Lopez Trascasa, Margarita margarita.lopez@uam.es

Publications

Properdin deficiency associated with systemic meningococcal disease due to a novel p.Cys337Arg pathogenic variant

  • Gonzalez-Sanchez, Laura
  • Agudo, Ana Mei
  • van den Rym, Anne
  • Begiristain, Maria Isabel
  • Saizar, Alazne
  • de Diego, Rebeca Perez
  • Nozal, Pilar
  • Lopez-Lera, Alberto
  • Lopez-Trascasa, Margarita
  • Corvillo, Fernando
... View more Collapse

Genes And Diseases - 1/11/2024

10.1016/j.gendis.2023.101134 View at source

  • ISSN 23523042

Characterization and Clinical Association of Autoantibodies Against Perilipin 1 in Patients with Acquired Generalized Lipodystrophy

  • Corvillo, F
  • Abel, BS
  • López-Lera, A
  • Ceccarini, G
  • Magno, S
  • Santini, F
  • Araújo-Vilar, D
  • Brown, RJ
  • Nozal, P
  • López-Trascasa, M
... View more Collapse

Diabetes (p. 71-84) - 1/1/2023

10.2337/db21-1086

  • ISSN 00121797
  • iMarina

Complement factor d (Adipsin) levels are elevated in acquired partial lipodystrophy (barraquer–simons syndrome)

  • Corvillo F
  • González-Sánchez L
  • López-Lera A
  • Arjona E
  • Ceccarini G
  • Santini F
  • Araújo-Vilar D
  • Brown RJ
  • Villarroya J
  • Villarroya F
  • de Córdoba SR
  • Caballero T
  • Nozal P
  • López-Trascasa M
... View more Collapse

International Journal Of Molecular Sciences - 2/6/2021

10.3390/ijms22126608 View at source

  • ISSN 14220067

Thrombin in the Activation of the Fluid Contact Phase in Patients with Hereditary Angioedema Carrying the F12 P.Thr309Lys Variant

  • Lopez-Galvez, R.
  • de la Morena-Barrio, M. E.
  • Minano, A.
  • Pathak, M.
  • Marcos, C.
  • Emsley, J.
  • Caballero, T.
  • Lopez-Trascasa, M.
  • Vicente, V.
  • Corral, J.
  • Lopez-Lera, A.;
... View more Collapse

Clinical Reviews In Allergy & Immunology (p. 357-368) - 1/6/2021

10.1007/s12016-021-08840-x View at source

  • ISSN 10800549

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

  • Marcos-Jimenez, Ana
  • Sanchez-Alonso, Santiago
  • Alcaraz-Serna, Ana
  • Esparcia, Laura
  • Lopez-Sanz, Celia
  • Sampedro-Nunez, Miguel
  • Mateu-Albero, Tamara
  • Sanchez-Cerrillo, Ildefonso
  • Martinez-Fleta, Pedro
  • Gabrie, Ligia
  • del Campo Guerola, Luciana
  • Rodriguez-Frade, Jose Miguel
  • Casasnovas, Jose M
  • Reyburn, Hugh T
  • Vales-Gomez, Mar
  • Lopez-Trascasa, Margarita
  • Martin-Gayo, Enrique
  • Calzada, Maria Jose
  • Castaneda, Santos
  • de la Fuente, Hortensia
  • Gonzalez-Alvaro, Isidoro
  • Sanchez-Madrid, Francisco
  • Munoz-Calleja, Cecilia
  • Alfranca, Arantzazu
... View more Collapse

European Journal Of Immunology (p. 634-647) - 1/3/2021

10.1002/eji.202048858 View at source

  • ISSN 00142980

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

  • López-Trascasa M
  • Alonso-Melgar Á
  • Melgosa-Hijosa M
  • Espinosa-Román L
  • Lledín-Barbancho MD
  • García-Fernández E
  • Rodríguez de Córdoba S
  • Sánchez-Corral P
... View more Collapse

