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Long term follow-up of hyperimmunoglobulin M syndrome cases

dc.contributor.authorCinar, Suzan Adin
dc.contributor.authorBarlan, Isil B.
dc.contributor.authorBARIŞ, SAFA
dc.contributor.authorDENİZ, Günnur
dc.contributor.authorBahceciler, Nerin N.
dc.contributor.authorAYDINER, ELİF
dc.contributor.authorÖZDEMİR, Cevdet
dc.contributor.authorKeles, Sevgi
dc.date.accessioned2021-12-10T10:37:38Z
dc.date.available2021-12-10T10:37:38Z
dc.date.issued2010
dc.identifier.citationAYDINER E., ÖZDEMİR C., Keles S., BARIŞ S., Cinar S. A. , DENİZ G., Bahceciler N. N. , Barlan I. B. , "Long term follow-up of hyperimmunoglobulin M syndrome cases", ASTIM ALLERJI IMMUNOLOJI, cilt.8, sa.2, ss.101-107, 2010
dc.identifier.othervv_1032021
dc.identifier.otherav_4a738260-1c2d-4099-b39d-9062f6162c3f
dc.identifier.urihttp://hdl.handle.net/20.500.12627/170265
dc.description.abstractObjective: Hyperimmunoglobulin M (HIGM) syndromes are primary immunodeficiencies characterized by normal or elevated serum IgM levels with decreased levels of other immunoglobulin isotypes. Over the past decade rapid progress has been made in the molecular and genetic basis of HIGM and five distinct subgroups have been described.
dc.language.isoeng
dc.subjectHealth Sciences
dc.subjectTıp
dc.subjectImmunology and Allergy
dc.subjectSağlık Bilimleri
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectALERJİ
dc.titleLong term follow-up of hyperimmunoglobulin M syndrome cases
dc.typeMakale
dc.relation.journalASTIM ALLERJI IMMUNOLOJI
dc.contributor.departmentMarmara Üniversitesi , ,
dc.identifier.volume8
dc.identifier.issue2
dc.identifier.startpage101
dc.identifier.endpage107
dc.contributor.firstauthorID2695332


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