Authors:
Giacaglia, LR
Mendonca, BB
Madureira, G
Melo, KFF
Suslik, CA
Arnhold, IJP
Bachega, TASS
Citation: Lr. Giacaglia et al., Adrenal nodules in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: Regression after adequate hormonal control, J PED END M, 14(4), 2001, pp. 415-419
Authors:
Bachega, TASS
Billerbeck, AEC
Marcondes, JAM
Madureira, G
Arnhold, IJP
Mendonca, BB
Citation: Tass. Bachega et al., Influence of different genotypes on 17-hydroxyprogesterone levels in patients with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency, CLIN ENDOCR, 52(5), 2000, pp. 601-607
Authors:
Billerbeck, AEC
Bachega, TASS
Frazzatto, ET
Nishi, MY
Goldberg, AC
Marin, MLC
Madureira, G
Monte, O
Arnhold, IJP
Mendonca, BB
Citation: Aec. Billerbeck et al., A novel missense mutation, GLY424SER, in Brazilian patients with 21-hydroxylase deficiency, J CLIN END, 84(8), 1999, pp. 2870-2872
Authors:
Bachega, TASS
Billerbeck, AEC
Madureira, G
Arnhold, IJP
Medeiros, MA
Marcondes, JAM
Longui, CA
Nicolau, W
Bloise, W
Mendonca, BB
Citation: Tass. Bachega et al., Low frequency of CYP21B deletions in Brazilian patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency, HUMAN HERED, 49(1), 1999, pp. 9-14
Authors:
Bachega, TASS
Billerbeck, EC
Madureira, G
Marcondes, JAM
Longui, CA
Leite, MV
Arnhold, IJP
Mendonca, BB
Citation: Tass. Bachega et al., Molecular genotyping in Brazilian patients with the classical and nonclassical forms of 21-hydroxylase deficiency, J CLIN END, 83(12), 1998, pp. 4416-4419