science
Journal of Applied Oral Science, Vol 27, Iss 0 (2019)
Journal of Applied Oral Science v.27 2019
Journal of applied oral science
Universidade de São Paulo (USP)
instacron:USP
Journal of Applied Oral Science, Volume: 27, Article number: e20180276, Published: 20 MAY 2019
Journal of Applied Oral Science, Vol 27, Iss 0 (2019)
Journal of Applied Oral Science v.27 2019
Journal of applied oral science
Universidade de São Paulo (USP)
instacron:USP
Journal of Applied Oral Science, Volume: 27, Article number: e20180276, Published: 20 MAY 2019
Objective: The aim of this study was to investigate possible malformations in the soft, bone and/or dental tissues in patients with congenital Zika Virus (ZIKV) by clinical and x-ray evaluation. Methodology: Thirty children born with ZIKV and 30 chil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1abb6bae9984cbe4c28d343261a0665c
https://pubmed.ncbi.nlm.nih.gov/31116278
https://pubmed.ncbi.nlm.nih.gov/31116278
Autor:
Krishnamurti M. Carvalho, Cláudia F. Santos, Ellaine Dóris Fernandes Carvalho, Marla Rochana Braga Monteiro, Bruno A. Cardi, Geissy I M C Feitosa, Edivaldo B S Coelho, Paulo Tárcio Aded da Silva, Rafael L Medeiros, Nilberto R.F. Nascimento, Isabella Fernandes Carvalho, Daniel Esdras de Andrade Uchoa, Doris Maria Fernandes Carvalho, Maria-Denise F Carvalho, Edilberto R. Silveira
Publikováno v:
Repositório Institucional da Universidade Federal do Ceará (UFC)
Universidade Federal do Ceará (UFC)
instacron:UFC
PAIN Reports, Vol 4, Iss 6, p e791 (2019)
Pain Reports
Universidade Federal do Ceará (UFC)
instacron:UFC
PAIN Reports, Vol 4, Iss 6, p e791 (2019)
Pain Reports
Introduction:. In recent decades, several researches have been conducted in search of new analgesics that do not present the side effects of opioids. In this context, animal venoms contain natural painkillers that have been used for the development o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9e7aa31a849536d7648c176334f7479
https://doi.org/10.1097/pr9.0000000000000791
https://doi.org/10.1097/pr9.0000000000000791