Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Rafaela Cabral Gonçalves Fabiano"'
Autor:
Sergio Veloso Brant Pinheiro, Raphael Figuiredo Dias, Rafaela Cabral Gonçalves Fabiano, Stanley de Almeida Araujo, Ana Cristina Simões e Silva
Publikováno v:
Brazilian Journal of Nephrology, Iss 0 (2018)
Abstract Involvement of the kidneys by lupus nephritis (LN) is one of the most severe clinical manifestations seen in individuals with systemic lupus erythematosus (SLE). LN is more frequent and severe in pediatric patients and has been associated wi
Externí odkaz:
https://doaj.org/article/1fd78fa070d449e8af74f467fe35a412
Autor:
Roberta Oliveira de Paula e Silva, Rafaela Cabral Gonçalves Fabiano, Moisés Salgado Pedrosa, José Roberto Lambertucci, Luciana Cristina dos Santos Silva
Publikováno v:
Revista da Sociedade Brasileira de Medicina Tropical, Vol 44, Iss 1, Pp 119-121 (2011)
We present the case of a 31-year-old man with acute manifestation of progressive multifocal leukoencephalopathy (PML) as an AIDS-defining disease. The patient presented with a three-day history of neurological disease, brain lesions without mass effe
Externí odkaz:
https://doaj.org/article/f6a856dd15214019a132cdaf471f3861
Autor:
Eduardo Alves Bambirra, Sérgio Veloso Brant Pinheiro, Rafaela Cabral Gonçalves Fabiano, Eduardo A. Oliveira, Stanley de Almeida Araújo, Ana Cristina Simões e Silva
Publikováno v:
Pediatric Nephrology. 32:1211-1220
Data on the risk factors for chronic kidney disease in children with immunoglobulin A nephropathy (IgAN) are scarce. This study was aimed at investigating whether glomerular C4d immunostaining is a prognostic marker in pediatric IgAN. In this retrosp
Autor:
Rafaela Cabral Gonçalves Fabiano, Stanley de Almeida Araújo, Sérgio Veloso Brant Pinheiro, Ana Cristina Simões e Silva
Publikováno v:
Nephrology. 21:995-1002
IgA nephropathy (IgAN) is one of the leading causes of glomerulonephritis characterized by the findings of IgA and IgG immune deposits in the mesangium of kidney biopsies from patients with persistent microscopic haematuria. IgAN is frequently detect
Autor:
Raphael Figuiredo Dias, Ana Cristina Simões e Silva, Sérgio Veloso Brant Pinheiro, Rafaela Cabral Gonçalves Fabiano, Stanley de Almeida Araújo
Publikováno v:
Brazilian Journal of Nephrology, Issue: ahead, Published: 14 NOV 2018
Brazilian Journal of Nephrology, Iss 0 (2018)
Brazilian Journal of Nephrology v.41 n.2 2019
Jornal Brasileiro de Nefrologia
Sociedade Brasileira de Nefrologia (SBN)
instacron:SBN
Brazilian Journal of Nephrology, Volume: 41, Issue: 2, Pages: 252-265, Published: 14 NOV 2018
Brazilian Journal of Nephrology, Iss 0 (2018)
Brazilian Journal of Nephrology v.41 n.2 2019
Jornal Brasileiro de Nefrologia
Sociedade Brasileira de Nefrologia (SBN)
instacron:SBN
Brazilian Journal of Nephrology, Volume: 41, Issue: 2, Pages: 252-265, Published: 14 NOV 2018
Involvement of the kidneys by lupus nephritis (LN) is one of the most severe clinical manifestations seen in individuals with systemic lupus erythematosus (SLE). LN is more frequent and severe in pediatric patients and has been associated with higher
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe341f300dbb3adcb05ab68a31cfdcfa
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002018005041102&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002018005041102&lng=en&tlng=en
Publikováno v:
Inflammation research : official journal of the European Histamine Research Society ... [et al.]. 65(10)
IgA nephropathy is one of the leading causes of primary glomerulonephritis worldwide and an important etiology of renal disease in young adults. IgA nephropathy is considered an immune complex-mediated disease. This review article summarizes recent e
Autor:
Rafaela Cabral Gonçalves Fabiano, Stanley de Almeida Araújo, Eduardo Alves Bambirra, Eduardo Araújo Oliveira, Ana Cristina Simões e Silva, Sérgio Veloso Brant Pinheiro
Publikováno v:
Pediatric Nephrology. 32:1283-1283
Autor:
Luciana Cristina dos Santos Silva, Rafaela Cabral Gonçalves Fabiano, Moisés Salgado Pedrosa, Roberta Oliveira de Paula e Silva, José Roberto Lambertucci
Publikováno v:
Revista da Sociedade Brasileira de Medicina Tropical, Vol 44, Iss 1, Pp 119-121 (2011)
We present the case of a 31-year-old man with acute manifestation of progressive multifocal leukoencephalopathy (PML) as an AIDS-defining disease. The patient presented with a three-day history of neurological disease, brain lesions without mass effe
Autor:
Eduardo A. Oliveira, Eduardo Alves Bambirra, Stanley de Almeida Araújo, Ana Cristina Simões e Silva, Rafaela Cabral Gonçalves Fabiano, Sérgio Veloso Brant Pinheiro
Publikováno v:
Jornal de Pediatria, Vol 93, Iss 4, Pp 389-397
Jornal de Pediatria, Vol 93, Iss 4, Pp 389-397 (2017)
Jornal de Pediatria v.93 n.4 2017
Jornal de Pediatria
Sociedade Brasileira de Pediatria (SBP)
instacron:SBPE
Repositório Institucional da UFOP
Universidade Federal de Ouro Preto (UFOP)
instacron:UFOP
Jornal de Pediatria (Versão em Português), Vol 93, Iss 4, Pp 389-397 (2017)
Jornal de Pediatria, Vol 93, Iss 4, Pp 389-397 (2017)
Jornal de Pediatria v.93 n.4 2017
Jornal de Pediatria
Sociedade Brasileira de Pediatria (SBP)
instacron:SBPE
Repositório Institucional da UFOP
Universidade Federal de Ouro Preto (UFOP)
instacron:UFOP
Jornal de Pediatria (Versão em Português), Vol 93, Iss 4, Pp 389-397 (2017)
Objective: The Oxford Classification for Immunoglobulin A nephropathy (IgAN) identifies pathological variables that may predict the decline of renal function. This study aimed to evaluate the Oxford Classification variables as predictors of renal dys
Publikováno v:
Biblioteca Digital de Teses e Dissertações da UFMGUniversidade Federal de Minas GeraisUFMG.
IgA nephropathy (IgAN) is the most common glomerulonephritis worldwide. IgAN is characterized by a highly variable course ranging from a totally benign condition to end-stage renal disease (ESRD), although a rapidly progressive course in uncommon. As
Externí odkaz:
http://hdl.handle.net/1843/BUBD-9ZPG9U