Arnhold IJ - Search Results

1

Spironolactone-reversible rickets associated with 11 beta-hydroxysteroid dehydrogenase deficiency syndrome.

Batista MC, Mendonça BB, Kater CE, Arnhold IJ, Rocha A, Nicolau W, Bloise W. Batista MC, et al. Among authors: arnhold ij. J Pediatr. 1986 Dec;109(6):989-93. doi: 10.1016/s0022-3476(86)80282-7. J Pediatr. 1986. PMID: 3023598

2

Male pseudohermaphroditism due to nonsalt-losing 3 beta-hydroxysteroid dehydrogenase deficiency: gender role change and absence of gynecomastia at puberty.

Mendonca BB, Bloise W, Arnhold IJ, Batista MC, Toledo SP, Drummond MC, Nicolau W, Mattar E. Mendonca BB, et al. Among authors: arnhold ij. J Steroid Biochem. 1987 Dec;28(6):669-75. doi: 10.1016/0022-4731(87)90396-7. J Steroid Biochem. 1987. PMID: 2826919

3

Low-dose oral clonidine: effective growth hormone releasing agent in children but not in adolescents.

Batista MC, Arnhold IJ, Mendonça BB, D'Abronzo FH, Bloise W, Nicolau W. Batista MC, et al. Among authors: arnhold ij. J Pediatr. 1987 Oct;111(4):564-7. doi: 10.1016/s0022-3476(87)80123-3. J Pediatr. 1987. PMID: 3309234 No abstract available.

4

Male pseudohermaphroditism resulting from Leydig cell hypoplasia.

Arnhold IJ, Mendonça BB, Bloise W, Toledo SP. Arnhold IJ, et al. J Pediatr. 1985 Jun;106(6):1057. doi: 10.1016/s0022-3476(85)80268-7. J Pediatr. 1985. PMID: 3998941 No abstract available.

5

Mutation in 3 beta-hydroxysteroid dehydrogenase type II associated with pseudohermaphroditism in males and premature pubarche or cryptic expression in females.

Mendonça BB, Russell AJ, Vasconcelos-Leite M, Arnhold IJ, Bloise W, Wajchenberg BL, Nicolau W, Sutcliffe RG, Wallace AM. Mendonça BB, et al. Among authors: arnhold ij. J Mol Endocrinol. 1994 Feb;12(1):119-22. doi: 10.1677/jme.0.0120119. J Mol Endocrinol. 1994. PMID: 8185809

6

17Beta-hydroxysteroid dehydrogenase 3 deficiency in women.

Mendonca BB, Arnhold IJ, Bloise W, Andersson S, Russell DW, Wilson JD. Mendonca BB, et al. Among authors: arnhold ij. J Clin Endocrinol Metab. 1999 Feb;84(2):802-4. doi: 10.1210/jcem.84.2.5477. J Clin Endocrinol Metab. 1999. PMID: 10022457

7

Male pseudohermaphroditism due to 17 beta-hydroxysteroid dehydrogenase 3 deficiency. Diagnosis, psychological evaluation, and management.

Mendonca BB, Inacio M, Arnhold IJ, Costa EM, Bloise W, Martin RM, Denes FT, Silva FA, Andersson S, Lindqvist A, Wilson JD. Mendonca BB, et al. Among authors: arnhold ij. Medicine (Baltimore). 2000 Sep;79(5):299-309. doi: 10.1097/00005792-200009000-00003. Medicine (Baltimore). 2000. PMID: 11039078 Free article.

8

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. J Endocrinol Invest. 1988 Apr;11(4):319-22. doi: 10.1007/BF03350158. J Endocrinol Invest. 1988. PMID: 3166023

9

Premature thelarche in girls after growth hormone therapy.

Carvalho LR, Mimura LY, Arnhold IJ, Mendonca BB. Carvalho LR, et al. Among authors: arnhold ij. J Pediatr. 2001 Mar;138(3):448-9. doi: 10.1067/mpd.2001.109106. J Pediatr. 2001. PMID: 11241065 No abstract available.

10

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

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