Hemoglobin I-Toulouse: A rare hemoglobinopathy presenting with low oxygen saturations.
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VCAM1, HMOX1 and NOS3 differential endothelial expression may impact sickle cell anemia vasculopathy. Up-regulation of miR-130a is related to leg ulcers in sickle cell anaemia.īatista THC, Santana RM, Sobreira MJ, Arcanjo GS, Domingos IF, Pereira-Martins DA, Falcão DA, Oliveira JMF, Batista JVGF, Weinhӓuser I, Hatzlhofer BL, Júnior WLB, Araujo AS, Dos Anjos AC, Costa FF, Saad MJA, Carvalho BM, Vasconcelos LRS, Lucena-Araujo AR, Bezerra MA Giordano P, Vecchio GCD, Russo G, Palmieri VV, Piacente L, Fidone C, Urbano F, Faienza MF High Dickkopf-1 levels are associated with chronic inflammation in children with sickle cell disease. Youssry I, Saad N, Madboly M, Samy RM, Hamed ST, Tawfik H, Elbatrawy SR, Kaddah N, Abd Elaziz D Luo S, Chen X, Zeng D, Tang N, Yuan D, Zhong Q, Mao A, Xu R, Yan Tīone health in pediatric transfusion-dependent beta-thalassemia: Circulating osteoprotegerin and RANKL system. The value of single-molecule real-time technology in the diagnosis of rare thalassemia variants and analysis of phenotype-genotype correlation. Zhou X, Chen T, Zhang Q, Qi M, Zhang L, Du J, Chi H, Shen B, Xu X, Lu Y De novo HBB frameshift mutation in a patient with dominant β-thalassemia major.
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