Frontiers In Immunology - 14/10/2021

10.3389/fimmu.2021.751093 View at source

  • ISSN 16643224

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

  • Corvillo F
  • Morena-Barrio MEdl
  • Marcos-Bravo C
  • López-Trascasa M
  • Vicente V
  • Emsley J
  • Caballero T
  • Corral J
  • López-Lera A
... View more Collapse

Frontiers In Genetics - 10/9/2020

10.3389/fgene.2020.01033 View at source

  • ISSN 16648021

Novel homozygous variants in theSERPING1gene in two Turkish families with hereditary angioedema of recessive inheritance

  • Gokmen, Nihal Mete
  • Rodriguez-Alcalde, Cesar
  • Gulbahar, Okan
  • Lopez-Trascasa, Margarita
  • Onay, Huseyin
  • Lopez-Lera, Alberto;

Immunology And Cell Biology (p. 693-699) - 1/9/2020

10.1111/imcb.12362 View at source

  • ISSN 08189641

Erratum: Correction to: Immunological features of patients affected by Barraquer-Simons syndrome (Orphanet journal of rare diseases (2020) 15 1 (9))

  • Corvillo F
  • Ceccarini G
  • Nozal P
  • Magno S
  • Pelosini C
  • Garrido S
  • López-Lera A
  • Moraru M
  • Vilches C
  • Fornaciari S
  • Gabbriellini S
  • Santini F
  • Araújo-Vilar D
  • López-Trascasa M
... View more Collapse

Orphanet Journal Of Rare Diseases - 30/3/2020

10.1186/s13023-020-1350-8 View at source

  • ISSN 17501172

Newborn Screening for Presymptomatic Diagnosis of Complement and Phagocyte Deficiencies

  • Dezfouli M
  • Bergström S
  • Skattum L
  • Abolhassani H
  • Neiman M
  • Torabi-Rahvar M
  • Franco Jarava C
  • Martin-Nalda A
  • Ferrer Balaguer JM
  • Slade CA
  • Roos A
  • Fernandez Pereira LM
  • López-Trascasa M
  • Gonzalez-Granado LI
  • Allende-Martinez LM
  • Mizuno Y
  • Yoshida Y
  • Friman V
  • Lundgren Å
  • Aghamohammadi A
  • Rezaei N
  • Hernández-Gonzalez M
  • von Döbeln U
  • Truedsson L
  • Hara T
  • Nonoyama S
  • Schwenk JM
  • Nilsson P
  • Hammarström L
... View more Collapse

Frontiers In Immunology - 17/3/2020

10.3389/fimmu.2020.00455 View at source

  • ISSN 16643224

This researcher has no books.

5.3 Deficiencias congénitas del complemento.

  • Deyà Martínez, Àngela
  • López Trascasa, Margarita

Manual De Pediatría (p. 301-306) - 1/1/2019

  • iMarina

Angioedema Adquirido con niveles normales de C1q

  • López Lera, Alberto
  • Gil Herrera, J
  • Marbán, Esther
  • Rivero Paparoni, Daniela
  • Garrido Elustondo, S
  • Caballero Molina, María Teresa
  • López Trascasa, Margarita
... View more Collapse

Inmunodeficiencias: Casos Clínicos Comentados / José Miguel Sempere Ortells (Ed. Lit.), Adolfo Campos Ferrer (Ed. Lit.), Pascual Martínez Peinado (Ed. Lit.), Sandra Pascual García (Ed. Lit.) (p. 43-46-46) - 1/1/2016

  • iMarina

An retrospective analysis of genetic diagnosis in Atypical Hemolytic Uremic Syndrome (aHUS) and C3 glomerulopathy (C3G). Where we are now and where we are moving to

  • Perez Perez, J.
  • Olavarrieta Scappini, L.
  • Vilches Arroyo, S.
  • Diaz Jauregui, T.
  • Lopez-Trascasa, M.
  • Sanchez-Corral, P.
  • Arjona Bolanos, E.
  • Rodriguez De Cordoba, S.;
... View more Collapse

