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444 results
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Deletion mapping of chromosome 17 in benign and malignant adrenocortical tumors associated with the Arg337His mutation of the p53 tumor suppressor protein.
Pinto EM, Billerbeck AE, Fragoso MC, Mendonca BB, Latronico AC. Pinto EM, et al. Among authors: mendonca bb. J Clin Endocrinol Metab. 2005 May;90(5):2976-81. doi: 10.1210/jc.2004-0963. Epub 2005 Mar 1. J Clin Endocrinol Metab. 2005. PMID: 15741269
Detection of gsp somatic mutation through direct sequencing of heteroduplex alleles disclosed by denaturing gradient gel electrophoresis.
Fragoso MC, Lando VS, Latronico AC, Frazzatto ET, Russell AJ, Mendonca BB. Fragoso MC, et al. Among authors: mendonca bb. Med Sci Monit. 2002 Jan;8(1):BR15-8. Med Sci Monit. 2002. PMID: 11782667
Poor reproducibility of IGF-I and IGF binding protein-3 generation test in children with short stature and normal coding region of the GH receptor gene.
Jorge AA, Souza SC, Arnhold IJ, Mendonca BB. Jorge AA, et al. Among authors: mendonca bb. J Clin Endocrinol Metab. 2002 Feb;87(2):469-72. doi: 10.1210/jcem.87.2.8191. J Clin Endocrinol Metab. 2002. PMID: 11836270
Variable ACTH-stimulated 17-hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations.
Bachega TA, Brenlha EM, Billerbeck AE, Marcondes JA, Madureira G, Arnhold IJ, Mendonca BB. Bachega TA, et al. Among authors: mendonca bb. J Clin Endocrinol Metab. 2002 Feb;87(2):786-90. doi: 10.1210/jcem.87.2.8247. J Clin Endocrinol Metab. 2002. PMID: 11836321
Detection of Y-specific sequences in 122 patients with Turner syndrome: nested PCR is not a reliable method.
Nishi MY, Domenice S, Medeiros MA, Mendonca BB, Billerbeck AE. Nishi MY, et al. Among authors: mendonca bb. Am J Med Genet. 2002 Feb 1;107(4):299-305. doi: 10.1002/ajmg.10168. Am J Med Genet. 2002. PMID: 11840486 Clinical Trial.
Female pseudohermaphroditism caused by a novel homozygous missense mutation of the GR gene.
Mendonca BB, Leite MV, de Castro M, Kino T, Elias LL, Bachega TA, Arnhold IJ, Chrousos GP, Latronico AC. Mendonca BB, et al. J Clin Endocrinol Metab. 2002 Apr;87(4):1805-9. doi: 10.1210/jcem.87.4.8379. J Clin Endocrinol Metab. 2002. PMID: 11932321
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: mendonca bb. 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.
Three novel mutations in CYP21 gene in Brazilian patients with the classical form of 21-hydroxylase deficiency due to a founder effect.
Billerbeck AE, Mendonca BB, Pinto EM, Madureira G, Arnhold IJ, Bachega TA. Billerbeck AE, et al. Among authors: mendonca bb. J Clin Endocrinol Metab. 2002 Sep;87(9):4314-7. doi: 10.1210/jc.2001-011939. J Clin Endocrinol Metab. 2002. PMID: 12213891
Pituitary magnetic resonance imaging and function in patients with growth hormone deficiency with and without mutations in GHRH-R, GH-1, or PROP-1 genes.
Osorio MG, Marui S, Jorge AA, Latronico AC, Lo LS, Leite CC, Estefan V, Mendonca BB, Arnhold IJ. Osorio MG, et al. Among authors: mendonca bb. J Clin Endocrinol Metab. 2002 Nov;87(11):5076-84. doi: 10.1210/jc.2001-011936. J Clin Endocrinol Metab. 2002. PMID: 12414875
Adrenocortical tumors: results of treatment and study of Weiss's score as a prognostic factor.
Lucon AM, Pereira MA, Mendonça BB, Zerbini MC, Saldanha LB, Arap S. Lucon AM, et al. Among authors: mendonca bb. Rev Hosp Clin Fac Med Sao Paulo. 2002 Nov-Dec;57(6):251-6. doi: 10.1590/s0041-87812002000600002. Epub 2003 Feb 17. Rev Hosp Clin Fac Med Sao Paulo. 2002. PMID: 12612756
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