Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Mauricio Barcelos Costa"'
Autor:
Mariane Martins Araújo Stefani, Patricia Sammarco Rosa, Mauricio Barcelos Costa, Antônio Pedro Mendes Schetinni, Igor Manhães, Maria Araci Andrade Pontes, Patricia Costa, Luciana Raquel Vincenzi Fachin, Ida Maria Foschiani Dias Batista, Marcos Virmond, Emília Pereira, Maria Lucia Fernandes Penna, Gerson Oliveira Penna
Publikováno v:
PLoS ONE, Vol 14, Iss 1, p e0209491 (2019)
There is evidence that in southern US, leprosy is a zoonosis infecting wild Dasypus novemcinctus armadillos but the extent of this finding is unknown. This ecological study investigated leprosy in rural communities and in wild armadillos from the Bra
Externí odkaz:
https://doaj.org/article/34157d3cb19040d6884d589f54e796b0
Autor:
Danielle de Freitas Mizoguti, Emerith Mayra Hungria, Aline Araújo Freitas, Regiane Morillas Oliveira, Ludimila Paula Vaz Cardoso, Mauricio Barcelos Costa, Ana Lúcia Maroclo Sousa, Malcolm S Duthie, Mariane Martins Araújo Stefani
Publikováno v:
Memorias do Instituto Oswaldo Cruz, Vol 110, Iss 7, Pp 914-920 (2015)
Leprosy inflammatory episodes [type 1 (T1R) and type 2 (T2R) reactions] represent the major cause of irreversible nerve damage. Leprosy serology is known to be influenced by the patient’s bacterial index (BI) with higher positivity in multibacillar
Externí odkaz:
https://doaj.org/article/3e46115665d448beb3e9b391b720474e
Autor:
Talita Alves Teixeira, Fernanda Coelho Barbosa da Cruz Fiori, Marilene Chaves Silvestre, Camilla de Barros Borges, Vanessa Gomes Maciel, Mauricio Barcelos Costa
Publikováno v:
Anais Brasileiros de Dermatologia, Vol 86, Iss 4, Pp 133-136 (2011)
O Pênfigo Foliáceo Endêmico é doença bolhosa autoimune crônica da pele. Geralmente, o tratamento com prednisona tem excelente resposta, mas existem formas refratárias, sendo necessária terapêutica alternativa. Apresentamos paciente adolescen
Externí odkaz:
https://doaj.org/article/b9df96efb62e4cc3893325697e95fb2f
Autor:
Talita Alves, Teixeira, Fernanda Coelho Barbosa da Cruz, Fiori, Marilene Chaves, Silvestre, Camilla de Barros, Borges, Vanessa Gomes, Maciel, Mauricio Barcelos, Costa
Publikováno v:
Anais brasileiros de dermatologia. 86(4 Suppl 1)
Endemic Pemphigus Foliaceous is a chronic autoimmune bullous skin disease. Treatment with prednisone often produces excellent results, but resistant forms exist, requiring alternative therapy. Alternative treatments have been used in cases of cortico
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ff703478a04e3b67ec3bc49dca9b8108
https://pubmed.ncbi.nlm.nih.gov/22068793
https://pubmed.ncbi.nlm.nih.gov/22068793
Autor:
Maurício Barcelos Costa, Emerith Mayra Hungria, Aline Araújo Freitas, Ana Lúcia O M Sousa, Juliano Jampietro, Fernando A Soares, Mariane M A Stefani
Publikováno v:
PLoS ONE, Vol 13, Iss 6, p e0196853 (2018)
Leprosy is a complex chronic, infectious dermato-neurological disease that affects the skin and peripheral nerves especially during immuno-inflammatory episodes known as type 1/T1R and type 2/T2R reactions. This study investigated the in situ express
Externí odkaz:
https://doaj.org/article/e531f6fef3824110b145038d309c3443
Autor:
