Silvia Parajes
Birmingham, ENG B152TT, United Kingdom
Last Updated: 09/26/2026
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Found 9 publications
5α-Reductase Type 2 Regulates Glucocorticoid Action and Metabolic Phenotype in Human Hepatocytes.
Journal: Endocrinology
Published: May 15, 2015
Low estriol levels in the maternal marker screen as a predictor of X-linked adrenal hypoplasia congenita: case report.
Journal: Srpski arhiv za celokupno lekarstvo
Published: March 04, 2015
Influence of 17-Hydroxyprogesterone, Progesterone and Sex Steroids on Mineralocorticoid Receptor Transactivation in Congenital Adrenal Hyperplasia.
Journal: Hormone research in paediatrics
Published: October 15, 2014
Characterization of the molecular genetic pathology in patients with 11β-hydroxylase deficiency.
Journal: Clinical endocrinology
Published: October 14, 2014
A diagnosis not to be missed: nonclassic steroid 11β-hydroxylase deficiency presenting with premature adrenarche and hirsutism.
Journal: The Journal of clinical endocrinology and metabolism
Published: August 14, 2013
Genotype-phenotype correlation in 153 adult patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: analysis of the United Kingdom Congenital adrenal Hyperplasia Adult Study Executive (CaHASE) cohort.
Journal: The Journal of clinical endocrinology and metabolism
Published: January 23, 2013
Delayed diagnosis of adrenal insufficiency in a patient with severe penoscrotal hypospadias due to two novel P450 side-change cleavage enzyme (CYP11A1) mutations (p.R360W; p.R405X).
Journal: European journal of endocrinology
Published: September 13, 2012
Showing 1-9 of 9
Last Updated: 09/26/2026