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Clinical applications of a gas chromatographic method for the combined determination of testosterone and epitestosterone glucuronide in urine

The journal of clinical endocrinology and metabolism, 1965-11, Vol.25 (11), p.1451-1456

1965

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A Randomized Safety and Efficacy Study of Somavaratan (VRS-317), a Long-Acting rhGH, in Pediatric Growth Hormone Deficiency

The journal of clinical endocrinology and metabolism, 2016-03, Vol.101 (3), p.1091-1097

2016

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Safety Outcomes During Pediatric GH Therapy: Final Results From the Prospective GeNeSIS Observational Program

The journal of clinical endocrinology and metabolism, 2019-02, Vol.104 (2), p.379-389

2019

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Recombinant Insulin-Like Growth Factor (IGF)-I Treatment in Short Children with Low IGF-I Levels: First-Year Results from a Randomized Clinical Trial

The journal of clinical endocrinology and metabolism, 2010-02, Vol.95 (2), p.611-619

2010

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Nonclassic Lipoid Congenital Adrenal Hyperplasia Masquerading as Familial Glucocorticoid Deficiency

The journal of clinical endocrinology and metabolism, 2009-10, Vol.94 (10), p.3865-3871

2009

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Evaluation and Treatment of Adult Growth Hormone Deficiency: An Endocrine Society Clinical Practice Guideline

The journal of clinical endocrinology and metabolism, 2006-05, Vol.91 (5), p.1621-1634

2006

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Leukocyte Telomere Length in Children With Congenital Adrenal Hyperplasia

The journal of clinical endocrinology and metabolism, 2023-01, Vol.108 (2), p.443-452

2023

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Long-Term Efficacy of T3 Analogue Triac in Children and Adults With MCT8 Deficiency: A Real-Life Retrospective Cohort Study

The journal of clinical endocrinology and metabolism, 2022-02, Vol.107 (3), p.e1136-e1147

2022

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Prediction of Autoantibody Positivity and Progression to Type 1 Diabetes: Diabetes Autoimmunity Study in the Young (DAISY)

The journal of clinical endocrinology and metabolism, 2004-08, Vol.89 (8), p.3896-3902

2004

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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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Diagnosis of hidden central hypothyroidism in survivors of childhood cancer

The journal of clinical endocrinology and metabolism, 1999-12, Vol.84 (12), p.4472-4479

1999

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The hypoplastic inferior petrosal sinus : A potential source of false-negative results in petrosal sampling for Cushing's disease

The journal of clinical endocrinology and metabolism, 1999-02, Vol.84 (2), p.533-540

1999

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Hypothalamic-pituitary-adrenal axis dysregulation in sexually abused girls

The journal of clinical endocrinology and metabolism, 1994-02, Vol.78 (2), p.249-255

1994

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Absence of Increased Height Velocity in the First Year of Life in Untreated Children with Simple Virilizing Congenital Adrenal Hyperplasia

The journal of clinical endocrinology and metabolism, 2006-04, Vol.91 (4), p.1205-1209

2006

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Endocrine and Immunogenetic Testing in Individuals with Type 1 Diabetes and 21-Hydroxylase Autoantibodies: Addison’s Disease in a High-Risk Population

The journal of clinical endocrinology and metabolism, 2005-01, Vol.90 (1), p.128-134

2005

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Screening Strategies for the Identification of Multiple Antibody-Positive Relatives of Individuals with Type 1 Diabetes

The journal of clinical endocrinology and metabolism, 2003-01, Vol.88 (1), p.103-108

2003

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Morbidity and mortality in follicular thyroid cancer

The journal of clinical endocrinology and metabolism, 1995-10, Vol.80 (10), p.2946-2953

1995

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Antiislet autoantibodies usually develop sequentially rather than simultaneously

The journal of clinical endocrinology and metabolism, 1996-12, Vol.81 (12), p.4264-4267

