Detalhe da pesquisa
1.
Sex dimorphism of weight and length at birth: evidence based on disorders of sex development.
Ann Hum Biol
; 49(7-8): 274-279, 2022 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-36218438
2.
Two Novel Mutations in the Thyroid Hormone Receptor ß in Patients with Resistance to Thyroid Hormone (RTH ß): Clinical, Biochemical, and Molecular Data.
Horm Metab Res
; 47(12): 889-94, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25738994
3.
The effect of fetal androgen metabolism-related gene variants on external genitalia virilization in congenital adrenal hyperplasia.
Clin Genet
; 84(5): 482-8, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-22978668
4.
OCT4 immunohistochemistry may be necessary to identify the real risk of gonadal tumors in patients with Turner syndrome and Y chromosome sequences.
Hum Reprod
; 26(12): 3450-5, 2011 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-21930534
5.
Effects of growth hormone on body proportions in Turner syndrome compared with non-treated patients and normal women.
J Endocrinol Invest
; 33(10): 691-5, 2010 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-20354352
6.
Complement 4 phenotypes and genotypes in Brazilian patients with classical 21-hydroxylase deficiency.
Clin Exp Immunol
; 155(2): 182-8, 2009 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19137635
7.
Inhibition of CYP21A2 enzyme activity caused by novel missense mutations identified in Brazilian and Scandinavian patients.
J Clin Endocrinol Metab
; 93(6): 2416-20, 2008 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-18381579
8.
The influence of parental origin of X chromosome genes on the stature of patients with 45 X Turner syndrome.
Genet Mol Res
; 6(1): 1-7, 2007 Jan 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-17278084
9.
Inhibin alpha-subunit (INHA) gene and locus changes in paediatric adrenocortical tumours from TP53 R337H mutation heterozygote carriers.
J Med Genet
; 41(5): 354-9, 2004 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-15121773
10.
Gonadotropin-independent precocious puberty due to luteinizing hormone receptor mutations in Brazilian boys: a novel constitutively activating mutation in the first transmembrane helix.
J Clin Endocrinol Metab
; 85(12): 4799-805, 2000 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-11134146
11.
H28+C insertion in the CYP21 gene: a novel frameshift mutation in a Brazilian patient with the classical form of 21-hydroxylase deficiency.
J Clin Endocrinol Metab
; 86(12): 5877-80, 2001 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-11739456
12.
Family-based association of HLA class II alleles and haplotypes with type I diabetes in Brazilians reveals some characteristics of a highly diversified population.
Hum Immunol
; 62(11): 1226-33, 2001 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-11704284
13.
Turner's syndrome and thyroid disease: a transverse study of pediatric patients in Brazil.
J Pediatr Endocrinol Metab
; 13(4): 357-62, 2000 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-10776989
14.
Pre-operative control of arterial hypertension using ketoconazole in pediatric patients with adrenocortical tumors.
J Pediatr Endocrinol Metab
; 13(2): 201-4, 2000 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-10711667
15.
Validity of the use of a few hand-wrist bones for assessing bone age.
J Pediatr Endocrinol Metab
; 16(4): 541-4, 2003.
Artigo
em Inglês
| MEDLINE | ID: mdl-12793606
16.
True hermaphrodites in the southeastern region of Brazil: a different cytogenetic and gonadal profile.
J Pediatr Endocrinol Metab
; 11(4): 519-24, 1998.
Artigo
em Inglês
| MEDLINE | ID: mdl-9777572
17.
Beckwith-Wiedemann syndrome and virilizing cortical adrenal tumor in a child.
J Pediatr Surg
; 35(8): 1269-71, 2000 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-10945711
18.
Mutation distribution and CYP21/C4 locus variability in Brazilian families with the classical form of the 21-hydroxylase deficiency.
Acta Paediatr
; 88(3): 275-83, 1999 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-10229037
19.
Female pseudohermaphroditism due to classical 21-hydroxylase deficiency in a girl with Turner syndrome.
Clin Genet
; 51(5): 351-3, 1997 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-9212186
20.
The influence of parental origin of X chromosome genes on the stature of patients with 45 X Turner syndrome
Genet. mol. res. (Online)
; 6(1): 1-7, 2007. tab
Artigo
em Inglês
| LILACS | ID: lil-440615