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Authors: WALTER L. MILLER
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Journal Article
Disordered Electron Transfer: New Forms of Defective Steroidogenesis and Mitochondriopathy Open Access
Walter L Miller and others
The Journal of Clinical Endocrinology & Metabolism, Volume 110, Issue 3, March 2025, Pages e574–e582, https://doi.org/10.1210/clinem/dgae815
Published: 22 November 2024
Journal Article
Response to Letter to the Editor: “Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline” Free
Phyllis W Speiser and others
The Journal of Clinical Endocrinology & Metabolism, Volume 104, Issue 6, June 2019, Page 1928, https://doi.org/10.1210/jc.2018-02629
Published: 17 December 2018
Journal Article
Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline Free
Phyllis W Speiser and others
The Journal of Clinical Endocrinology & Metabolism, Volume 103, Issue 11, November 2018, Pages 4043–4088, https://doi.org/10.1210/jc.2018-01865
Published: 27 September 2018
Journal Article
In Memoriam: Melvin M. Grumbach (1925–2016) Free
Walter L. Miller
The Journal of Clinical Endocrinology & Metabolism, Volume 101, Issue 12, 1 December 2016, Pages 4497–4499, https://doi.org/10.1210/jc.2016-3492
Published: 06 December 2016
Journal Article
Quantitation of CYP24A1 Enzymatic Activity With a Simple Two-Hybrid System
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Amy Mugg and others
The Journal of Clinical Endocrinology & Metabolism, Volume 100, Issue 2, 1 February 2015, Pages 684–688, https://doi.org/10.1210/jc.2014-3365
Published: 01 February 2015
Journal Article
Cortisol Response to Operative Stress With Anesthesia in Healthy Children
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Lisa K. Taylor and others
The Journal of Clinical Endocrinology & Metabolism, Volume 98, Issue 9, 1 September 2013, Pages 3687–3693, https://doi.org/10.1210/jc.2013-2148
Published: 01 September 2013
Journal Article
Varied Clinical Presentations of Seven Patients With Mutations in CYP11A1 Encoding the Cholesterol Side-Chain Cleavage Enzyme, P450scc
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Meng Kian Tee and others
The Journal of Clinical Endocrinology & Metabolism, Volume 98, Issue 2, 1 February 2013, Pages 713–720, https://doi.org/10.1210/jc.2012-2828
Published: 01 February 2013
Journal Article
Congenital Adrenal Hyperplasia—More Dogma Bites the Dust
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Richard J. Auchus and Walter L. Miller
The Journal of Clinical Endocrinology & Metabolism, Volume 97, Issue 3, 1 March 2012, Pages 772–775, https://doi.org/10.1210/jc.2012-1080
Published: 01 March 2012
Journal Article
The Syndrome of 17,20 Lyase Deficiency
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Walter L. Miller
The Journal of Clinical Endocrinology & Metabolism, Volume 97, Issue 1, 1 January 2012, Pages 59–67, https://doi.org/10.1210/jc.2011-2161
Published: 01 January 2012
Journal Article
Partial Defect in the Cholesterol Side-Chain Cleavage Enzyme P450scc (CYP11A1) Resembling Nonclassic Congenital Lipoid Adrenal Hyperplasia
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Taninee Sahakitrungruang and others
The Journal of Clinical Endocrinology & Metabolism, Volume 96, Issue 3, 1 March 2011, Pages 792–798, https://doi.org/10.1210/jc.2010-1828
Published: 01 March 2011
Journal Article
Clinical, Biochemical, and Molecular Characterization of Macronodular Adrenocortical Hyperplasia of the Zona Reticularis: A New Syndrome
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Hans K. Ghayee and others
The Journal of Clinical Endocrinology & Metabolism, Volume 96, Issue 2, 1 February 2011, Pages E243–E250, https://doi.org/10.1210/jc.2010-1222
Published: 01 February 2011
Journal Article
Naturally-Occurring Mutation in the Calcium-Sensing Receptor Reveals the Significance of Extracellular Domain Loop III Region for Class C G-Protein-Coupled Receptor Function
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Qing Dong and others
The Journal of Clinical Endocrinology & Metabolism, Volume 95, Issue 10, 1 October 2010, Pages E245–E252, https://doi.org/10.1210/jc.2010-0559
Published: 01 October 2010
Includes: Multimedia
Journal Article
Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline Open Access
Phyllis W. Speiser and others
The Journal of Clinical Endocrinology & Metabolism, Volume 95, Issue 9, 1 September 2010, Pages 4133–4160, https://doi.org/10.1210/jc.2009-2631
Published: 01 September 2010
Journal Article
Clinical, Genetic, and Functional Characterization of Four Patients Carrying Partial Loss-of-Function Mutations in the Steroidogenic Acute Regulatory Protein (StAR)
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Taninee Sahakitrungruang and others
The Journal of Clinical Endocrinology & Metabolism, Volume 95, Issue 7, 1 July 2010, Pages 3352–3359, https://doi.org/10.1210/jc.2010-0437
Published: 01 July 2010
Journal Article
Clinical, Genetic, and Enzymatic Characterization of P450 Oxidoreductase Deficiency in Four Patients
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Taninee Sahakitrungruang and others
The Journal of Clinical Endocrinology & Metabolism, Volume 94, Issue 12, 1 December 2009, Pages 4992–5000, https://doi.org/10.1210/jc.2009-1460
Published: 01 December 2009
Journal Article
Novel P450c17 Mutation H373D Causing Combined 17α-Hydroxylase/17,20-Lyase Deficiency
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Taninee Sahakitrungruang and others
The Journal of Clinical Endocrinology & Metabolism, Volume 94, Issue 8, 1 August 2009, Pages 3089–3092, https://doi.org/10.1210/jc.2009-0645
Published: 01 August 2009
Journal Article
Extraadrenal 21-Hydroxylation by CYP2C19 and CYP3A4: Effect on 21-Hydroxylase Deficiency
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Larissa G. Gomes and others
The Journal of Clinical Endocrinology & Metabolism, Volume 94, Issue 1, 1 January 2009, Pages 89–95, https://doi.org/10.1210/jc.2008-1174
Published: 01 January 2009
Journal Article
Homozygous Mutation G539R in the Gene for P450 Oxidoreductase in a Family Previously Diagnosed as Having 17,20-Lyase Deficiency
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Eli Hershkovitz and others
The Journal of Clinical Endocrinology & Metabolism, Volume 93, Issue 9, 1 September 2008, Pages 3584–3588, https://doi.org/10.1210/jc.2008-0051
Published: 01 September 2008
Journal Article
The Common P450 Oxidoreductase Variant A503V Is Not a Modifier Gene for 21-Hydroxylase Deficiency
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Larissa G. Gomes and others
The Journal of Clinical Endocrinology & Metabolism, Volume 93, Issue 7, 1 July 2008, Pages 2913–2916, https://doi.org/10.1210/jc.2008-0304
Published: 01 July 2008
Journal Article
Severe Combined Adrenal and Gonadal Deficiency Caused by Novel Mutations in the Cholesterol Side Chain Cleavage Enzyme, P450scc
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Chan Jong Kim and others
The Journal of Clinical Endocrinology & Metabolism, Volume 93, Issue 3, 1 March 2008, Pages 696–702, https://doi.org/10.1210/jc.2007-2330
Published: 01 March 2008
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