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Does absolute excess of alpha chains compromise the benefit of splenectomy in patients with thalassemia intermedia?

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dc.contributor.author Graziadei G.
dc.contributor.author Refaldi C.
dc.contributor.author Barcellini W.
dc.contributor.author Cesaretti C.
dc.contributor.author Cassinero E.
dc.contributor.author Musallam K.M.
dc.contributor.author Cappellini M.D.
dc.contributor.editor
dc.date 2012
dc.date.accessioned 2017-10-05T15:39:55Z
dc.date.available 2017-10-05T15:39:55Z
dc.date.issued 2012
dc.identifier 10.3324/haematol.2011.046730
dc.identifier.isbn
dc.identifier.issn 03906078
dc.identifier.uri http://hdl.handle.net/10938/17153
dc.description.abstract [No abstract available]
dc.format.extent
dc.format.extent Pages: (151-153)
dc.language English
dc.publisher PAVIA
dc.relation.ispartof Publication Name: Haematologica; Publication Year: 2012; Volume: 97; no. 1; Pages: (151-153);
dc.relation.ispartofseries
dc.relation.uri
dc.source Scopus
dc.subject.other
dc.title Does absolute excess of alpha chains compromise the benefit of splenectomy in patients with thalassemia intermedia?
dc.type Letter
dc.contributor.affiliation Graziadei, G., Hereditary Anemia Center, Department of Internal Medicine, Fondazione IRCCS 'Ca' Granda' Ospedale Maggiore Policlinico, Università di Milano, Granelli, Via Francesco Sforza, 35 20122, Milano, Italy
dc.contributor.affiliation Refaldi, C., Hereditary Anemia Center, Department of Internal Medicine, Fondazione IRCCS 'Ca' Granda' Ospedale Maggiore Policlinico, Università di Milano, Granelli, Via Francesco Sforza, 35 20122, Milano, Italy
dc.contributor.affiliation Barcellini, W., Hematology Unit, Fondazione IRCCS 'Ca' Granda' Ospedale Maggiore Policlinico, Università di Milano, Milano, Italy
dc.contributor.affiliation Cesaretti, C., UOSD Genetica Medica, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milano, Italy
dc.contributor.affiliation Cassinero, E., Hereditary Anemia Center, Department of Internal Medicine, Fondazione IRCCS 'Ca' Granda' Ospedale Maggiore Policlinico, Università di Milano, Granelli, Via Francesco Sforza, 35 20122, Milano, Italy
dc.contributor.affiliation Musallam, K.M., Department of Internal Medicine, American University of Beirut Medical Center, Beirut, Lebanon
dc.contributor.affiliation Cappellini, M.D., Hereditary Anemia Center, Department of Internal Medicine, Fondazione IRCCS 'Ca' Granda' Ospedale Maggiore Policlinico, Università di Milano, Granelli, Via Francesco Sforza, 35 20122, Milano, Italy
dc.contributor.authorAddress Cappellini, M. D.; Hereditary Anemia Center, Department of Internal Medicine, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Università di Milano, Granelli, Via Francesco Sforza, 35 20122, Milano, Italy; email: maria.cappellini@unimi.it
dc.contributor.authorCorporate University: American University of Beirut Medical Center; Faculty: Faculty of Medicine; Department: Internal Medicine;
dc.contributor.authorDepartment Internal Medicine
dc.contributor.authorDivision
dc.contributor.authorEmail maria.cappellini@unimi.it
dc.contributor.authorFaculty Faculty of Medicine
dc.contributor.authorInitials Graziadei, G
dc.contributor.authorInitials Refaldi, C
dc.contributor.authorInitials Barcellini, W
dc.contributor.authorInitials Cesaretti, C
dc.contributor.authorInitials Cassinero, E
dc.contributor.authorInitials Musallam, KM
dc.contributor.authorInitials Cappellini, MD
dc.contributor.authorOrcidID
dc.contributor.authorReprintAddress Cappellini, MD (reprint author), Univ Milan, Fdn IRCSS Ca Granda Osped Maggiore Policlin, Dept Internal Med, Hereditary Anemia Ctr, Via Francesco Sforza 35, I-20122 Milan, Italy.
