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Budd-Chiari syndrome in a paroxysmal nocturnal hemoglobinuria patient with coexistence of factor II and MTHFR mutations [14]

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dc.contributor.author Shamseddine A.I.
dc.contributor.author Otrock Z.K.
dc.contributor.author Mahfouz R.A.R.
dc.contributor.author Makarem J.A.
dc.contributor.author Taher A.T.
dc.contributor.editor
dc.date May-2005
dc.date.accessioned 2017-10-05T15:59:38Z
dc.date.available 2017-10-05T15:59:38Z
dc.date.issued 2005
dc.identifier 10.1111/j.1538-7836.2005.01283.x
dc.identifier.isbn
dc.identifier.issn 15387933
dc.identifier.uri http://hdl.handle.net/10938/19133
dc.description.abstract [No abstract available]
dc.format.extent
dc.language English
dc.publisher OXFORD
dc.relation.ispartof Publication Name: Journal of Thrombosis and Haemostasis; Publication Year: 2005; Volume: 3; no. 5; Pages: (1111
dc.relation.ispartofseries
dc.relation.uri
dc.source Scopus
dc.subject.other
dc.title Budd-Chiari syndrome in a paroxysmal nocturnal hemoglobinuria patient with coexistence of factor II and MTHFR mutations [14]
dc.type Letter
dc.contributor.affiliation Shamseddine, A.I., Department of Internal Medicine, American University of Beirut Medical Center, Beirut, Lebanon
dc.contributor.affiliation Otrock, Z.K., Department of Internal Medicine, American University of Beirut Medical Center, Beirut, Lebanon
dc.contributor.affiliation Mahfouz, R.A.R., Department of Pathology and Laboratory Medicine, American University of Beirut Medical Center, Beirut, Lebanon
dc.contributor.affiliation Makarem, J.A., Department of Internal Medicine, American University of Beirut Medical Center, Beirut, Lebanon
dc.contributor.affiliation Taher, A.T., Department of Internal Medicine, American University of Beirut Medical Center, Beirut, Lebanon, Hematology-Oncology Division, Department of Internal Medicine, American University of Beirut, PO Box 113-0236, Beirut, Lebanon
dc.contributor.authorAddress Taher, A.T.; Hematology-Oncology Division, Department of Internal Medicine, American University of Beirut, PO Box 113-0236, Beirut, Lebanon; email: ataher@aub.edu.lb
dc.contributor.authorCorporate University: American University of Beirut Medical Center; Faculty: Faculty of Medicine; Department: Pathology and Laboratory Medicine;
dc.contributor.authorDepartment Pathology and Laboratory Medicine
dc.contributor.authorDivision
dc.contributor.authorEmail ataher@aub.edu.lb
dc.contributor.authorFaculty Faculty of Medicine
dc.contributor.authorInitials Shamseddine, AI
dc.contributor.authorInitials Otrock, ZK
dc.contributor.authorInitials Mahfouz, RAR
dc.contributor.authorInitials Makarem, JA
dc.contributor.authorInitials Taher, AT
dc.contributor.authorOrcidID
dc.contributor.authorReprintAddress Taher, AT (reprint author), Amer Univ Beirut, Div Hematol Oncol, Dept Internal Med, Med Ctr, POB 113-0236, Beirut, Lebanon.
dc.contributor.authorResearcherID
dc.contributor.authorUniversity American University of Beirut Medical Center
dc.description.cited Almawi WY, 2004, AM J HEMATOL, V76, P85, DOI 10.1002-ajh.20047; Dahlback B, 1997, THROMB HAEMOSTASIS, V78, P483; Graham IM, 1997, JAMA-J AM MED ASSOC, V277, P1775, DOI 10.1001-jama.277.22.1775; Poort SR, 1996, BLOOD, V88, P3698; Rotoli B, 1989, Baillieres Clin Haematol, V2, P113, DOI 10.1016-S0950-3536(89)80010-1; Smith Larry J, 2004, Clin Lab Sci, V17, P172; Taher A, 2003, THROMB HAEMOSTASIS, V89, P945
dc.description.citedCount 2
dc.description.citedTotWOSCount 2
dc.description.citedWOSCount 2
dc.format.extentCount -1110
dc.identifier.articleNo
dc.identifier.coden JTHOA
dc.identifier.pubmedID 15869626
dc.identifier.scopusID 23844473045
dc.identifier.url
dc.publisher.address 108 COWLEY RD, OXFORD OX4 1JF, OXON, ENGLAND
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 J. Thromb. Haemost.
