Integration of Genetic Testing and Pathology for the Diagnosis of Adults with FSGS.

Yao, Tony; Udwan, Khalil; John, Rohan; Rana, Akanchaya; Haghighi, Amirreza; Xu, Lizhen; Hack, Saidah; Reich, Heather N; Hladunewich, Michelle Adrienne; Cattran, Daniel C; Paterson, Andrew D; Pei, York; Barua, Moumita

Yao, Tony; Udwan, Khalil; John, Rohan; Rana, Akanchaya; Haghighi, Amirreza; Xu, Lizhen; Hack, Saidah; Reich, Heather N; Hladunewich, Michelle Adrienne; Cattran, Daniel C; Paterson, Andrew D; Pei, York; Barua, Moumita.

Afiliação

Yao T; Division of Nephrology and.
Udwan K; Toronto General Hospital Research Institute, Toronto General Hospital, Toronto, Canada.
John R; Division of Nephrology and.
Rana A; Toronto General Hospital Research Institute, Toronto General Hospital, Toronto, Canada.
Haghighi A; Department of Pathology, University Health Network, Toronto, Canada.
Xu L; Division of Nephrology and.
Hack S; Toronto General Hospital Research Institute, Toronto General Hospital, Toronto, Canada.
Reich HN; Institute of Medical Sciences.
Hladunewich MA; Division of Nephrology and.
Cattran DC; The Centre for Applied Genomics and.
Paterson AD; Division of Nephrology and.
Pei Y; Toronto General Hospital Research Institute, Toronto General Hospital, Toronto, Canada.
Barua M; Division of Nephrology and.

Clin J Am Soc Nephrol ; 14(2): 213-223, 2019 02 07.

Article em En | MEDLINE | ID: mdl-30647093

Assuntos

Membrana Basal Glomerular/patologia; Glomerulosclerose Segmentar e Focal/genética; Glomerulosclerose Segmentar e Focal/patologia; Falência Renal Crônica/etiologia; Adolescente; Adulto; Autoantígenos/genética; Colágeno Tipo IV/genética; Anormalidades Congênitas/genética; Feminino; Testes Genéticos; Glomerulosclerose Segmentar e Focal/diagnóstico; Humanos; Masculino; Pessoa de Meia-Idade; Podócitos; Taxa de Sobrevida; Sistema Urinário/anormalidades; Sequenciamento do Exoma; Adulto Jovem

Palavras-chave

Cohort Studies; FSGS; Genetic Testing; Glomerular Basement Membrane; Kidney Failure, Chronic; Podocytes; Registries; Renal Insufficiency; Urogenital Abnormalities; Whole Exome Sequencing; glomerulonephritis; human genetics; idiopathic nephrotic syndrome; kidney; nephrotic syndrome; renal development; type 4A collagen; vesico-ureteral reflux

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Glomerulosclerose Segmentar e Focal / Membrana Basal Glomerular / Falência Renal Crônica Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Clin J Am Soc Nephrol Assunto da revista: NEFROLOGIA Ano de publicação: 2019 Tipo de documento: Article País de publicação: Estados Unidos

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