Lopez Trascasa, Margarita margarita.lopez@uam.es
Publications
- Articles 140
- Books 0
- Book chapters 2
- Conferences 9
- Working papers 1
- Technical reports 0
- Research projects 0
- Supervised theses 21
- Patent or software license 0
First case of homozygous C1 inhibitor deficiency
- Blanch A
- Roche O
- Urrutia I
- Gamboa P
- Fontán G
- López-Trascasa M
Journal Of Allergy And Clinical Immunology (p. 1330-1335) - 1/1/2006
10.1016/j.jaci.2006.07.035 View at source
- ISSN 00916749
Hereditary angioedema: The mutation spectrum of SERPING1/C1NH in a large Spanish cohort
- Roche O
- Blanch A
- Duponchel C
- Fontán G
- Tosi M
- López-Trascasa M
Human Mutation (p. 135-144) - 1/8/2005
10.1002/humu.20197 View at source
- ISSN 10597794
Erratum: Predisposition to atypical hemolytic uremic syndrome involves the concurrence of different susceptibility alleles in the regulators of complement activation of gene cluster in 1q32 (Human Molecular Genetics (2005) vol. 14 (703-712))
- Esparza-Gordillo, J
- de Jorge, EG
- Buil, A
- Berges, LC
- Lopez-Trascasa, M
- Sanchez-Corral, P
- de Cordoba, SR;
Human Molecular Genetics (p. 1107-1107) - 15/4/2005
10.1093/hmg/ddi099 View at source
- ISSN 14602083
Predisposition to atypical hemolytic uremic syndrome involves the concurrence of different susceptibility alleles in the regulators of complement activation gene cluster in 1q32
- Esparza-Gordillo, J
- de Jorge, EG
- Buil, A
- Berges, LC
- Lopez-Trascasa, M
- Sanchez-Corral, P
- de Cordoba, SR;
Human Molecular Genetics (p. 703-712) - 1/3/2005
10.1093/hmg/ddi066 View at source
- ISSN 14602083
Hereditary angioedema due to C1 inhibitor deficiency: Patient registry and approach to the prevalence in Spain
- Roche O
- Blanch A
- Caballero T
- Sastre N
- Callejo D
- López-Trascasa M
Annals Of Allergy Asthma & Immunology (p. 498-503) - 1/1/2005
- ISSN 10811206
- iMarina
C5 complement deficiency in a Spanish family: Molecular characterization of the double mutation responsible for the defect
- Delgado-Cerviño E
- Fontán G
- López-Trascasa M
Molecular Immunology (p. 105-111) - 1/1/2005
10.1016/j.molimm.2004.06.036 View at source
- ISSN 01615890
Angioedema hereditario de comienzo tardío
- Ferreira, A
- López Trascasa, Margarita
- Roche, O
- Blanch, A
Anales De Medicina Interna (Madrid, Spain : 1984) (p. 468-469) - 1/9/2004
10.4321/s0212-71992004000900017
- ISSN 02127199
- iMarina
The human complement factor H: Functional roles, genetic variations and disease associations
- de Cordoba, SR
- Esparza-Gordillo, J
- de Jorge, EG
- Lopez-Trascasa, M
- Sanchez-Corral, P;
Molecular Immunology (p. 355-367) - 1/6/2004
10.1016/j.molimm.2004.02.005 View at source
- ISSN 01615890
Functional analysis in serum from atypical Hemolytic Uremic Syndrome patients reveals impaired protection of host cells associated with mutations in factor H
- Sanchez-Corral, P
- Gonzalez-Rubio, C
- de Cordoba, SR
- Lopez-Trascasa, M;
Molecular Immunology (p. 81-84) - 1/5/2004
10.1016/j.molimm.2004.01.003 View at source
- ISSN 01615890
Complement component C7 deficiency in two Spanish families
- Vazquez-Bermudez, MF
- Barroso, S
- Walter, K
- Alvarez, AJ
- Alarcon, A
- Lopez-Trascasa, M
- Wichmann, I
- Aguilar, F
- Nunez-Roldan, A
- Sanchez, B;
Immunology (p. 518-523) - 1/12/2004
10.1111/j.1365-2567.2004.01997.x View at source
- ISSN 13652567
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
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.;
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;
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;
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.;
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.;
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
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)
- Lopez Trascasa, Margarita (Autor o Coautor)
- Suarez Fernandez, M Carmen (Autor o Coautor)
- Gomez Cerezo, Jorge Francisco (Autor o Coautor)
- Juan José Ríos Blanco (Director)
- Dora Pascual Salcedo (Director) Doctorando: Alexandru Danie Vlagea
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
This researcher has no patents or software licenses.
Researcher profiles
-
ORCID
-
Publons
-
Scopus Author ID
-
Dialnet id