Emília Vieira

New variants, challenges and pitfalls in DMD genotyping: implications in diagnosis, prognosis and therapy

Rosário Santos, Ana Gonçalves, Jorge Oliveira et al. · Journal of Human Genetics · 2014 · 40 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Analysis of the UDP-glucuronosyltransferase gene in Portuguese patients with a clinical diagnosis of Gilbert and Crigler–Najjar syndromes

Elı́sio Costa, Emília Vieira, Márcia Martins et al. · Blood Cells Molecules and Diseases · 2005 · 32 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

The Polymorphism c.-3279T>G in the Phenobarbital-Responsive Enhancer Module of the Bilirubin UDP-Glucuronosyltransferase Gene Is Associated with Gilbert Syndrome

Elı́sio Costa, Emília Vieira, Rosário Santos · Clinical Chemistry · 2005 · 29 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Impact of UGT1A1 gene variants on total bilirubin levels in Gilbert syndrome patients and in healthy subjects

Carina Rodrigues, Emília Vieira, Rosário Santos et al. · Blood Cells Molecules and Diseases · 2012 · 27 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

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

Sandra Ribeiro, Maria Faria, Gil Silva et al. · Hemodialysis International · 2012 · 24 citations

Medicine, Biochemistry, Nephrology +16