Complement Interaction with Trypanosomatid Promastigotes in Normal Human Serum

por Domínguez, Mercedes, Moreno, Inmaculada, López-Trascasa, Margarita, Toraño, Alfredo
Publicado 2002

Self-Damage Caused by Dysregulation of the Complement Alternative Pathway: Relevance of the Factor H Protein Family

por Sánchez-Corral, Pilar, Pouw, Richard B., López-Trascasa, Margarita, Józsi, Mihály
Publicado 2018

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 def...

por López-Lera, Alberto, Pernia, Olga, López-Trascasa, Margarita, Ibanez de Caceres, Inmaculada
Publicado 2014

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

por López-Lera, Alberto, Cabo, Fátima Sánchez, Garrido, Sofía, Dopazo, Ana, López-Trascasa, Margarita
Publicado 2013

Nephritic Factors: An Overview of Classification, Diagnostic Tools and Clinical Associations

por Corvillo, Fernando, Okrój, Marcin, Nozal, Pilar, Melgosa, Marta, Sánchez-Corral, Pilar, López-Trascasa, Margarita
Publicado 2019

Autoantibodies Against Perilipin 1 as a Cause of Acquired Generalized Lipodystrophy

por Corvillo, Fernando, Aparicio, Verónica, López-Lera, Alberto, Garrido, Sofía, Araújo-Vilar, David, de Miguel, María P., López-Trascasa, Margarita
Publicado 2018

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

por Nozal, Pilar, Strobel, Stefanie, Ibernon, Meritxell, López, Dolores, Sánchez-Corral, Pilar, Rodríguez de Córdoba, Santiago, Józsi, Mihály, López-Trascasa, Margarita
Publicado 2012

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

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

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

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

The FXII c.-4T>C Polymorphism as a Disease Modifier in Patients With Hereditary Angioedema Due to the FXII p.Thr328Lys Variant

por Corvillo, Fernando, de la Morena-Barrio, María Eugenia, Marcos-Bravo, Carmen, López-Trascasa, Margarita, Vicente, Vicente, Emsley, Jonas, Caballero, Teresa, Corral, Javier, López-Lera, Alberto
Publicado 2020

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

por Paixão-Cavalcante, Danielle, López-Trascasa, Margarita, Skattum, Lillemor, Giclas, Patricia C, Goodship, Timothy H, de Córdoba, Santiago Rodríguez, Truedsson, Lennart, Morgan, B Paul, Harris, Claire L
Publicado 2012

Case Report: Combined Liver-Kidney Transplantation to Correct a Mutation in Complement Factor B in an Atypical Hemolytic Uremic Syndrome Patient

por López-Trascasa, Margarita, Alonso-Melgar, Ángel, Melgosa-Hijosa, Marta, Espinosa-Román, Laura, Lledín-Barbancho, María Dolores, García-Fernández, Eugenia, Rodríguez de Córdoba, Santiago, Sánchez-Corral, Pilar
Publicado 2021

Testing the Activity of Complement Convertases in Serum/Plasma for Diagnosis of C4NeF-Mediated C3 Glomerulonephritis

por Blom, Anna M., Corvillo, Fernando, Magda, Michal, Stasiłojć, Grzegorz, Nozal, Pilar, Pérez-Valdivia, Miguel Ángel, Cabello-Chaves, Virginia, Rodríguez de Córdoba, Santiago, López-Trascasa, Margarita, Okrój, Marcin
Publicado 2016

The molecular and structural bases for the association of complement C3 mutations with atypical hemolytic uremic syndrome

por Martínez-Barricarte, Rubén, Heurich, Meike, López-Perrote, Andrés, Tortajada, Agustin, Pinto, Sheila, López-Trascasa, Margarita, Sánchez-Corral, Pilar, Morgan, B. Paul, Llorca, Oscar, Harris, Claire L., Rodríguez de Córdoba, Santiago
Publicado 2015

