AUB ScholarWorks

Celiac disease, Behçet, and idiopathic thrombocytopenic purpura in siblings of a patient with multiple sclerosis

Show simple item record

dc.contributor.author Yamout B.
dc.contributor.author Usta J.
dc.contributor.author Itani S.
dc.contributor.author Yaghi S.
dc.contributor.editor
dc.date Nov-2009
dc.date.accessioned 2017-10-05T15:37:41Z
dc.date.available 2017-10-05T15:37:41Z
dc.date.issued 2009
dc.identifier 10.1177/1352458509345908
dc.identifier.isbn
dc.identifier.issn 13524585
dc.identifier.uri http://hdl.handle.net/10938/15874
dc.description.abstract Multiple sclerosis (MS) is a demyelinating disease of uncertain etiology. Many genetic and environmental risk factors have been associated with this disease including certain human leukocyte antigen haplotypes, Epstein-Barr virus infection, and vitamin D deficiency. We report a 30-year-old woman with MS, the product of consanguineous marriage, and three siblings with three different autoimmune diseases: idiopathic thrombocytopenic purpura, celiac disease, and Behçet's disease. © The Author(s) 2009.
dc.format.extent
dc.format.extent Pages: (1368-1371)
dc.language English
dc.publisher LONDON
dc.relation.ispartof Publication Name: Multiple Sclerosis; Publication Year: 2009; Volume: 15; no. 11; Pages: (1368-1371);
dc.relation.ispartofseries
dc.relation.uri
dc.source Scopus
dc.subject.other
dc.title Celiac disease, Behçet, and idiopathic thrombocytopenic purpura in siblings of a patient with multiple sclerosis
dc.type Article
dc.contributor.affiliation Yamout, B., Department of Internal Medicine, American University of Beirut - Medical Center, Beirut, Lebanon
dc.contributor.affiliation Usta, J., Department of Family Medicine, American University of Beirut - Medical Center, Beirut, Lebanon
dc.contributor.affiliation Itani, S., Department of Internal Medicine, American University of Beirut - Medical Center, Beirut, Lebanon
dc.contributor.affiliation Yaghi, S., Department of Internal Medicine, American University of Beirut - Medical Center, Beirut, Lebanon, American University of Beirut - Medical Center, P.O. Box 11-0236, Riad El Solh 1107 2020 Beirut, Lebanon
dc.contributor.authorAddress Yaghi, S.; American University of Beirut - Medical Center, P.O. Box 11-0236, Riad El Solh 1107 2020 Beirut, Lebanon; email: shadiyaghi@yahoo.com
dc.contributor.authorCorporate University: American University of Beirut Medical Center; Faculty: Faculty of Medicine; Department: Internal Medicine; Division: Neurology;
dc.contributor.authorDepartment Internal Medicine
dc.contributor.authorDivision Neurology
dc.contributor.authorEmail shadiyaghi@yahoo.com
dc.contributor.authorFaculty Faculty of Medicine
dc.contributor.authorInitials Yamout, B
dc.contributor.authorInitials Usta, J
dc.contributor.authorInitials Itani, S
dc.contributor.authorInitials Yaghi, S
dc.contributor.authorOrcidID
dc.contributor.authorReprintAddress Yaghi, S (reprint author), Amer Univ Beirut, Med Ctr, Dept Internal Med, POB 11-0236,Riad El Solh 1107 2020, Beirut, Lebanon.
dc.contributor.authorResearcherID
dc.contributor.authorUniversity American University of Beirut Medical Center
