Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Fabiano Bichuette Custodio"'
Publikováno v:
Brazilian Journal of Nephrology, Vol 35, Iss 2, Pp 142-146 (2013)
Cerca de 10% dos pacientes em unidade de terapia intensiva que desenvolvem injúria renal aguda irão depender de terapia renal substitutiva. Embora não existam dados que comprovem redução da mortalidade, quando comparadas às terapias intermitent
Externí odkaz:
https://doaj.org/article/b86431baed7c4927877307ddf93fe7e3
Publikováno v:
Atualizações em Nefropatologia ISBN: 9786584626003
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a872430c4e7bc296750214c98b36d56
https://doi.org/10.53924/nefropat.06
https://doi.org/10.53924/nefropat.06
Autor:
Maria Luíza Gonçalves dos Reis Monteiro, Fabiano Bichuette Custódio, Precil Diego Miranda de Menezes Neves, Frederico Moraes Ferreira, Elieser Hitoshi Watanabe, Antônio Marcondes Lerário, Liliane Silvano de Araújo, Bruno Eduardo Pedroso Balbo, Vívian Christine Dourado Pinto, Lívia Maria Gruli Barbosa, Vilmar de Paiva Marques, Juliana Reis Machado, Marlene Antônia Reis, Luiz Fernando Onuchic
Publikováno v:
BMC Nephrology, Vol 20, Iss 1, Pp 1-6 (2019)
Abstract Background Glomerulopathy with fibronectin deposits is an autosomal dominant disease associated with proteinuria, hematuria, hypertension and renal function decline. Forty percent of the cases are caused by mutations in FN1, the gene that en
Externí odkaz:
https://doaj.org/article/0424c73a2b9441a887536f839ea624cd
Autor:
Precil Diego Miranda de Menezes Neves, Juliana Reis Machado, Fabiano Bichuette Custódio, Maria Luíza Gonçalves dos Reis Monteiro, Shigueo Iwamoto, Marlene Freire, Marisa França Ferreira, Marlene Antônia dos Reis
Publikováno v:
BMC Nephrology, Vol 18, Iss 1, Pp 1-7 (2017)
Abstract Background Fabry Disease (FD) is a genetic disorder caused by alpha-galactosidase A deficiency. Certain drugs, such as hydroxychloroquine, can produce renal deposits that mimic morphological findings seen in FD, characterizing a type of drug
Externí odkaz:
https://doaj.org/article/d3c4d5c55aba43c7ada96cc6dc729fbb
Autor:
Crislaine Aparecida da Silva, Fabiano Bichuette Custódio, Maria Luíza Gonçalves dos Reis Monteiro, Stanley de Almeida Araújo, Liliane Silvano Araújo, Rosana Rosa Miranda Côrrea, Marlene Antônia dos Reis, Juliana Reis Machado
Publikováno v:
Brazilian Journal of Nephrology, Iss 0 (2019)
Abstract Introduction: Some cases of membranous nephropathy (MGN) present focal segmental glomerulosclerosis (FSGS) typically associated with disease progression. However, we report a case of a patient who seemed to have MGN and FSGS, both primary. C
Externí odkaz:
https://doaj.org/article/2d32e47d1f5545df8e541bd844fbb777
Autor:
Lethícia Borges Oliveira, Eliangela de Castro Cobo, Juliana Reis Machado, Fabiano Bichuette Custódio, Marcos Vinícius da Silva, Flávia Aparecida de Oliveira, Rosana Rosa Miranda Correa, Marlene Antônia dos Reis
Publikováno v:
Brazilian Journal of Nephrology, Vol 37, Iss 2, Pp 166-170 (2015)
Resumo Introdução: Atualmente, a população idosa do Brasil está sofrendo aumento significativo. O envelhecimento é um processo fisiológico que causa alterações nos diversos órgãos, inclusive no rim. A biópsia renal é de suma importância
Externí odkaz:
https://doaj.org/article/d27acdb460324b349f3af345865c186a
Autor:
Fabiano Bichuette Custódio, Crislaine Aparecida da Silva, Fernanda Rodrigues Helmo, Juliana Reis Machado, Marlene Antônia dos Reis
Publikováno v:
Brazilian Journal of Nephrology, Vol 39, Iss 4, Pp 370-375
Abstract Introduction: Membranous nephropathy (MN) is one of the major causes of nephrotic syndrome. The complement system plays a key role in the pathophysiology of MN. Objectives: To identify the complement pathway possibly activated in MN cases an
Externí odkaz:
https://doaj.org/article/5ad206d995f7493aaabe8d77b5f4b18a