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Postreceptor insulin resistance contributes to human dyslipidemia and hepatic steatosis

The Journal of clinical investigation, 2009-02, Vol.119 (2), p.315-322

2009

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A new variant in signal peptide of the human luteinizing hormone receptor (LHCGR) affects receptor biogenesis causing leydig cell hypoplasia

Human molecular genetics, 2015-11, Vol.24 (21), p.6003-6012

2015

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Relationship of CYP21A2 genotype and serum 17-hydroxyprogesterone and cortisol levels in a large cohort of Italian children with premature pubarche

European journal of endocrinology, 2011-08, Vol.165 (2), p.307-314

2011

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Clinical Significance of the Parental Origin of the X Chromosome in Turner Syndrome

The journal of clinical endocrinology and metabolism, 2007-03, Vol.92 (3), p.846-852

2007

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Natural Glucocorticoid Receptor Mutants Causing Generalized Glucocorticoid Resistance: Molecular Genotype, Genetic Transmission, and Clinical Phenotype

The journal of clinical endocrinology and metabolism, 2004-04, Vol.89 (4), p.1939-1949

2004

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Familial/Sporadic Glucocorticoid Resistance Syndrome and Hypertension

Annals of the New York Academy of Sciences, 2002-09, Vol.970 (1), p.101-111

2002

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Prevalence of pathogenetic MC4R mutations in Italian children with early onset obesity, tall stature and familial history of obesity

BMC medical genetics, 2009-03, Vol.10 (1), p.25-25, Article 25

2009

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Evidence for Epigenetic Abnormalities of the Androgen Receptor Gene in Foreskin from Children with Hypospadias

The journal of clinical endocrinology and metabolism, 2011-12, Vol.96 (12), p.E1953-E1962

2011

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Corticotropin-Releasing Hormone (CRH) Inhibits Steroid Biosynthesis by Cultured Human Granulosa-Lutein Cells in a CRH and Interleukin-1 Receptor-Mediated Fashion

Endocrinology (Philadelphia), 1997-11, Vol.138 (11), p.4806-4811

1997

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Ghrelin Inhibits Steroid Biosynthesis by Cultured Granulosa-Lutein Cells

The journal of clinical endocrinology and metabolism, 2008-04, Vol.93 (4), p.1476-1481

2008

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Mitochondrial dysfunction in patients with primary congenital insulin resistance

The Journal of clinical investigation, 2011-06, Vol.121 (6), p.2457-2461

2011

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L’induzione della pubertà

L'Endocrinologo, 2014-04, Vol.15 (2), p.65-71

2014

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Leptin, Cortisol, and GH Secretion Interactions in Short Normal Prepubertal Children

The journal of clinical endocrinology and metabolism, 2001-08, Vol.86 (8), p.3729-3734

2001

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The Human Glucocorticoid Receptor (hGR) β Isoform Suppresses the Transcriptional Activity of hGRα by Interfering with Formation of Active Coactivator Complexes

Molecular endocrinology (Baltimore, Md.), 2005-01, Vol.19 (1), p.52-64

2005

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A Novel, C-Terminal Dominant Negative Mutation of the GR Causes Familial Glucocorticoid Resistance through Abnormal Interactions with p160 Steroid Receptor Coactivators

The journal of clinical endocrinology and metabolism, 2002-06, Vol.87 (6), p.2658-2667

2002

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Diagnosi e terapia della malattia di Cushing in età pediatrica

L'Endocrinologo, 2011-06, Vol.12 (3), p.117-121

2011

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New Aspects of the Physiology of the GH-IGF-1 Axis

Endocrine development, 2013, Vol.24, p.96-105

2013

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High constitutive glucocorticoid receptor beta in human neutrophils enables them to reduce their spontaneous rate of cell death in response to corticosteroids

The Journal of experimental medicine, 2001-03, Vol.193 (5), p.585-594

2001

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Association of glucocorticoid insensitivity with increased expression of glucocorticoid receptor beta

The Journal of experimental medicine, 1997-11, Vol.186 (9), p.1567-1574

1997

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Progress in Pediatrics in 2012: choices in allergy, endocrinology, gastroenterology, hematology, infectious diseases, neurology, nutrition and respiratory tract illnesses

