dc.contributor.author | Badr, Mohamed | |
dc.contributor.author | Al Hawsawi, Zakaria | |
dc.contributor.author | KILINÇ, YURDANUR | |
dc.contributor.author | Yesilipek, M. Akif | |
dc.contributor.author | Elsafy, Usama | |
dc.contributor.author | Karakas, Zeynep | |
dc.contributor.author | Tricta, Fernando | |
dc.contributor.author | Temin, Noemi Toiber | |
dc.contributor.author | Stilman, Anne | |
dc.contributor.author | Shebl, Shebl | |
dc.contributor.author | Rahman, Yousryeia Abdel | |
dc.contributor.author | Salama, Mostafa | |
dc.contributor.author | Elalfy, Mohssen | |
dc.contributor.author | Wali, Yasser A. | |
dc.contributor.author | Qari, Mohamad | |
dc.contributor.author | Al Damanhouri, Ghazi | |
dc.contributor.author | Al-Tonbary, Youssef | |
dc.contributor.author | Yazman, Dilek | |
dc.date.accessioned | 2021-03-04T12:30:45Z | |
dc.date.available | 2021-03-04T12:30:45Z | |
dc.date.issued | 2014 | |
dc.identifier.citation | Elalfy M., Wali Y. A. , Qari M., Al Damanhouri G., Al-Tonbary Y., Yazman D., Al Hawsawi Z., Karakas Z., KILINÇ Y., Yesilipek M. A. , et al., "Deviating From Safety Guidelines During Deferiprone Therapy in Clinical Practice May Not be Associated With Higher Risk of Agranulocytosis", PEDIATRIC BLOOD & CANCER, cilt.61, sa.5, ss.879-884, 2014 | |
dc.identifier.issn | 1545-5009 | |
dc.identifier.other | vv_1032021 | |
dc.identifier.other | av_77a7ee39-1b50-4533-b5c1-19878f612f67 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/82133 | |
dc.identifier.uri | https://doi.org/10.1002/pbc.24920 | |
dc.description.abstract | BackgroundA risk associated with the iron chelator deferiprone is the development of neutropenia or agranulocytosis. Accordingly, the product label recommends weekly blood monitoring and immediate interruption of treatment upon detection of an absolute neutrophil count (ANC) <1.5x10(9)/L, out of concern that continued therapy might lead to a more severe drop. However, it is uncertain how these recommendations are followed under real-life conditions and, if they are not followed, whether continuation of therapy results in increased incidence of agranulocytosis. | |
dc.language.iso | eng | |
dc.subject | Klinik Tıp | |
dc.subject | HEMATOLOJİ | |
dc.subject | İç Hastalıkları | |
dc.subject | Hematoloji | |
dc.subject | Onkoloji | |
dc.subject | ONKOLOJİ | |
dc.subject | Sağlık Bilimleri | |
dc.subject | Tıp | |
dc.subject | PEDİATRİ | |
dc.subject | Dahili Tıp Bilimleri | |
dc.subject | Çocuk Sağlığı ve Hastalıkları | |
dc.subject | Klinik Tıp (MED) | |
dc.title | Deviating From Safety Guidelines During Deferiprone Therapy in Clinical Practice May Not be Associated With Higher Risk of Agranulocytosis | |
dc.type | Makale | |
dc.relation.journal | PEDIATRIC BLOOD & CANCER | |
dc.contributor.department | Ain Shams University , , | |
dc.identifier.volume | 61 | |
dc.identifier.issue | 5 | |
dc.identifier.startpage | 879 | |
dc.identifier.endpage | 884 | |
dc.contributor.firstauthorID | 214628 | |