Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Vania Mesquita Gadelha, Prazeres"'
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:
null Cleiton Fantin, null Isabella Cristina Amaral Dantas, null Daniella Yleane Gadelha Viana, null Vania Mesquita Gadelha Prazeres, null Natalia Dayane Moura Carvalho
Publikováno v:
Journal of Pharmacy and Pharmacology. 10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c54fa3d63a9d6045bbbcd7ebd722f76
https://doi.org/10.17265/2328-2150/2022.09.001
https://doi.org/10.17265/2328-2150/2022.09.001
Autor:
Natalia Dayane Moura Carvalho, Isabella Cristina Amaral Dantas, Vania Mesquita Gadelha Prazeres, Cleiton Fantin
Publikováno v:
Saúde e Desenvolvimento Humano. 10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1e1871985381cb95e1f9879c628980e
https://doi.org/10.18316/sdh.v10i2.8274
https://doi.org/10.18316/sdh.v10i2.8274
Autor:
Tirciana Carvalho Passos, Cleiton Fantin, Natalia Dayane Moura Carvalho, Vania Mesquita Gadelha Prazeres
Publikováno v:
Revista de Ciências Médicas e Biológicas. 20:341-343
Introduction: Ovotesticular disorder of sex development is a rare condition by the concomitant presence of testicular and ovarian tissue, and usually presents genital ambiguity. Are chromosomally heterogeneous, and cytogenetic analyses is relevant. O
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::145c9f3063031c5f4a4c8b3de59ee433
https://doi.org/10.9771/cmbio.v20i2.44045
https://doi.org/10.9771/cmbio.v20i2.44045
Publikováno v:
Saúde e Desenvolvimento Humano. 9
Introducao Translocacao corresponde a troca de segmentos entre cromossomos nao homologos, decorrendo novas mutacoes ou herdadas. Na maioria dos casos, translocacoes estao associadas com cromossomo derivativo. Assim, objetivou-se relatar paciente com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7958fca540f66df48272db3b0f494db9
https://doi.org/10.18316/sdh.v9i2.6896
https://doi.org/10.18316/sdh.v9i2.6896
Autor:
Isy Lima Peixoto, Ana Maria Carreno, Vania Mesquita Gadelha Prazeres, Caroline Albuquerque Rodrigues Chirano, Gabriel Maroja Ihara, Patricia Bandeira de Melo Akel
Publikováno v:
Anais Brasileiros de Dermatologia, Vol 89, Iss 6, Pp 1005-1006 (2014)
Costello syndrome (CS) is a rare genetic disorder, first described by Costello in 1971, caused by mutations in the HRAS proto-oncogene. Clinical findings include facial dysmorphism, skin disorders, cognitive impairment, cardiac and musculoskeletal de
Externí odkaz:
https://doaj.org/article/c8ea44f581d04585b1688a308d7d3faa
Autor:
Isy Lima, Peixoto, Ana Maria, Carreno, Vania Mesquita Gadelha, Prazeres, Caroline Albuquerque Rodrigues, Chirano, Gabriel Maroja, Ihara, Patricia Bandeira de Melo, Akel
Publikováno v:
Anais Brasileiros de Dermatologia
Costello syndrome (CS) is a rare genetic disorder, first described by Costello in 1971, caused by mutations in the HRAS proto-oncogene. Clinical findings include facial dysmorphism, skin disorders, cognitive impairment, cardiac and musculoskeletal de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a4842c9ed7ba6bca65ecb6eb4002150e
https://pubmed.ncbi.nlm.nih.gov/25387514
https://pubmed.ncbi.nlm.nih.gov/25387514
Autor:
Vania Mesquita Gadelha Prazeres, Patrícia Bandeira de Melo Akel, Ana Maria Carreño, Gabriel Maroja Ihara, Caroline Albuquerque Rodrigues Chirano, Isy Lima Peixoto
Publikováno v:
Anais Brasileiros de Dermatologia, Vol 89, Iss 6, Pp 1005-1006 (2014)
Costello syndrome (CS) is a rare genetic disorder, first described by Costello in 1971, caused by mutations in the HRAS proto-oncogene. Clinical findings include facial dysmorphism, skin disorders, cognitive impairment, cardiac and musculoskeletal de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::056747a58de7f681713981851b1995db
https://doi.org/10.1590/abd1806-4841.20143062
https://doi.org/10.1590/abd1806-4841.20143062