Adrenal incidentaloma and patients with homozygous or heterozygous congenital adrenal hyperplasia.

Genotyping steroid 21-hydroxylase deficiency: hormonal reference data

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Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society* Clinical Practice Guideline

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The clinically inapparent adrenal mass: update in diagnosis and management

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Prevalence and natural history of adrenal incidentalomas

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Congenital adrenal hyperplasia.

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Congenital Adrenal Hyperplasia—Current Insights in Pathophysiology, Diagnostics, and Management

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Approach to the patient with an adrenal incidentaloma

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Increased mortality in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

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An update of congenital adrenal hyperplasia

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Adrenal Steroidogenesis and Congenital Adrenal Hyperplasia

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The molecular pathogenesis of hereditary and sporadic adrenocortical and adrenomedullary tumors

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Molecular genetics of adrenocortical tumours, from familial to sporadic diseases

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MANAGEMENT OF ENDOCRINE DISEASE: diagnosis and management of the patient with non-classic CAH due to 21-hydroxylase deficiency

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Future Directions in the Study and Management of Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

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Clinical guidelines for the management of adrenal incidentaloma

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INCIDENTALOMAS

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Nonclassic congenital adrenal hyperplasia due to 21-hydroxylase deficiency: clinical presentation, diagnosis, treatment, and outcome

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Clonal analysis of human adrenocortical carcinomas and secreting adenomas

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Study of glucose tolerance in consecutive patients harbouring incidental adrenal tumours

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11-Oxygenated Androgens are Biomarkers of Adrenal Volume and Testicular Adrenal Rest Tumors in 21-Hydroxylase Deficiency

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High frequency of adrenal myelolipomas and testicular adrenal rest tumours in adult Norwegian patients with classical congenital adrenal hyperplasia because of 21-hydroxylase deficiency: <i>Adrenal tumours and TART in 21-OHD</i>

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Management of endocrine disease: differential diagnosis, investigation and therapy of bilateral adrenal incidentalomas

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Total Adrenal Volume But Not Testicular Adrenal Rest Tumor Volume Is Associated with Hormonal Control in Patients with 21-Hydroxylase Deficiency

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MANAGEMENT APPROACHES TO ADRENAL INCIDENTALOMAS

Mantero, F., & Arnaldi, G. (2000) · Endocrinology and Metabolism Clinics of North America · doi:10.1016/s0889-8529(05)70119-5 · Cited by 83 · see citing works

Phenotypic profiling of parents with cryptic nonclassic congenital adrenal hyperplasia: findings in 145 unrelated families

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Mortality in patients with congenital adrenal hyperplasia: a cohort study

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Prevalence and Characteristics of Adrenal Tumors and Myelolipomas in Congenital Adrenal Hyperplasia: A Systematic Review and Meta-Analysis

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Evaluation of hormonal function in a series of incidentally discovered adrenal masses.

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Congenital adrenal hyperplasia due to 21-hydroxylase deficiency presenting as adrenal incidentaloma: a systematic review and meta-analysis

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Steroid 21 hydroxylase deficiency congenital adrenal hyperplasia

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The natural history of incidentally discovered adrenocortical adenomas: a retrospective evaluation.

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Non-classic congenital adrenal hyperplasia

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Increased 17<i>a</i>‐hydroxyprogesterone response to ACTH in silent adrenal adenoma: cause or effect?

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Lesions of the adrenal cortex

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The role of 21-hydroxylase in the pathogenesis of adrenal masses: review of the literature and focus on our own experience

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Adrenal morphology and associated comorbidities in congenital adrenal hyperplasia

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