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GSTT1, GSTM1, and GSTP1 polymorphisms and chemotherapy response in locally advanced breast cancer

Genetics and molecular research, 2010-01, Vol.9 (2), p.1045-1053

2010

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DIAGNÓSTICO OCASIONAL DE LEUCEMIA LINFOIDE AGUDA EM PACIENTE COM DOENÇA DE GRAVES: UM RELATO DE CASO

Hematology, Transfusion and Cell Therapy, 2022-10, Vol.44, p.S196-S197

2022

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DIAGNÓSTICO OCASIONAL DE LEUCEMIA LINFOIDE AGUDA EM PACIENTE COM DOENÇA DE GRAVES: UM RELATO DE CASO

Hematology, Transfusion and Cell Therapy, 2022-10, Vol.44, p.S196-S197

2022

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The effect of fetal androgen metabolism-related gene variants on external genitalia virilization in congenital adrenal hyperplasia

Clinical genetics, 2013-11, Vol.84 (5), p.482-488

2013

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P450c17 Deficiency in Brazilian Patients: Biochemical Diagnosis through Progesterone Levels Confirmed by CYP17 Genotyping

The journal of clinical endocrinology and metabolism, 2003-12, Vol.88 (12), p.5739-5746

2003

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Androgen receptor-mediated hypersensitivity to androgens in women with nonhyperandrogenic hirsutism : Skewing of X-chromosome inactivation

The journal of clinical endocrinology and metabolism, 1999-03, Vol.84 (3), p.1091-1095

1999

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Quantitation of glucocorticoid receptor alpha and NF-κB pathway mRNA and its correlation with disease activity in rheumatoid arthritis patients

Genetics and molecular research, 2010-01, Vol.9 (4), p.2300-2310

2010

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Imbalanced Expression of the Glucocorticoid Receptor Isoforms in Cultured Lymphocytes from a Patient with Systemic Glucocorticoid Resistance and Chronic Lymphocytic Leukemia

Biochemical and biophysical research communications, 1999-01, Vol.254 (3), p.559-565

1999

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Inhibin α-subunit (INHA) gene and locus changes in paediatric adrenocortical tumours from TP53 R337H mutation heterozygote carriers

Journal of medical genetics, 2004-05, Vol.41 (5), p.354-359

2004

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Low Glucocorticoid Receptor α/β Ratio in T-cell Lymphoblastic Leukemia

Hormone and metabolic research, 2000-10, Vol.32 (10), p.401-406

2000

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Molecular genotyping in Brazilian patients with the classical and nonclassical forms of 21-hydroxylase deficiency

The journal of clinical endocrinology and metabolism, 1998-12, Vol.83 (12), p.4416-4419

1998

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Myocilin mt.1 gene promoter single nucleotide polymorphism (-1000C>G) in Brazilian patients with primary open angle glaucoma

Ophthalmic genetics, 2011-03, Vol.32 (1), p.18-23

2011

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Real-time PCR quantitation of glucocorticoid receptor alpha isoform

BMC molecular biology, 2004-10, Vol.5 (1), p.19-19, Article 19

2004

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A novel mutation in DAX1 gene causing different phenotypes in three siblings with adrenal hypoplasia congenita

Genetics and molecular research, 2007-01, Vol.6 (2), p.277-283

2007

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The influence of parental origin of X chromosome genes on the stature of patients with 45 X Turner syndrome

Genetics and molecular research, 2007-01, Vol.6 (1), p.1-7

2007

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Size of the exon 1-CAG repeats of the androgen receptor gene employed as a molecular marker in the diagnosis of Turner syndrome in girls with short stature

Genetics and molecular research, 2008-01, Vol.7 (1), p.43-49

2008

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Structural evaluation of type 3 dopaminergic receptor gene (DRD3) in chronic anovulatory women

Genetics and molecular research, 2008-01, Vol.7 (1), p.140-151

2008

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Transdermal estradiol priming during clonidine stimulation test in non-growth hormone deficient children with short stature: a pilot study

Journal of Pediatric Endocrinology and Metabolism, 2006-03, Vol.19 (3), p.223

2006

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Southwickʼs head-shaft angles: normal standards and abnormal values observed in obesity and in patients with epiphysiolysis

