Madureira G - Search Results

1

Prepubertal male pseudohermaphroditism due to 17-ketosteroid reductase deficiency: diagnostic value of a hCG test and lack of HLA association.

Arnhold IJ, Mendonça BB, Diaz JA, Nogueira C, Batista MC, Madureira G, Oliveira D, Nicolau W, Bloise W. Arnhold IJ, et al. Among authors: madureira g. J Endocrinol Invest. 1988 Apr;11(4):319-22. doi: 10.1007/BF03350158. J Endocrinol Invest. 1988. PMID: 3166023

2

Male pseudohermaphroditism due to 5 alpha reductase deficiency associated with gynecomastia.

Mendonça BB, Batista MC, Arnhold IJ, Nicolau W, Madureira G, Lando VS, Kohek MB, Carvalho DG, Bloise W. Mendonça BB, et al. Among authors: madureira g. Rev Hosp Clin Fac Med Sao Paulo. 1987 Mar-Apr;42(2):66-8. Rev Hosp Clin Fac Med Sao Paulo. 1987. PMID: 3441728 No abstract available.

3

Low frequency of CYP2B deletions in Brazilian patients with congenital adrenal hyperplasia due to 21-hydroxylas deficiency.

Bachega TA, Billerbeck AE, Madureira G, Arnhold IJ, Medeiros MA, Marcondes JA, Longui CA, Nicolau W, Bloise W, Mendonca BB. Bachega TA, et al. Among authors: madureira g. Hum Hered. 1999 Jan;49(1):9-14. doi: 10.1159/000022833. Hum Hered. 1999. PMID: 10189236

4

Endocrine interaction between zinc and prolactin. An interpretative review.

Brandão-Neto J, Madureira G, Mendonça BB, Bloise W, Castro AV. Brandão-Neto J, et al. Among authors: madureira g. Biol Trace Elem Res. 1995 Aug-Sep;49(2-3):139-49. doi: 10.1007/BF02788963. Biol Trace Elem Res. 1995. PMID: 8562282 Review.

5

Molecular genotyping in Brazilian patients with the classical and nonclassical forms of 21-hydroxylase deficiency.

Bachega TA, Billerbeck AE, Madureira G, Marcondes JA, Longui CA, Leite MV, Arnhold IJ, Mendonca BB. Bachega TA, et al. Among authors: madureira g. J Clin Endocrinol Metab. 1998 Dec;83(12):4416-9. doi: 10.1210/jcem.83.12.5350. J Clin Endocrinol Metab. 1998. PMID: 9851787

6

A novel missense mutation, GLY424SER, in Brazilian patients with 21-hydroxylase deficiency.

Billerbeck AE, Bachega TA, Frazatto ET, Nishi MY, Goldberg AC, Marin ML, Madureira G, Monte O, Arnhold IJ, Mendonca BB. Billerbeck AE, et al. Among authors: madureira g. J Clin Endocrinol Metab. 1999 Aug;84(8):2870-2. doi: 10.1210/jcem.84.8.5937. J Clin Endocrinol Metab. 1999. PMID: 10443693

7

Influence of different genotypes on 17-hydroxyprogesterone levels in patients with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Bachega TA, Billerbeck AE, Marcondes JA, Madureira G, Arnhold IJ, Mendonca BB. Bachega TA, et al. Among authors: madureira g. Clin Endocrinol (Oxf). 2000 May;52(5):601-7. doi: 10.1046/j.1365-2265.2000.00995.x. Clin Endocrinol (Oxf). 2000. PMID: 10792340

8

21-Hydroxylase deficiency in Brazil.

Bachega TA, Billerbeck AE, Madureira G, Marcondes JA, Longui CA, Leite MV, Arnhold IJ, Mendonça BB. Bachega TA, et al. Among authors: madureira g. Braz J Med Biol Res. 2000 Oct;33(10):1211-6. doi: 10.1590/s0100-879x2000001000011. Braz J Med Biol Res. 2000. PMID: 11004722 Free article.

9

Adrenal nodules in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: regression after adequate hormonal control.

Giacaglia LR, Mendonca BB, Madureira G, Melo KF, Suslik CA, Arnhold IJ, Bachega TA. Giacaglia LR, et al. Among authors: madureira g. J Pediatr Endocrinol Metab. 2001 Apr;14(4):415-9. doi: 10.1515/jpem.2001.14.4.415. J Pediatr Endocrinol Metab. 2001. PMID: 11327375

10

Effect of acute and chronic oral zinc administration in hyperprolactinemic patients.

Madureira G, Bloise W, Mendonca BB, Brandão-Neto J. Madureira G, et al. Met Based Drugs. 1999;6(3):159-62. doi: 10.1155/MBD.1999.159. Met Based Drugs. 1999. PMID: 18472906 Free PMC article.

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