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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.977-984

2011

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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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Future Directions in the Study and Management of Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

Annals of internal medicine, 2002-02, Vol.136 (4), p.320

2002

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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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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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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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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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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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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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THE RISK FACTORS FOR ARRHYTHMIC DEATH IN A SAMPLE OF MEN FOLLOWED FOR 20 YEARS

American journal of epidemiology, 1988-03, Vol.127 (3), p.500-515

1988

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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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An Increased Capacity for Adrenal DHEA Release is Associated with Decreased Avoidance and Negative Mood Symptoms in Women with PTSD

Neuropsychopharmacology (New York, N.Y.), 2004-08, Vol.29 (8), p.1546-1557

2004

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Renal receptors and effects of atrial natriuretic factor in compensatory renal hypertrophy

Kidney international, 1992-07, Vol.42 (1), p.75-82

1992

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Cardiovascular Risk Factors and Ultrasound Evaluation of Intima-Media Thickness at Common Carotids, Carotid Bulbs, and Femoral and Abdominal Aorta Arteries in Patients with Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

The journal of clinical endocrinology and metabolism, 2007-03, Vol.92 (3), p.1015-1018

2007

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Normal Bone Mineral Density and Lean Body Mass, but Increased Fat Mass, in Young Adult Patients with Congenital Adrenal Hyperplasia

The journal of clinical endocrinology and metabolism, 2003-03, Vol.88 (3), p.1036-1042

2003

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Reduced Bone Mineral Density and Increased Bone Metabolism Rate in Young Adult Patients with 21-Hydroxylase Deficiency

The journal of clinical endocrinology and metabolism, 2006-11, Vol.91 (11), p.4453-4458

2006

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Monitoring of menstrual cycles, ovulation, and adrenal suppression by saliva sampling in female patients with 21-hydroxylase deficiency

Fertility and sterility, 2003-10, Vol.80 (4), p.1030-1036

2003

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Mild cutaneous manifestation in two young women with extraordinary hyperandrogenemia

Dermatology (Basel), 2005, Vol.210 (1), p.49-52

2005

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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

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

Future Directions in the Study and Management of Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

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

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

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

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

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

THE RISK FACTORS FOR ARRHYTHMIC DEATH IN A SAMPLE OF MEN FOLLOWED FOR 20 YEARS

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

An Increased Capacity for Adrenal DHEA Release is Associated with Decreased Avoidance and Negative Mood Symptoms in Women with PTSD

Renal receptors and effects of atrial natriuretic factor in compensatory renal hypertrophy

Cardiovascular Risk Factors and Ultrasound Evaluation of Intima-Media Thickness at Common Carotids, Carotid Bulbs, and Femoral and Abdominal Aorta Arteries in Patients with Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

Normal Bone Mineral Density and Lean Body Mass, but Increased Fat Mass, in Young Adult Patients with Congenital Adrenal Hyperplasia

Reduced Bone Mineral Density and Increased Bone Metabolism Rate in Young Adult Patients with 21-Hydroxylase Deficiency

Monitoring of menstrual cycles, ovulation, and adrenal suppression by saliva sampling in female patients with 21-hydroxylase deficiency

Mild cutaneous manifestation in two young women with extraordinary hyperandrogenemia

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