Margarita López-Trascasa

Papers authored by Margarita López-Trascasa

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2015 Pilar Nozal, Sofía Garrido, Jorge Martínez-Ara, María Luz Picazo, Laura Yébenes, Rita Álvarez-Doforno, Sheila Pinto, Santiago Rodríguez de Córdoba, Margarita López-Trascasa

, Margarita López Trascasa

Case report: lupus nephritis with autoantibodies to complement alternative pathway proteins and C3 gene mutation

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C. Gomez Traseira, E. Perez Fernandez, López Serrano Mc, M. C. García-Ara, García Ara Mc, M. Pedrosa, M. López Trascasa

, M. López-Trascasa, T. Caballero

Clinical Pattern and Acute and Long-term Management of Hereditary Angioedema Due to C1-Esterase Inhibitor Deficiency

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This paper was not found in any repository; the policy of its publisher is unknown or unclear.

M. Bravo García Morato, B. Padilla Merlano, P. Nozal, M. Espiño, C. Juárez, Villar Lm, M. López Trascasa

, En Nombre del grupo de Inmunoquímica de la Sociedad Española de Inmunología

Laboratory guidelines for the diagnosis and follow-up of patients with monoclonal gammopathies.

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2014 D. Charignon, A. Ghannam, F. Defendi, D. Ponard, N. Monnier, M. López Trascasa

, D. Launay, T. Caballero, K. Djenouhat, O. Fain, S. Cichon, L. Martin, C. Drouet

Hereditary angioedema withF12mutation: factors modifying the clinical phenotype

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Daniel Sánchez Chinchilla, Sheila Pinto, Bernd Hoppe, Marta Adragna, Laura Lopez, Maria Luisa Justa Roldan, Antonia Peña, Margarita Lopez Trascasa

, Pilar Sánchez-Corral, Santiago Rodríguez de Córdoba

Complement Mutations in Diacylglycerol Kinase-ε–Associated Atypical Hemolytic Uremic Syndrome

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Alberto López-Lera, Inmaculada Ibanez de Caceres, Olga Pernia, Margarita López-Trascasa

, Inmaculada Ibanez de Caceres

Expression of the SERPING1 gene is not regulated by promoter hypermethylation in peripheral blood mononuclear cells from patients with hereditary angioedema due to C1-inhibitor deficiency

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Ana Sánchez-Moreno, Santiago Rodríguez de Córdoba, Francisco De la Cerda, Rocío Cabrera, Julia Fijo, Margarita López-Trascasa

, Rafael Bedoya, Santiago Rodríguez de Córdoba

, Patricia Ybot-González

Eculizumab in dense-deposit disease after renal transplantation

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Mihály Józsi, Stefanie Reuter, Pilar Nozal, Margarita Lopez-Trascasa

, Pilar Sanchez-Corral, Zoltán Prohászka, Barbara Uzonyi

Autoantibodies to complement components in C3 glomerulopathy and atypical hemolytic uremic syndrome.

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A. M. Blom, E. B. Volokhina

, V. Fransson, P. Stromberg, L. Berghard, M. Viktorelius, T. E. Mollnes, M. Lopez-Trascasa

, L. P. van den Heuvel, B. van den Heuvel, T. H. Goodship, K. J. Marchbank

, M. Okroj

A novel method for direct measurement of complement convertases activity in human serum

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2013 Pilar Nozal, Santiago Rodríguez de Córdoba, Sofía Garrido, María Alba-Domínguez, Laura Espinosa, Antonia Peña, Santiago Rodríguez de Córdoba, Pilar Sánchez-Corral, Margarita López -Trascasa, Margarita López-Trascasa

An ELISA assay with two monoclonal antibodies allows the estimation of free factor H and identifies patients with acquired deficiency of this complement regulator

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López-Lera Alberto, Juan M. Torres-Canizales, Torres-Canizalesjuan Manuel, Sofía Garrido, Adelaida Morales, Margarita López-Trascasa

Rothmund–Thomson Syndrome and Glomerulonephritis in a Homozygous C1q-Deficient Patient Due to a Gly164Ser C1qC Mutation

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Carmen Gómez-Traseira, Alberto López-Lera, Christian Drouet, Margarita López-Trascasa

, Elia Pérez-Fernández, Bertrand Favier, Nieves Prior, Teresa Caballero

Hereditary angioedema caused by the p.Thr309Lys mutation in the F12 gene: A multifactorial disease

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Elena Román-Ortiz, Santiago Rodríguez de Cordoba, Santiago Mendizabal Oteiza, Sheila Pinto, Margarita López-Trascasa

, Pilar Sánchez-Corral, Santiago Rodríguez de Cordoba

Eculizumab long-term therapy for pediatric renal transplant in aHUS with CFH/CFHR1 hybrid gene

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Agustín Tortajada, Santiago Rodríguez de Córdoba, Hugo Yébenes, Cynthia Abarrategui-Garrido, Jaouad Anter, Jesús M. García-Fernández, Rubén Martínez-Barricarte, María Alba-Domínguez, Talat H. Malik, Rafael Bedoya, Rocío Cabrera Pérez, Margarita López Trascasa

, Matthew C. Pickering

, Claire L. Harris, Pilar Sánchez-Corral and 2 other authors

C3 glomerulopathy–associated CFHR1 mutation alters FHR oligomerization and complement regulation

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Alberto López-Lera, Fátima Sánchez Cabo, Fátima Sánchez Cabo, Sofía Garrido, Ana Dopazo, Margarita López-Trascasa

Disease-modifying factors in hereditary angioedema: an RNA expression-based screening

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This paper was not found in any repository, but could be made available legally by the author.

2012 Agustin Tortajada, Maria Alba, Sheila Pinto, Margarita Lopez-Trascasa

, Pilar Sanchez-Corral, Claire L. Harris, Santiago Rodriguez de Cordoba

CFHR1 gene variants and their pathophysiological relevance

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Maria Alba-Dominguez, Ruben Martinez-Barricarte, Sheila Pinto, Cynthia Abarrategui-Garrido, Margarita Lopez-Trascasa

, Santiago Rodriguez de Cordoba, Pilar Sanchez-Corral

Abnormal factor H/FHRS proteins in sera from aHUS patients reveal novel CFH/CFHRS gene rearrangements of potential pathological relevance

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Danielle Paixão-Cavalcante, Margarita López-Trascasa

, Lillemor Skattum, Patricia C. Giclas, Timothy H. Goodship, Santiago Rodríguez de Córdoba

, Santiago Rodriguez de Cordoba, Lennart Truedsson, B. Paul Morgan, B. Paul Morgan, Claire L. Harris

Sensitive and specific assays for C3 nephritic factors clarify mechanisms underlying complement dysregulation

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Carmen Marcos, Alberto López Lera, Alberto López Lera, Susana Varela, Tania Liñares, Marimar G. Alvarez Eire, Margarita López-Trascasa

Clinical, biochemical, and genetic characterization of type III hereditary angioedema in 13 Northwest Spanish families

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Anne Kopp, Stefanie Strobel, Agustín Tortajada, Santiago Rodriguez de Cordoba

, P. Sanchez-Corral, Pilar Sánchez-Corral, Zoltán Prohaszka, Margarita Lopez-Trascasa

, Mihály Jozsi

Atypical Hemolytic Uremic Syndrome-Associated Variants and Autoantibodies Impair Binding of Factor H and Factor H-Related Protein 1 to Pentraxin 3

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Papers authored by Margarita López-Trascasa