Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Rafaela B Pinheiro"'
Autor:
Precil D Neves, Ramaiane A Bridi, Janaína A Ramalho, Lectícia B Jorge, Elieser H Watanabe, Andreia Watanabe, Luis Yu, Viktoria Woronik, Rafaela B Pinheiro, Leonardo A Testagrossa, Lívia B Cavalcante, Denise M Malheiros, Cristiane B Dias, Luiz F Onuchic
Publikováno v:
PLoS Neglected Tropical Diseases, Vol 14, Iss 10, p e0008582 (2020)
BackgroundSchistosoma mansoni schistosomiasis (SM) remains a public health problem in Brazil. Renal involvement is classically manifested as a glomerulopathy, most often membranoproliferative glomerulonephritis or focal and segmental glomeruloscleros
Externí odkaz:
https://doaj.org/article/b3da16565a04432f9badbda9d9798932
Autor:
Precil Diego Miranda de Menezes Neves, Rafael A Souza, Fábio M Torres, Fábio A Reis, Rafaela B Pinheiro, Cristiane B Dias, Luis Yu, Viktoria Woronik, Luzia S Furukawa, Lívia B Cavalcante, Stanley de Almeida Araújo, David Campos Wanderley, Denise M Malheiros, Lectícia B Jorge
Publikováno v:
PLoS ONE, Vol 15, Iss 11, p e0233199 (2020)
IntroductionIgA nephropathy (IgAN) is the most common primary glomerulopathy worldwide. According to the Oxford Classification, changes in the kidney vascular compartment are not related with worse outcomes. This paper aims to assess the impact of th
Externí odkaz:
https://doaj.org/article/837d490d3d794ed8a0a32ae8a08159eb
Autor:
Denise Maria Avancini Costa Malheiros, Bernardo Vergara Reichert, Rafaela B. Pinheiro, Cristiane Bitencourt Dias, Precil Diego Miranda de Menezes Neves, Viktoria Woronik, Leonardo de Abreu Testagrossa, Luis Yu, Lectícia Barbosa Jorge, Lívia Barreira Cavalcante, Ramaiane A. Bridi
Publikováno v:
BMC Nephrology, Vol 21, Iss 1, Pp 1-6 (2020)
BMC Nephrology
BMC Nephrology
Background Sickle cell disease (SCD) is a highly prevalent genetic disease worldwide. In the natural evolution of SCD, glomerular lesions can develop, presenting histopathological patterns of segmental or focal membranoproliferative glomerulosclerosi
Autor:
Luzia S. Furukawa, Fábio Augusto Gomes Vieira Reis, Lectícia Barbosa Jorge, Viktoria Woronik, Luis Yu, Rafaela B. Pinheiro, Rafael de Abreu e Souza, Fábio M. Torres, Denise Maria Avancini Costa Malheiros, Precil Diego Miranda de Menezes Neves, Cristiane B. Dias, Lívia Barreira Cavalcante
IntroductionIgA nephropathy (IgAN) is the most common primary glomerulopathy worldwide. According to the Oxford Classification, changes in the kidney vascular compartment are not related with worse outcomes. This paper aims to assess the impact of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8851cdb48f9d664db03d1fd42db830e8
https://doi.org/10.1101/2020.05.01.072074
https://doi.org/10.1101/2020.05.01.072074
Autor:
Lectícia Barbosa Jorge, Lívia Barreira Cavalcante, Luzia S. Furukawa, Luis Yu, Fábio Augusto Gomes Vieira Reis, Rafaela B. Pinheiro, Fábio M. Torres, Rafael de Abreu e Souza, Viktoria Woronik, David Campos Wanderley, Precil Diego Miranda de Menezes Neves, Denise Maria Avancini Costa Malheiros, Stanley de Almeida Araújo, Cristiane B. Dias
Publikováno v:
PLoS ONE, Vol 15, Iss 11, p e0233199 (2020)
PLoS ONE
PLoS ONE
IntroductionIgA nephropathy (IgAN) is the most common primary glomerulopathy worldwide. According to the Oxford Classification, changes in the kidney vascular compartment are not related with worse outcomes. This paper aims to assess the impact of th
Autor:
Luiz F. Onuchic, Lectícia Barbosa Jorge, Cristiane B. Dias, Luis Yu, Elieser H. Watanabe, Rafaela B. Pinheiro, Viktoria Woronik, Lívia Barreira Cavalcante, Ramaiane A. Bridi, Denise Maria Avancini Costa Malheiros, Andreia Watanabe, Leonardo de Abreu Testagrossa, Janaina Ramalho, Precil Diego Miranda de Menezes Neves
Publikováno v:
PLoS Neglected Tropical Diseases
PLoS Neglected Tropical Diseases, Vol 14, Iss 10, p e0008582 (2020)
PLoS Neglected Tropical Diseases, Vol 14, Iss 10, p e0008582 (2020)
Background Schistosoma mansoni schistosomiasis (SM) remains a public health problem in Brazil. Renal involvement is classically manifested as a glomerulopathy, most often membranoproliferative glomerulonephritis or focal and segmental glomerulosclero
Autor:
Rafael Futoshi Mizutani, Rafaela B. Pinheiro, Ubiratan de Paula Santos, Fernanda Coccolin, Cristiane B. Dias, Mario Terra-Filho, Fernando Augusto Soares, Marcos Roberto Vieira Garcia
Publikováno v:
Occupational and Environmental Health.
Introduction: there is evidence linking silicosis and autoimmune diseases, such as systemic lupus erythematosus, systemic sclerosis, and rheumatoid arthritis. More recently, there are some reports and studies associating chronic kidney disease and si
Autor:
Bruno Eduardo Pedroso Balbo, Viktoria Woronik, Luiz F. Onuchic, Luis Yu, Leonardo de Abreu Testagrossa, Rafaela B. Pinheiro, Lectícia Barbosa Jorge, Antonio M. Lerario, Precil Diego Miranda de Menezes Neves, Cristiane B. Dias, Denise Maria Avancini Costa Malheiros, Mariana Pigozzi Veloso
Publikováno v:
Nephron. 136(2)
Alport syndrome (AS) is a disorder of collagen IV, a component of glomerular basement membrane (GBM). The association of AS and immunocomplex nephropathies is uncommon. This is a case of a 37-year-old woman with family history of X-linked AS, includi