Arnhold IJ - Search Results

1

Bachega TA, Billerbeck AE, Madureira G, Marcondes JA, Longui CA, Leite MV, Arnhold IJ, Mendonça BB. Bachega TA, et al. Among authors: arnhold ij. 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.

2

Clinical and molecular characterization of Brazilian patients with growth hormone gene deletions.

Arnhold IJ, Osorio MG, Oliveira SB, Estefan V, Kamijo T, Krishnamani MR, Cogan JD, Phillips JA 3rd, Mendonca BB. Arnhold IJ, et al. Braz J Med Biol Res. 1998 Apr;31(4):491-7. doi: 10.1590/s0100-879x1998000400003. Braz J Med Biol Res. 1998. PMID: 9698799

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. Among authors: arnhold ij. 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. Among authors: arnhold ij. 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. Among authors: arnhold ij. 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. Among authors: arnhold ij. 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

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: arnhold ij. 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

8

Identification of nonclassical 21-hydroxylase deficiency in girls with precocious pubarche.

Leite MV, Mendonça BB, Arnhold IJ, Estefan V, Nunes C, Nicolau W, Bloise W. Leite MV, et al. Among authors: arnhold ij. J Endocrinol Invest. 1991 Jan;14(1):11-5. doi: 10.1007/BF03350247. J Endocrinol Invest. 1991. PMID: 1646249

9

Longitudinal hormonal and pituitary imaging changes in two females with combined pituitary hormone deficiency due to deletion of A301,G302 in the PROP1 gene.

Mendonca BB, Osorio MG, Latronico AC, Estefan V, Lo LS, Arnhold IJ. Mendonca BB, et al. Among authors: arnhold ij. J Clin Endocrinol Metab. 1999 Mar;84(3):942-5. doi: 10.1210/jcem.84.3.5537. J Clin Endocrinol Metab. 1999. PMID: 10084575

10

A novel point mutation (R840S) in the androgen receptor in a Brazilian family with partial androgen insensitivity syndrome.

Melo KF, Latronico AC, Costa EM, Billerbeck AE, Mendonca BB, Arnhold IJ. Melo KF, et al. Among authors: arnhold ij. Hum Mutat. 1999 Oct;14(4):353. doi: 10.1002/(SICI)1098-1004(199910)14:4<353::AID-HUMU16>3.0.CO;2-7. Hum Mutat. 1999. PMID: 10502786

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