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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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Modified-Release Hydrocortisone to Provide Circadian Cortisol Profiles

The journal of clinical endocrinology and metabolism, 2009-05, Vol.94 (5), p.1548-1554

2009

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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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Psychiatric characterization of children with genetic causes of hyperandrogenism

European journal of endocrinology, 2010-11, Vol.163 (5), p.801

2010

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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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An oral multiparticulate, modified-release, hydrocortisone replacement therapy that provides physiological cortisol exposure

Clinical endocrinology (Oxford), 2014-04, Vol.80 (4), p.554-561

2014

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Junction Site Analysis of Chimeric CYP21A1P/CYP21A2 Genes in 21-Hydroxylase Deficiency

Clinical chemistry (Baltimore, Md.), 2012-02, Vol.58 (2), p.421-430

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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In Boys with Abnormal Developmental Tempo, Maturation of the Skeleton and the Hypothalamic-Pituitary-Gonadal Axis Remains Synchronous

The journal of clinical endocrinology and metabolism, 2004-01, Vol.89 (1), p.236-241

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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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 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 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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Endocrinologic and Psychologic Evaluation of 21-Hydroxylase Deficiency Carriers and Matched Normal Subjects: Evidence for Physical and/or Psychologic Vulnerability to Stress

The journal of clinical endocrinology and metabolism, 2004-05, Vol.89 (5), p.2228-2236

2004

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NEW IDEAS FOR MEDICAL TREATMENT OF CONGENITAL ADRENAL HYPERPLASIA

Endocrinology and metabolism clinics of North America, 2001-03, Vol.30 (1), p.121-135

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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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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Early puberty: a cautionary tale

Pediatrics (Evanston), 2000-01, Vol.105 (1 Pt 1), p.115

2000

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Novel CYP11B1 Mutations in Congenital Adrenal Hyperplasia due to Steroid 11β-Hydroxylase Deficiency

The journal of clinical endocrinology and metabolism, 1998-01, Vol.83 (1), p.270-273

1998

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

Modified-Release Hydrocortisone to Provide Circadian Cortisol Profiles

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

Psychiatric characterization of children with genetic causes of hyperandrogenism

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

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

An oral multiparticulate, modified-release, hydrocortisone replacement therapy that provides physiological cortisol exposure

Junction Site Analysis of Chimeric CYP21A1P/CYP21A2 Genes in 21-Hydroxylase Deficiency

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

In Boys with Abnormal Developmental Tempo, Maturation of the Skeleton and the Hypothalamic-Pituitary-Gonadal Axis Remains Synchronous

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

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

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

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

Endocrinologic and Psychologic Evaluation of 21-Hydroxylase Deficiency Carriers and Matched Normal Subjects: Evidence for Physical and/or Psychologic Vulnerability to Stress

NEW IDEAS FOR MEDICAL TREATMENT OF 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

Early puberty: a cautionary tale

Novel CYP11B1 Mutations in Congenital Adrenal Hyperplasia due to Steroid 11β-Hydroxylase Deficiency

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