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Molecular Basis of Factor H R1210C Association with Ocular and Renal Diseases.
Recalde, Sergio; Tortajada, Agustin; Subias, Marta; Anter, Jaouad; Blasco, Miquel; Maranta, Ramona; Coco, Rosa; Pinto, Sheila; Noris, Marina; García-Layana, Alfredo; Rodríguez de Córdoba, Santiago.
Afiliación
  • Recalde S; Department of Ophthalmology, University Clinic of Navarra, Pamplona, Navarra, Spain;
  • Tortajada A; Department of Cellular and Molecular Medicine, Center for Biological Research and Center for Biomedical Network Research on Rare Diseases, Madrid, Spain;
  • Subias M; Department of Cellular and Molecular Medicine, Center for Biological Research and Center for Biomedical Network Research on Rare Diseases, Madrid, Spain;
  • Anter J; Department of Cellular and Molecular Medicine, Center for Biological Research and Center for Biomedical Network Research on Rare Diseases, Madrid, Spain;
  • Blasco M; Nephrology and Kidney Transplant Unit, Hospital Clinic, University of Barcelona, Barcelona, Spain;
  • Maranta R; Mario Negri Institute for Pharmacology Research, Aldo and Cele Daccò Clinical Research Center for Rare Diseases, Ranica, Bergamo, Italy; and.
  • Coco R; Institute of Applied Ophthalmology, University of Valladolid, Valladolid, Spain.
  • Pinto S; Department of Cellular and Molecular Medicine, Center for Biological Research and Center for Biomedical Network Research on Rare Diseases, Madrid, Spain;
  • Noris M; Mario Negri Institute for Pharmacology Research, Aldo and Cele Daccò Clinical Research Center for Rare Diseases, Ranica, Bergamo, Italy; and.
  • García-Layana A; Department of Ophthalmology, University Clinic of Navarra, Pamplona, Navarra, Spain;
  • Rodríguez de Córdoba S; Department of Cellular and Molecular Medicine, Center for Biological Research and Center for Biomedical Network Research on Rare Diseases, Madrid, Spain; srdecordoba@cib.csic.es.
J Am Soc Nephrol ; 27(5): 1305-11, 2016 05.
Article en En | MEDLINE | ID: mdl-26376859
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Complemento C3 / Síndrome Hemolítico Urémico Atípico / Enfermedades Renales / Glomérulos Renales / Degeneración Macular / Mutación Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male / Middle aged Idioma: En Revista: J Am Soc Nephrol Asunto de la revista: NEFROLOGIA Año: 2016 Tipo del documento: Article Pais de publicación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Complemento C3 / Síndrome Hemolítico Urémico Atípico / Enfermedades Renales / Glomérulos Renales / Degeneración Macular / Mutación Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male / Middle aged Idioma: En Revista: J Am Soc Nephrol Asunto de la revista: NEFROLOGIA Año: 2016 Tipo del documento: Article Pais de publicación: Estados Unidos