Teresa C. Vieira

A Novel Mutation in the Anion Exchanger 1 Gene Is Associated With Familial Distal Renal Tubular Acidosis and Nephrocalcinosis

Lara Cheidde, Teresa C. Vieira, Paulo Roberto Moura Lima et al. · PEDIATRICS · 2003 · 61 citations

Mutations linked to familial hypokalaemic periodic paralysis in the calcium channel α1 subunit gene (Ca_v1·1) are not associated with thyrotoxic hypokalaemic periodic paralysis

Magnus R. Dias‐da‐Silva, Janete M. Cerutti, Célia Harumi Tengan et al. · Clinical Endocrinology · 2002 · 50 citations · Full text

Familial Combined Pituitary Hormone Deficiency due to a Novel Mutation R99Q in the Hot Spot Region of Prophet of Pit-1 Presenting as Constitutional Growth Delay

Teresa C. Vieira, Magnus R. Dias‐da‐Silva, Janete M. Cerutti et al. · The Journal of Clinical Endocrinology & Metabolism · 2003 · 47 citations · Full text

Molecular analysis of PROP1, PIT1, HESX1, LHX3, and LHX4 shows high frequency of PROP1 mutations in patients with familial forms of combined pituitary hormone deficiency

Teresa C. Vieira, Valter Tadeu Boldarine, Júlio Abucham · Arquivos Brasileiros de Endocrinologia & Metabologia · 2007 · 42 citations · Full text

Hereditary corticosteroid‐binding globulin deficiency due to a missense mutation (Asp367Asn, CBG Lyon) in a Brazilian kindred

Elisa Brunner, Jader Baima, Teresa C. Vieira et al. · Clinical Endocrinology · 2003 · 32 citations