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See Latest ArticlesClinically guided genetic screening in a large cohort of Italian patients with pheochromocytomas and/or functional or non-functional paragangliomas
Journal of Clinical Endocrinology and Metabolism, 02/19/09
Mannelli M et al. - The frequency of the hereditary forms of pheochromocytoma/paraganglioma varies depending on the family history and the clinical presentation. A positive family history and an accurate clinical evaluation of patients are strong indicators of which genes should be screened first.
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Epidemiology of adrenal crisis in chronic adrenal insufficiency – the need for new prevention strategies
European Journal of Endocrinology, 12/15/09
miR-195 and miR-483-5p Identified as Predictors of Poor Prognosis in Adrenocortical Cancer
Clinical Cancer Research, 12/15/09
Diagnosis, management and therapeutic outcome in prepubertal Cushing’s disease
European Journal of Endocrinology, 12/15/09
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