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APOL1 in an ethnically diverse pediatric population with nephrotic syndrome: implications in focal segmental glomerulosclerosis and other diagnoses.
Watanabe, Andreia; Guaragna, Mara Sanches; Belangero, Vera Maria Santoro; Casimiro, Fernanda Maria Serafim; Pesquero, João Bosco; de Santis Feltran, Luciana; Palma, Lilian Monteiro Pereira; Varela, Patrícia; de Menezes Neves, Precil Diego Miranda; Lerario, Antonio Marcondes; de Souza, Marcela Lopes; de Mello, Maricilda Palandi; de Brito Lutaif, Anna Cristina Gervásio; Ferrari, Cassio Rodrigues; Sampson, Matthew Gordon; Onuchic, Luiz Fernando; Nogueira, Paulo Cesar Koch.
Afiliação
  • Watanabe A; Department of Pediatrics, University of São Paulo School of Medicine, São Paulo, Brazil.
  • Guaragna MS; Division of Molecular Medicine, University of São Paulo School of Medicine, São Paulo, Brazil.
  • Belangero VMS; Center for Molecular Biology and Genetic Engineering, State University of Campinas, Campinas, Brazil.
  • Casimiro FMS; Department of Pediatrics, State University of Campinas, Campinas, Brazil. vmsbelangero@gmail.com.
  • Pesquero JB; Center for Diagnosis and Research on Genetic Diseases, Department of Biophysics, Federal University of São Paulo School of Medicine, São Paulo, Brazil.
  • de Santis Feltran L; Center for Diagnosis and Research on Genetic Diseases, Department of Biophysics, Federal University of São Paulo School of Medicine, São Paulo, Brazil.
  • Palma LMP; Department of Nephrology, Federal University of São Paulo School of Medicine, São Paulo, Brazil.
  • Varela P; Department of Pediatrics, State University of Campinas, Campinas, Brazil.
  • de Menezes Neves PDM; Center for Diagnosis and Research on Genetic Diseases, Department of Biophysics, Federal University of São Paulo School of Medicine, São Paulo, Brazil.
  • Lerario AM; Division of Molecular Medicine, University of São Paulo School of Medicine, São Paulo, Brazil.
  • de Souza ML; Division of Nephrology, University of São Paulo School of Medicine, São Paulo, Brazil.
  • de Mello MP; Division of Endocrinology, University of Michigan, Ann Arbor, MI, USA.
  • de Brito Lutaif ACG; Center for Molecular Biology and Genetic Engineering, State University of Campinas, Campinas, Brazil.
  • Ferrari CR; Center for Molecular Biology and Genetic Engineering, State University of Campinas, Campinas, Brazil.
  • Sampson MG; Department of Pediatrics, State University of Campinas, Campinas, Brazil.
  • Onuchic LF; Department of Pediatrics, State University of Campinas, Campinas, Brazil.
  • Nogueira PCK; Division of Pediatric Nephrology, Boston Children's Hospital, Boston, MA, USA.
Pediatr Nephrol ; 36(8): 2327-2336, 2021 08.
Article em En | MEDLINE | ID: mdl-33585978
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Glomerulosclerose Segmentar e Focal / Insuficiência Renal Crônica / Síndrome Nefrótica Tipo de estudo: Clinical_trials / Diagnostic_studies / Risk_factors_studies Limite: Child / Humans Idioma: En Revista: Pediatr Nephrol Assunto da revista: NEFROLOGIA / PEDIATRIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Brasil
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Glomerulosclerose Segmentar e Focal / Insuficiência Renal Crônica / Síndrome Nefrótica Tipo de estudo: Clinical_trials / Diagnostic_studies / Risk_factors_studies Limite: Child / Humans Idioma: En Revista: Pediatr Nephrol Assunto da revista: NEFROLOGIA / PEDIATRIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Brasil