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Femoral head necrosis treatment with autologous stem cells in sickle cell disease
(Sociedade Brasileira de Ortopedia e Traumatologia, 2008)
PURPOSE: To assess the efficacy and safety of autologous bone-marrow mononuclear cells (BMMC) implantation in necrotic lesions of the femoral head in patients with sickle cell disease. METHODS: We studied eight patients ...
Sub capsular splenic hematoma in a sickle cell trait carrier. case report Hematoma subcapsular esplénico en paciente portador de rasgo falciforme
(2011)
Drepanocytic anemia is an uncommon hereditary disease in Chile. The heterozygous state of drepanocytic anemia or "sickle trait" has a frequency of 8% among Afro-Americans. A small number of patients carrying hemoglobin S ...
Extensive spondylodiscitis with epidural abscess causing fever and lower limbs pain in a child with sickle cell disease
(2008)
Spondylodiscitis is an unusual diagnosis among children and consequent abscess formation is even rarer. A 6-year-old girl with fever, hip pain, and refusal to walk was evaluated. The neurologic examination was normal. ...
The Association of Serum 25-Hydroxyvitamin D With Biomarkers of Hemolysis in Pediatric Patients With Sickle Cell Disease
(Lippincott Williams & Wilkins, 2018)
Although vitamin D deficiency (VDD) has been linked to anemia among sickle cell disease (SCD), its relationship with hemolysis is unclear. Serum 25-hydroxyvitamin D and biomarkers of hemolysis (hemoglobin [Hb]/hematocrit, ...
Multiple Primary Choledocholithiasis in Sickle Cell Disease
(Japan Soc Internal Medicine, 2008-01-01)
Choledocholithiasis can be caused by either primary or secondary bile duct stones. Although patients with sickle cell disease (SCD) are at high risk of development of pigmented gallstones due to chronic hemolysis, primary ...
Sickle-cell erythrocytes in the placentas of dengue-infected women
(Elsevier, 2017)