Pediatric Nephrology (p. 1871-1871) - 1/1/2016

  • ISSN 0931041X
  • iMarina

FAMILY DEFECTS IN FACTOR H/FHRS OF THE COMPLEMENT IN IGA NEPHROPATHY

  • Olea, Teresa
  • Bernabeu-Herrero, Maria E.
  • Rodriguez-Gayo, Lucia
  • Selgas, Rafael
  • Lopez-Trascasa, Margarita
  • Sanchez-Corral, Pilar;

Nephrology Dialysis Transplantation (p. 383-383) - 1/1/2016

  • ISSN 13125257
  • iMarina

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

  • Alba-Dominguez, Maria
  • Martinez-Barricarte, Ruben
  • Pinto, Sheila
  • Abarrategui-Garrido, Cynthia
  • Lopez-Trascasa, Margarita
  • Rodriguez de Cordoba, Santiago
  • Sanchez-Corral, Pilar;
... View more Collapse

Immunobiology (p. 1134-1135) - 1/1/2012

10.1016/j.imbio.2012.08.017 View at source

  • ISSN 01712985

CFHR1 gene variants and their pathophysiological relevance

  • Tortajada, Agustin
  • Alba, Maria
  • Pinto, Sheila
  • Lopez-Trascasa, Margarita
  • Sanchez-Corral, Pilar
  • Harris, Claire L.
  • Rodriguez de Cordoba, Santiago;
... View more Collapse

Immunobiology (p. 1149-1149) - 1/1/2012

10.1016/j.imbio.2012.08.058 View at source

  • ISSN 01712985

Clinical and radiological course of simple renal cysts in children

  • Aguirre, M.
  • Mateos, J.
  • Abarrategui, C.
  • Lopez-Bayon, J.
  • Lopez-Trascasa, M.
  • Ariceta, G.;

Pediatric Nephrology (p. 1676-1676) - 1/1/2011

  • ISSN 0931041X
  • iMarina

Eculizumab pharmacokinetics and efficacy in a newborn with aHUS: an option in no-candidates to plasmaexchange

  • Aguirre, M.
  • Arrizabalaga, B.
  • Abarrategui, C.
  • Morteruel, E.
  • Lopez-Trascasa, M.
  • Areses, R.
  • Quintela, M. J.
  • Ariceta, G.;
... View more Collapse

Pediatric Nephrology (p. 1676-1677) - 1/1/2011

  • ISSN 0931041X
  • iMarina

Early diagnosis of deap-hus followed by complete renal recovery: case report

  • Aguirre, M.
  • Mateos, J.
  • Abarrategui, C.
  • Lopez-Bayon, J.
  • Lopez-Trascasa, M.
  • Ariceta, G.;

Pediatric Nephrology (p. 1676-1676) - 1/1/2011

  • ISSN 0931041X
  • iMarina

Anti-nucleosome antibodies as a marker of active proliferative lupus nephritis

  • Bigler, C.
  • Lopez-Trascasa, M.
  • Potlukova, E.
  • Moll, S.
  • Danner, D.
  • Schaller, M.
  • Trendelenburg, M.;
... View more Collapse

Swiss Medical Weekly (p. 53S-53S) - 1/1/2008

  • ISSN 14247860
  • iMarina

Report of the III workshop on immunochemistry of the Spanish Society of Immunology

  • Rodríguez Molina JJ
  • Sequí Navarro J
  • Villar Guimerans LM
  • Juárez Rubio C
  • Martínez Cáceres EM
  • Amengual Guedaní MJ
  • Rodrigo Anoro MJ
  • Cámara Hijón C
  • Fernández Pereira L
  • Sanchez Mozo P
  • Alarcón Torres I
  • González Parqué P
  • Varela Peña P
  • Allende Martínez L
  • Sentchordi Izquierdo MJ
  • Jiménez Garófano C
  • Muñoz Calleja C
  • López Trascasa M
  • Fernández Arcas N
  • Álvarez López R
  • Ferrer Balaguer J
  • López Hoyos M
  • Larrad Mur L
... View more Collapse

Inmunologia (p. 57-66) - 1/1/2006

  • ISSN 02139626
  • iMarina

Successful renal transplantation in a patient with atypical hemolytic uremic syndrome carrying mutations in both factor I and MCP

  • Cruzado JM, de Córdoba SR, Melilli E, Bestard O, Rama I, Sánchez-Corral P, López-Trascasa M, Navarro I, Torras J, Gomà M, Grinyó JM

American Journal Of Transplantation (p. 1477-1483) - 1/6/2009

10.1111/j.1600-6143.2009.02647.x View at source

  • ISSN 16006135

This researcher has no technical reports.

