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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorStepien, Karolina M.
dc.contributor.authorKieć-Wilk, Beata
dc.contributor.authorLampe, Christina
dc.contributor.authorTangeraas, Trine
dc.contributor.authorCefalo, Graziella
dc.contributor.authorBelmatoug, Nadia
dc.contributor.authordel Toro Riera, Mireia
dc.date.accessioned2022-03-14T13:33:18Z
dc.date.available2022-03-14T13:33:18Z
dc.date.issued2021-02
dc.identifier.citationStepien KM, Kieć-Wilk B, Lampe C, Tangeraas T, Cefalo G, Belmatoug N, et al. Challenges in Transition From Childhood to Adulthood Care in Rare Metabolic Diseases: Results From the First Multi-Center European Survey. Front Med. 2021 Feb;8:652358.
dc.identifier.issn2296-858X
dc.identifier.urihttps://hdl.handle.net/11351/7172
dc.descriptionMalalties metabòliques hereditàries; Malaltia rara; Procés de transició
dc.description.sponsorshipThis work was generated within the European Reference Network for Rare Hereditary Metabolic Disorders (MetabERN), co-funded by the European Union within the framework of the Third Health Programme ERN-2016 - Framework Partnership Agreement 2017–2021, Project ID No. 739543.
dc.language.isoeng
dc.publisherFrontiers Media
dc.relation.ispartofseriesFrontiers in Medicine;8
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScientia
dc.subjectMetabolisme - Trastorns - Aspectes genètics
dc.subjectDiàtesi
dc.subject.meshMetabolic Diseases
dc.subject.mesh/genetics
dc.subject.meshGenetic Predisposition to Disease
dc.titleChallenges in Transition From Childhood to Adulthood Care in Rare Metabolic Diseases: Results From the First Multi-Center European Survey
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.3389/fmed.2021.652358
dc.subject.decsenfermedades metabólicas
dc.subject.decs/genética
dc.subject.decspredisposición genética a la enfermedad
dc.relation.publishversionhttps://doi.org/10.3389/fmed.2021.652358
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Stepien KM] Adult Inherited Metabolic Diseases, Salford Royal NHS Foundation Trust, Salford, United Kingdom. [Kieć-Wilk B] Department of Metabolic Diseases and Diabetes, Krakow University Hospital, Krakow, Poland. Department of Metabolic Diseases, Medical College, Jagiellonian University, Krakow, Poland. [Lampe C] Department of Child Neurology, Center for Rare Diseases Giessen (ZSEGI), Justus-Liebig University, Giessen, Germany. [Tangeraas T] Norwegian National Unit for Newborn Screening, Division of Paediatric and Adolescent Medicine, Oslo University Hospital, Oslo, Norway. [Cefalo G] Department of Maternal and Child Health, San Paolo Hospital, University of Milan, ASST Santi Paolo e Carlo, Milan, Italy. [Belmatoug N] Referral Center for Lysosomal Diseases, AP-HP Nord, Beaujon Hospital, Paris University, Clichy, France. [Del Toro M] Servei de Neurologia Pediàtrica, Vall d'Hebron Hospital Universitari, Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain
dc.identifier.pmid33738294
dc.identifier.wos000629292700001
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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