Found: 29
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Taxoid side-chain structure determination by electrospray ionization tandem mass spectrometry.
- Published in:
- Rapid Communications in Mass Spectrometry: RCM, 1993, v. 7, n. 10, p. 891, doi. 10.1002/rcm.1290071007
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- Publication type:
- Article
Steroid Sulfatase Deficiency and Androgen Activation Before and After Puberty.
- Published in:
- 2016
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- Publication type:
- journal article
Evidence for Increased 5α-Reductase Activity During Early Childhood in Daughters of Women With Polycystic Ovary Syndrome.
- Published in:
- 2016
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- Publication type:
- journal article
Diminished 11β-hydroxysteroid dehydrogenase type 2 activity is associated with decreased weight and weight gain across the first year of life.
- Published in:
- 2014
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- Publication type:
- journal article
Prenatal diagnosis of congenital adrenal hyperplasia caused by P450 oxidoreductase deficiency.
- Published in:
- 2013
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- Publication type:
- journal article
A missense mutation in the human cytochrome b5 gene causes 46,XY disorder of sex development due to true isolated 17,20 lyase deficiency.
- Published in:
- 2012
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- Publication type:
- journal article
Urine steroid metabolomics as a biomarker tool for detecting malignancy in adrenal tumors.
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- 2011
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- Publication type:
- journal article
Pubertal presentation in seven patients with congenital adrenal hyperplasia due to P450 oxidoreductase deficiency.
- Published in:
- 2011
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- Publication type:
- journal article
Dehydro-oestriol and dehydropregnanetriol are candidate analytes for prenatal diagnosis of Smith-Lemli-Opitz syndrome.
- Published in:
- 2001
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- Publication type:
- journal article
Steroid sulphatase deficiency is the major cause of extremely low oestriol production at mid-pregnancy: a urinary steroid assay for the discrimination of steroid sulphatase deficiency from other causes.
- Published in:
- Prenatal Diagnosis, 1998, v. 18, n. 8, p. 789, doi. 10.1002/(SICI)1097-0223(199808)18:8<789::AID-PD345>3.0.CO;2-9
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- Publication type:
- Article
Concomitant mutations in the P450 oxidoreductase and androgen receptor genes presenting with 46,XY disordered sex development and androgenization at adrenarche.
- Published in:
- 2010
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- Publication type:
- journal article
Steroid biomarkers and genetic studies reveal inactivating mutations in hexose-6-phosphate dehydrogenase in patients with cortisone reductase deficiency.
- Published in:
- 2008
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- Publication type:
- journal article
Low-Dose Growth Hormone Inhibits 11β-Hydroxysteroid Dehydrogenase Type 1 but Has No Effect upon Fat Mass in Patients with Simple Obesity.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2003, v. 88, n. 5, p. 2113, doi. 10.1210/jc.2002-021894
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- Publication type:
- Article
5α-Reductase and 11β-Hydroxysteroid Dehydrogenase Activity in Prepubertal Hispanic Girls with Premature Adrenarche.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 10, p. 4647, doi. 10.1210/jc.2001-012045
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- Publication type:
- Article
The Diagnosis of Congenital Adrenal Hyperplasia in the Newborn by Gas Chromatography/Mass Spectrometry Analysis of Random Urine Specimens.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 8, p. 3682, doi. 10.1210/jcem.87.8.8712
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- Publication type:
- Article
Cortisol Metabolism in Human Obesity: Impaired Cortisone3Cortisol Conversion in Subjects with Central Adiposity.
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- Journal of Clinical Endocrinology & Metabolism, 1999, v. 84, n. 3, p. 1022, doi. 10.1210/jcem.84.3.5538
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- Publication type:
- Article
Equine Type Estrogens Produced by a Pregnant Woman Carrying a Smith-Lemli-Opitz Syndrome Fetus.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 1999, v. 84, n. 3, p. 1157, doi. 10.1210/jcem.84.3.5660
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- Publication type:
- Article
The Identification of 5α-Reductase-2 and 17β Hydroxysteroid Dehydrogenase-3 Gene Defects in Male Pseudohermaphrodites from a Turkish Kindred.
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- Journal of Clinical Endocrinology & Metabolism, 1998, v. 83, n. 2, p. 560, doi. 10.1210/jc.83.2.560
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- Publication type:
- Article
Apparent Cortisone Reductase Deficiency: A Unique Form of Hypercortisolism.
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- Journal of Clinical Endocrinology & Metabolism, 1996, v. 81, n. 11, p. 3855, doi. 10.1210/jcem.81.11.8923828
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- Publication type:
- Article
Metabolism of 5αDihydroprogesterone in Women and Men: 3β- and 3α-,6α-Dihydroxy-5α-Pregnan-2O-Ones Are Major Urinary Metabolites.
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- Journal of Clinical Endocrinology & Metabolism, 1996, v. 81, n. 10, p. 3644, doi. 10.1210/jc.81.10.3644
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- Publication type:
- Article
Urinary free cortisone and the assessment of 11β-hydroxysteroid dehydrogenase activity in man.
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- Clinical Endocrinology, 1996, v. 45, n. 5, p. 605, doi. 10.1046/j.1365-2265.1996.00853.x
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- Publication type:
- Article
Deficient inactivation of cortisol by 11β-hydroxysteroid dehydrogenase in essential hypertension.
- Published in:
- Clinical Endocrinology, 1993, v. 39, n. 2, p. 221, doi. 10.1111/j.1365-2265.1993.tb01778.x
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- Publication type:
- Article
The broad phenotypic spectrum of 17α-hydroxylase/17,20-lyase (CYP17A1) deficiency: a case series.
- Published in:
- European Journal of Endocrinology, 2021, v. 185, n. 5, p. 729, doi. 10.1530/EJE-21-0152
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- Publication type:
- Article
Failure of Steroid Sulfatase to Desulfate Vitamin D<sub>3</sub> Sulfate.
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- Journal of Investigative Dermatology, 1983, v. 80, n. 6, p. 514, doi. 10.1111/1523-1747.ep12535105
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- Publication type:
- Article
Steroid Metabolome Analysis in Disorders of Adrenal Steroid Biosynthesis and Metabolism.
- Published in:
- Endocrine Reviews, 2019, v. 40, n. 6, p. 1605, doi. 10.1210/er.2018-00262
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- Article
Prevalence of steroid sulfatase deficiency in California according to race and ethnicity.
- Published in:
- Prenatal Diagnosis, 2010, v. 30, n. 9, p. 893, doi. 10.1002/pd.2588
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- Publication type:
- Article
Maternal urine and serum steroid measurements to identify steroid sulfatase deficiency (STSD) in second trimester pregnancies.
- Published in:
- Prenatal Diagnosis, 2009, v. 29, n. 8, p. 771, doi. 10.1002/pd.2284
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- Publication type:
- Article
Identifying Smith-Lemli-Opitz syndrome in conjunction with prenatal screening for Down syndrome.
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- Prenatal Diagnosis, 2006, v. 26, n. 9, p. 842, doi. 10.1002/pd.1518
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- Publication type:
- Article
Increased central adiposity and decreased subcutaneous adipose tissue 11β‐hydroxysteroid dehydrogenase type 1 are associated with deterioration in glucose tolerance—A longitudinal cohort study.
- Published in:
- Clinical Endocrinology, 2019, v. 91, n. 1, p. 72, doi. 10.1111/cen.13939
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- Publication type:
- Article