1996

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A single midnight serum cortisol measurement distinguishes Cushing's syndrome from pseudo-cushing states

The Journal of clinical endocrinology and metabolism, 1998-04, Vol.83 (4), p.1163-1167

1998

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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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Female pseudohermaphroditism caused by a novel homozygous missense mutation of the GR gene

The journal of clinical endocrinology and metabolism, 2002-04, Vol.87 (4), p.1805-1809

2002

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DRB104 and DQ alleles : Expression of 21-hydroxylase autoantibodies and risk of progression to Addison's disease

The journal of clinical endocrinology and metabolism, 1999, Vol.84 (1), p.328-335

1999

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Specific Human Leukocyte Antigen DQ Influence on Expression of Antiislet Autoantibodies and Progression to Type 1 Diabetes

The journal of clinical endocrinology and metabolism, 2006-05, Vol.91 (5), p.1705-1713

2006

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Basal and Cosyntropin-Stimulated Plasma Cortisol Concentrations, as Measured by High-Performance Liquid Chromatography, in Children Aged 5 Months to Younger than 6 Years

The journal of clinical endocrinology and metabolism, 2007-06, Vol.92 (6), p.2125-2129

2007

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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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Clinical applications of a gas chromatographic method for the combined determination of testosterone and epitestosterone glucuronide in urine

A Randomized Safety and Efficacy Study of Somavaratan (VRS-317), a Long-Acting rhGH, in Pediatric Growth Hormone Deficiency

Safety Outcomes During Pediatric GH Therapy: Final Results From the Prospective GeNeSIS Observational Program

Recombinant Insulin-Like Growth Factor (IGF)-I Treatment in Short Children with Low IGF-I Levels: First-Year Results from a Randomized Clinical Trial

Nonclassic Lipoid Congenital Adrenal Hyperplasia Masquerading as Familial Glucocorticoid Deficiency

Evaluation and Treatment of Adult Growth Hormone Deficiency: An Endocrine Society Clinical Practice Guideline

Leukocyte Telomere Length in Children With Congenital Adrenal Hyperplasia

Long-Term Efficacy of T3 Analogue Triac in Children and Adults With MCT8 Deficiency: A Real-Life Retrospective Cohort Study

Prediction of Autoantibody Positivity and Progression to Type 1 Diabetes: Diabetes Autoimmunity Study in the Young (DAISY)

Children Experience Cognitive Decline Despite Reversal of Brain Atrophy One Year After Resolution of Cushing Syndrome

Diagnosis of hidden central hypothyroidism in survivors of childhood cancer

The hypoplastic inferior petrosal sinus : A potential source of false-negative results in petrosal sampling for Cushing's disease

Hypothalamic-pituitary-adrenal axis dysregulation in sexually abused girls

Absence of Increased Height Velocity in the First Year of Life in Untreated Children with Simple Virilizing Congenital Adrenal Hyperplasia

Endocrine and Immunogenetic Testing in Individuals with Type 1 Diabetes and 21-Hydroxylase Autoantibodies: Addison’s Disease in a High-Risk Population

Screening Strategies for the Identification of Multiple Antibody-Positive Relatives of Individuals with Type 1 Diabetes

Morbidity and mortality in follicular thyroid cancer

Antiislet autoantibodies usually develop sequentially rather than simultaneously

A single midnight serum cortisol measurement distinguishes Cushing's syndrome from pseudo-cushing states

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

Female pseudohermaphroditism caused by a novel homozygous missense mutation of the GR gene

DRB104 and DQ alleles : Expression of 21-hydroxylase autoantibodies and risk of progression to Addison's disease

Specific Human Leukocyte Antigen DQ Influence on Expression of Antiislet Autoantibodies and Progression to Type 1 Diabetes

Basal and Cosyntropin-Stimulated Plasma Cortisol Concentrations, as Measured by High-Performance Liquid Chromatography, in Children Aged 5 Months to Younger than 6 Years

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

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