dc.contributor | Vall d'Hebron Barcelona Hospital Campus |
dc.contributor.author | Argudo-Ramírez, Ana |
dc.contributor.author | Martín Nalda, Andrea |
dc.contributor.author | Pajares Garcia, Sonia |
dc.contributor.author | García Prat, Marina |
dc.contributor.author | Colobran Oriol, Roger |
dc.contributor.author | Rivière, Jacques |
dc.contributor.author | Soler Palacín, Pere |
dc.contributor.author | Marin Soria, José Luis |
dc.contributor.author | Lopez Galera, Rosa Maria |
dc.contributor.author | González de Aledo Castillo, José Manuel |
dc.contributor.author | Martínez Gallo, Mónica |
dc.date.accessioned | 2020-09-07T10:33:36Z |
dc.date.available | 2020-09-07T10:33:36Z |
dc.date.issued | 2019-10-22 |
dc.identifier.citation | Argudo-Ramírez A, Martín-Nalda A, Marín-Soria JL, López-Galera RM, Pajares-García S, González de Aledo-Castillo JM, et al. First universal newborn screening program for severe combined immunodeficiency in Europe: two-years' experience in Catalonia (Spain). Front Immunol. 2019 Oct 22;10:2406. |
dc.identifier.issn | 1664-3224 |
dc.identifier.uri | https://hdl.handle.net/11351/5217 |
dc.description | Cribratge de nadons; Immunodeficiència combinada greu; Cercles d'excisió de receptors de cèl·lules T |
dc.language.iso | eng |
dc.publisher | Frontiers Media |
dc.relation.ispartofseries | Frontiers in Immunology;10 |
dc.rights | Attribution 4.0 International |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ |
dc.source | Scientia |
dc.subject | Cribatge (Medicina) |
dc.subject | Síndromes de deficiència immunitària en els infants - Epidemiologia - Catalunya |
dc.subject.mesh | Neonatal Screening |
dc.subject.mesh | Severe Combined Immunodeficiency |
dc.subject.mesh | /epidemiology |
dc.subject.mesh | Catalonia |
dc.title | First universal newborn screening program for severe combined immunodeficiency in Europe: two-years' experience in Catalonia (Spain) |
dc.type | info:eu-repo/semantics/article |
dc.identifier.doi | 10.3389/fimmu.2019.02406 |
dc.subject.decs | cribado neonatal |
dc.subject.decs | inmunodeficiencia combinada grave |
dc.subject.decs | /epidemiología |
dc.subject.decs | Cataluña |
dc.relation.publishversion | https://www.frontiersin.org/articles/10.3389/fimmu.2019.02406/full |
dc.type.version | info:eu-repo/semantics/publishedVersion |
dc.audience | Professionals |
dc.contributor.authoraffiliation | [Argudo-Ramírez A, Marín-Soria JL, López-Galera RM, Pajares-García S, González de Aledo-Castillo JM] Newborn Screening Laboratory, Inborn Errors of Metabolism Division, Biochemistry and Molecular Genetics Department, Hospital Clínic, Barcelona, Spain. [Martín-Nalda A, García-Prat M, Riviere JG, Soler-Palacín P] Unitat de Patologia Infecciosa i Immunodeficiències de Pediatria, Vall d'Hebron Hospital Universitari, Barcelona, Spain. Jeffrey Modell Diagnostic and Research Center for Primary Immunodeficiencies, Barcelona, Spain. Universitat Autònoma de Barcelona, Barcelona, Spain. [Martínez-Gallo M] Servei d’ Immunologia, Vall d'Hebron Hospital Universitari, Barcelona, Spain. Jeffrey Modell Diagnostic and Research Center for Primary Immunodeficiencies, Barcelona, Spain. Universitat Autònoma de Barcelona, Barcelona, Spain. [Colobran R] Servei d’ Immunologia, Vall d'Hebron Hospital Universitari, Barcelona, Spain. Jeffrey Modell Diagnostic and Research Center for Primary Immunodeficiencies, Barcelona, Spain. Universitat Autònoma de Barcelona, Barcelona, Spain. Servei de Genètica Clínica i Molecular, Vall d'Hebron Hospital Universitari, Barcelona, Spain |
dc.identifier.pmid | 31695692 |
dc.identifier.wos | 000497335000001 |
dc.rights.accessrights | info:eu-repo/semantics/openAccess |