Mariona Pascal

Research group

Clinical and experimental respiratory immunoallergy Accredited researcher (R3A)

mpascal@clinic.cat 0000-0003-0549-9720

Featured publications

Role of Art v 3 in pollinosis of patients allergic to Pru p 3

Authors:
Sanchez-Lopez, Jaime; Tordesillas, Leticia; Pascal, Mariona; Munoz-Cano, Rosa; Garrido, Maria;

(...)

Vilella, Ramon; Valero, Antonio; Diaz-Perales, Araceli; Picado, Cesar; Bartra, Joan.

Reference: Journal Of Allergy And Clinical Immunology 2014.
Gene Expression Profiling Of Food-Induced Anaphylaxis Associated With Non-Steroidal Anti-Inflammatory Drugs (NSAIDs)

Authors:
Munoz-Cano, Rosa M; Bartra, Joan; Scheffel, Jorg; Pascal, Mariona; Dema, Barbara;

Valero, Antonio; Olivera, Ana; Picado, Cesar; Rivera, Juan.

Reference: Journal Of Allergy And Clinical Immunology 2014.
Serum allergen-specific IgA is not associated with natural or induced tolerance to egg in children

Authors:
Vazquez-Ortiz, M; Pascal, M; Juan, M; Alsina, L; Martin-Mateos, M A;

Plaza, A M.

Reference: Allergy 2013.
Massively parallel sequencing reveals maternal somatic IL2RG mosaicism in an X-linked severe combined immunodeficiency family

Authors:
Alsina, Laia; Gonzalez-Roca, Eva; Teresa Giner, Maria; Piquer, Monica; Puga, Irene;

(...)

Cerutti, Andrea; Juan, Manel; Yaguee, Jordi; Plaza, Ana M; Arostegui, Juan I.

Reference: Journal Of Allergy And Clinical Immunology 2013.
Lipid transfer protein syndrome: clinical pattern, cofactor effect and profile of molecular sensitization to plant-foods and pollens

Authors:
Pascal, M; Munoz-Cano, R; Reina, Z; Palacin, A; Vilella, R;

(...)

Rueda, M; Salcedo, G; Valero, A; Yaguee, J; Bartra, J.

Reference: Clinical And Experimental Allergy 2012.
A somatic NLRP3 mutation as a cause of a sporadic case of chronic infantile neurologic, cutaneous, articular syndrome/neonatal-onset multisystem inflammatory disease: Novel evidence of the role of low-level mosaicism as the pathophysiologic mechanism underlying mendelian inherited diseases

Authors:
Arostegui, Juan I; Lopez Saldana, Ma Dolores; Clemente, Daniel; Balaguer, Francesc; Goel, Ajay;

Fournier del Castillo, Concepcion; Lopez Robledillo, Juan Carlos; Ibanez, Mercedes.

Reference: Arthritis And Rheumatism 2010.
Influence of mannose-binding lectin gene polymorphisms on the invasiveness of cytomegalovirus disease after solid organ transplantation

Authors:
Cervera, C; Lozano, F; Linares, L; Anton Pagarolas, Andres; Anton, A;

(...)

Navasa, M; Roig, E; Marcos, M A; Pumarola, T; Moreno, A.

Reference: Transplantation Proceedings 2009.
Novel And Recurrent Mutations In NLRP3 Gene Encoding Cryopyrin in Patients With Cryopyrinopathies: Experience from a Spanish Cohort

Authors:
Pascal, Mariona; Ignacio Arostegui, Juan; Modesto, Consuelo; Arguelles, Federico; Cinta Cid, Maria;

(...)

Sol Camacho, Mari; Plaza, Susana; Rius, Josefina; Yaguee, Jordi; Juan, Manel.

Reference: Clinical Immunology 2009.
Pyogenic bacterial infections in humans with MyD88 deficiency

Authors:
Von Bernuth, Horst; Picard, Capucine; Jin, Zhongbo; Pankla, Rungnapa; Xiao, Hui;

(...)

Abel, Laurent; Li, Xiaoxia; Chaussabel, Damien; Puel, Anne; Casanova, Jean-Laurent.

Reference: Science 2008.
Combined Spanish cohort and international Blau syndrome registry: Report on the expanding phenotype of patients with NOD-2 mutation

Authors:
Rose, Carlos D; Arostegui, Juan I; Martin, Tammy; Espada, Graciela; Scalzi, Lisabeth;

(...)

Ramos, Eduardo; Naranjo, Antonio; Pascal, Mariona; Yague, Jordi; Wouters, Carine H.

Reference: Arthritis And Rheumatism 2008.

Featured Projects

Asma, Reacciones Adversas y Alérgicas (ARADYAL).

Principal investigator: Joan Bartra Tomas

Funder: INSTITUTO CARLOS III(MINECO)

Code: RD16/0006/0007

Duration: 01/01/2017 - 31/12/2021
Síndrome LTP: Identificación y caracterización clínica de los epítopos inmunodominantes B y T y su presentación antigénica HLA.

Principal investigator: Mariona Pascal

Funder: Ministerio de Economia y Competitividad (MINECO)

Code: PI16/00344

Duration: 01/01/2017 - 31/12/2019
PI19/00710. Estratificación del riesgo de gravedad y patrón de reconocimiento en el Síndrome LTP: papel de la afinidad, clonalidad BCR/TCR y la presentación facilitada de antígeno

Principal investigator: Lopez G

Funder: Institut d`Investigacions Biomèdiques August Pi i Sunyer (Sede o evento); Instituto de Salud Carlos III

Duration: 01/01/2020 - 31/12/2022
PI16/00344. Síndrome LTP: identificación y caracterización clínica de los epítopos inmunodominantes B y T y su presentación antigénica HLA

Principal investigator: Joan Bartra Tomás

Funder: HOSPITAL CLINICO Y PROVINCIAL DE BARCELONA (Sede o evento); Instituto de Salud Carlos III

Duration: 01/01/2017 - 01/01/2019
RETIC - Red de Investigación Asma, reacciones adversas y alérgicas (ARADyAL)

Principal investigator: Margarita Martin

Funder: HOSPITAL CLINICO Y PROVINCIAL DE BARCELONA (Sede o evento); Asma, reacciones adversas y alérgicas (ARADyAL) (Programa financiador competitivo)

Duration: 01/01/2017 - 01/01/2021

Mariona Pascal

Research group

Featured publications

Combined Spanish cohort and international Blau syndrome registry: Report on the expanding phenotype of patients with NOD-2 mutation

Featured Projects

Asma, Reacciones Adversas y Alérgicas (ARADYAL).

Síndrome LTP: Identificación y caracterización clínica de los epítopos inmunodominantes B y T y su presentación antigénica HLA.

PI19/00710. Estratificación del riesgo de gravedad y patrón de reconocimiento en el Síndrome LTP: papel de la afinidad, clonalidad BCR/TCR y la presentación facilitada de antígeno

PI16/00344. Síndrome LTP: identificación y caracterización clínica de los epítopos inmunodominantes B y T y su presentación antigénica HLA

RETIC - Red de Investigación Asma, reacciones adversas y alérgicas (ARADyAL)

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