Sickle Cell Trait
Renal dysfunction in patients with sickle cell anemia or sickle cell trait
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Confidencialidade, aconselhamento genético e saúde pública: um estudo de caso sobre o traço falciforme Confidentiality, genetic counseling, and public health: a case study on sickle cell trait
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J. Bras. Patol. Med. Lab. vol.51 número4
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Renal tubular dysfunction in sickle cell disease
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Int. braz j urol. vol.33 número5
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Maternal anaemia at delivery and haemoglobin evolution in children during their first 18 months of life using latent class analysis.
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S -Haplotypes in sickle cell anemia
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Rev. Bras. Hematol. Hemoter. vol.38 número3
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J. Bras. Patol. Med. Lab. vol.49 número4
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Sickle cell disease and associated problems: Case study of Homozygous sicklers
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Self-care of men with priapism and sickle cell disease
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Comparison of oxidative stress and the frequency of polymorphisms in the HFE gene between hemoglobin S trait blood donors and sickle cell disease patients
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Cerebral Vasculopathy in Children with Sickle Cell Disease
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Men with Sickle Cell Anemia and Priapism Exhibit Increased Hemolytic Rate, Decreased Red Blood Cell Deformability and Increased Red Blood Cell Aggregate Strength.
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Mobile applications for sickle cell disease management: an integrative review
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Risk factors for alloimmunization by patients with sickle cell disease
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Hepatitis C virus infection in a Brazilian population with sickle-cell anemia
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The pain of children with sickle cell disease: the nursing approach
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Fatores de risco para aloimunização em pacientes com anemia falciforme
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