A rare syndrome that can easily be missed: May-Hegglin anomaly
dc.authorscopusid | 56264100700 | |
dc.authorscopusid | 7004568106 | |
dc.authorscopusid | 6603472555 | |
dc.authorscopusid | 8617232800 | |
dc.authorscopusid | 8617232900 | |
dc.authorscopusid | 8617233000 | |
dc.contributor.author | Aydo?du I. | |
dc.contributor.author | Kaya E. | |
dc.contributor.author | Kuku I. | |
dc.contributor.author | Ali Erkurt M. | |
dc.contributor.author | Görgel A. | |
dc.contributor.author | Özhan O. | |
dc.date.accessioned | 2024-08-04T20:01:09Z | |
dc.date.available | 2024-08-04T20:01:09Z | |
dc.date.issued | 2005 | |
dc.department | İnönü Üniversitesi | en_US |
dc.description.abstract | May-Hegglin is a rare disease characterized by macrothrombocytopenia and presence of Döhle-like bodies in white cells. We present a patient treated with acute myeloid leukemia had pale-blue colored inclusion bodies assuming Döhle in his neutrophils. | en_US |
dc.identifier.endpage | 93 | en_US |
dc.identifier.issn | 1300-7777 | |
dc.identifier.issue | 2 | en_US |
dc.identifier.scopus | 2-s2.0-22644433057 | en_US |
dc.identifier.scopusquality | Q3 | en_US |
dc.identifier.startpage | 91 | en_US |
dc.identifier.uri | https://hdl.handle.net/11616/91298 | |
dc.identifier.volume | 22 | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.language.iso | en | en_US |
dc.relation.ispartof | Turkish Journal of Haematology | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Leukemia | en_US |
dc.subject | May-Hegglin | en_US |
dc.subject | Thrombocytopenia | en_US |
dc.title | A rare syndrome that can easily be missed: May-Hegglin anomaly | en_US |
dc.type | Article | en_US |