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The common P450 oxidoreductase variant A503V is not a modifier gene for 21-hydroxylase deficiency.
Insulinoma and gastrinoma syndromes from a single intrapancreatic neuroendocrine tumor.
Severe combined adrenal and gonadal deficiency caused by novel mutations in the cholesterol side chain cleavage enzyme, P450scc.
Vitamin D 1alpha-hydroxylase gene mutations in patients with 1alpha-hydroxylase deficiency.
Apparent manifesting heterozygosity in P450 oxidoreductase deficiency and its effect on coexisting 21-hydroxylase deficiency.
Nonclassic congenital lipoid adrenal hyperplasia: a new disorder of the steroidogenic acute regulatory protein with very late presentation and normal male genitalia.
Dietary phosphorus regulates serum fibroblast growth factor-23 concentrations in healthy men.
Elevated peptide YY levels in adolescent girls with anorexia nervosa.
A genetic isolate of congenital lipoid adrenal hyperplasia with atypical clinical findings.