Bloise W - 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: bloise w. 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: bloise w. 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: bloise w. 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. Among authors: bloise w. 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: bloise w. 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: bloise w. 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: bloise w. 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. Among authors: bloise w. J Endocrinol Invest. 1988 Apr;11(4):319-22. doi: 10.1007/BF03350158. J Endocrinol Invest. 1988. PMID: 3166023

9

Male pseudohermaphroditism due to 5 alpha reductase deficiency associated with gynecomastia.

Mendonça BB, Batista MC, Arnhold IJ, Nicolau W, Madureira G, Lando VS, Kohek MB, Carvalho DG, Bloise W. Mendonça BB, et al. Among authors: bloise w. Rev Hosp Clin Fac Med Sao Paulo. 1987 Mar-Apr;42(2):66-8. Rev Hosp Clin Fac Med Sao Paulo. 1987. PMID: 3441728 No abstract available.

10

Molecular genetics and pathophysiology of 17 beta-hydroxysteroid dehydrogenase 3 deficiency.

Andersson S, Geissler WM, Wu L, Davis DL, Grumbach MM, New MI, Schwarz HP, Blethen SL, Mendonca BB, Bloise W, Witchel SF, Cutler GB Jr, Griffin JE, Wilson JD, Russel DW. Andersson S, et al. Among authors: bloise w. J Clin Endocrinol Metab. 1996 Jan;81(1):130-6. doi: 10.1210/jcem.81.1.8550739. J Clin Endocrinol Metab. 1996. PMID: 8550739 Free article.

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