Martin RM - Search Results

1

Familial hyperestrogenism in both sexes: clinical, hormonal, and molecular studies of two siblings.

Martin RM, Lin CJ, Nishi MY, Billerbeck AE, Latronico AC, Russell DW, Mendonca BB. Martin RM, et al. J Clin Endocrinol Metab. 2003 Jul;88(7):3027-34. doi: 10.1210/jc.2002-021780. J Clin Endocrinol Metab. 2003. PMID: 12843139

2

Origin of an ovarian steroid cell tumor causing isosexual pseudoprecocious puberty demonstrated by the expression of adrenal steroidogenic enzymes and adrenocorticotropin receptor.

Lin CJ, Jorge AA, Latronico AC, Marui S, Fragoso MC, Martin RM, Carvalho FM, Arnhold IJ, Mendonca BB. Lin CJ, et al. Among authors: martin rm. J Clin Endocrinol Metab. 2000 Mar;85(3):1211-4. doi: 10.1210/jcem.85.3.6454. J Clin Endocrinol Metab. 2000. PMID: 10720064

3

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: martin rm. Medicine (Baltimore). 2000 Sep;79(5):299-309. doi: 10.1097/00005792-200009000-00003. Medicine (Baltimore). 2000. PMID: 11039078 Free article.

4

An inherited mutation outside the highly conserved DNA-binding domain of the p53 tumor suppressor protein in children and adults with sporadic adrenocortical tumors.

Latronico AC, Pinto EM, Domenice S, Fragoso MC, Martin RM, Zerbini MC, Lucon AM, Mendonca BB. Latronico AC, et al. Among authors: martin rm. J Clin Endocrinol Metab. 2001 Oct;86(10):4970-3. doi: 10.1210/jcem.86.10.7957. J Clin Endocrinol Metab. 2001. PMID: 11600572

5

An unusual phenotype of Frasier syndrome due to IVS9 +4C>T mutation in the WT1 gene: predominantly male ambiguous genitalia and absence of gonadal dysgenesis.

Melo KF, Martin RM, Costa EM, Carvalho FM, Jorge AA, Arnhold IJ, Mendonca BB. Melo KF, et al. Among authors: martin rm. J Clin Endocrinol Metab. 2002 Jun;87(6):2500-5. doi: 10.1210/jcem.87.6.8521. J Clin Endocrinol Metab. 2002. PMID: 12050205 Review.

6

Cushing's syndrome secondary to adrenocorticotropin-independent macronodular adrenocortical hyperplasia due to activating mutations of GNAS1 gene.

Fragoso MC, Domenice S, Latronico AC, Martin RM, Pereira MA, Zerbini MC, Lucon AM, Mendonca BB. Fragoso MC, et al. Among authors: martin rm. J Clin Endocrinol Metab. 2003 May;88(5):2147-51. doi: 10.1210/jc.2002-021362. J Clin Endocrinol Metab. 2003. PMID: 12727968

7

P450c17 deficiency in Brazilian patients: biochemical diagnosis through progesterone levels confirmed by CYP17 genotyping.

Martin RM, Lin CJ, Costa EM, de Oliveira ML, Carrilho A, Villar H, Longui CA, Mendonca BB. Martin RM, et al. J Clin Endocrinol Metab. 2003 Dec;88(12):5739-46. doi: 10.1210/jc.2003-030988. J Clin Endocrinol Metab. 2003. PMID: 14671162

8

Assessment of the role of transcript for GATA-4 as a marker of unfavorable outcome in human adrenocortical neoplasms.

Barbosa AS, Giacaglia LR, Martin RM, Mendonca BB, Lin CJ. Barbosa AS, et al. Among authors: martin rm. BMC Endocr Disord. 2004 Jul 7;4(1):3. doi: 10.1186/1472-6823-4-3. BMC Endocr Disord. 2004. PMID: 15239841 Free PMC article.

9

Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion.

Abrão MG, Leite MV, Carvalho LR, Billerbeck AE, Nishi MY, Barbosa AS, Martin RM, Arnhold IJ, Mendonca BB. Abrão MG, et al. Among authors: martin rm. Clin Endocrinol (Oxf). 2006 Sep;65(3):294-300. doi: 10.1111/j.1365-2265.2006.02592.x. Clin Endocrinol (Oxf). 2006. PMID: 16918947 Review.

10

An inhibin B and estrogen-secreting adrenocortical carcinoma leading to selective FSH suppression.

Fragoso MC, Kohek MB, Martin RM, Latronico AC, Lucon AM, Zerbini MC, Longui CA, Mendonca BB, Domenice S. Fragoso MC, et al. Among authors: martin rm. Horm Res. 2007;67(1):7-11. doi: 10.1159/000095806. Epub 2006 Sep 15. Horm Res. 2007. PMID: 16974107

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