Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Laura Viñas-Giménez"'
Autor:
Laura Viñas-Giménez, Rafael Rincón, Roger Colobran, Xavier de la Cruz, Verónica Paola Celis, José Luis Dapena, Laia Alsina, Joan Sayós, Mónica Martínez-Gallo
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening hyperinflammatory disorder. HLH can be considered as a threshold disease depending on the trigger and the residual NK-cell cytotoxicity. In this study, we analyzed the molecular and funct
Externí odkaz:
https://doaj.org/article/adad2843b85d4f1691acf851788361af
Autor:
Anaís Mariscal, Milena Milán, Andrés Baucells, Maria Angeles Martínez, Andrea Garcia Guillen, Ernesto Trallero-Araguás, Marcelo Alvarado-Cardenas, Laura Martínez-Martínez, Leticia Alserawan, Teresa Franco-Leyva, María Teresa Sanz-Martínez, Laura Viñas-Giménez, Hector Corominas, Cándido Juárez, Iván Castellví, Albert Selva-O’Callaghan
Publikováno v:
Frontiers in Immunology, Vol 11 (2021)
ObjectivesAnti-TIF-1γ autoantibody detection is important for cancer screening in patients with dermatomyositis. The gold standard for anti-TIF-1γ detection, immunoprecipitation, is only available from a few specialized laboratories worldwide, so c
Externí odkaz:
https://doaj.org/article/970cd372a1fc433a847d93f4139961d2
Autor:
Laura Viñas-Giménez, Natàlia Padilla, Laura Batlle-Masó, Ferran Casals, Jacques G. Rivière, Mónica Martínez-Gallo, Xavier de la Cruz, Roger Colobran
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
Background: Primary immunodeficiencies (PIDs) are a heterogeneous group of disorders. The lack of comprehensive disease-specific mutation databases may hinder or delay classification of the genetic variants found in samples from these patients. This
Externí odkaz:
https://doaj.org/article/aa915b4130a44308a82e0f9dd6a1bf13
Autor:
Laura Donadeu, Laura Viñas-Giménez, Albert Català, Elena Álvarez de la Campa, Mónica Martínez-Gallo, Xavier de la Cruz, Rafael Rincón, Joan Sayós, Roger Colobran, Ana Esteve-Solé, Laia Alsina
Publikováno v:
International Journal of Hematology. 111:440-450
The presence of mutations in PRF1, UNC13D, STX11 and STXBP2 genes in homozygosis or compound heterozygosis results in immune deregulation. Most such cases lead to clinical manifestations of haemophagocytic lymphohistiocytosis (HLH). In the present st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5de6642c47c2fe845cf9242b8d9d74dc
https://doi.org/10.1007/s12185-019-02796-7
https://doi.org/10.1007/s12185-019-02796-7
Autor:
Maria Teresa Sanz-Martínez, Laura Viñas-Giménez, Kishore Malyavantham, Chelsea Bentow, Albert Selva-O'Callaghan, Ariadna Anunciacion-Llunell, Andrea Seaman, Michael Mahler
Publikováno v:
Scientia
Diagnostics
Diagnostics; Volume 11; Issue 12; Pages: 2246
Diagnostics, Vol 11, Iss 2246, p 2246 (2021)
Diagnostics
Diagnostics; Volume 11; Issue 12; Pages: 2246
Diagnostics, Vol 11, Iss 2246, p 2246 (2021)
Autoantibodies; Dermatomyositis; Diagnosis Autoanticuerpos; Dermatomiositis; Diagnóstico Autoanticossos; Dermatomiositis; Diagnòstic (1) Background: Myositis specific antibodies (MSA) represent important diagnostic and stratification tools in idiop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e185b548b2caa95640b1fc60241c598
https://hdl.handle.net/11351/7616
https://hdl.handle.net/11351/7616
Autor:
Laura Viñas-Giménez, Natàlia Padilla, Laura Batlle-Masó, Ferran Casals, Jacques G. Rivière, Mónica Martínez-Gallo, Xavier de la Cruz, Roger Colobran
Publikováno v:
Frontiers in Immunology
Frontiers in Immunology, Vol 11 (2020)
Digital.CSIC. Repositorio Institucional del CSIC
instname
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Frontiers in Immunology, Vol 11 (2020)
Digital.CSIC. Repositorio Institucional del CSIC
instname
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Background: Primary immunodeficiencies (PIDs) are a heterogeneous group of disorders. The lack of comprehensive disease-specific mutation databases may hinder or delay classification of the genetic variants found in samples from these patients. This
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c10b5d7b81ec7a21f30c272560ed459b
https://pubmed.ncbi.nlm.nih.gov/32076423
https://pubmed.ncbi.nlm.nih.gov/32076423
Autor:
Michael Mahler, Kishore Malyavantham, Andrea Seaman, Chelsea Bentow, Ariadna Anunciacion-Llunell, María Teresa Sanz-Martínez, Laura Viñas-Gimenez, Albert Selva-O’Callaghan
Publikováno v:
Diagnostics, Vol 11, Iss 12, p 2246 (2021)
(1) Background: Myositis specific antibodies (MSA) represent important diagnostic and stratification tools in idiopathic inflammatory myositis (IIM) patients. Here we aimed to evaluate the clinical performance of MSA profiled by a novel particle base
Externí odkaz:
https://doaj.org/article/f3b280542e2943a8be6617b971ed2bac