Gerson Oliveira Penna, Samira Bührer-Sékula, Lígia Regina Sansigolo Kerr, Mariane Martins de Araújo Stefani, Laura Cunha Rodrigues, Marcelo Grossi de Araújo, Andrea Machado Coelho Ramos, Ana Regina Coelho de Andrade, Maurício Barcelos Costa, Patricia Sammarco Rosa, Heitor de Sá Gonçalves, Rossilene Cruz, Maurício Lima Barreto, Maria Araci de Andrade Pontes, Maria Lúcia Fernandes Penna
Publikováno v:
PLoS Neglected Tropical Diseases, Vol 11, Iss 7, p e0005725 (2017)
BACKGROUND:Leprosy control is based on early diagnosis and multidrug therapy. For treatment purposes, leprosy patients can be classified as paucibacillary (PB) or multibacillary (MB), according to the number of skin lesions. Studies regarding a unifo
Externí odkaz:
https://doaj.org/article/340d5cea4d57402682d56d5c94e41c9a
Autor:
Mariane Martins de Araújo Stefani, Adriano Badotti Grassi, Lucas Henrique Sampaio, Ana Lúcia Osório Maroclo de Sousa, Maurício Barcelos Costa, Pauline Scheelbeek, Kapil D Neupane, Deanna A Hagge, Murdo Macdonald, Sang-Nae Cho, Linda Oskam, Samira Bührer-Sékula
Publikováno v:
Memorias do Instituto Oswaldo Cruz, Vol 107, Iss suppl 1, Pp 124-131 (2012)
The diagnosis of leprosy continues to be based on clinical symptoms and early diagnosis and treatment are critical to preventing disability and transmission. Sensitive and specific laboratory tests are not available for diagnosing leprosy. Despite th
Externí odkaz:
https://doaj.org/article/16f7967839fd4d39a230363040613bd5
Autor:
Emerith Mayra Hungria, Regiane Morillas de Oliveira, Ana Lúcia Osório Maroclo de Souza, Maurício Barcelos Costa, Vânia Nieto Brito de Souza, Eliane Aparecida Silva, Fátima Regina Vilani Moreno, Maria Esther Salles Nogueira, Maria Renata Sales Nogueira Costa, Sônia Maria Usó Ruiz Silva, Samira Bührer-Sékula, Steven G Reed, Malcolm S Duthie, Mariane Martins de Araújo Stefani
Publikováno v:
Memorias do Instituto Oswaldo Cruz, Vol 107, Iss suppl 1, Pp 104-111 (2012)
New Mycobacterium leprae protein antigens can contribute to improved serologic tests for leprosy diagnosis/classification and multidrug therapy (MDT) monitoring. This study describes seroreactivity to M. leprae proteins among participants from three
Externí odkaz:
https://doaj.org/article/a7873e878f264884a4c4ca90c60fb87d
Autor:
Lana Bezerra Fernandes, Jackeline Gomes Guerra, Maurício Barcelos Costa, Isadora Guimarães Paiva, Fernanda Paglia Duran, Diogo Neves Jacó
Publikováno v:
Anais Brasileiros de Dermatologia, Vol 86, Iss 4, Pp 78-81 (2011)
A histiocitose de células de Langerhans é representante de um raro grupo de síndromes histiocitárias, sendo caracterizada pela proliferação das células de Langerhans. Suas manifestações variam de lesão solitária a envolvimento multissistê
Externí odkaz:
https://doaj.org/article/1df944f17af1435cacf77c58f9f25346
Autor:
Wanessa Simão Barbosa, Camila Martins Rodarte, Jackeline Gomes Guerra, Vanessa Gomes Maciel, Luiz Fernando Fróes Fleury Júnior, Maurício Barcelos Costa
Publikováno v:
Anais Brasileiros de Dermatologia, Vol 86, Iss 4, Pp 92-95 (2011)
O lúpus eritematoso sistêmico bolhoso é um subtipo raro do lúpus eritematoso sistêmico, que ocorre ainda de forma mais incomum nos pacientes pediátricos. Relatamos o caso de uma adolescente de 12 anos, apresentando lesões vésico-bolhosas em f
Externí odkaz:
https://doaj.org/article/2746289c90e3446fa0866cce4a1dc88d