Congenital adrenal hyperplasia
El-Maouche, Diala, MD, Arlt, Wiebke, Prof, Merke, Deborah P, Dr Prof
Published in The Lancet (British edition) (11.11.2017)
Published in The Lancet (British edition) (11.11.2017)
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Journal Article
Diagnosis and Treatment of Primary Adrenal Insufficiency: An Endocrine Society Clinical Practice Guideline
Bornstein, Stefan R, Allolio, Bruno, Arlt, Wiebke, Barthel, Andreas, Don-Wauchope, Andrew, Hammer, Gary D, Husebye, Eystein S, Merke, Deborah P, Murad, M. Hassan, Stratakis, Constantine A, Torpy, David J
Published in The journal of clinical endocrinology and metabolism (01.02.2016)
Published in The journal of clinical endocrinology and metabolism (01.02.2016)
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Journal Article
Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline
Speiser, Phyllis W, Arlt, Wiebke, Auchus, Richard J, Baskin, Laurence S, Conway, Gerard S, Merke, Deborah P, Meyer-Bahlburg, Heino F L, Miller, Walter L, Murad, M Hassan, Oberfield, Sharon E, White, Perrin C
Published in The journal of clinical endocrinology and metabolism (01.11.2018)
Published in The journal of clinical endocrinology and metabolism (01.11.2018)
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Journal Article
Adrenal-derived 11-oxygenated 19-carbon steroids are the dominant androgens in classic 21-hydroxylase deficiency
Turcu, Adina F, Nanba, Aya T, Chomic, Robert, Upadhyay, Sunil K, Giordano, Thomas J, Shields, James J, Merke, Deborah P, Rainey, William E, Auchus, Richard J
Published in European journal of endocrinology (01.05.2016)
Published in European journal of endocrinology (01.05.2016)
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Journal Article
Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline
Speiser, Phyllis W, Azziz, Ricardo, Baskin, Laurence S, Ghizzoni, Lucia, Hensle, Terry W, Merke, Deborah P, Meyer-Bahlburg, Heino F. L, Miller, Walter L, Montori, Victor M, Oberfield, Sharon E, Ritzen, Martin, White, Perrin C
Published in The journal of clinical endocrinology and metabolism (01.09.2010)
Published in The journal of clinical endocrinology and metabolism (01.09.2010)
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Journal Article
Genetics of Congenital Adrenal Hyperplasia
Hannah-Shmouni, Fady, Chen, Wuyan, Merke, Deborah P
Published in Endocrinology and metabolism clinics of North America (01.06.2017)
Published in Endocrinology and metabolism clinics of North America (01.06.2017)
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Journal Article
Management of adolescents with congenital adrenal hyperplasia
Merke, Deborah P, Dr, Poppas, Dix P, Prof
Published in The lancet. Diabetes & endocrinology (01.12.2013)
Published in The lancet. Diabetes & endocrinology (01.12.2013)
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Journal Article
Modified-Release Hydrocortisone to Provide Circadian Cortisol Profiles
Debono, Miguel, Ghobadi, Cyrus, Rostami-Hodjegan, Amin, Huatan, Hiep, Campbell, Michael J, Newell-Price, John, Darzy, Ken, Merke, Deborah P, Arlt, Wiebke, Ross, Richard J
Published in The journal of clinical endocrinology and metabolism (01.05.2009)
Published in The journal of clinical endocrinology and metabolism (01.05.2009)
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Journal Article
Course of COVID-19 infection in patients with congenital adrenal hyperplasia
Javaid, Rida, Sinaii, Ninet, Kollender, Sarah, Desai, Jay, Moon, Amy, Merke, Deborah P
Published in Frontiers in endocrinology (Lausanne) (09.02.2024)
Published in Frontiers in endocrinology (Lausanne) (09.02.2024)
