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Adrenal-derived 11-oxygenated 19-carbon steroids are the dominant androgens in classic 21-hydroxylase deficiency

European journal of endocrinology, 2016-05, Vol.174 (5), p.601

2016

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Pubertal and Gender-Related Changes in the Sympathoadrenal System in Healthy Children

The journal of clinical endocrinology and metabolism, 2002-11, Vol.87 (11), p.5038-5043

2002

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Morphologic and Molecular Characterization of Adrenals and Adrenal Rest Affected by Congenital Adrenal Hyperplasia

Frontiers in endocrinology (Lausanne), 2021-09, Vol.12, p.730947-730947

2021

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Cardiovascular Disease Risk Factors and Metabolic Morbidity in a Longitudinal Study of Congenital Adrenal Hyperplasia

The journal of clinical endocrinology and metabolism, 2021-12, Vol.106 (12), p.e5247-e5257

2021

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Adrenomedullary Dysplasia and Hypofunction in Patients with Classic 21-Hydroxylase Deficiency

The New England journal of medicine, 2000-11, Vol.343 (19), p.1362-1368

2000

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Longitudinal Assessment of Illnesses, Stress Dosing, and Illness Sequelae in Patients With Congenital Adrenal Hyperplasia

The journal of clinical endocrinology and metabolism, 2018-06, Vol.103 (6), p.2336-2345

2018

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11-Oxygenated Androgens Are Biomarkers of Adrenal Volume and Testicular Adrenal Rest Tumors in 21-Hydroxylase Deficiency

The journal of clinical endocrinology and metabolism, 2017-08, Vol.102 (8), p.2701-2710

2017

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Characterization of the CYP11A1 Nonsynonymous Variant p.E314K in Children Presenting With Adrenal Insufficiency

The journal of clinical endocrinology and metabolism, 2019-02, Vol.104 (2), p.269-276

2019

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Clinical Characteristics of a Cohort of 244 Patients with Congenital Adrenal Hyperplasia

The journal of clinical endocrinology and metabolism, 2012-12, Vol.97 (12), p.4429-4438

2012

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Adrenomedullary Function May Predict Phenotype and Genotype in Classic 21-Hydroxylase Deficiency

The journal of clinical endocrinology and metabolism, 2002-07, Vol.87 (7), p.3031-3037

2002

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Aplasia cutis congenita following in utero methimazole exposure

Journal of pediatric endocrinology & metabolism : JPEM, 2007-05, Vol.20 (5), p.585

2007

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Quality of life in children and adolescents 1-year after cure of Cushing syndrome: a prospective study

Clinical endocrinology (Oxford), 2009-09, Vol.71 (3), p.326-333

2009

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Hydrocortisone suspension and hydrocortisone tablets are not bioequivalent In the treatment of children with congenital adrenal hyperplasia

The journal of clinical endocrinology and metabolism, 2001, Vol.86 (1), p.441-445

2001

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Children with Classic Congenital Adrenal Hyperplasia Have Elevated Serum Leptin Concentrations and Insulin Resistance: Potential Clinical Implications

The journal of clinical endocrinology and metabolism, 2002-05, Vol.87 (5), p.2114-2120

2002

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Children with Classic Congenital Adrenal Hyperplasia Have Decreased Amygdala Volume: Potential Prenatal and Postnatal Hormonal Effects

The journal of clinical endocrinology and metabolism, 2003-04, Vol.88 (4), p.1760-1765

2003

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The adrenal life cycle: the fetal and adult cortex and the remaining questions

Journal of pediatric endocrinology & metabolism : JPEM, 2006-11, Vol.19 (11), p.1299

2006

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Testicular adrenal rest tissue in congenital adrenal hyperplasia: comparison of MR imaging and sonographic findings

American journal of roentgenology (1976), 1999-04, Vol.172 (4), p.1003

1999

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A preliminary study of flutamide, testolactone, and reduced hydrocortisone dose in the treatment of congenital adrenal hyperplasia

The journal of clinical endocrinology and metabolism, 1996-10, Vol.81 (10), p.3535-3539

1996

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Puberty-related influences on brain development

Molecular and cellular endocrinology, 2006-07, Vol.254, p.154-162

2006

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First Morning Pregnanetriol and 17-Hydroxyprogesterone Correlated Significantly in 21-Hydroxylase Deficiency

