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dc.rights.licenseopenen_US
hal.structure.identifierLaboratory of Hematology, Bordeaux University Hospital, Avenue de Magellan, 33604, Pessac
dc.contributor.authorMOUTHON, Paul
hal.structure.identifierBiologie des maladies cardiovasculaires = Biology of Cardiovascular Diseases
hal.structure.identifierLaboratory of Hematology, Bordeaux University Hospital, Avenue de Magellan, 33604, Pessac
dc.contributor.authorGUY, Alexandre
dc.contributor.authorD'OIRON, Roseline
dc.contributor.authorHARROCHE, Annie
dc.contributor.authorLEBRETON, Aurélien
dc.contributor.authorGOURGUECHON, Clément
dc.contributor.authorOUDOT-CHALLARD, Caroline
dc.contributor.authorHUGUENIN, Yoann
dc.date.accessioned2024-03-25T14:31:23Z
dc.date.available2024-03-25T14:31:23Z
dc.date.issued2024-02-01
dc.identifier.issn1365-2141en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/188960
dc.description.abstractEnAcquired haemophilia A (AHA) is a rare haemorrhagic disease characterised by new-onset haemorrhagic symptoms associated with a dramatic decrease in factor VIII levels and an anti-factor VIII neutralising autoantibody concentration >0.6 Bethesda units. Elderly people are often affected, whereas children are rarely affected; the paediatric incidence reported in the literature is about 0.045 case/million/year. For some time, the paediatric standard of care has been that for adults, but clinicians have often reported poor outcomes. Here, we describe the largest retrospective paediatric AHA cohort assembled to date, including eight patients diagnosed in France from 2000 to 2020.
dc.language.isoENen_US
dc.rightsAttribution-NonCommercial 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/us/*
dc.subject.enAdult
dc.subject.enHumans
dc.subject.enChild
dc.subject.enAged
dc.subject.enHemophilia A
dc.subject.enRetrospective Studies
dc.subject.enHemorrhage
dc.subject.enAutoantibodies
dc.subject.enFactor VIII
dc.title.enAcquired haemophilia A in paediatric patients: A retrospective French cohort of eight cases.
dc.title.alternativeBr J Haematolen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1111/bjh.19285en_US
dc.subject.halSciences du Vivant [q-bio]/Médecine humaine et pathologieen_US
dc.identifier.pubmed38192055en_US
bordeaux.journalBritish Journal of Haematologyen_US
bordeaux.page606-611en_US
bordeaux.volume204en_US
bordeaux.hal.laboratoriesBiologie des maladies cardiovasculaires (BMC) - UMR 1034en_US
bordeaux.issue2en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-04520216
hal.version1
hal.date.transferred2024-03-25T14:31:25Z
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exporttrue
workflow.import.sourcepubmed
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=British%20Journal%20of%20Haematology&rft.date=2024-02-01&rft.volume=204&rft.issue=2&rft.spage=606-611&rft.epage=606-611&rft.eissn=1365-2141&rft.issn=1365-2141&rft.au=MOUTHON,%20Paul&GUY,%20Alexandre&D'OIRON,%20Roseline&HARROCHE,%20Annie&LEBRETON,%20Aur%C3%A9lien&rft.genre=article


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