Italian journal of pediatrics, 2013-05, Vol.39 (1), p.26-26

2013

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A novel, C-terminal dominant negative mutation of the GR causes familial glucocorticoid resistance through abnormal interactions with p160 steroid receptor coactivators

The journal of clinical endocrinology and metabolism, 2002-06, Vol.87 (6), p.2658-2667

2002

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Progress in pediatrics in 2013: choices in allergology, endocrinology, gastroenterology, hypertension, infectious diseases, neonatology, neurology, nutrition and respiratory tract illnesses

Italian journal of pediatrics, 2014-07, Vol.40 (1), p.62-62, Article 62

2014

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A novel mutation in the NR0B1 gene in a family with monozygotic twin sisters and congenital adrenal hypoplasia affected children

Hormones (Athens, Greece), 2015-01, Vol.14 (1), p.160-166

2015

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Final Height in Girls with Central Idiopathic Precocious Puberty Treated with Gonadotropin-Releasing Hormone Analog and Oxandrolone

The journal of clinical endocrinology and metabolism, 2006-04, Vol.91 (4), p.1284-1287

2006

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The aromatase excess syndrome is associated with feminization of both sexes and autosomal dominant transmission of aberrant P450 aromatase gene transcription

The journal of clinical endocrinology and metabolism, 1998-04, Vol.83 (4), p.1348-1357

1998

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Postreceptor insulin resistance contributes to human dyslipidemia and hepatic steatosis

A new variant in signal peptide of the human luteinizing hormone receptor (LHCGR) affects receptor biogenesis causing leydig cell hypoplasia

Relationship of CYP21A2 genotype and serum 17-hydroxyprogesterone and cortisol levels in a large cohort of Italian children with premature pubarche

Clinical Significance of the Parental Origin of the X Chromosome in Turner Syndrome

Natural Glucocorticoid Receptor Mutants Causing Generalized Glucocorticoid Resistance: Molecular Genotype, Genetic Transmission, and Clinical Phenotype

Familial/Sporadic Glucocorticoid Resistance Syndrome and Hypertension

Prevalence of pathogenetic MC4R mutations in Italian children with early onset obesity, tall stature and familial history of obesity

Evidence for Epigenetic Abnormalities of the Androgen Receptor Gene in Foreskin from Children with Hypospadias

Corticotropin-Releasing Hormone (CRH) Inhibits Steroid Biosynthesis by Cultured Human Granulosa-Lutein Cells in a CRH and Interleukin-1 Receptor-Mediated Fashion

Ghrelin Inhibits Steroid Biosynthesis by Cultured Granulosa-Lutein Cells

Mitochondrial dysfunction in patients with primary congenital insulin resistance

L’induzione della pubertà

Leptin, Cortisol, and GH Secretion Interactions in Short Normal Prepubertal Children

The Human Glucocorticoid Receptor (hGR) β Isoform Suppresses the Transcriptional Activity of hGRα by Interfering with Formation of Active Coactivator Complexes

A Novel, C-Terminal Dominant Negative Mutation of the GR Causes Familial Glucocorticoid Resistance through Abnormal Interactions with p160 Steroid Receptor Coactivators

Diagnosi e terapia della malattia di Cushing in età pediatrica

New Aspects of the Physiology of the GH-IGF-1 Axis

High constitutive glucocorticoid receptor beta in human neutrophils enables them to reduce their spontaneous rate of cell death in response to corticosteroids

Association of glucocorticoid insensitivity with increased expression of glucocorticoid receptor beta

Progress in Pediatrics in 2012: choices in allergy, endocrinology, gastroenterology, hematology, infectious diseases, neurology, nutrition and respiratory tract illnesses

A novel, C-terminal dominant negative mutation of the GR causes familial glucocorticoid resistance through abnormal interactions with p160 steroid receptor coactivators

Progress in pediatrics in 2013: choices in allergology, endocrinology, gastroenterology, hypertension, infectious diseases, neonatology, neurology, nutrition and respiratory tract illnesses

A novel mutation in the NR0B1 gene in a family with monozygotic twin sisters and congenital adrenal hypoplasia affected children

Final Height in Girls with Central Idiopathic Precocious Puberty Treated with Gonadotropin-Releasing Hormone Analog and Oxandrolone

The aromatase excess syndrome is associated with feminization of both sexes and autosomal dominant transmission of aberrant P450 aromatase gene transcription

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