dc.relation.ispartOfIssue 5
dc.relation.ispartOfPart
dc.relation.ispartofPubTitle Journal of Thrombosis and Haemostasis
dc.relation.ispartofPubTitleAbbr J. Thromb. Haemost.
dc.relation.ispartOfSpecialIssue
dc.relation.ispartOfSuppl
dc.relation.ispartOfVolume 3
dc.source.ID WOS:000229132000054
dc.type.publication Journal
dc.subject.otherAuthKeyword
dc.subject.otherChemCAS 5,10 methylenetetrahydrofolate reductase (FADH2), 9028-69-7
dc.subject.otherChemCAS heparin, 37187-54-5, 8057-48-5, 8065-01-8, 9005-48-5
dc.subject.otherChemCAS prothrombin, 9001-26-7
dc.subject.otherChemCAS warfarin, 129-06-6, 2610-86-8, 3324-63-8, 5543-58-8, 81-81-2
dc.subject.otherChemCAS blood clotting factor 5, 9001-24-5, 9013-23-4
dc.subject.otherChemCAS methylenetetrahydrofolate dehydrogenase (NAD), 82062-90-6
dc.subject.otherChemCAS Factor V, 9001-24-5
dc.subject.otherChemCAS Methylenetetrahydrofolate Dehydrogenase (NAD+), EC 1.5.1.15
dc.subject.otherChemCAS Prothrombin, 9001-26-7
dc.subject.otherChemCAS Warfarin, 81-81-2
dc.subject.otherIndex 5,10 methylenetetrahydrofolate reductase (FADH2)
dc.subject.otherIndex heparin
dc.subject.otherIndex prothrombin
dc.subject.otherIndex warfarin
dc.subject.otherIndex blood clotting factor 5
dc.subject.otherIndex methylenetetrahydrofolate dehydrogenase (NAD)
dc.subject.otherIndex prothrombin
dc.subject.otherIndex warfarin
dc.subject.otherIndex adult
dc.subject.otherIndex anamnesis
dc.subject.otherIndex ascites
dc.subject.otherIndex Budd Chiari syndrome
dc.subject.otherIndex case report
dc.subject.otherIndex computer assisted tomography
dc.subject.otherIndex disease association
dc.subject.otherIndex genotype
dc.subject.otherIndex hepatosplenomegaly
dc.subject.otherIndex human
dc.subject.otherIndex incidence
dc.subject.otherIndex letter
dc.subject.otherIndex male
dc.subject.otherIndex paroxysmal nocturnal hemoglobinuria
dc.subject.otherIndex point mutation
dc.subject.otherIndex priority journal
dc.subject.otherIndex risk factor
dc.subject.otherIndex treatment outcome
dc.subject.otherIndex vein thrombosis
dc.subject.otherIndex genetics
dc.subject.otherIndex hemoglobinuria
dc.subject.otherIndex heterozygote
dc.subject.otherIndex international normalized ratio
dc.subject.otherIndex liver vein thrombosis
dc.subject.otherIndex mutation
dc.subject.otherIndex paroxysmal nocturnal hemoglobinuria
dc.subject.otherIndex radiography
dc.subject.otherIndex spleen
dc.subject.otherIndex thrombophilia
dc.subject.otherIndex time
dc.subject.otherIndex Adult
dc.subject.otherIndex Ascites
dc.subject.otherIndex Factor V
dc.subject.otherIndex Hemoglobinuria
dc.subject.otherIndex Hemoglobinuria, Paroxysmal
dc.subject.otherIndex Hepatic Vein Thrombosis
dc.subject.otherIndex Heterozygote
dc.subject.otherIndex Humans
dc.subject.otherIndex International Normalized Ratio
dc.subject.otherIndex Male
dc.subject.otherIndex Methylenetetrahydrofolate Dehydrogenase (NAD+)
dc.subject.otherIndex Mutation
dc.subject.otherIndex Prothrombin
dc.subject.otherIndex Spleen
dc.subject.otherIndex Thrombophilia
dc.subject.otherIndex Time Factors
dc.subject.otherIndex Tomography, X-Ray Computed
dc.subject.otherIndex Warfarin
dc.subject.otherKeywordPlus VENOUS THROMBOSIS
dc.subject.otherKeywordPlus RISK-FACTOR
dc.subject.otherKeywordPlus GENE
dc.subject.otherWOS Hematology
dc.subject.otherWOS Peripheral Vascular Disease


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