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Novel P450c17 mutation H373D causing combined 17alpha-hydroxylase/17,20-lyase deficiency.
Relative growth hormone deficiency and cortisol excess are associated with increased cardiovascular risk markers in obese adolescent girls.
Blood pressure in pediatric patients with Cushing syndrome.
Extensive and largely reversible ischemic cerebral infarctions in a prepubertal child with hypertension and Cushing disease.
Patient guide to the prevention and management of pediatric obesity.
Extraadrenal 21-hydroxylation by CYP2C19 and CYP3A4: effect on 21-hydroxylase deficiency.
Prevention and treatment of pediatric obesity: an endocrine society clinical practice guideline based on expert opinion.
Homozygous mutation G539R in the gene for P450 oxidoreductase in a family previously diagnosed as having 17,20-lyase deficiency.
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.