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Thrombotic Microangiopathy in Inverted Formin 2-Mediated Renal Disease.
Challis, Rachel C; Ring, Troels; Xu, Yaobo; Wong, Edwin K S; Flossmann, Oliver; Roberts, Ian S D; Ahmed, Saeed; Wetherall, Michael; Salkus, Giedrius; Brocklebank, Vicky; Fester, Julian; Strain, Lisa; Wilson, Valerie; Wood, Katrina M; Marchbank, Kevin J; Santibanez-Koref, Mauro; Goodship, Timothy H J; Kavanagh, David.
Afiliación
  • Challis RC; National Renal Complement Therapeutics Centre, Institutes of *Genetic Medicine and.
  • Ring T; Department of Nephrology, Aalborg University Hospital and.
  • Xu Y; National Renal Complement Therapeutics Centre, Institutes of *Genetic Medicine and.
  • Wong EK; National Renal Complement Therapeutics Centre, Institutes of *Genetic Medicine and.
  • Flossmann O; Renal Unit, Royal Berkshire Hospital, Reading, United Kingdom.
  • Roberts IS; Department of Cellular Pathology, Oxford University Hospitals National Health Service Trust, Oxford, United Kingdom.
  • Ahmed S; Department of Nephrology, City Hospitals Sunderland National Health Service Foundation Trust, Sunderland, United Kingdom.
  • Wetherall M; Department of Pathology, Gateshead Health National Health Service Foundation Trust, Gateshead, United Kingdom.
  • Salkus G; Department of Pathology, Aalborg University Hospital, Aalborg, Denmark.
  • Brocklebank V; National Renal Complement Therapeutics Centre, Institutes of *Genetic Medicine and.
  • Fester J; Egton Surgery, Whitby, United Kingdom; and.
  • Strain L; National Renal Complement Therapeutics Centre, Northern Molecular Genetics Service and.
  • Wilson V; National Renal Complement Therapeutics Centre, Northern Molecular Genetics Service and.
  • Wood KM; Department of Cellular Pathology, Newcastle upon Tyne Hospitals National Health Service Foundation Trust, Newcastle upon Tyne, United Kingdom.
  • Marchbank KJ; Cellular Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.
  • Santibanez-Koref M; National Renal Complement Therapeutics Centre, Institutes of *Genetic Medicine and.
  • Goodship TH; National Renal Complement Therapeutics Centre, Institutes of *Genetic Medicine and.
  • Kavanagh D; National Renal Complement Therapeutics Centre, Institutes of *Genetic Medicine and david.kavanagh@ncl.ac.uk.
J Am Soc Nephrol ; 28(4): 1084-1091, 2017 Apr.
Article en En | MEDLINE | ID: mdl-27974406
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Microangiopatías Trombóticas / Síndrome Hemolítico Urémico Atípico / Proteínas de Microfilamentos / Mutación Límite: Adolescent / Child / Female / Humans Idioma: En Revista: J Am Soc Nephrol Asunto de la revista: NEFROLOGIA Año: 2017 Tipo del documento: Article
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Microangiopatías Trombóticas / Síndrome Hemolítico Urémico Atípico / Proteínas de Microfilamentos / Mutación Límite: Adolescent / Child / Female / Humans Idioma: En Revista: J Am Soc Nephrol Asunto de la revista: NEFROLOGIA Año: 2017 Tipo del documento: Article