Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/105544
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dc.contributor.authorPlompen, Elisabeth P.C.-
dc.contributor.authorValk, Peter J.M.-
dc.contributor.authorChu, Isabel-
dc.contributor.authorMurad, Sarwa D.-
dc.contributor.authorPlessier, Aurélie-
dc.contributor.authorTuron, Fanny-
dc.contributor.authorTrebicka, Jonel-
dc.contributor.authorPrimignani, Massimo-
dc.contributor.authorGarcía Pagán, Juan Carlos-
dc.contributor.authorValla, Dominique-
dc.contributor.authorJanssen, Harry L.A.-
dc.contributor.authorLeebeek, Frank W. G.-
dc.date.accessioned2017-01-12T17:49:38Z-
dc.date.available2017-01-12T17:49:38Z-
dc.date.issued2015-06-
dc.identifier.issn0390-6078-
dc.identifier.urihttp://hdl.handle.net/2445/105544-
dc.descriptionCarta a l'editor-
dc.description.abstractWe studied the role of the recently identified CALR mutations in 141 patients with Budd-Chiari Syndrome (BCS) or portal vein thrombosis (PVT) in a large multinational cohort. A CALR mutation was present in one of the 141 patients (0.7%). This patient was previously diagnosed with primary myelofibrosis. This results in CALR positivity in one out of 44 (2.3%) patients with myeloproliferative neoplasm (MPN), and in one of 11 (9.1%) JAK2V617F negative patients diagnosed with MPN. We suggest that analysis of CALR mutations should be performed in JAK2V617F negative BCS and PVT patients...-
dc.format.extent3 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherFerrata Storti Foundation-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.3324/haematol.2014.120857-
dc.relation.ispartofHaematologica, 2015, vol. 100, num. 6, p. e226-8-
dc.relation.urihttps://doi.org/10.3324/haematol.2014.120857-
dc.rights(c) Ferrata Storti Foundation, 2015-
dc.sourceArticles publicats en revistes (Medicina)-
dc.subject.classificationHipertensió portal-
dc.subject.classificationMalalties del fetge-
dc.subject.classificationMutació (Biologia)-
dc.subject.classificationSíndrome de Budd-Chiari-
dc.subject.otherPortal hypertension-
dc.subject.otherLiver diseases-
dc.subject.otherMutation (Biology)-
dc.subject.otherBudd–Chiari syndrome-
dc.titleSomatic calreticulin mutations in patients with Budd-Chiari syndrome and portal vein thrombosis-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.identifier.idgrec650907-
dc.date.updated2017-01-12T17:49:38Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid25682604-
Appears in Collections:Articles publicats en revistes (Medicina)

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