Immunological features of patients affected by Barraquer-Simons syndrome

por Corvillo, Fernando, Ceccarini, Giovanni, Nozal, Pilar, Magno, Silvia, Pelosini, Caterina, Garrido, Sofía, López-Lera, Alberto, Moraru, Manuela, Vilches, Carlos, Fornaciari, Silvia, Gabbriellini, Sabrina, Santini, Ferruccio, Araújo-Vilar, David, López-Trascasa, Margarita
Publicado 2020

Correction to: Immunological features of patients affected by Barraquer-Simons syndrome

por Corvillo, Fernando, Ceccarini, Giovanni, Nozal, Pilar, Magno, Silvia, Pelosini, Caterina, Garrido, Sofía, López-Lera, Alberto, Moraru, Manuela, Vilches, Carlos, Fornaciari, Silvia, Gabbriellini, Sabrina, Santini, Ferruccio, Araújo-Vilar, David, López-Trascasa, Margarita
Publicado 2020

SERPING1 Variants and C1-INH Biological Function: A Close Relationship With C1-INH-HAE

por Drouet, Christian, López-Lera, Alberto, Ghannam, Arije, López-Trascasa, Margarita, Cichon, Sven, Ponard, Denise, Parsopoulou, Faidra, Grombirikova, Hana, Freiberger, Tomáš, Rijavec, Matija, Veronez, Camila L., Pesquero, João Bosco, Germenis, Anastasios E.
Publicado 2022

Complement Factor D (adipsin) Levels Are Elevated in Acquired Partial Lipodystrophy (Barraquer–Simons syndrome)

por Corvillo, Fernando, González-Sánchez, Laura, López-Lera, Alberto, Arjona, Emilia, Ceccarini, Giovanni, Santini, Ferruccio, Araújo-Vilar, David, Brown, Rebecca J, Villarroya, Joan, Villarroya, Francesc, Rodríguez de Córdoba, Santiago, Caballero, Teresa, Nozal, Pilar, López-Trascasa, Margarita
Publicado 2021

Deregulated cellular circuits driving immunoglobulins and complement consumption associate with the severity of COVID‐19 patients

por Marcos‐Jiménez, Ana, Sánchez‐Alonso, Santiago, Alcaraz‐Serna, Ana, Esparcia, Laura, López‐Sanz, Celia, Sampedro‐Núñez, Miguel, Mateu‐Albero, Tamara, Sánchez‐Cerrillo, Ildefonso, Martínez‐Fleta, Pedro, Gabrie, Ligia, del Campo Guerola, Luciana, Rodríguez‐Frade, José Miguel, Casasnovas, José M., Reyburn, Hugh T., Valés‐Gómez, Mar, López‐Trascasa, Margarita, Martín‐Gayo, Enrique, Calzada, María José, Castañeda, Santos, de la Fuente, Hortensia, González‐Álvaro, Isidoro, Sánchez‐Madrid, Francisco, Muñoz‐Calleja, Cecilia, Alfranca, Arantzazu
Publicado 2021

Newborn Screening for Presymptomatic Diagnosis of Complement and Phagocyte Deficiencies

por Dezfouli, Mahya, Bergström, Sofia, Skattum, Lillemor, Abolhassani, Hassan, Neiman, Maja, Torabi-Rahvar, Monireh, Franco Jarava, Clara, Martin-Nalda, Andrea, Ferrer Balaguer, Juana M., Slade, Charlotte A., Roos, Anja, Fernandez Pereira, Luis M., López-Trascasa, Margarita, Gonzalez-Granado, Luis I., Allende-Martinez, Luis M., Mizuno, Yumi, Yoshida, Yusuke, Friman, Vanda, Lundgren, Åsa, Aghamohammadi, Asghar, Rezaei, Nima, Hernández-Gonzalez, Manuel, von Döbeln, Ulrika, Truedsson, Lennart, Hara, Toshiro, Nonoyama, Shigeaki, Schwenk, Jochen M., Nilsson, Peter, Hammarström, Lennart
Publicado 2020