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Severe macrothrombocytopenia with platelet CD9 deficiency responsive to romiplostim
dc.contributor.authorSeddiq, Marjilla
dc.contributor.authorGadgeel, Manisha
dc.contributor.authorPersaud, Yogindra
dc.contributor.authorLafferty, Jennifer
dc.contributor.authorSavaşan, Süreyya
dc.date.accessioned2020-09-02T14:59:23Z
dc.date.availableWITHHELD_12_MONTHS
dc.date.available2020-09-02T14:59:23Z
dc.date.issued2020-08
dc.identifier.citationSeddiq, Marjilla; Gadgeel, Manisha; Persaud, Yogindra; Lafferty, Jennifer; Savaşan, Süreyya (2020). "Severe macrothrombocytopenia with platelet CD9 deficiency responsive to romiplostim." British Journal of Haematology 190(4): e239-e242.
dc.identifier.issn0007-1048
dc.identifier.issn1365-2141
dc.identifier.urihttps://hdl.handle.net/2027.42/156447
dc.publisherWiley Periodicals, Inc.
dc.subject.othersevere
dc.subject.otherbleeding
dc.subject.otherplatelet CD9 deficiency
dc.subject.otherromiplostim
dc.subject.othermacrothrombocytopenia
dc.titleSevere macrothrombocytopenia with platelet CD9 deficiency responsive to romiplostim
dc.typeArticle
dc.rights.robotsIndexNoFollow
dc.subject.hlbsecondlevelOncology and Hematology
dc.subject.hlbtoplevelHealth Sciences
dc.description.peerreviewedPeer Reviewed
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/156447/2/bjh16812_am.pdfen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/156447/1/bjh16812.pdfen_US
dc.identifier.doi10.1111/bjh.16812
dc.identifier.sourceBritish Journal of Haematology
dc.identifier.citedreferenceLambert MP. Inherited platelet disorders: a modern approach to evaluation and treatment. Hematol Oncol Clin North Am. 2019; 33: 471 - 87.
dc.identifier.citedreferenceBeltrame MP, Malvezzi M, Zanis J, Pasquini R. Flow cytometry as a tool in the diagnosis of bernard- Soulier syndrome in brazilian patients. Platelets. 2009; 20: 229 - 34.
dc.identifier.citedreferenceBoeckelmann D, Hengartner H, Greinacher A, Nowak- Göttl U, Sachs UJ, Peter K, et al. Patients with Bernard- Soulier syndrome and different severity of the bleeding phenotype. Blood Cell Mol Dis. 2017; 67: 69 - 74.
dc.identifier.citedreferenceNoris P, Biino G, Pecci A, Civaschi E, Savoia A, Seri M, et al. Platelet diameters in inherited thrombocytopenias: analysis of 376 patients with all known disorders. Blood. 2014; 124: 4 - 11.
dc.identifier.citedreferenceJennings LK, Crossno JT, Fox CF, White MM, Green CA. Platelet p24/CD9, a Member of the Tetraspanin Family of Proteins. Ann NY Acad Sci. 1994; 714: 175 - 84.
dc.identifier.citedreferenceSlupsky JR, Kamiguti AS, Rhodes NP, Cawley JC, Shaw ARE, Zuzel M. The platelet antigens CD9, CD42 and integrin α(IIb)β(IIIa) can be topographically associated and transduce functionally similar signals. Eur J Biochem. 1997; 244: 168 - 75.
dc.identifier.citedreferenceCharrin S, Jouannet S, Boucheix C, Rubinstein E. Tetraspanins at a glance. J Cell Sci. 2014; 127: 3641 - 8.
dc.identifier.citedreferenceZaninetti C, Gresele P, Bertomoro A, Klersy C, de Candia E, Veneri D, et al. Eltrombopag for the treatment of inherited thrombocytopenias: a phase II clinical trial. Haematologica. 2020; 105: 820 - 8.
dc.identifier.citedreferenceRodeghiero F, Pecci A, Balduini CL. Thrombopoietin receptor agonists in hereditary thrombocytopenias. J Thromb Haemost. 2018; 16: 1700 - 10.
dc.identifier.citedreferenceQiao J, Davis AK, Morel- Kopp MC, Ward CM, Gardiner EE, Andrews RK. Low levels of CD9 coincidental with a novel nonsense mutation in glycoprotein Ibβ in a patient with Bernard- Soulier syndrome. Ann Hematol. 2015; 94: 2069 - 71.
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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