Folate supplementation and twinning in patients with sickle cell disease
โ Scribed by Samir K. Ballas; Jason K. Baxter; Gaye Riddick
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 72 KB
- Volume
- 81
- Category
- Article
- ISSN
- 0361-8609
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๐ SIMILAR VOLUMES
The transfusion histories over a 33-month period of 50 patients with sickle cell disease were reviewed to determine the frequency of alloimmunization to red cell antigens following transfusion in these patients. There were 30 females and 20 males, aged 19--49 years. Eighteen (36%) were immunized of
Using homocysteine as a functional marker, we determined optimal folic acid, vitamin B 12 , and vitamin B 6 dosages in 21 pediatric sickle cell disease (SCD) patients (11 HbSS, 10 HbSC;(7)(8)(9)(10)(11)(12)(13)(14)(15)(16). Daily supplements of folic acid (400, 700, or 1,000 lg), vitamin B 12 (1, 3,
The ability of circulating progenitor cells to develop erythroid colonies was studied in vitro in the presence or absence of growth factors (5637-CM and erythropoietin) in 63 patients with sickle cell disease (SCD) (36 homozygotes for hemoglobin [Hb] S, 13 double heterozygotes for Hb S and beta thal