Inmunología, Oftalmología y ORL
Departamento
Margarita
López Trascasa
Publicaciones en las que colabora con Margarita López Trascasa (24)
2020
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Newborn Screening for Presymptomatic Diagnosis of Complement and Phagocyte Deficiencies
Frontiers in Immunology, Vol. 11
2019
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Complement as a diagnostic tool in immunopathology
Seminars in Cell and Developmental Biology, Vol. 85, pp. 86-97
2018
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Acquired angioedema with anti–C1-inhibitor autoantibodies during assisted reproduction techniques
Journal of Investigational Allergology and Clinical Immunology
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Common and rare genetic variants of complement components in human disease
Molecular Immunology, Vol. 102, pp. 42-57
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Human plasma C3 is essential for the development of memory B, but not T, lymphocytes
Journal of Allergy and Clinical Immunology, Vol. 141, Núm. 3, pp. 1151-1154.e14
2017
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Elevated factor H–related protein 1 and factor H pathogenic variants decrease complement regulation in IgA nephropathy
Kidney International, Vol. 92, Núm. 4, pp. 953-963
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Multimarker risk stratification approach at multiple sclerosis onset
Clinical Immunology, Vol. 181, pp. 43-50
2016
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Serum properdin consumption as a biomarker of C5 convertase dysregulation in C3 glomerulopathy
Clinical and Experimental Immunology, Vol. 184, Núm. 1, pp. 118-125
2015
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The molecular and structural bases for the association of complement C3 mutations with atypical hemolytic uremic syndrome
Molecular Immunology, Vol. 66, Núm. 2, pp. 263-273
2013
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C3 glomerulopathy-associated CFHR1 mutation alters FHR oligomerization and complement regulation
Journal of Clinical Investigation, Vol. 123, Núm. 6, pp. 2434-2446
2012
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Atypical hemolytic uremic syndrome-associated variants and autoantibodies impair binding of factor H and factor H-related protein 1 to pentraxin 3
Journal of Immunology, Vol. 189, Núm. 4, pp. 1858-1867
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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
Kidney International, Vol. 81, Núm. 1, pp. 56-63
2010
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Human C3 mutation reveals a mechanism of dense deposit disease pathogenesis and provides insights into complement activation and regulation
Journal of Clinical Investigation, Vol. 120, Núm. 10, pp. 3702-3712
2008
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Mutations in Proteins of the Alternative Pathway of Complement and the Pathogenesis of Atypical Hemolytic Uremic Syndrome
American Journal of Kidney Diseases, Vol. 52, Núm. 1, pp. 171-180
2007
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Erratum: Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome (Proceeding of the National Academy of Science of the United States of America (January 2007) 104, (240-245))
Proceedings of the National Academy of Sciences of the United States of America
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Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome
Proceedings of the National Academy of Sciences of the United States of America, Vol. 104, Núm. 1, pp. 240-245
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The interactive factor H-atypical hemolytic uremic syndrome mutation database and website: Update and integration of membrane cofactor protein and factor I mutations with structural models
Human Mutation, Vol. 28, Núm. 3, pp. 222-234
2006
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Análisis de parámetros inmunoquímicos y paraproteínas. Informe del III taller de inmunoquímica de la Sociedad Española de Inmunología
Inmunologia
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Insights into hemolytic uremic syndrome: Segregation of three independent predisposition factors in a large, multiple affected pedigree
Molecular Immunology, Vol. 43, Núm. 11, pp. 1769-1775