Detalhe da pesquisa
1.
Partial remission in Brazilian children and adolescents with type 1 diabetes. Association with a haplotype of class II human leukocyte antigen and synthesis of autoantibodies.
Pediatr Diabetes
; 21(4): 606-614, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32078220
2.
Phase 2 study of neoadjuvant enzalutamide and paclitaxel for luminal androgen receptor-enriched TNBC: Trial results and insights into "ARness".
Cell Rep Med
; 5(6): 101595, 2024 Jun 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-38838676
3.
Two distinct WT1 mutations identified in patients and relatives with isolated nephrotic proteinuria.
Biochem Biophys Res Commun
; 441(2): 371-6, 2013 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24161391
4.
Screening of Y chromosome microdeletions in 46,XY partial gonadal dysgenesis and in patients with a 45,X/46,XY karyotype or its variants.
BMC Med Genet
; 14: 115, 2013 Nov 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-24192396
5.
Anthropometry and physical appearance can be associated with quality of life in Brazilian women with Turner syndrome.
Arch Endocrinol Metab
; 67(1): 126-135, 2023 Jan 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-36468921
6.
Normal ambulatory blood pressure in young adults with 21-hydroxylase enzyme deficiency undergoing glucocorticoid replacement therapy.
Arch Endocrinol Metab
; 67(1): 64-72, 2023 Jan 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-35929901
7.
Screening of autosomal gene deletions in patients with hypogonadotropic hypogonadism using multiplex ligation-dependent probe amplification: detection of a hemizygosis for the fibroblast growth factor receptor 1.
Clin Endocrinol (Oxf)
; 72(3): 371-6, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-19489874
8.
Spontaneous final height in Turner's syndrome in Brazil.
J Pediatr Endocrinol Metab
; 20(11): 1207-14, 2007 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-18183792
9.
A Single Nucleotide Variant in the Promoter Region of 17ß-HSD Type 5 Gene Influences External Genitalia Virilization in Females with 21-Hydroxylase Deficiency.
Horm Res Paediatr
; 85(5): 333-8, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27082632
10.
Clinical and molecular data from 61 Brazilian cases of Congenital Hyperinsulinemic Hypoglycemia.
Diabetol Metab Syndr
; 7: 5, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25972930
11.
[Turner syndrome: the patients' view]. / A percepção da doença em portadoras da síndrome de Turner.
J Pediatr (Rio J)
; 80(4): 309-14, 2004.
Artigo
em Português
| MEDLINE | ID: mdl-15309233
12.
[Multicentric study of Brazilian patients with 21-hydroxylase deficiency: a genotype-phenotype correlation]. / Estudo multicêntrico de pacientes brasileiros com deficiência da 21-hidroxilase: correlação do genótipo com o fenótipo.
Arq Bras Endocrinol Metabol
; 48(5): 697-704, 2004 Oct.
Artigo
em Português
| MEDLINE | ID: mdl-15761541
13.
Performance of phalangeal quantitative ultrasound parameters in the evaluation of reduced bone mineral density assessed by DX in patients with 21 hydroxylase deficiency.
Ultrasound Med Biol
; 40(7): 1414-9, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24726797
14.
Éxodo en personal de Atención Primaria de Salud / Exodus on Primary Health Care personnel
Rev. cienc. méd. La Habana (En línea)
; 18(2)2012. tab
Artigo
em Espanhol
| LILACS | ID: lil-731350
15.
Severe hypertriglyceridemia is related to episodes of epididymitis.
J Clin Lipidol
; 3(3): 201-4, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-21291815
16.
Labioscrotal island flap in feminizing genitoplasty.
J Pediatr Surg
; 39(7): 1030-3, 2004 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-15213892
17.
Bone mineralization in Turner syndrome: a transverse study of the determinant factors in 58 patients.
J Bone Miner Metab
; 20(5): 294-7, 2002.
Artigo
em Inglês
| MEDLINE | ID: mdl-12203035
18.
Classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a cross-sectional study of factors involved in bone mineral density.
J Bone Miner Metab
; 21(6): 396-401, 2003.
Artigo
em Inglês
| MEDLINE | ID: mdl-14586796