Publications by authors named "Sheila Pinto"

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The role of the complement system in Shiga toxin-associated hemolytic uremic syndrome.
Victoria Bocanegra, Mariana Luna, Valeria V Costantino, Andrea F Gil Lorenzo, Raul Marino, Sheila Pinto

Pediatr Nephrol· May 2025

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Novel immunochromatographic test for rapid detection of anti-factor H autoantibodies with an assessment of its clinical relevance.
Santiago Rodríguez de Córdoba, Andrea Reparaz, Daniel Sanchez, Sheila Pinto, Lucia Juana Lopez

Front Immunol· May 2025

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Statistical Validation of Rare Complement Variants Provides Insights into the Molecular Basis of Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy.
Amy J Osborne, Matteo Breno, Nicolo Ghiringhelli Borsa, Fengxiao Bu, Véronique Frémeaux-Bacchi, Sheila Pinto

J Immunol· April 2018

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Elevated factor H-related protein 1 and factor H pathogenic variants decrease complement regulation in IgA nephropathy.
Agustín Tortajada, Eduardo Gutiérrez, Elena Goicoechea de Jorge, Jaouad Anter, Alfons Segarra, Sheila Pinto

Kidney Int· October 2017

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Molecular Basis of Factor H R1210C Association with Ocular and Renal Diseases.
Sergio Recalde, Agustin Tortajada, Marta Subias, Jaouad Anter, Miquel Blasco, Sheila Pinto

J Am Soc Nephrol· May 2016

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Complement factor H, FHR-3 and FHR-1 variants associate in an extended haplotype conferring increased risk of atypical hemolytic uremic syndrome.
Maria E Bernabéu-Herrero, Miguel Jiménez-Alcázar, Jaouad Anter, Sheila Pinto, Daniel Sánchez Chinchilla

Mol Immunol· October 2015

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The molecular and structural bases for the association of complement C3 mutations with atypical hemolytic uremic syndrome.
Rubén Martínez-Barricarte, Meike Heurich, Andrés López-Perrote, Agustin Tortajada, Sheila Pinto

Mol Immunol· August 2015

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Case report: lupus nephritis with autoantibodies to complement alternative pathway proteins and C3 gene mutation.
Pilar Nozal, Sofía Garrido, Jorge Martínez-Ara, María Luz Picazo, Laura Yébenes, Sheila Pinto

BMC Nephrol· March 2015

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Complement mutations in diacylglycerol kinase-ε-associated atypical hemolytic uremic syndrome.
Daniel Sánchez Chinchilla, Sheila Pinto, Bernd Hoppe, Marta Adragna, Laura Lopez

Clin J Am Soc Nephrol· September 2014

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Genetics of atypical hemolytic uremic syndrome (aHUS).
Santiago Rodríguez de Córdoba, Marta Subías Hidalgo, Sheila Pinto, Agustín Tortajada

Semin Thromb Hemost· June 2014

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Eculizumab long-term therapy for pediatric renal transplant in aHUS with CFH/CFHR1 hybrid gene.
Elena Román-Ortiz, Santiago Mendizabal Oteiza, Sheila Pinto, Margarita López-Trascasa, Pilar Sánchez-Corral

Pediatr Nephrol· January 2014

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Combined complement gene mutations in atypical hemolytic uremic syndrome influence clinical phenotype.
Elena Bresin, Erica Rurali, Jessica Caprioli, Pilar Sanchez-Corral, Veronique Fremeaux-Bacchi, Sheila Pinto

J Am Soc Nephrol· February 2013

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Complement factor H variants I890 and L1007 while commonly associated with atypical hemolytic uremic syndrome are polymorphisms with no functional significance.
Agustín Tortajada, Sheila Pinto, Jorge Martínez-Ara, Margarita López-Trascasa, Pilar Sánchez-Corral

Kidney Int· January 2012

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Human C3 mutation reveals a mechanism of dense deposit disease pathogenesis and provides insights into complement activation and regulation.
Rubén Martínez-Barricarte, Meike Heurich, Francisco Valdes-Cañedo, Eduardo Vazquez-Martul, Eva Torreira, Sheila Pinto

J Clin Invest· October 2010

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Changes in NPY and POMC, but not serotonin transporter, following a restricted feeding/repletion protocol in rats.
Nuria Lauzurica, Luis García-García, Sheila Pinto, José A Fuentes, Mercedes Delgado

Brain Res· February 2010

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Influence of environmental variables on the shrub and tree species distribution in two Semideciduous Forest sites in Viçosa, Minas Gerais, Brazil.
Sheila Isabel do C Pinto, Sebastião V Martins, Nairam F de Barros, Herly Carlos T Dias, Sustanis H Kunz

Rev Biol Trop· September 2008

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