This researcher has no research projects.

Estudio genético de inmunodeficiencias primarias: Desarrollo e implementación de algoritmos diagnósticos

  • Rodríguez Pena, Rebeca (Director)
  • Vallespín García, Elena (Director)
  • Lopez Trascasa, Margarita (Tutor) Doctorando: Bravo García-Morato, María

15/3/2019

  • iMarina

Estudio de los mecanismos inmunopatológicos en lipodistrofias adquiridas de tipo parcial y generalizado

  • Herranz de la Morena, Lucrecia (Autor o Coautor)
  • Arnalich Fernandez, Francisco (Autor o Coautor)
  • Lopez Trascasa, Margarita (Director) Doctorando: Fernando Corvillo Rodríguez

22/6/2018

  • iMarina

Evaluación del perfil inmunitario postrasplante autólogo de progenitores hematopoyéticos, en pacientes con mieloma múltiple en remisión completa de larga duración

  • Lopez Trascasa, Margarita (Autor o Coautor)
  • Cabrera Marin, Jose R (Autor o Coautor)
  • CECILIA MUÑOZ CALLEJA (Director)
  • Adrián Alegre Amor (Director)
  • Alegre Amor, Adrian (Autor o Coautor) Doctorando: Ana Rosa Arteche López

19/1/2018

  • iMarina

SPLICING ALTERNATIVO EN SERPING1: Expresión del ARNm total y de dos variantes alternativas del mensajero del gen del inhibidor de C1 en pacientes con angioedema hereditario

  • Sainz Anding, Bruno (Autor o Coautor)
  • Fernandez Piqueras, Jose (Autor o Coautor)
  • Lopez Trascasa, Margarita (Director) Doctorando: MARIA ROCIO MENA DE LA CRUZ

21/3/2017

  • iMarina

Estudio sobre los anticuerpos no clasificatorios presentes en el síndrome antifosfolipídico: Búsqueda de nuevos marcadores de laboratorio: anticuerpos anti-complejo fosfatidilserina/protrombina (aPS/PT) y isotipo IgA de los anticuerpos anti-ß2 glicoproteína I(IgA aß2GPI)

  • Pascual-Salcedo, Dora (Codirector)
  • Rios Blanco, Juan Jose (Codirector) Doctorando: Vlagea, Alexandru Daniel

1/1/2017

  • iMarina

Autoanticuerpos frente a proteínas de la vía alternativa del complemento en patologías renales

  • Lopez Trascasa, Margarita (Director) Doctorando: Nozal Aranda, Pilar

13/9/2016

  • iMarina

Autoanticuerpos frente a proteínas de la vía alternativa del complemento en enfermedades renales

  • Arnalich Fernandez, Francisco (Autor o Coautor)
  • Margarita López Trascasa (Director) Doctorando: Pilar Nozal Aranda

1/1/2016

  • iMarina

El angioedema hereditario estudio genético de la población española y análisis funcionales en pacientes homocigotos para la deficiencia de C1 inhibidor

  • Lopez Trascasa, Margarita (Director) Doctorando: Lopez Lera, Alberto

29/11/2010

  • iMarina

Caracterización molecular de la deficiencia del factor I en dos familias españolas

  • Lopez Trascasa, Margarita (Director) Doctorando: Ponce Castro, Isabel María

16/7/2007

  • iMarina

Caracterizacion molecular de la deficiencia del factor 1 en dos familiar

  • Fontan Casariego, Gumersindo (Autor o Coautor)
  • Margarita López Trascasa (Director) Doctorando: Isabel María Ponce Castro

1/1/2007

  • iMarina

This researcher has no patents or software licenses.

Last data update: 8/28/24 3:10 PM