1-19 of 19
Authors: SONGYA PANG
Journal Article
The Hormonal Phenotype of Nonclassic 3β-Hydroxysteroid Dehydrogenase (HSD3B) Deficiency in Hyperandrogenic Females Is Associated with Insulin-Resistant Polycystic Ovary Syndrome and Is Not a Variant of Inherited HSD3B2 Deficiency Get access
The Journal of Clinical Endocrinology & Metabolism, Volume 89, Issue 2, 1 February 2004, Pages 783–794, https://doi.org/10.1210/jc.2003-030934
Published: 01 February 2004
Journal Article
A Novel Nonstop Mutation in the Stop Codon and a Novel Missense Mutation in the Type II 3β-Hydroxysteroid Dehydrogenase (3β-HSD) Gene Causing, Respectively, Nonclassic and Classic 3β-HSD Deficiency Congenital Adrenal Hyperplasia Get access
The Journal of Clinical Endocrinology & Metabolism, Volume 87, Issue 6, 1 June 2002, Pages 2556–2563, https://doi.org/10.1210/jcem.87.6.8559
Published: 01 June 2002
Journal Article
Newly Proposed Hormonal Criteria via Genotypic Proof for Type II 3β-Hydroxysteroid Dehydrogenase Deficiency Get access
The Journal of Clinical Endocrinology & Metabolism, Volume 87, Issue 6, 1 June 2002, Pages 2611–2622, https://doi.org/10.1210/jcem.87.6.8615
Published: 01 June 2002
Journal Article
Missense Mutations Cluster within the Carboxyl-Terminal Region of DAX-1 and Impair Transcriptional Repression Get access
The Journal of Clinical Endocrinology & Metabolism, Volume 86, Issue 7, 1 July 2001, Pages 3171–3175, https://doi.org/10.1210/jcem.86.7.7660
Published: 01 July 2001
Journal Article
Characterization of Two Novel Homozygous Missense Mutations Involving Codon 6 and 259 of Type II 3β-Hydroxysteroid Dehydrogenase (3βHSD) Gene Causing, Respectively, Nonsalt-Wasting and Salt-Wasting 3βHSD Deficiency Disorder Get access
The Journal of Clinical Endocrinology & Metabolism, Volume 85, Issue 4, 1 April 2000, Pages 1678–1685, https://doi.org/10.1210/jcem.85.4.6539
Published: 01 April 2000
Journal Article
Clinical and Functional Effects of Mutations in the DAX-1 Gene in Patients with Adrenal Hypoplasia Congenita Get access
The Journal of Clinical Endocrinology & Metabolism, Volume 84, Issue 2, 1 February 1999, Pages 504–511, https://doi.org/10.1210/jcem.84.2.5468
Published: 01 February 1999
Journal Article
3α-Androstanediol Glucuronide in Virilizing Congenital Adrenal Hyperplasia: A Useful Serum Metabolic Marker of Integrated Adrenal Androgen Secretion Get access
The Journal of Clinical Endocrinology & Metabolism, Volume 73, Issue 1, 1 July 1991, Pages 166–174, https://doi.org/10.1210/jcem-73-1-166
Published: 01 July 1991
Journal Article
3α-Androstanediol Glucuronide in Premature and Normal Pubarche Get access
The Journal of Clinical Endocrinology & Metabolism, Volume 72, Issue 1, 1 January 1991, Pages 46–50, https://doi.org/10.1210/jcem-72-1-46
Published: 01 January 1991
Journal Article
Morning Salivary 17-Hydroxyprogesterone Is a Useful Screening Test for Nonclassical 21-Hydroxylase Deficiency Get access
The Journal of Clinical Endocrinology & Metabolism, Volume 65, Issue 2, 1 August 1987, Pages 227–232, https://doi.org/10.1210/jcem-65-2-227
Published: 01 August 1987
Journal Article
Adrenal Androgen Response to Metyrapone, Adrenocorticotropin, and Corticotropin-Releasing Hormone Stimulation in Children with Hypopituitarism Get access
The Journal of Clinical Endocrinology & Metabolism, Volume 65, Issue 2, 1 August 1987, Pages 282–289, https://doi.org/10.1210/jcem-65-2-282
Published: 01 August 1987
Journal Article
Genetic Defects of Steroidogenesis in Premature Pubarche Get access
The Journal of Clinical Endocrinology & Metabolism, Volume 64, Issue 3, 1 March 1987, Pages 609–617, https://doi.org/10.1210/jcem-64-3-609
Published: 01 March 1987
Journal Article
Pitfalls of Prenatal Diagnosis of 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia Get access
The Journal of Clinical Endocrinology & Metabolism, Volume 61, Issue 1, 1 July 1985, Pages 89–97, https://doi.org/10.1210/jcem-61-1-89
Published: 01 July 1985
Journal Article
Late-Onset Adrenal Steroid 3β-Hydroxysteroid Dehydrogenase Deficiency. I. A Cause of Hirsutism in Pubertal and Postpubertal Women Get access
The Journal of Clinical Endocrinology & Metabolism, Volume 60, Issue 3, 1 March 1985, Pages 428–439, https://doi.org/10.1210/jcem-60-3-428
Published: 01 March 1985
Journal Article
Antepartum Diagnosis of Goitrous Hypothyroidism by Fetal Ultrasonography and Amniotic Fluid Thyrotropin Concentration Get access
The Journal of Clinical Endocrinology & Metabolism, Volume 59, Issue 5, 1 November 1984, Pages 1016–1018, https://doi.org/10.1210/jcem-59-5-1016
Published: 01 November 1984
Journal Article
Genotyping Steroid 21-Hydroxylase Deficiency: Hormonal Reference Data Get access
The Journal of Clinical Endocrinology & Metabolism, Volume 57, Issue 2, 1 August 1983, Pages 320–326, https://doi.org/10.1210/jcem-57-2-320
Published: 01 August 1983
Journal Article
Nonsalt-Losing Congenital Adrenal Hyperplasia due to 3β-Hydroxysteroid Dehydrogenase Deficiency with Normal Glomerulosa Function Get access
The Journal of Clinical Endocrinology & Metabolism, Volume 56, Issue 4, 1 April 1983, Pages 808–818, https://doi.org/10.1210/jcem-56-4-808
Published: 01 April 1983
Journal Article
Late-Onset Steroid 21-Hydroxylase Deficiency: A Variant of Classical Congenital Adrenal Hyperplasia Get access
The Journal of Clinical Endocrinology & Metabolism, Volume 55, Issue 5, 1 November 1982, Pages 817–827, https://doi.org/10.1210/jcem-55-5-817
Published: 01 November 1982
Journal Article
A Pilot Newborn Screening for Congenital Adrenal Hyperplasia in Alaska Get access
The Journal of Clinical Endocrinology & Metabolism, Volume 55, Issue 3, 1 September 1982, Pages 413–420, https://doi.org/10.1210/jcem-55-3-413
Published: 01 September 1982
Journal Article
Genetic and Hormonal Characterization of Cryptic 21-Hydroxylase Deficiency Get access
The Journal of Clinical Endocrinology & Metabolism, Volume 53, Issue 6, 1 December 1981, Pages 1193–1197, https://doi.org/10.1210/jcem-53-6-1193
Published: 01 December 1981
