Serum Steroid Profile Captures Metabolic Phenotypes in Adults with Classic Congenital Adrenal Hyperplasia

[1]  A. Mallappa,et al.  Management challenges and therapeutic advances in congenital adrenal hyperplasia , 2022, Nature Reviews Endocrinology.

[2]  Mariska A M Schröder,et al.  Novel treatments for congenital adrenal hyperplasia , 2022, Reviews in Endocrine and Metabolic Disorders.

[3]  Young Ah Lee,et al.  Epidemiology and Long-Term Adverse Outcomes in Korean Patients with Congenital Adrenal Hyperplasia: A Nationwide Study , 2022, Endocrinology and metabolism.

[4]  Chang Ho Ahn,et al.  Long-Term Health Outcomes of Korean Adults With Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency , 2021, Frontiers in Endocrinology.

[5]  B. Keevil,et al.  11-oxygenated androgens and their relation to hypothalamus-pituitary-gonadal-axis disturbances in adults with congenital adrenal hyperplasia , 2021, The Journal of Steroid Biochemistry and Molecular Biology.

[6]  P. White,et al.  Congenital adrenal hyperplasia - current insights in pathophysiology, diagnostics and management. , 2021, Endocrine reviews.

[7]  Jay R. Desai,et al.  Cardiovascular Disease Risk Factors and Metabolic Morbidity in a Longitudinal Study of Congenital Adrenal Hyperplasia. , 2021, The Journal of clinical endocrinology and metabolism.

[8]  2. Classification and Diagnosis of Diabetes: Standards of Medical Care in Diabetes-2021. , 2020, Diabetes care.

[9]  J. H. Kim,et al.  Selective LC-MRM/SIM-MS based profiling of adrenal steroids reveals metabolic signatures of 17α-hydroxylase deficiency , 2020, The Journal of Steroid Biochemistry and Molecular Biology.

[10]  M. Bidlingmaier,et al.  Effect of androgen excess and glucocorticoid exposure on metabolic risk profiles in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency , 2019, The Journal of Steroid Biochemistry and Molecular Biology.

[11]  W. Miller.  Congenital Adrenal Hyperplasia: Time to Replace 17OHP with 21-Deoxycortisol , 2019, Hormone Research in Paediatrics.

[12]  P. Span,et al.  Glucocorticoid activity of adrenal steroid precursors in untreated patients with congenital adrenal hyperplasia. , 2019, The Journal of clinical endocrinology and metabolism.

[13]  J. Kang,et al.  2018 Korean Society for the Study of Obesity Guideline for the Management of Obesity in Korea , 2019, Journal of obesity & metabolic syndrome.

[14]  M. Murad,et al.  Cardiovascular and Metabolic Outcomes in Congenital Adrenal Hyperplasia: A Systematic Review and Meta-Analysis , 2018, The Journal of clinical endocrinology and metabolism.

[15]  M. Murad,et al.  Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline. , 2018, The Journal of clinical endocrinology and metabolism.

[16]  W. Arlt,et al.  MECHANISMS IN ENDOCRINOLOGY: The sexually dimorphic role of androgens in human metabolic disease , 2017, European journal of endocrinology.

[17]  A. Tsodikov,et al.  11-Oxygenated Androgens Are Biomarkers of Adrenal Volume and Testicular Adrenal Rest Tumors in 21-Hydroxylase Deficiency , 2017, The Journal of clinical endocrinology and metabolism.

[18]  T. Giordano,et al.  Adrenal-derived 11-oxygenated 19-carbon steroids are the dominant androgens in classic 21-hydroxylase deficiency. , 2016, European journal of endocrinology.

[19]  M. Polak,et al.  Determining clinical and biological indicators for health outcomes in adult patients with childhood onset of congenital adrenal hyperplasia. , 2015, European journal of endocrinology.

[20]  P. Span,et al.  Adrenal Steroid Metabolites Accumulating in Congenital Adrenal Hyperplasia Lead to Transactivation of the Glucocorticoid Receptor. , 2015, Endocrinology.

[21]  H. Falhammar,et al.  Increased Cardiovascular and Metabolic Morbidity in Patients With 21-Hydroxylase Deficiency: A Swedish Population-Based National Cohort Study. , 2015, The Journal of clinical endocrinology and metabolism.

[22]  Sheree M. Schrager,et al.  Increased Abdominal Adiposity in Adolescents and Young Adults With Classical Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency. , 2015, The Journal of clinical endocrinology and metabolism.

[23]  Jacques Young,et al.  Clinical Outcome, Hormonal Status, Gonadotrope Axis, and Testicular Function in 219 Adult Men Born With Classic 21-Hydroxylase Deficiency. A French National Survey. , 2015, The Journal of clinical endocrinology and metabolism.

[24]  B. Walker,et al.  Treatment and health outcomes in adults with congenital adrenal hyperplasia , 2014, Nature Reviews Endocrinology.

[25]  Yasuhiro Nakamura,et al.  Liquid chromatography-tandem mass spectrometry analysis of human adrenal vein 19-carbon steroids before and after ACTH stimulation. , 2013, The Journal of clinical endocrinology and metabolism.

[26]  M. Nishitani,et al.  Clinical characteristics of a cohort of 244 patients with congenital adrenal hyperplasia. , 2012, The Journal of clinical endocrinology and metabolism.

[27]  J. Connell,et al.  Health Status of Adults with Congenital Adrenal Hyperplasia: A Cohort Study of 203 Patients , 2010, The Journal of clinical endocrinology and metabolism.

[28]  A. Dauber,et al.  Monitoring of therapy in congenital adrenal hyperplasia. , 2010, Clinical chemistry.

[29]  R. Norman,et al.  Assessment of cardiovascular risk and prevention of cardiovascular disease in women with the polycystic ovary syndrome: a consensus statement by the Androgen Excess and Polycystic Ovary Syndrome (AE-PCOS) Society. , 2010, The Journal of clinical endocrinology and metabolism.

[30]  D. Merke.  Approach to the adult with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. , 2008, The Journal of clinical endocrinology and metabolism.

[31]  R. Krauss,et al.  Diagnosis and Management of the Metabolic Syndrome: An American Heart Association/National Heart, Lung, and Blood Institute Scientific Statement , 2005, Current opinion in cardiology.

[32]  Paul Zimmet,et al.  The metabolic syndrome—a new worldwide definition , 2005, The Lancet.

[33]  J. Popović,et al.  Congenital adrenal hyperplasia due to 21-hydroxylase deficiency. , 2005, Journal for specialists in pediatric nursing : JSPN.

[34]  A. Häkkinen,et al.  Body fat distribution and cortisol metabolism in healthy men: enhanced 5beta-reductase and lower cortisol/cortisone metabolite ratios in men with fatty liver. , 2003, The Journal of clinical endocrinology and metabolism.

[35]  A. Boulton,et al.  Cortisol metabolism in human obesity: impaired cortisone-->cortisol conversion in subjects with central adiposity. , 1999, The Journal of clinical endocrinology and metabolism.

[36]  Jackson T. Wright,et al.  Evidence-Based Guideline for the Management of High Blood Pressure in Adults , 2012 .