Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Antonia Peña - Carrión"'
Autor:
Johnson S, Stojanovic J, Ariceta G, Bitzan M, Besbas N, Frieling M, Karpman D, Landau D, Langman C, Licht C, Pecoraro C, Riedl M, Siomou E, van de Kar N Walle JV, Loirat C, Taylor CM, Anne-Laure Adra, Klaus Arbeiter, Yelda Bilginer, Heiko Billing, Maria Bitsori, Bernard Boudailliez, Francisco de la Cerda – Ojeda, Gérard Champion, Amit Dagan, Bradley Dixon, Philippe Eckart, Israel Eisenstein, Arnaud Garnier, Clara Gomes, Karsten Häffner, Jerome Harambat, Carol Inward, Rafael Krmar, Theresa Kwon, Anne-Laure Lapeyraque, Sebastian Loos, Meeta Malik, Mignon McCulloch, David Milford, Danko Milosevic, Carla Nester, François Nobili, Pedro J Ortega, Fotios Papachristou, Antonia Peña - Carrión, Ludmila Podracká, Nikoleta Printza, Bruno Ranchin, Christopher Reid, Caroline Rousset-Rouvière, Rémi Salomon, Anne-Laure Sellier-Leclerc, James Springate, Sophie Taque, Despoina Tramma, Sibylle Tschumi, Ulrike Walden, Kay Tyerman, Aoife Waters, Donald J Weaver Jr
Publikováno v:
Pediatric Nephrology, 29, 10, pp. 1967-78
Pediatric Nephrology, 29, 1967-78
Pediatric Nephrology, 29, 1967-78
Item does not contain fulltext BACKGROUND: In 2009, the European Paediatric Study Group for Haemolytic Uraemic Syndrome (HUS) published a clinical practice guideline for the investigation and initial therapy of diarrhea-negative HUS (now more widely
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7cfc2ff06baa3cd6fd37ac75199a0be
https://hdl.handle.net/2066/138690
https://hdl.handle.net/2066/138690
Autor:
Santiago Rodríguez de Córdoba, Antonia Peña-Carrión, Margarita López-Trascasa, Elena Goicoechea de Jorge, Marta Melgosa, Cynthia Abarrategui-Garrido, Pilar Sánchez-Corral
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
10 páginas, 5 figuras, 1 tabla -- PAGS nros. 171-180
Atypical hemolytic uremic syndrome is associated with mutations in the complement proteins factor H, factor I, factor B, C3, or membrane cofactor protein in about 50% of patients. The evoluti
Atypical hemolytic uremic syndrome is associated with mutations in the complement proteins factor H, factor I, factor B, C3, or membrane cofactor protein in about 50% of patients. The evoluti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc255df8d3d2d763045f86a6a88477f1
http://hdl.handle.net/10261/56597
http://hdl.handle.net/10261/56597