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Non-lupus full-house nephropathy-immune dysregulation as a rare cause of pediatric nephrotic syndrome: Answers.
Horváth, Orsolya; Reusz, György S; Goda, Veronika; Kelen, Kata; Balogh, István; Kardos, Magdolna; Kállay, Krisztián; Cseh, Áron; Szabó, Attila J; Kriván, Gergely.
Afiliación
  • Horváth O; 1St Department of Pediatrics, Semmelweis University, 53-54 Bókay János Street, Budapest, 1083, Hungary.
  • Reusz GS; Pediatric Hematology and Stem Cell Transplantation Unit, Central Hospital of Southern Pest, National Institute of Hematology and Infectious Diseases, Budapest, Hungary.
  • Goda V; 1St Department of Pediatrics, Semmelweis University, 53-54 Bókay János Street, Budapest, 1083, Hungary. reusz.gyorgy@med.semmelweis-univ.hu.
  • Kelen K; Pediatric Hematology and Stem Cell Transplantation Unit, Central Hospital of Southern Pest, National Institute of Hematology and Infectious Diseases, Budapest, Hungary.
  • Balogh I; 1St Department of Pediatrics, Semmelweis University, 53-54 Bókay János Street, Budapest, 1083, Hungary.
  • Kardos M; Department of Laboratory Medicine, Division of Clinical Genetics, Department of Human Genetics, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
  • Kállay K; 2Nd Department of Pathology, Semmelweis University, Budapest, Hungary.
  • Cseh Á; Pediatric Hematology and Stem Cell Transplantation Unit, Central Hospital of Southern Pest, National Institute of Hematology and Infectious Diseases, Budapest, Hungary.
  • Szabó AJ; 1St Department of Pediatrics, Semmelweis University, 53-54 Bókay János Street, Budapest, 1083, Hungary.
  • Kriván G; 1St Department of Pediatrics, Semmelweis University, 53-54 Bókay János Street, Budapest, 1083, Hungary.
Pediatr Nephrol ; 37(5): 1053-1056, 2022 05.
Article en En | MEDLINE | ID: mdl-34919150
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedades Genéticas Ligadas al Cromosoma X / Diabetes Mellitus Tipo 1 / Enfermedades del Sistema Inmune / Síndrome Nefrótico Tipo de estudio: Diagnostic_studies / Etiology_studies Límite: Child / Female / Humans / Male Idioma: En Revista: Pediatr Nephrol Asunto de la revista: NEFROLOGIA / PEDIATRIA Año: 2022 Tipo del documento: Article País de afiliación: Hungria
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedades Genéticas Ligadas al Cromosoma X / Diabetes Mellitus Tipo 1 / Enfermedades del Sistema Inmune / Síndrome Nefrótico Tipo de estudio: Diagnostic_studies / Etiology_studies Límite: Child / Female / Humans / Male Idioma: En Revista: Pediatr Nephrol Asunto de la revista: NEFROLOGIA / PEDIATRIA Año: 2022 Tipo del documento: Article País de afiliación: Hungria