Journal of pediatric orthopaedics. B, 2004-07, Vol.13 (4), p.244-247

2004

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Partial glucocorticoid resistance in obese children detected by very low dose dexamethasone suppression test

Journal of Pediatric Endocrinology and Metabolism, 2003-12, Vol.16 (9), p.1277

2003

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Fast acquisition sagittal T1 magnetic resonance imaging (FAST1-MRI): a new imaging approach for the diagnosis of growth hormone deficiency

Journal of pediatric endocrinology & metabolism : JPEM, 2004-08, Vol.17 (8), p.1111

2004

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Requirement of FAT and DCHS protocadherins during hypothalamic-pituitary development

Yearbook of Paediatric Endocrinology, 2021-09

2021

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Adrenal steroids synthesis during acute infectious diseases in infants

Journal of Pediatric Endocrinology and Metabolism, 2002-11, Vol.15 (9), p.1515

2002

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Plasma cortisol responses after intramuscular corticotropin 1–24 in healthy men

Metabolism, clinical and experimental, 1998-11, Vol.47 (11), p.1419-1422

1998

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Abnormal inhibin A and inhibin B secretion in obese women with and without insulin resistance

Gynecological endocrinology, 2005-07, Vol.21 (1), p.7-11

2005

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GSTT1, GSTM1, and GSTP1 polymorphisms and chemotherapy response in locally advanced breast cancer

DIAGNÓSTICO OCASIONAL DE LEUCEMIA LINFOIDE AGUDA EM PACIENTE COM DOENÇA DE GRAVES: UM RELATO DE CASO

DIAGNÓSTICO OCASIONAL DE LEUCEMIA LINFOIDE AGUDA EM PACIENTE COM DOENÇA DE GRAVES: UM RELATO DE CASO

The effect of fetal androgen metabolism-related gene variants on external genitalia virilization in congenital adrenal hyperplasia

P450c17 Deficiency in Brazilian Patients: Biochemical Diagnosis through Progesterone Levels Confirmed by CYP17 Genotyping

Androgen receptor-mediated hypersensitivity to androgens in women with nonhyperandrogenic hirsutism : Skewing of X-chromosome inactivation

Quantitation of glucocorticoid receptor alpha and NF-κB pathway mRNA and its correlation with disease activity in rheumatoid arthritis patients

Imbalanced Expression of the Glucocorticoid Receptor Isoforms in Cultured Lymphocytes from a Patient with Systemic Glucocorticoid Resistance and Chronic Lymphocytic Leukemia

Inhibin α-subunit (INHA) gene and locus changes in paediatric adrenocortical tumours from TP53 R337H mutation heterozygote carriers

Low Glucocorticoid Receptor α/β Ratio in T-cell Lymphoblastic Leukemia

Molecular genotyping in Brazilian patients with the classical and nonclassical forms of 21-hydroxylase deficiency

Myocilin mt.1 gene promoter single nucleotide polymorphism (-1000C>G) in Brazilian patients with primary open angle glaucoma

Real-time PCR quantitation of glucocorticoid receptor alpha isoform

A novel mutation in DAX1 gene causing different phenotypes in three siblings with adrenal hypoplasia congenita

The influence of parental origin of X chromosome genes on the stature of patients with 45 X Turner syndrome

Size of the exon 1-CAG repeats of the androgen receptor gene employed as a molecular marker in the diagnosis of Turner syndrome in girls with short stature

Structural evaluation of type 3 dopaminergic receptor gene (DRD3) in chronic anovulatory women

Transdermal estradiol priming during clonidine stimulation test in non-growth hormone deficient children with short stature: a pilot study

Southwickʼs head-shaft angles: normal standards and abnormal values observed in obesity and in patients with epiphysiolysis

Partial glucocorticoid resistance in obese children detected by very low dose dexamethasone suppression test

Fast acquisition sagittal T1 magnetic resonance imaging (FAST1-MRI): a new imaging approach for the diagnosis of growth hormone deficiency

Requirement of FAT and DCHS protocadherins during hypothalamic-pituitary development

Adrenal steroids synthesis during acute infectious diseases in infants

Plasma cortisol responses after intramuscular corticotropin 1–24 in healthy men

Abnormal inhibin A and inhibin B secretion in obese women with and without insulin resistance

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