Total antioxidant status in sickle cell anemia

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Oxidative status in sickle cell anemia

177 xxx They analyzed 651 patients with APL of whom 72 expressed CD56 (11%). CD56 + APL was significantly associated with high white blood cell counts, low albumin levels, the BCR3 isoform and coexpression of the CD2, CD34, CD7, HLA-DR, CD15 and CD117 antigens. For CD56 + APL, the 5-year relapse rate was 22% compared with a 10% relapse rate for CD56-APL (p-value = 0.006). CD56 + APL also showed...

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Nitric oxide status in sickle cell anemia

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Side Effects of Hydroxyurea in Patients with Sickle Cell Anemia

Background: Hemoglobin S arises is the result of a point mutation (A-T) in the sixth codon on the -globin gene on chromosome 11 causing sickle cell anemia. The presence of fetal hemoglobin in infancy plays a relatively protective role for vaso-occlusive symptoms that are the major contributor for the morbidity and mortality among patients with sickle cell anemia. hydroxyurea, an s-phase-specif...

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Oxidant-antioxidant status in Egyptian children with sickle cell anemia: a single center based study.

OBJECTIVE the present study was conducted to investigate the oxidant-antioxidant status in Egyptian children with sickle cell anemia. METHODS the serum levels of total antioxidant capacity (TAO), paraoxonase (PON), vitamin E, nitrite, and malondialdehyde (MDA) were measured in 40 steady state children with homozygous sickle cell anemia (24 males and 16 females) and 20 apparently healthy age- ...

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ژورنال

عنوان ژورنال: Saudi Journal for Health Sciences

سال: 2018

ISSN: 2278-0521

DOI: 10.4103/sjhs.sjhs_34_18