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Results: 1-7 |
Results: 7
A multicenter study of women with nonclassical congenital adrenal hyperplasia: Relationship between genotype and phenotype
Authors: Speiser, PW Knochenhauer, ES Dewailly, D Fruzzetti, F Marcondes, JAM Azziz, R
Citation: Pw. Speiser et al., A multicenter study of women with nonclassical congenital adrenal hyperplasia: Relationship between genotype and phenotype, MOL GEN MET, 71(3), 2000, pp. 527-534
Influence of different genotypes on 17-hydroxyprogesterone levels in patients with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency
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
21-hydroxylase deficiency in Brazil
Authors: Bachega, TASS Billerbeck, AEC Madureira, G Marcondes, JAM Longui, CA Leite, MV Arnhold, IJP Mendonca, BB
Citation: Tass. Bachega et al., 21-hydroxylase deficiency in Brazil, BRAZ J MED, 33(10), 2000, pp. 1211-1216
21-Hydroxylase-deficient nonclassic adrenal hyperplasia is a progressive disorder: A multicenter study
Authors: Moran, C Azziz, R Carmina, E Dewailly, D Fruzzetti, F Ibanez, L Knochenhauer, ES Marcondes, JAM Mendonca, BB Pignatelli, D Pugeat, M Rohmer, V Speiser, PW Witchel, SF
Citation: C. Moran et al., 21-Hydroxylase-deficient nonclassic adrenal hyperplasia is a progressive disorder: A multicenter study, AM J OBST G, 183(6), 2000, pp. 1468-1474
Analysis of gonadotropin pulsatility in hirsute women with normal menstrual cycles and in women with polycystic ovary syndrome
Authors: Minanni, SL Marcondes, JAM Wajchenberg, BL Cavaleiro, AM Fortes, MAHZ Rego, MA Vezozzo, DP Robard, D Giannella-Neto, D
Citation: Sl. Minanni et al., Analysis of gonadotropin pulsatility in hirsute women with normal menstrual cycles and in women with polycystic ovary syndrome, FERT STERIL, 71(4), 1999, pp. 675-683
Low frequency of CYP21B deletions in Brazilian patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
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
Molecular genotyping in Brazilian patients with the classical and nonclassical forms of 21-hydroxylase deficiency
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
Risultati: 1-7 |