dc.description.cited Alemany-Rodriguez MJ, 2005, REV NEUROLOGIA, V40, P594; Banwell Brenda L, 2004, Curr Neurol Neurosci Rep, V4, P245, DOI 10.1007-s11910-004-0045-1; Barcellos LF, 2006, LANCET NEUROL, V5, P924, DOI 10.1016-S1474-4422(06)70552-X; BRAY PF, 1992, NEUROLOGY, V42, P1798; Broadley SA, 2000, BRAIN, V123, P1102, DOI 10.1093-brain-123.6.1102; Heward J, 1997, CLIN SCI, V93, P479; Kristiansen OP, 2000, GENES IMMUN, V1, P170, DOI 10.1038-sj.gene.6363655; Nielsen NM, 2008, MULT SCLER J, V14, P823, DOI 10.1177-1352458508088936; Ramagopalan SV, 2009, PLOS GENET, V5, P1; Willer CJ, 2003, P NATL ACAD SCI USA, V100, P12877, DOI 10.1073-pnas.1932604100
dc.description.citedCount 1
dc.description.citedTotWOSCount 0
dc.description.citedWOSCount 0
dc.format.extentCount 4
dc.identifier.articleNo
dc.identifier.coden MUSCF
dc.identifier.pubmedID 19825890
dc.identifier.scopusID 70450173100
dc.identifier.url
dc.publisher.address 1 OLIVERS YARD, 55 CITY ROAD, LONDON EC1Y 1SP, 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 Mult. Scler.
dc.relation.ispartOfIssue 11
dc.relation.ispartOfPart
dc.relation.ispartofPubTitle Multiple Sclerosis
dc.relation.ispartofPubTitleAbbr Mult. Scler.
dc.relation.ispartOfSpecialIssue
dc.relation.ispartOfSuppl
dc.relation.ispartOfVolume 15
dc.source.ID WOS:000271536400017
dc.type.publication Journal
dc.subject.otherAuthKeyword Autoimmune diseases
dc.subject.otherAuthKeyword Behçet's disease
dc.subject.otherAuthKeyword Celiac disease
dc.subject.otherAuthKeyword Consanguineous
dc.subject.otherAuthKeyword Idiopathic thrombocytopenic
dc.subject.otherAuthKeyword Multiple sclerosis
dc.subject.otherAuthKeyword Purpura
dc.subject.otherChemCAS gadolinium, 7440-54-2
dc.subject.otherIndex beta interferon
dc.subject.otherIndex gadolinium
dc.subject.otherIndex leukocyte antigen
dc.subject.otherIndex steroid
dc.subject.otherIndex adult
dc.subject.otherIndex article
dc.subject.otherIndex Behcet disease
dc.subject.otherIndex case report
dc.subject.otherIndex celiac disease
dc.subject.otherIndex cerebrospinal fluid
dc.subject.otherIndex clinical feature
dc.subject.otherIndex consanguineous marriage
dc.subject.otherIndex dizziness
dc.subject.otherIndex family history
dc.subject.otherIndex female
dc.subject.otherIndex human
dc.subject.otherIndex idiopathic thrombocytopenic purpura
dc.subject.otherIndex multiple sclerosis
dc.subject.otherIndex nerve paralysis
dc.subject.otherIndex nuclear magnetic resonance imaging
dc.subject.otherIndex parent
dc.subject.otherIndex physical examination
dc.subject.otherIndex sibling
dc.subject.otherIndex unsteadiness
dc.subject.otherIndex walking difficulty
dc.subject.otherIndex weakness
dc.subject.otherIndex Adult
dc.subject.otherIndex Autoimmune Diseases
dc.subject.otherIndex Behcet Syndrome
dc.subject.otherIndex Brain
dc.subject.otherIndex Celiac Disease
dc.subject.otherIndex Consanguinity
dc.subject.otherIndex Demyelinating Diseases
dc.subject.otherIndex Female
dc.subject.otherIndex Humans
dc.subject.otherIndex Magnetic Resonance Imaging
dc.subject.otherIndex Multiple Sclerosis
dc.subject.otherIndex Pedigree
dc.subject.otherIndex Platelet Count
dc.subject.otherIndex Purpura, Thrombocytopenic, Idiopathic
dc.subject.otherIndex Siblings
dc.subject.otherKeywordPlus AUTOIMMUNE-DISEASES
dc.subject.otherKeywordPlus 1ST-DEGREE RELATIVES
dc.subject.otherKeywordPlus SUSCEPTIBILITY
dc.subject.otherWOS Clinical Neurology


Files in this item

Files Size Format View

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record

Search AUB ScholarWorks


Browse

My Account