Arnhold IJ - Search Results

1

Molecular analysis of SRY gene in Brazilian 46,XX sex reversed patients: absence of SRY sequence in gonadal tissue.

Domenice S, Nishi MY, Billerbeck AE, Carvalho FM, Frade EM, Latronico AC, Arnhold IJ, Mendonca BB. Domenice S, et al. Among authors: arnhold ij. Med Sci Monit. 2001 Mar-Apr;7(2):238-41. Med Sci Monit. 2001. PMID: 11257728

2

Gonadal agenesis in XX and XY sisters: evidence for the involvement of an autosomal gene.

Mendonça BB, Barbosa AS, Arnhold IJ, McElreavey K, Fellous M, Moreira-Filho CA. Mendonça BB, et al. Among authors: arnhold ij. Am J Med Genet. 1994 Aug 1;52(1):39-43. doi: 10.1002/ajmg.1320520108. Am J Med Genet. 1994. PMID: 7977459

3

Ovarian resistance to luteinizing hormone: a novel cause of amenorrhea and infertility.

Arnhold IJ, Latronico AC, Batista MC, Carvalho FM, Chrousos GP, Mendonça BB. Arnhold IJ, et al. Fertil Steril. 1997 Feb;67(2):394-7. doi: 10.1016/s0015-0282(97)81929-2. Fertil Steril. 1997. PMID: 9022621 Free article.

4

A homozygous microdeletion in helix 7 of the luteinizing hormone receptor associated with familial testicular and ovarian resistance is due to both decreased cell surface expression and impaired effector activation by the cell surface receptor.

Latronico AC, Chai Y, Arnhold IJ, Liu X, Mendonca BB, Segaloff DL. Latronico AC, et al. Among authors: arnhold ij. Mol Endocrinol. 1998 Mar;12(3):442-50. doi: 10.1210/mend.12.3.0077. Mol Endocrinol. 1998. PMID: 9514160

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: 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

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: 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

7

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

8

Clinical features of women with resistance to luteinizing hormone.

Arnhold IJ, Latronico AC, Batista MC, Izzo CR, Mendonca BB. Arnhold IJ, et al. Clin Endocrinol (Oxf). 1999 Dec;51(6):701-7. doi: 10.1046/j.1365-2265.1999.00863.x. Clin Endocrinol (Oxf). 1999. PMID: 10619974

9

Mutations in the type II 3beta-hydroxysteroid dehydrogenase (HSD3B2) gene can cause premature pubarche in girls.

Marui S, Castro M, Latronico AC, Elias LL, Arnhold IJ, Moreira AC, Mendonca BB. Marui S, et al. Among authors: arnhold ij. Clin Endocrinol (Oxf). 2000 Jan;52(1):67-75. doi: 10.1046/j.1365-2265.2000.00873.x. Clin Endocrinol (Oxf). 2000. PMID: 10651755

10

The effect of distinct activating mutations of the luteinizing hormone receptor gene on the pituitary-gonadal axis in both sexes.

Latronico AC, Lins TS, Brito VN, Arnhold IJ, Mendonca BB. Latronico AC, et al. Among authors: arnhold ij. Clin Endocrinol (Oxf). 2000 Nov;53(5):609-13. doi: 10.1046/j.1365-2265.2000.01135.x. Clin Endocrinol (Oxf). 2000. PMID: 11106922

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