dc.contributor.authorResearcherID
dc.contributor.authorUniversity American University of Beirut Medical Center
dc.description.cited Camaschella C, 1997, AM J HEMATOL, V55, P83, DOI 10.1002-(SICI)1096-8652(199706)55:283::AID-AJH63.3.CO;2-M; Cappellini MD, 2010, ANN NY ACAD SCI, V1202, P231, DOI 10.1111-j.1749-6632.2010.05548.x; Cappellini MD, 2000, BRIT J HAEMATOL, V111, P467, DOI 10.1046-j.1365-2141.2000.02376.x; Harteveld CL, 2008, BLOOD CELL MOL DIS, V40, P312, DOI 10.1016-j.bcmd.2007.11.006; Harteveld CL, 2005, J MED GENET, V42, P922, DOI 10.1136-jmg.2005.033597; MANNU F, 1995, BLOOD, V86, P2014; SAMPIETRO M, 1983, BRIT J HAEMATOL, V55, P709, DOI 10.1111-j.1365-2141.1983.tb02854.x; SHINAR E, 1990, SEMIN HEMATOL, V27, P70; Sollaino MC, 2009, HAEMATOL-HEMATOL J, V94, P1445, DOI 10.3324-haematol.2009.005728; Taher AT, 2011, BRIT J HAEMATOL, V152, P512, DOI 10.1111-j.1365-2141.2010.08486.x; Taher AT, 2010, J THROMB HAEMOST, V8, P2152, DOI 10.1111-j.1538-7836.2010.03940.x
dc.description.citedCount 1
dc.description.citedTotWOSCount 1
dc.description.citedWOSCount 1
dc.format.extentCount 3
dc.identifier.articleNo
dc.identifier.coden HAEMA
dc.identifier.pubmedID 21993684
dc.identifier.scopusID 84855249050
dc.identifier.url
dc.publisher.address VIA GIUSEPPE BELLI 4, 27100 PAVIA, ITALY
dc.relation.ispartofConference
dc.relation.ispartofConferenceCode
dc.relation.ispartofConferenceDate
dc.relation.ispartofConferenceHosting
dc.relation.ispartofConferenceLoc
dc.relation.ispartofConferenceSponsor
dc.relation.ispartofConferenceTitle
dc.relation.ispartofFundingAgency
dc.relation.ispartOfISOAbbr Haematol-Hematol. J.
dc.relation.ispartOfIssue 1
dc.relation.ispartOfPart
dc.relation.ispartofPubTitle Haematologica
dc.relation.ispartofPubTitleAbbr Haematologica
dc.relation.ispartOfSpecialIssue
dc.relation.ispartOfSuppl
dc.relation.ispartOfVolume 97
dc.source.ID WOS:000299870500026
dc.type.publication Journal
dc.subject.otherAuthKeyword Adverse outcome
dc.subject.otherAuthKeyword Alpha chains
dc.subject.otherAuthKeyword Excess
dc.subject.otherAuthKeyword Splenectomy
dc.subject.otherAuthKeyword Thalassemia intermedia
dc.subject.otherChemCAS hemoglobin, 9008-02-0
dc.subject.otherChemCAS alpha-Globins
dc.subject.otherIndex alpha globin
dc.subject.otherIndex hemoglobin
dc.subject.otherIndex adolescent
dc.subject.otherIndex adult
dc.subject.otherIndex alpha chain
dc.subject.otherIndex alpha globin gene
dc.subject.otherIndex anemia
dc.subject.otherIndex beta globin gene
dc.subject.otherIndex blood transfusion
dc.subject.otherIndex case report
dc.subject.otherIndex chelation therapy
dc.subject.otherIndex DNA determination
dc.subject.otherIndex father
dc.subject.otherIndex female
dc.subject.otherIndex gene
dc.subject.otherIndex hemoglobin blood level
dc.subject.otherIndex human
dc.subject.otherIndex Italy
dc.subject.otherIndex letter
dc.subject.otherIndex male
dc.subject.otherIndex mother
dc.subject.otherIndex sibling
dc.subject.otherIndex splenectomy
dc.subject.otherIndex thalassemia
dc.subject.otherIndex thalassemia intermedia
dc.subject.otherIndex treatment response
dc.subject.otherIndex Adolescent
dc.subject.otherIndex Adult
dc.subject.otherIndex alpha-Globins
dc.subject.otherIndex beta-Thalassemia
dc.subject.otherIndex Female
dc.subject.otherIndex Humans
dc.subject.otherIndex Male
dc.subject.otherIndex Middle Aged
dc.subject.otherIndex Sibling Relations
dc.subject.otherIndex Splenectomy
dc.subject.otherIndex Young Adult
dc.subject.otherKeywordPlus HETEROZYGOUS BETA-THALASSEMIA
dc.subject.otherKeywordPlus PHENOTYPES
dc.subject.otherWOS Hematology


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