Nascimento, H., Vieira, E., Coimbra, S., Catarino, C., et al. (2016). Adipokine gene single-nucleotide polymorphisms in Portuguese obese adolescents: Associations with plasma concentrations of adiponectin, resistin, IL-6, IL-1?, and TNF-?. Childhood Obesity, 12(4), 300 - 313.

Rodrigues, C., Rocha, S., Nascimento, H., Vieira, E., et al. (2013). Bilirubin levels and redox status in a young healthy population. Acta Haematologica, 130(1), 57 - 60.

Rodrigues, C., Vieira, E., Santos, R., de Carvalho, J., et al. (2012). Impact of UGT1A1 gene variants on total bilirubin levels in Gilbert syndrome patients and in healthy subjects. Blood Cells, Molecules, and Diseases, 48(3), 166 - 172.

Ribeiro, S., Faria, M. D. S., Silva, G., Nascimento, H., et al. (2012). Oxidized low-density lipoprotein and lipoprotein(a) levels in chronic kidney disease patients under hemodialysis: Influence of adiponectin and of a polymorphism in the apolipoprotein(a) gene. Hemodialysis International, 16(4), 481 - 490.

Vernengo, L., Oliveira, J., Krahn, M., Vieira, E., et al. (2011). Novel ancestral Dysferlin splicing mutation which migrated from the Iberian peninsula to South America. Neuromuscular Disorders, 21(5), 328 - 337.

Santos, R., Oliveira, J., Vieira, E., Coelho, T., et al. (2010). Private dysferlin exon skipping mutation (c.5492G > A) with a founder effect reveals further alternative splicing involving exons 49-51. Journal of Human Genetics, 55(8), 546 - 549.

Nascimento, H., Silva, L. L., Lourenço, P., Vieira, E., et al. (2009). Lipoprotein(a) levels in obese portuguese children and adolescents: Contribution of the pentanucleotide repeat (TTTTA)n polymorphism in the apolipoprotein(a) gene. Archives of Pediatrics and Adolescent Medicine, 163(4), 393 - 394.

Cruz, C. D., Charrua, A., Vieira, E., Valente, J., et al. (2008). Intrathecal delivery of resiniferatoxin (RTX) reduces detrusor overactivity and spinal expression of TRPV1 in spinal cord injured animals. Experimental Neurology, 214(2), 301 - 308.

Oliveira, J., Santos, R., Soares-Silva, I., Jorge, P., et al. (2008). LAMA2 gene analysis in a cohort of 26 congenital muscular dystrophy patients. Clinical Genetics, 74(6), 502 - 512.