Werner's syndrome: a quite rare disease for differential diagnosis of scleroderma

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dc.authorid0000-0003-1710-7018en_US
dc.authorid0000-0002-1730-2991
dc.contributor.authorBeş, Cemal
dc.contributor.authorVardı, Şeref
dc.contributor.authorGüven, Melih
dc.contributor.authorSoy, Mehmet
dc.date.accessioned2021-06-23T19:27:08Z
dc.date.available2021-06-23T19:27:08Z
dc.date.issued2010
dc.departmentBAİBÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümüen_US
dc.description.abstractWerner's syndrome (WS) is an autosomal recessive disorder characterized by premature aging. The main features of the disease are scleroderma-like skin appearance, premature atherosclerosis, short stature, diabetes mellitus, early osteoporosis and early aging. Herein, we describe a patient with WS, who has scleroderma-like skin changes and discuss the literature about WS as a disease in the differential diagnosis of systemic sclerosis.en_US
dc.identifier.doi10.1007/s00296-009-0982-8
dc.identifier.endpage698en_US
dc.identifier.issn0172-8172
dc.identifier.issn1437-160X
dc.identifier.issue5en_US
dc.identifier.pmid19495768en_US
dc.identifier.scopus2-s2.0-77951023059en_US
dc.identifier.scopusqualityQ2en_US
dc.identifier.startpage695en_US
dc.identifier.urihttps://doi.org/10.1007/s00296-009-0982-8
dc.identifier.urihttps://hdl.handle.net/20.500.12491/6742
dc.identifier.volume30en_US
dc.identifier.wosWOS:000274634400022en_US
dc.identifier.wosqualityQ3en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.institutionauthorBeş, Cemal
dc.language.isoenen_US
dc.publisherSpringer Heidelbergen_US
dc.relation.ispartofRheumatology Internationalen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectWerner Syndromeen_US
dc.subjectSclerodermaen_US
dc.subjectDigital Ulcersen_US
dc.titleWerner's syndrome: a quite rare disease for differential diagnosis of sclerodermaen_US
dc.typeArticleen_US

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