1-12 of 12
Authors: Carlos E Fardella
Journal Article
Progressive 11β-Hydroxysteroid Dehydrogenase Type 2 Insufficiency as Kidney Function Declines Get access
The Journal of Clinical Endocrinology & Metabolism, Volume 110, Issue 4, April 2025, Pages 1037–1043, https://doi.org/10.1210/clinem/dgae663
Published: 23 September 2024
Journal Article
Classic and Nonclassic Apparent Mineralocorticoid Excess Syndrome Free
The Journal of Clinical Endocrinology & Metabolism, Volume 105, Issue 4, April 2020, Pages e924–e936, https://doi.org/10.1210/clinem/dgz315
Published: 31 December 2019
Journal Article
Clinical, Biochemical, and Genetic Characteristics of “Nonclassic” Apparent Mineralocorticoid Excess Syndrome Free
The Journal of Clinical Endocrinology & Metabolism, Volume 104, Issue 2, February 2019, Pages 595–603, https://doi.org/10.1210/jc.2018-01197
Published: 14 September 2018
Journal Article
A Novel Adrenocorticotropin Receptor Mutation Alters Its Structure and Function, Causing Familial Glucocorticoid Deficiency Get access
The Journal of Clinical Endocrinology & Metabolism, Volume 93, Issue 8, 1 August 2008, Pages 3097–3105, https://doi.org/10.1210/jc.2008-0048
Published: 01 August 2008
Journal Article
Novel Intronic Mutation of MEN1 Gene Causing Familial Isolated Primary Hyperparathyroidism Get access
The Journal of Clinical Endocrinology & Metabolism, Volume 89, Issue 8, 1 August 2004, Pages 4124–4129, https://doi.org/10.1210/jc.2003-032101
Published: 01 August 2004
Journal Article
Increased Diagnosis of Primary Aldosteronism, Including Surgically Correctable Forms, in Centers from Five Continents Get access
The Journal of Clinical Endocrinology & Metabolism, Volume 89, Issue 3, 1 March 2004, Pages 1045–1050, https://doi.org/10.1210/jc.2003-031337
Published: 01 March 2004
Journal Article
Congenital Lipoid Adrenal Hyperplasia Caused by a Novel Splicing Mutation in the Gene for the Steroidogenic Acute Regulatory Protein Get access
The Journal of Clinical Endocrinology & Metabolism, Volume 89, Issue 2, 1 February 2004, Pages 946–951, https://doi.org/10.1210/jc.2003-030345
Published: 01 February 2004
Journal Article
Two Homozygous Mutations in the 11β-Hydroxysteroid Dehydrogenase Type 2 Gene in a Case of Apparent Mineralocorticoid Excess Get access
The Journal of Clinical Endocrinology & Metabolism, Volume 88, Issue 6, 1 June 2003, Pages 2501–2507, https://doi.org/10.1210/jc.2002-021909
Published: 01 June 2003
Journal Article
Genetic Study of Patients with Dexamethasone-Suppressible Aldosteronism without the Chimeric CYP11B1/CYP11B2 Gene Get access
The Journal of Clinical Endocrinology & Metabolism, Volume 86, Issue 10, 1 October 2001, Pages 4805–4807, https://doi.org/10.1210/jcem.86.10.7920
Published: 01 October 2001
Journal Article
Authors’ Response: Prevalence of Primary Aldosteronism in Unselected Hypertensive Populations—Screening and Definitive Diagnosis Get access
The Journal of Clinical Endocrinology & Metabolism, Volume 86, Issue 8, 1 August 2001, Pages 4003–4004, https://doi.org/10.1210/jcem.86.8.9994
Published: 01 August 2001
Journal Article
Primary Hyperaldosteronism in Essential Hypertensives: Prevalence, Biochemical Profile, and Molecular Biology Get access
The Journal of Clinical Endocrinology & Metabolism, Volume 85, Issue 5, 1 May 2000, Pages 1863–1867, https://doi.org/10.1210/jcem.85.5.6596
Published: 01 May 2000
Journal Article
Salt-Wasting Congenital Adrenal Hyperplasia: Detection of Mutations in CYP21B Gene in a Chilean Population Get access
The Journal of Clinical Endocrinology & Metabolism, Volume 83, Issue 9, 1 September 1998, Pages 3357–3360, https://doi.org/10.1210/jcem.83.9.5071
Published: 01 September 1998
