| dc.contributor.author | Karakuş, Volkan | |
| dc.contributor.author | Kaya, Egemen | |
| dc.contributor.author | Dere, Yelda | |
| dc.contributor.author | Şahin, Fahri | |
| dc.date.accessioned | 2022-09-20T11:19:19Z | |
| dc.date.available | 2022-09-20T11:19:19Z | |
| dc.date.issued | 2021 | en_US |
| dc.identifier.uri | https://hdl.handle.net/20.500.12868/1638 | |
| dc.identifier.uri | https://www.italjmed.org/index.php/ijm/article/view/itjm.2021.1319 | |
| dc.identifier.uri | https://doi.org/10.4081/itjm.2021.1319 | |
| dc.description.abstract | Paroxysmal nocturnal hemoglobinuria (PNH) is a clonal stem cell disease that manifests with chronic intravascular hemolysis, thrombosis, and bone marrow failure. Various degrees of cytopenias accompany the disease. Although laboratory and clinical findings are similar, the disease may show different courses and require different treatments. Herein, we report two different courses of PNH with similar clinical and laboratory findings. | en_US |
| dc.language.iso | eng | en_US |
| dc.relation.isversionof | 10.4081/itjm.2021.1319 | en_US |
| dc.rights | info:eu-repo/semantics/openAccess | en_US |
| dc.subject | Paroxysmal nocturnal hemoglobinuria | en_US |
| dc.subject | Thrombocytopeniaaplastic anemia | en_US |
| dc.title | Different clinical courses with the same findings: two cases of paroxysmal nocturnal hemoglobinuria presenting with thrombocytopenia | en_US |
| dc.type | article | en_US |
| dc.contributor.department | ALKÜ, Fakülteler, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü | en_US |
| dc.identifier.volume | 15 | en_US |
| dc.identifier.issue | 3 | en_US |
| dc.identifier.startpage | 188 | en_US |
| dc.identifier.endpage | 190 | en_US |
| dc.relation.journal | Italian Journal of Medicine | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
