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

Clinical endocrinology (Oxford), 2006-09, Vol.65 (3), p.294-300

2006

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A novel missense mutation, GLY424SER, in Brazilian patients with 21-hydroxylase deficiency

The journal of clinical endocrinology and metabolism, 1999-08, Vol.84 (8), p.2870-2872

1999

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Influence of different genotypes on 17-hydroxyprogesterone levels in patients with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Clinical endocrinology (Oxford), 2000-05, Vol.52 (5), p.601-607

2000

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Germline mutation analysis of Tpit in Poodle dogs with ACTH-dependent hyperadrenocorticism

Arquivo brasileiro de medicina veterinária e zootecnia, 2012-08, Vol.64 (4), p.853-859

2012

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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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Detection of Leptospira DNA in Patients with Aseptic Meningitis by PCR

Journal of Clinical Microbiology, 1998-05, Vol.36 (5), p.1453-1455

1998

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Genetic linkage studies of thyroid peroxidase (TPO) gene in families with TPO deficiency

The journal of clinical endocrinology and metabolism, 1991-02, Vol.72 (2), p.471-476

1991

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A 138-nucleotide deletion in the thyroglobulin ribonucleic acid messenger in a congenital goiter with defective thyroglobulin synthesis

The journal of clinical endocrinology and metabolism, 1995-11, Vol.80 (11), p.3356-3360

1995

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Gene and Genotype Frequencies for HLA-DQA1 in Caucasians and Mulattoes in Brazil

Journal of forensic sciences, 1999-09, Vol.44 (5), p.1051-1052

1999

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Low Frequency of CYP21B Deletions in Brazilian Patients with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

Human heredity, 1999-01, Vol.49 (1), p.9-14

1999

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Characterization of 8 Point Mutations in the Cyp21b Gene in Brazilian Patients With Congenital Adrenal Hyperplasia (Cah) Due To 21-Hydroxylase Deficiency 31

Pediatric research, 1998-02, Vol.43 (2), p.300-300

1998

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Frequency of Deletions and Gene Conversions in Brazilian Patients With Congenital Adrenal Hyperplasia Due To 21-Hydroxylase Deficiency

Pediatric research, 1997-02, Vol.41 (2), p.302-302

1997

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Investigations of the ZFY gene in XX true hermaphroditism and Swyer syndrome

Human genetics, 1990, Vol.85 (1), p.85-88

1990

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Effects of Cymbopogon nardus (L.) W. Watson essential oil on the growth and morphogenesis of Aspergillus niger

Canadian journal of microbiology, 2001-01, Vol.47 (1), p.9-17

2001

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A Microdeletion in the Ligand Binding Domain of Human Steroidogenic Factor 1 Causes XY Sex Reversal without Adrenal Insufficiency

The journal of clinical endocrinology and metabolism, 2004-04, Vol.89 (4), p.1767-1772

2004

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SHOX mutations in idiopathic short stature and Leri-Weill dyschondrosteosis: frequency and phenotypic variability

Clinical endocrinology (Oxford), 2007-01, Vol.66 (1), p.130-135

2007

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Usefulness of MLPA in the detection of SHOX deletions

European journal of medical genetics, 2010-09, Vol.53 (5), p.234-238

2010

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Analysis of a novel erm(T)- and cadDX-carrying plasmid from methicillin-susceptible Staphylococcus aureus ST398-t571 of human origin

Journal of antimicrobial chemotherapy, 2013-02, Vol.68 (2), p.471-473

2013

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O112 GENERATION OF MICE WITH SYNGENEIC HUMAN LIVER AND IMMUNE SYSTEM TO STUDY CELLULAR IMMUNITY TO HEPATITIS B VIRUS

Journal of hepatology, 2014-04, Vol.60 (1), p.S46-S46

2014

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Three Novel Mutations in CYP21 Gene in Brazilian Patients with the Classical Form of 21-Hydroxylase Deficiency Due to a Founder Effect

The journal of clinical endocrinology and metabolism, 2002-09, Vol.87 (9), p.4314-4317

2002

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A unique constitutively activating mutation in third transmembrane helix of luteinizing hormone receptor causes sporadic male gonadotropin-independent precocious puberty

The journal of clinical endocrinology and metabolism, 1998-07, Vol.83 (7), p.2435-2440

1998

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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

The journal of clinical endocrinology and metabolism, 2005-05, Vol.90 (5), p.2976-2981

2005

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A novel missense mutation (S18N) in the 5' non-HMG box region of the SRY gene in a patient with partial gonadal dysgenesis and his normal male relatives

Human genetics, 1998-02, Vol.102 (2), p.213-215

1998

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Variable ACTH-stimulated 17-hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations

The journal of clinical endocrinology and metabolism, 2002-02, Vol.87 (2), p.786-790

2002

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Nongenetic Male Pseudohermaphroditism and Reduced Prenatal Growth

The New England journal of medicine, 2001-10, Vol.345 (15), p.1135-1135

2001

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

A novel missense mutation, GLY424SER, in Brazilian patients with 21-hydroxylase deficiency

Influence of different genotypes on 17-hydroxyprogesterone levels in patients with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Germline mutation analysis of Tpit in Poodle dogs with ACTH-dependent hyperadrenocorticism

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

Detection of Leptospira DNA in Patients with Aseptic Meningitis by PCR

Genetic linkage studies of thyroid peroxidase (TPO) gene in families with TPO deficiency

A 138-nucleotide deletion in the thyroglobulin ribonucleic acid messenger in a congenital goiter with defective thyroglobulin synthesis

Gene and Genotype Frequencies for HLA-DQA1 in Caucasians and Mulattoes in Brazil

Low Frequency of CYP21B Deletions in Brazilian Patients with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

Characterization of 8 Point Mutations in the Cyp21b Gene in Brazilian Patients With Congenital Adrenal Hyperplasia (Cah) Due To 21-Hydroxylase Deficiency 31

Frequency of Deletions and Gene Conversions in Brazilian Patients With Congenital Adrenal Hyperplasia Due To 21-Hydroxylase Deficiency

Investigations of the ZFY gene in XX true hermaphroditism and Swyer syndrome

Effects of Cymbopogon nardus (L.) W. Watson essential oil on the growth and morphogenesis of Aspergillus niger

A Microdeletion in the Ligand Binding Domain of Human Steroidogenic Factor 1 Causes XY Sex Reversal without Adrenal Insufficiency

SHOX mutations in idiopathic short stature and Leri-Weill dyschondrosteosis: frequency and phenotypic variability

Usefulness of MLPA in the detection of SHOX deletions

Analysis of a novel erm(T)- and cadDX-carrying plasmid from methicillin-susceptible Staphylococcus aureus ST398-t571 of human origin

O112 GENERATION OF MICE WITH SYNGENEIC HUMAN LIVER AND IMMUNE SYSTEM TO STUDY CELLULAR IMMUNITY TO HEPATITIS B VIRUS

Three Novel Mutations in CYP21 Gene in Brazilian Patients with the Classical Form of 21-Hydroxylase Deficiency Due to a Founder Effect

A unique constitutively activating mutation in third transmembrane helix of luteinizing hormone receptor causes sporadic male gonadotropin-independent precocious puberty

Deletion Mapping of Chromosome 17 in Benign and Malignant Adrenocortical Tumors Associated with the Arg337His Mutation of the p53 Tumor Suppressor Protein

A novel missense mutation (S18N) in the 5' non-HMG box region of the SRY gene in a patient with partial gonadal dysgenesis and his normal male relatives

Variable ACTH-stimulated 17-hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations

Nongenetic Male Pseudohermaphroditism and Reduced Prenatal Growth

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