Search Results - "Dos Anjos, Ana C"

Influence of UGT1A1 promoter polymorphism, α-thalassemia and βs haplotype in bilirubin levels and cholelithiasis in a large sickle cell anemia cohort by Batista, Jéssica V. G. F., Arcanjo, Gabriela S., Batista, Thais H. C., Sobreira, Marcondes J., Santana, Rodrigo M., Domingos, Igor F., Hatzlhofer, Betânia L., Falcão, Diego A., Pereira-Martins, Diego A., Oliveira, Jéssica M., Araujo, Amanda S., Laranjeira, Luana P. M., Medeiros, Fernanda S., Albuquerque, Flávia P., Albuquerque, Dulcinéia M., Santos, Magnun N., Hazin, Manuela F., dos Anjos, Ana C., Costa, Fernando F., Araujo, Aderson S., Lucena-Araujo, Antonio R., Bezerra, Marcos A.

“…Hyperbilirubinemia in patients with sickle cell anemia (SCA) as a result of enhanced erythrocyte destruction, lead to cholelithiasis development in a subset of…”
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Association of KLOTHO polymorphisms with clinical complications of sickle cell anemia by Batista, Jéssica V. G. F., Pereira-Martins, Diego A., Falcão, Diego A., Domingos, Igor F., Arcanjo, Gabriela S., Hatzlhofer, Betânia L., Weinhäuser, Isabel, Batista, Thais H. C., Cardoso, Pablo R. G., dos Anjos, Ana C., Hazin, Manuela F., Pitta, Maira G. R., Costa, Fernando F., Araujo, Aderson S., Lucena-Araujo, Antonio R., Bezerra, Marcos A.

“…The clinical and phenotypic heterogeneity of patients with sickle cell anemia (SCA) is influenced by environmental and genetic factors. Several genetic…”
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Up‐regulation of miR‐130a is related to leg ulcers in sickle cell anaemia by Batista, Thais H. C., Santana, Rodrigo M., Sobreira, Marcondes J., Arcanjo, Gabriela S., Domingos, Igor F., Pereira‐Martins, Diego A., Falcão, Diego A., Oliveira, Jéssica M. F., Batista, Jéssica V. G. F., Weinhӓuser, Isabel, Hatzlhofer, Betânia L., Júnior, Walter L. B., Araujo, Aderson S., dos Anjos, Ana C., Costa, Fernando F., Saad, Mario J. A., Carvalho, Bruno M., Vasconcelos, Luydson R. S., Lucena‐Araujo, Antonio R., Bezerra, Marcos A.

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A-296G variant of THBS1 gene (rs1478605) is associated with a lower frequency of stroke in a Brazilian population with sickle cell anemia by Oliveira, Jessica M F, Arcanjo, Gabriela S, Domingos, Igor F, Batista, Jéssica V G F, Pereira-Martins, Diego A, Batista, Thais H C, Hatzlhofer, Betânia L D, Falcão, Diego A, Diniz, Madi V, Silva, Alexsandro P, Pires, Bárbara C V, Dos Anjos, Ana C, Costa, Fernando F, Araujo, Aderson S, Lucena-Araujo, Antonio R, Bezerra, Marcos A

“…Stroke is a devastating clinical outcome that significantly contributes to the morbidity and mortality of sickle cell anemia (SCA) patients. Despite its…”
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Functional characterization of compound heterozygosity Hb S/Hb Deer Lodge in Brazil by Sobreira, Marcondes J, Batista, Thais H, Santana, Rodrigo M, Arcanjo, Gabriela S, Jorge, Susan E, Santos, Magnun N, Albuquerque, Dulcinéia M, Hatzlhofer, Betânia L, Dos Anjos, Ana C, Costa, Fernando F, Araujo, Aderson S, Sonati, Maria F, Lucena-Araujo, Antonio R, Bezerra, Marcos A

“…The Hb Deer Lodge (β2 His>Arg; HBB:c.8A>G) is a structural hemoglobin variant described in some populations around the world, characterized by increased oxygen…”
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