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Journal Article
Evidence of the Role of Inflammation and the Hormonal Environment in the Pathogenesis of Adrenal Myelolipomas in Congenital Adrenal Hyperplasia
Kolli, Vipula, Frucci, Emily, da Cunha, Isabela Werneck, Iben, James R, Kim, Sun A, Mallappa, Ashwini, Li, Tianwei, Faucz, Fabio Rueda, Kebebew, Electron, Nilubol, Naris, Quezado, Martha M, Merke, Deborah P
Published in International journal of molecular sciences (22.02.2024)
Published in International journal of molecular sciences (22.02.2024)
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Journal Article
Morphologic and Molecular Characterization of Adrenals and Adrenal Rest Affected by Congenital Adrenal Hyperplasia
Kolli, Vipula, da Cunha, Isabela Werneck, Kim, SunA, Iben, James R, Mallappa, Ashwini, Li, Tianwei, Gaynor, Alison, Coon, Steven L, Quezado, Martha M, Merke, Deborah P
Published in Frontiers in endocrinology (Lausanne) (20.09.2021)
Published in Frontiers in endocrinology (Lausanne) (20.09.2021)
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Journal Article
11-Oxygenated Androgens Useful in the Setting of Discrepant Conventional Biomarkers in 21-Hydroxylase Deficiency
Jha, Smita, Turcu, Adina F, Sinaii, Ninet, Brookner, Brittany, Auchus, Richard J, Merke, Deborah P
Published in Journal of the Endocrine Society (01.02.2021)
Published in Journal of the Endocrine Society (01.02.2021)
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Journal Article
Pseudogene TNXA Variants May Interfere with the Genetic Testing of CAH-X
Lao, Qizong, Zhou, Kiet, Parker, Megan, Faucz, Fabio R, Merke, Deborah P
Published in Genes (19.01.2023)
Published in Genes (19.01.2023)
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Journal Article
24-Hour Profiles of 11-Oxygenated C19 Steroids and Δ5-Steroid Sulfates during Oral and Continuous Subcutaneous Glucocorticoids in 21-Hydroxylase Deficiency
Turcu, Adina F., Mallappa, Ashwini, Nella, Aikaterini A., Chen, Xuan, Zhao, Lili, Nanba, Aya T., Byrd, James Brian, Auchus, Richard J., Merke, Deborah P.
Published in Frontiers in endocrinology (Lausanne) (16.11.2021)
Published in Frontiers in endocrinology (Lausanne) (16.11.2021)
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Journal Article
A pharmacokinetic and pharmacodynamic study of delayed- and extended-release hydrocortisone (ChronocortTM) vs. conventional hydrocortisone (CortefTM) in the treatment of congenital adrenal hyperplasia
Verma, Somya, VanRyzin, Carol, Sinaii, Ninet, Kim, Mimi S., Nieman, Lynnette K., Ravindran, Shayna, Calis, Karim A., Arlt, Wiebke, Ross, Richard J., Merke, Deborah P.
Published in Clinical endocrinology (Oxford) (01.04.2010)
Published in Clinical endocrinology (Oxford) (01.04.2010)
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Journal Article
Congenital adrenal hyperplasia due to two rare CYP21A2 variant alleles, including a novel attenuated CYP21A1P/CYP21A2 chimera
Lao, Qizong, Burkardt, Deepika D., Kollender, Sarah, Faucz, Fabio R., Merke, Deborah P.
Published in Molecular genetics & genomic medicine (01.07.2023)
Published in Molecular genetics & genomic medicine (01.07.2023)
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Journal Article
Measurement of serum tenascin-X in patients with congenital adrenal hyperplasia at risk for Ehlers-Danlos contiguous gene deletion syndrome CAH-X
Kolli, Vipula, Kim, Hannah, Rao, Hamsini, Lao, Qizong, Gaynor, Alison, Milner, Joshua D, Merke, Deborah P
Published in BMC research notes (30.10.2019)
Published in BMC research notes (30.10.2019)
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