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Report of a rare co-incidence of congenital factor V deficiency and thalassemia intermedia in a family

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dc.contributor.author Mourad Y.A.
dc.contributor.author Shamseddine A.
dc.contributor.author Hamdan A.
dc.contributor.author Koussa S.
dc.contributor.author Taher A.
dc.contributor.editor
dc.date Jul-2004
dc.date.accessioned 2017-10-05T15:37:22Z
dc.date.available 2017-10-05T15:37:22Z
dc.date.issued 2004
dc.identifier
dc.identifier.isbn
dc.identifier.issn 02564947
dc.identifier.uri http://hdl.handle.net/10938/15672
dc.description.abstract [No abstract available]
dc.format.extent
dc.format.extent Pages: (301-302)
dc.language English
dc.publisher RIYADH
dc.relation.ispartof Publication Name: Annals of Saudi Medicine; Publication Year: 2004; Volume: 24; no. 4; Pages: (301-302);
dc.relation.ispartofseries
dc.relation.uri
dc.source Scopus
dc.subject.other
dc.title Report of a rare co-incidence of congenital factor V deficiency and thalassemia intermedia in a family
dc.type Article
dc.contributor.affiliation Mourad, Y.A., Division of Hematology-Oncology, American Univ. of Beirut-Med. Center, Box 113, 6044 Beirut, Lebanon
dc.contributor.affiliation Shamseddine, A., Division of Hematology-Oncology, American Univ. of Beirut-Med. Center, Box 113, 6044 Beirut, Lebanon
dc.contributor.affiliation Hamdan, A., Department of Internal Medicine, American Univ. of Beirut-Med. Center, Box 113, 6044 Beirut, Lebanon
dc.contributor.affiliation Koussa, S., Chronic Care Center, Hazmieha, Lebanon
dc.contributor.affiliation Taher, A., Division of Hematology-Oncology, American Univ. of Beirut-Med. Center, Box 113, 6044 Beirut, Lebanon
dc.contributor.authorAddress Taher, A.; Division of Hematology-Oncology, Department of Internal Medicine, American Univ. of Beirut-Med. Center, Box 113, 6044 Beirut, Lebanon; email: ataher@aub.edu.lb
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 ataher@aub.edu.lb
dc.contributor.authorFaculty Faculty of Medicine
dc.contributor.authorInitials Abou Mourad, Y
dc.contributor.authorInitials Shamseddine, A
dc.contributor.authorInitials Hamdan, A
dc.contributor.authorInitials Koussa, S
dc.contributor.authorInitials Taher, A
dc.contributor.authorOrcidID
dc.contributor.authorReprintAddress Taher, A (reprint author), Amer Univ Beirut, Med Ctr, Div Hematol and Oncol, Box 113-6044, Beirut, Lebanon.
dc.contributor.authorResearcherID
dc.contributor.authorUniversity American University of Beirut Medical Center
dc.description.cited CHIU HC, 1983, J CLIN INVEST, V72, P493, DOI 10.1172-JCI110997; CHIU HC, 1985, J CLIN INVEST, V75, P339, DOI 10.1172-JCI111706; Giannini E, 1998, ITAL J GASTROENTEROL, V30, P633; GIROLAMI A, 1985, CLIN HAEMATOL, V14, P385; Lak M, 1998, BRIT J HAEMATOL, V103, P1067; MANOTTI C, 1989, HAEMOSTASIS, V19, P331; Peyvandi F, 2002, HAEMOPHILIA, V8, P308, DOI 10.1046-j.1365-2516.2002.00633.x; Qatanani M, 2000, EUR J HAEMATOL, V64, P237, DOI 10.1034-j.1600-0609.2000.90087.x; Tuddenham EGD, 1994, MOL GENETICS HEMOSTA
dc.description.citedCount
dc.description.citedTotWOSCount 0
dc.description.citedWOSCount 0
dc.format.extentCount 2
dc.identifier.articleNo
dc.identifier.coden ANSME
dc.identifier.pubmedID 15387502
dc.identifier.scopusID 4344669894
dc.identifier.url
dc.publisher.address PUBLICATIONS OFFICE PO BOX 3354, RIYADH 11211, SAUDI ARABIA
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 Ann. Saudi Med.
dc.relation.ispartOfIssue 4
dc.relation.ispartOfPart
dc.relation.ispartofPubTitle Annals of Saudi Medicine
dc.relation.ispartofPubTitleAbbr Ann. Saudi Med.
dc.relation.ispartOfSpecialIssue
dc.relation.ispartOfSuppl
dc.relation.ispartOfVolume 24
dc.source.ID WOS:000223257700017
dc.type.publication Journal
dc.subject.otherAuthKeyword
dc.subject.otherChemCAS blood clotting factor 5, 9001-24-5, 9013-23-4
dc.subject.otherChemCAS hemoglobin, 9008-02-0
dc.subject.otherIndex beta1 integrin
dc.subject.otherIndex blood clotting factor 5
dc.subject.otherIndex fresh frozen plasma
dc.subject.otherIndex hemoglobin
dc.subject.otherIndex adult
dc.subject.otherIndex allogenic bone marrow transplantation
dc.subject.otherIndex article
dc.subject.otherIndex beta thalassemia
dc.subject.otherIndex blood clotting factor 5 deficiency
dc.subject.otherIndex blood transfusion
dc.subject.otherIndex case report
dc.subject.otherIndex comorbidity
dc.subject.otherIndex disease severity
dc.subject.otherIndex erythrocyte transfusion
dc.subject.otherIndex family study
dc.subject.otherIndex female
dc.subject.otherIndex genotype
dc.subject.otherIndex heart atrium septum defect
dc.subject.otherIndex heterozygosity
dc.subject.otherIndex homozygosity
dc.subject.otherIndex human
dc.subject.otherIndex inheritance
dc.subject.otherIndex male
dc.subject.otherIndex menorrhagia
dc.subject.otherIndex mother
dc.subject.otherIndex open heart surgery
dc.subject.otherIndex pericardial effusion
dc.subject.otherIndex priority journal
dc.subject.otherIndex reverse transcription polymerase chain reaction
dc.subject.otherIndex sibling
dc.subject.otherIndex Adolescent
dc.subject.otherIndex Adult
dc.subject.otherIndex Factor V Deficiency
dc.subject.otherIndex Family
dc.subject.otherIndex Female
dc.subject.otherIndex Genetic Predisposition to Disease
dc.subject.otherIndex Humans
dc.subject.otherIndex Male
dc.subject.otherIndex Thalassemia
dc.subject.otherKeywordPlus BETA-THALASSEMIA
dc.subject.otherKeywordPlus COAGULATION
dc.subject.otherWOS Medicine, General and Internal


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