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A mutation in the SAA1 promoter causes hereditary amyloid A amyloidosis.
Sikora, Jakub; Kmochová, Tereza; Musálková, Dita; Pohludka, Michal; Prikryl, Petr; Hartmannová, Hana; Hodanová, Katerina; Treslová, Helena; Nosková, Lenka; Mrázová, Lenka; Stránecký, Viktor; Lunová, Mariia; Jirsa, Milan; Honsová, Eva; Dasari, Surendra; McPhail, Ellen D; Leung, Nelson; Zivná, Martina; Bleyer, Anthony J; Rychlík, Ivan; Rysavá, Romana; Kmoch, Stanislav.
Afiliación
  • Sikora J; Research Unit for Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General Teaching Hospital in Prague, Prague, Czech Republic; Institute of Pathology, First Faculty of Medicine, Charles University in Prague and G
  • Kmochová T; Research Unit for Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General Teaching Hospital in Prague, Prague, Czech Republic.
  • Musálková D; Research Unit for Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General Teaching Hospital in Prague, Prague, Czech Republic.
  • Pohludka M; Research Unit for Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General Teaching Hospital in Prague, Prague, Czech Republic.
  • Prikryl P; Institute of Pathological Physiology, First Faculty of Medicine, Charles University in Prague, Prague, Czech Republic.
  • Hartmannová H; Research Unit for Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General Teaching Hospital in Prague, Prague, Czech Republic.
  • Hodanová K; Research Unit for Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General Teaching Hospital in Prague, Prague, Czech Republic.
  • Treslová H; Research Unit for Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General Teaching Hospital in Prague, Prague, Czech Republic.
  • Nosková L; Research Unit for Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General Teaching Hospital in Prague, Prague, Czech Republic.
  • Mrázová L; Research Unit for Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General Teaching Hospital in Prague, Prague, Czech Republic.
  • Stránecký V; Research Unit for Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General Teaching Hospital in Prague, Prague, Czech Republic.
  • Lunová M; Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
  • Jirsa M; Institute for Clinical and Experimental Medicine, Prague, Czech Republic; Institute of Clinical Biochemistry and Laboratory Diagnostics, First Faculty of Medicine, Charles University in Prague, Prague, Czech Republic.
  • Honsová E; Institute of Pathology, First Faculty of Medicine, Charles University in Prague and General Teaching Hospital in Prague, Prague, Czech Republic; AeskuLab Pathology, Prague, Czech Republic.
  • Dasari S; Department of Quantitative Health Sciences, Mayo Clinic, Rochester, Minnesota, USA.
  • McPhail ED; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.
  • Leung N; Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.
  • Zivná M; Research Unit for Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General Teaching Hospital in Prague, Prague, Czech Republic.
  • Bleyer AJ; Research Unit for Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General Teaching Hospital in Prague, Prague, Czech Republic; Section on Nephrology, Wake Forest School of Medicine, Winston-Salem, North Carolina,
  • Rychlík I; Department of Medicine, Third Faculty of Medicine, Charles University in Prague and Faculty Hospital Kralovske Vinohrady, Prague, Czech Republic.
  • Rysavá R; Department of Nephrology, First Faculty of Medicine, Charles University in Prague and General Teaching Hospital in Prague, Prague, Czech Republic. Electronic address: Romana.Rysava@vfn.cz.
  • Kmoch S; Research Unit for Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General Teaching Hospital in Prague, Prague, Czech Republic; Section on Nephrology, Wake Forest School of Medicine, Winston-Salem, North Carolina,
Kidney Int ; 101(2): 349-359, 2022 02.
Article en En | MEDLINE | ID: mdl-34560138
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Amiloidosis Tipo de estudio: Etiology_studies Límite: Humans Idioma: En Revista: Kidney Int Año: 2022 Tipo del documento: Article Pais de publicación: Estados Unidos
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Amiloidosis Tipo de estudio: Etiology_studies Límite: Humans Idioma: En Revista: Kidney Int Año: 2022 Tipo del documento: Article Pais de publicación: Estados Unidos