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Congenital adrenal hyperplasia

The Lancet (British edition), 2005-06, Vol.365 (9477), p.2125-2136

2005

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Approach to the Adult with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

The journal of clinical endocrinology and metabolism, 2008-03, Vol.93 (3), p.653-660

Merke, Deborah P

2008

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A pharmacokinetic and pharmacodynamic study of delayed- and extended-release hydrocortisone (ChronocortTM) vs. conventional hydrocortisone (CortefTM) in the treatment of congenital adrenal hyperplasia

Clinical endocrinology (Oxford), 2010-04, Vol.72 (4), p.441-447

2010

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Phenotypic profiling of parents with cryptic nonclassic congenital adrenal hyperplasia: findings in 145 unrelated families

European journal of endocrinology, 2011-06, Vol.164 (6), p.977

2011

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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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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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Patients with Classic Congenital Adrenal Hyperplasia Have Decreased Epinephrine Reserve and Defective Glucose Elevation in Response to High-Intensity Exercise

The journal of clinical endocrinology and metabolism, 2004-02, Vol.89 (2), p.591-597

2004

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Hypogonadotropic Hypogonadism in a Female Caused by an X-Linked Recessive Mutation in the DAX1 Gene

The New England journal of medicine, 1999-04, Vol.340 (16), p.1248-1252

1999

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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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Children experience cognitive decline despite reversal of brain atrophy one year after resolution of cushing syndrome

The journal of clinical endocrinology and metabolism, 2005-05, Vol.90 (5), p.2531-2536

2005

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Patients with Classic Congenital Adrenal Hyperplasia Have Decreased Epinephrine Reserve and Defective Glycemic Control during Prolonged Moderate-Intensity Exercise

The journal of clinical endocrinology and metabolism, 2007-08, Vol.92 (8), p.3019-3024

2007

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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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Incentive processing in Congenital Adrenal Hyperplasia (CAH): A reward-based antisaccade study

Psychoneuroendocrinology, 2013-05, Vol.38 (5), p.716-721

2013

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Amygdala function in adolescents with congenital adrenal hyperplasia: A model for the study of early steroid abnormalities

Neuropsychologia, 2007-01, Vol.45 (9), p.2104-2113

2007

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The phenotypic spectrum of contiguous deletion of CYP21A2 and tenascin XB: Quadricuspid aortic valve and other midline defects

American journal of medical genetics. Part A, 2009-12, Vol.149A (12), p.2803-2808

2009

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Stress Dose of Hydrocortisone Is Not Beneficial in Patients with Classic Congenital Adrenal Hyperplasia Undergoing Short-Term, High-Intensity Exercise

The journal of clinical endocrinology and metabolism, 2004-08, Vol.89 (8), p.3679-3684

2004

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Steroid abnormalities and the developing brain: Declarative memory for emotionally arousing and neutral material in children with congenital adrenal hyperplasia

Psychoneuroendocrinology, 2008-02, Vol.33 (2), p.238-245

2008

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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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Utility of plasma free metanephrines for detecting childhood pheochromocytoma

The journal of clinical endocrinology and metabolism, 2002-05, Vol.87 (5), p.1955-1960

2002

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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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Emotional Memory in Early Steroid Abnormalities: An fMRI Study of Adolescents With Congenital Adrenal Hyperplasia: Typical and Atypical Processing of Emotional and Social Cues Across the Lifespan

Developmental neuropsychology, 2011, Vol.36 (4), p.473-492

2011

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Flutamide decreases cortisol clearance in patients with congenital adrenal hyperplasia

The journal of clinical endocrinology and metabolism, 2002-07, Vol.87 (7), p.3197-3200

2002

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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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Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Socie Clinical Practice Guideline

The journal of clinical endocrinology and metabolism, 2010, Vol.95 (9), p.4133-4160

2010

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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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Congenital adrenal hyperplasia

Approach to the Adult with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

A pharmacokinetic and pharmacodynamic study of delayed- and extended-release hydrocortisone (ChronocortTM) vs. conventional hydrocortisone (CortefTM) in the treatment of congenital adrenal hyperplasia

Phenotypic profiling of parents with cryptic nonclassic congenital adrenal hyperplasia: findings in 145 unrelated families

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

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

Patients with Classic Congenital Adrenal Hyperplasia Have Decreased Epinephrine Reserve and Defective Glucose Elevation in Response to High-Intensity Exercise

Hypogonadotropic Hypogonadism in a Female Caused by an X-Linked Recessive Mutation in the DAX1 Gene

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

Children experience cognitive decline despite reversal of brain atrophy one year after resolution of cushing syndrome

Patients with Classic Congenital Adrenal Hyperplasia Have Decreased Epinephrine Reserve and Defective Glycemic Control during Prolonged Moderate-Intensity Exercise

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

Incentive processing in Congenital Adrenal Hyperplasia (CAH): A reward-based antisaccade study

Amygdala function in adolescents with congenital adrenal hyperplasia: A model for the study of early steroid abnormalities

The phenotypic spectrum of contiguous deletion of CYP21A2 and tenascin XB: Quadricuspid aortic valve and other midline defects

Stress Dose of Hydrocortisone Is Not Beneficial in Patients with Classic Congenital Adrenal Hyperplasia Undergoing Short-Term, High-Intensity Exercise

Steroid abnormalities and the developing brain: Declarative memory for emotionally arousing and neutral material in children with congenital adrenal hyperplasia

Children with classic congenital adrenal hyperplasia have elevated serum leptin concentrations and insulin resistance: Potential clinical implications

Utility of plasma free metanephrines for detecting childhood pheochromocytoma

Adrenomedullary function may predict phenotype and genotype in classic 21-hydroxylase deficiency

Emotional Memory in Early Steroid Abnormalities: An fMRI Study of Adolescents With Congenital Adrenal Hyperplasia: Typical and Atypical Processing of Emotional and Social Cues Across the Lifespan

Flutamide decreases cortisol clearance in patients with congenital adrenal hyperplasia

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

Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Socie Clinical Practice Guideline

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

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