Bachega TASS - Search Results

1

Steroid Screening Tools Differentiating Nonclassical Congenital Adrenal Hyperplasia and Polycystic Ovary Syndrome.

Maffazioli GDN, Bachega TASS, Hayashida SAY, Gomes LG, Valassi HPL, Marcondes JAM, Mendonca BB, Baracat EC, Maciel GAR. Maffazioli GDN, et al. Among authors: bachega tass. J Clin Endocrinol Metab. 2020 Aug 1;105(8):dgaa369. doi: 10.1210/clinem/dgaa369. J Clin Endocrinol Metab. 2020. PMID: 32530459

2

Protocol for rapid fetal sex determination in chorionic villus through polimerase chain reaction.

Domenice S, Billerbeck AE, Rocha RO, Nishi MY, Medeiros MA, Bachega TA, Budunki V, Mendonca BB. Domenice S, et al. Rev Hosp Clin Fac Med Sao Paulo. 1998 Mar-Apr;53(2):80-2. Rev Hosp Clin Fac Med Sao Paulo. 1998. PMID: 9699359

3

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. J Clin Endocrinol Metab. 1998 Dec;83(12):4416-9. doi: 10.1210/jcem.83.12.5350. J Clin Endocrinol Metab. 1998. PMID: 9851787

4

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. Hum Hered. 1999 Jan;49(1):9-14. doi: 10.1159/000022833. Hum Hered. 1999. PMID: 10189236

5

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. J Clin Endocrinol Metab. 1999 Aug;84(8):2870-2. doi: 10.1210/jcem.84.8.5937. J Clin Endocrinol Metab. 1999. PMID: 10443693

6

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. Clin Endocrinol (Oxf). 2000 May;52(5):601-7. doi: 10.1046/j.1365-2265.2000.00995.x. Clin Endocrinol (Oxf). 2000. PMID: 10792340

7

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. 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.

8

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. 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

9

Variable ACTH-stimulated 17-hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations.

Bachega TA, Brenlha EM, Billerbeck AE, Marcondes JA, Madureira G, Arnhold IJ, Mendonca BB. Bachega TA, et al. J Clin Endocrinol Metab. 2002 Feb;87(2):786-90. doi: 10.1210/jcem.87.2.8247. J Clin Endocrinol Metab. 2002. PMID: 11836321

10

Three novel mutations in CYP21 gene in Brazilian patients with the classical form of 21-hydroxylase deficiency due to a founder effect.

Billerbeck AE, Mendonca BB, Pinto EM, Madureira G, Arnhold IJ, Bachega TA. Billerbeck AE, et al. J Clin Endocrinol Metab. 2002 Sep;87(9):4314-7. doi: 10.1210/jc.2001-011939. J Clin Endocrinol Metab. 2002. PMID: 12213891

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