About Pyrimidine 5’-Nucleotidase Deficiency
Journal Title: Turkish Journal of Hematology - Year 2013, Vol 30, Issue 2
Abstract
To the Editor, Agapidou et al.’s case of pyrimidine 5’-nucleotidase defi ciency and heterozygous α-thalassemia was an interesting co-existence [1]. Did the authors have the chance to study the offspring for these hereditary conditions from birth?
Authors and Affiliations
Şinasi Özsoylu
Keywords
Related Articles
- EP ID EP111136
- DOI 10.4274/Tjh.2013.0050
- Views 89
- Downloads 0
Deviation from Normal Values of Leukocyte and Erythroblast Parameters in Complete Blood Count is a Messenger for Platelet Abnormalities
Pediatrik Akut Miyeloid Lösemili Hastada Yüksek Doz Sitarabin Uygulamasına Bağlı Korneal Epitel Mikrokistler
Sole Infrequent Karyotypic Aberration Trisomy 6 in a Patient with Acute Myeloid Leukemia and Breast Cancer in Remission
Sole Infrequent Karyotypic Aberration Trisomy 6 in a Patient with Acute Myeloid Leukemia and Breast Cancer in Remission
Megadose Methylprednisolone (MDMP) for the Treatment of Steroid Refractory Patient with Diamond-Blackfan (D-B) Anemia
To the Editor, Dr. Malbora [1] and his colleagues reported metoclopramide in addition to corticosteroid in the treatment of a patient with steroid refractory Diamond-Blackfan (D-B) anemia in the recent issue of the Jour...
Kronik Miyeloid Lösemi Hastasında Gelişen İnterstisyel Pnömoni