Bachega TASS - Search Results

1

Low Adrenomedullary Function Predicts Acute Illness in Infants With Classical Congenital Adrenal Hyperplasia.

Weber J, Tanawattanacharoen VK, Seagroves A, Liang MC, Koppin CM, Ross HM, Bachega TASS, Geffner ME, Serrano-Gonzalez M, Bhullar G, Kim MS. Weber J, et al. Among authors: bachega tass. J Clin Endocrinol Metab. 2022 Jan 1;107(1):e264-e271. doi: 10.1210/clinem/dgab600. J Clin Endocrinol Metab. 2022. PMID: 34397083 Free PMC article.

2

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

3

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

4

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

5

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

6

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

7

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

8

Adrenal steroids synthesis during acute infectious diseases in infants.

Longui CA, Zlochevsky ER, Bachega TA, Monte O. Longui CA, et al. J Pediatr Endocrinol Metab. 2002 Nov-Dec;15(9):1515-23. doi: 10.1515/jpem.2002.15.9.1515. J Pediatr Endocrinol Metab. 2002. PMID: 12503859

9

Substitutions in the CYP21A2 promoter explain the simple-virilizing form of 21-hydroxylase deficiency in patients harbouring a P30L mutation.

Araujo RS, Billerbeck AE, Madureira G, Mendonca BB, Bachega TA. Araujo RS, et al. Clin Endocrinol (Oxf). 2005 Feb;62(2):132-6. doi: 10.1111/j.1365-2265.2005.02184.x. Clin Endocrinol (Oxf). 2005. PMID: 15670187

10

The degree of external genitalia virilization in girls with 21-hydroxylase deficiency appears to be influenced by the CAG repeats in the androgen receptor gene.

Rocha RO, Billerbeck AE, Pinto EM, Melo KF, Lin CJ, Longui CA, Mendonca BB, Bachega TA. Rocha RO, et al. Clin Endocrinol (Oxf). 2008 Feb;68(2):226-32. doi: 10.1111/j.1365-2265.2007.03023.x. Epub 2007 Sep 4. Clin Endocrinol (Oxf). 2008. PMID: 17803691

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