Frontiers in endocrinology (Lausanne), 2022-01, Vol.12, p.808254-808254

2022

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Experience with long-term glucocorticoid treatment in congenital adrenal hyperplasia: growth pattern compared with genetic height potential

Journal of pediatric endocrinology & metabolism : JPEM, 2006-03, Vol.19 (3), p.245

2006

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Androgens concentrations and second-to fourth-digit ratio (2D:4D) in girls with congenital adrenal hyperplasia (21-hydroxylase deficiency)

Neuro-endocrinology letters, 2012, Vol.33 (8), p.787-791

2012

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Comparative study of prednisolone versus hydrocortisone acetate for treatment of patients with the classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Arquivos brasileiros de endocrinologia e metabologia, 2008-02, Vol.52 (1), p.101-108

2008

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Characterization and Management of Testicular Pathology in McCune-Albright Syndrome

The journal of clinical endocrinology and metabolism, 2012-09, Vol.97 (9), p.E1782-E1790

2012

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Salivary morning androstenedione and 17α-OH progesterone levels in childhood and puberty in patients with classic congenital adrenal hyperplasia

Clinical chemistry and laboratory medicine, 2015-02, Vol.53 (3), p.461

2015

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Zeitschrift / SerieInternational Journal Of Pediatric Endocrinology

ThemaAdrenal Hyperplasia, Congenital - Genetics

ThemaChild, Preschool

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Adrenal Hyperplasia, Congenital - Drug Therapy
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Adrenals. Adrenal Axis. Renin-Angiotensin System
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Endocrinopathies
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Non Tumoral Diseases. Target Tissue Resistance. Benign Neoplasms
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Adrenal-derived 11-oxygenated 19-carbon steroids are the dominant androgens in classic 21-hydroxylase deficiency

Pubertal and Gender-Related Changes in the Sympathoadrenal System in Healthy Children

Morphologic and Molecular Characterization of Adrenals and Adrenal Rest Affected by Congenital Adrenal Hyperplasia

Cardiovascular Disease Risk Factors and Metabolic Morbidity in a Longitudinal Study of Congenital Adrenal Hyperplasia

Adrenomedullary Dysplasia and Hypofunction in Patients with Classic 21-Hydroxylase Deficiency

Longitudinal Assessment of Illnesses, Stress Dosing, and Illness Sequelae in Patients With Congenital Adrenal Hyperplasia

11-Oxygenated Androgens Are Biomarkers of Adrenal Volume and Testicular Adrenal Rest Tumors in 21-Hydroxylase Deficiency

Characterization of the CYP11A1 Nonsynonymous Variant p.E314K in Children Presenting With Adrenal Insufficiency

Clinical Characteristics of a Cohort of 244 Patients with Congenital Adrenal Hyperplasia

Adrenomedullary Function May Predict Phenotype and Genotype in Classic 21-Hydroxylase Deficiency

Aplasia cutis congenita following in utero methimazole exposure

Quality of life in children and adolescents 1-year after cure of Cushing syndrome: a prospective study

Hydrocortisone suspension and hydrocortisone tablets are not bioequivalent In the treatment of children with congenital adrenal hyperplasia

Children with Classic Congenital Adrenal Hyperplasia Have Elevated Serum Leptin Concentrations and Insulin Resistance: Potential Clinical Implications

Children with Classic Congenital Adrenal Hyperplasia Have Decreased Amygdala Volume: Potential Prenatal and Postnatal Hormonal Effects

The adrenal life cycle: the fetal and adult cortex and the remaining questions

Testicular adrenal rest tissue in congenital adrenal hyperplasia: comparison of MR imaging and sonographic findings

A preliminary study of flutamide, testolactone, and reduced hydrocortisone dose in the treatment of congenital adrenal hyperplasia

Puberty-related influences on brain development

First Morning Pregnanetriol and 17-Hydroxyprogesterone Correlated Significantly in 21-Hydroxylase Deficiency

Experience with long-term glucocorticoid treatment in congenital adrenal hyperplasia: growth pattern compared with genetic height potential

Androgens concentrations and second-to fourth-digit ratio (2D:4D) in girls with congenital adrenal hyperplasia (21-hydroxylase deficiency)

Comparative study of prednisolone versus hydrocortisone acetate for treatment of patients with the classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Characterization and Management of Testicular Pathology in McCune-Albright Syndrome

Salivary morning androstenedione and 17α-OH progesterone levels in childhood and puberty in patients with classic congenital adrenal hyperplasia

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