Margarita López-Trascasa

Papers authored by Margarita López-Trascasa

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2012 María Alba-Domínguez, Alberto López-Lera, Sofía Garrido, Pilar Nozal, Ignacio González-Granado, Josefa Melero, Pere Soler-Palacín, Carmen Cámara, Margarita López-Trascasa

Complement factor I deficiency: a not so rare immune defect. Characterization of new mutations and the first large gene deletion

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P. Nozal, S. Strobel, M. Ibernon, D. Lopez, P. Sanchez Corral, S. Rodriguez de Cordoba

, M. Jozsi, M. Lopez Trascasa

Anti-factor H antibody affecting factor H cofactor activity in a patient with dense deposit disease

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Agustín Tortajada, Sheila Pinto, Jorge Martínez-Ara, Margarita López-Trascasa

, Pilar Sánchez-Corral, Santiago Rodríguez de Córdoba

Complement factor H variants I890 and L1007 while commonly associated with atypical hemolytic uremic syndrome are polymorphisms with no functional significance

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Rocío Mena de la Cruz, Alberto López-Lera, Margarita López-Trascasa

Analysis of SERPING1 expression on hereditary angioedema patients: Quantitative analysis of full-length and exon 3 splicing variants

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2011 Gema Ariceta, Beatriz Arrizabalaga, Mireia Aguirre, Elvira Morteruel, Margarita Lopez-Trascasa

Eculizumab in the Treatment of Atypical Hemolytic Uremic Syndrome in Infants

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Alberto López-Lera, Sofía Garrido, Olga Roche, Margarita López-Trascasa

SERPING1 mutations in 59 families with hereditary angioedema

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V. Abraira, J. C. Alvarez Cermeño, R. Arroyo, C. Cámara, B. Casanova, S. Cubillo, C. de Andrés, C. Espejo, O. Fernández, J. Ferrer, M. A. Figueredo, A. García Merino, M. I. García Sánchez, J. A. García Trujillo, M. Gómez and 27 other authors

Utility of oligoclonal IgG band detection for MS diagnosis in daily clinical practice

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Grupo Español de Estudio del Angioedema mediado por Bradicinina, T. Caballero, Baeza Ml, M. L. Baeza, R. Cabanas, A. Campos, S. Cimbollek, C. Gomez-Traseira, C. Gómez-Traseira, T. Gonzalez-Quevedo

, M. Guilarte, Jurado Palomo Gj, Larco Ji, J. Jurado-Palomo, López Serrano Mc and 11 other authors

Consensus Statement on the Diagnosis, Management, and Treatment of Angioedema Mediated by Bradykinin. Part I. Classification, Epidemiology, Pathophysiology, Genetics, Clinical Symptoms, and Diagnosis

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2010 Alberto López-Lera, Bertrand Favier, Rocío Mena de la Cruz, Sofía Garrido, Christian Drouet, Margarita López-Trascasa

A new case of homozygous C1-inhibitor deficiency suggests a role for Arg378 in the control of kinin pathway activation

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Rubén Martínez-Barricarte, Santiago Rodríguez de Córdoba, Meike Heurich, Francisco Valdes-Cañedo, Eduardo Vazquez-Martul, Eva Torreira, Tamara Montes, Agustín Tortajada, Sheila Pinto, Margarita Lopez-Trascasa

, B. Paul Morgan, Oscar Llorca, Claire L. Harris, Santiago Rodríguez de Córdoba

Human C3 mutation reveals a mechanism of dense deposit disease pathogenesis and provides insights into complement activation and regulation

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Nadia Leban, Sabra Aloui, Dalel Touati, Ramzy Lakhdhar, Habib Skhiri, Gerard Lefranc, Abdellatif Achour, Mezri Elmay, Margarita Lopez-Trascasa

, Pilar Sanchez-Corral, Jemni Chibani, Amel Haj Khelil

Atypical hemolytic uremic syndrome in the Tunisian population

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Sonia Barroso, Margarita López-Trascasa

, Dolores Merino, Antonia José Álvarez, Antonio Núñez-Roldán, Berta Sánchez

C7 Deficiency and Meningococcal Infection Susceptibility in Two Spanish Families

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2009 Cynthia Abarrategui-Garrido, Santiago Rodríguez de Córdoba, Rubén Martínez-Barricarte, Margarita López-Trascasa

, Santiago Rodriguez de Cordoba

, Pilar Sánchez-Corral

Characterization of complement factor H-related (CFHR) proteins in plasma reveals novel genetic variations of CFHR1 associated with atypical Hemolytic Uremic Syndrome

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Alberto López-Lera, Sofía Garrido, Rocío Mena de la Cruz, Gumersindo Fontán, Margarita López-Trascasa

Molecular characterization of three new mutations causing C5 deficiency in two non-related families

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J. M. Cruzado, S. Rodríguez de Córdoba

, S. Rodríguez de Córdoba, E. Melilli, O. Bestard, I. Rama, P. Sánchez Corral, M. López Trascasa

, I. Navarro, J. Torras, M. Gomà, J. M. Grinyo

Successful Renal Transplantation in a Patient with Atypical Hemolytic Uremic Syndrome Carrying Mutations in Both Factor I and MCP

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M. López Trascasa

, A. Gil Aguado, A. Capozzi, M. Sorice

Association of anti-C1 inhibitor and anti-protein S antibodies in a patient with primary antiphospholipid syndrome

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2008 Ineke G. A. Wagenaar-Bos, Christian Drouet, Emel Aygören-Pursun, Konrad Bork

, Christoph Bucher, Anette Bygum, Henriette Farkas, George Fust, Hanna Gregorek, C. Erik Hack, C. Erik Hack, Alaco Hickey, Helen I. Joller-Jemelka, Maria Kapusta, Wolfhart Kreuz and 14 other authors

Functional C1-inhibitor diagnostics in hereditary angioedema: assay evaluation and recommendations.

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Cynthia Abarrategui-Garrido, Marta Melgosa, Antonia Peña-Carrión, Elena Goicoechea de Jorge, Santiago Rodríguez de Córdoba

, Margarita López-Trascasa

, Pilar Sánchez-Corral

Mutations in Proteins of the Alternative Pathway of Complement and the Pathogenesis of Atypical Hemolytic Uremic Syndrome

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Isabel María Ponce-Castro, Carolina González-Rubio, Eva María Delgado-Cerviño, Cynthia Abarrategui-Garrido, Gumersindo Fontán, Pilar Sánchez-Corral, Margarita López-Trascasa

Molecular characterization of complement Factor I deficiency in two Spanish families

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Cornelia Bigler, Margarita Lopez-Trascasa

, Eliska Potlukova, Solange Moll, Doris Danner, Monica Schaller, Marten Trendelenburg

Antinucleosome Antibodies as a Marker of Active Proliferative Lupus Nephritis

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Papers authored by Margarita López-Trascasa