Full-house nephropathy associated with high expression of SPATA5L1 due to a genetic pathogenic variant.

de Carvalho, Luciana Martins; de Sousa, Graziella Ribeiro; Moura, Ronald; Saggioro, Fabiano; Facincani, Inalda; Costa, Roberto; Kahwage, Paola Pinheiro; Gomes de Paula Queiroz, Rosane; Valera, Elvis Terci; Crovella, Sergio; Sandrin-Garcia, Paula

de Carvalho, Luciana Martins; de Sousa, Graziella Ribeiro; Moura, Ronald; Saggioro, Fabiano; Facincani, Inalda; Costa, Roberto; Kahwage, Paola Pinheiro; Gomes de Paula Queiroz, Rosane; Valera, Elvis Terci; Crovella, Sergio; Sandrin-Garcia, Paula.

Afiliação

de Carvalho LM; Department of Pediatrics.
de Sousa GR; Division of Pediatric Rheumatology.
Moura R; Department of Genetics, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, Brazil.
Saggioro F; Department of Advanced Diagnostics, Institute for Maternal and Child Health-IRCCS "Burlo Garofolo", Trieste, Italy.
Facincani I; Department of Pathology, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto.
Costa R; Department of Pathology, Rede D'Or, São Paulo, SP.
Kahwage PP; Department of Pediatrics.
Gomes de Paula Queiroz R; Department of Medicine, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, Brazil.
Valera ET; Department of Pediatrics.
Crovella S; Division of Pediatric Rheumatology.
Sandrin-Garcia P; Department of Pediatrics.

Rheumatology (Oxford) ; 61(4): e84-e86, 2022 04 11.

Article em En | MEDLINE | ID: mdl-34864870

Assuntos

Nefropatias; Nefrite Lúpica; Humanos; Nefrite Lúpica/patologia

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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Nefrite Lúpica / Nefropatias Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: Rheumatology (Oxford) Assunto da revista: REUMATOLOGIA Ano de publicação: 2022 Tipo de documento: Article

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