Compound heterozygosity for hemoglobin S and D: what do we need to know? [PDF]
Rev Bras Hematol Hemoter, 2016 Bonini-Domingos CR.
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[Does glycaemic control improve in diabetic patients after introducing dipeptidyl peptidase-4 inhibitors into the treatment?]. [PDF]
Aten Primaria, 2013 Vila Arteaga P +2 more
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Prevalence of β(S)-globin gene haplotypes, α-thalassemia (3.7 kb deletion) and redox status in patients with sickle cell anemia in the state of Paraná, Brazil. [PDF]
Genet Mol Biol, 2015 Shimauti EL +5 more
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Hemoglobinopathies in newborns in the southern region of the Triângulo Mineiro, Brazil. Cross-sectional study. [PDF]
Sao Paulo Med J, 2015 Carlos AM +6 more
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Diagnóstico de hemoglobinopatías en el laboratorio clínico: hallazgo de una hemoglobina hofu oculta en HPLC. [PDF]
Adv Lab MedEcheverría Urroz M +3 more
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Interaction between Hb SS and alpha thalassemia (3.7 kb deletion): a familial study. [PDF]
Rev Bras Hematol Hemoter, 2011 Shimauti EL +2 more
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Clinical and metabolic effects of the etonogestrel-releasing implant on the puerperium of healthy women [PDF]
, 2009 BRITO, Milena Bastos
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Falso valor de HbA1c debido a la variante inusual hemoglobina Petie Salpetriere coheredada con talasemia alfa. [PDF]
Adv Lab MedLepe Balsalobre E +3 more
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Leg ulcers in sickle cell disease patients. [PDF]
J Vasc Bras, 2020 Granja PD +6 more
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