Associated Papers
The clinical characteristics and pathogenic variants of primary pigmented nodular adrenocortical disease in 210 patients: a systematic review.
Sun J et al.
Frontiers in Endocrinology, 2024
Familial Forms of Cushing Syndrome in Primary Pigmented Nodular Adrenocortical Disease Presenting with Short Stature and Insidious Symptoms: A Clinical Series.
Navarro Moreno C et al.
Hormone Research in Paediatrics, 2018
A novel PRKAR1A gene mutation associated with primary pigmented nodular adrenocortical disease.
Ran H et al.
The American Journal of the Medical Sciences, 2014
[A pedigree study of a patient with primary pigmented nodular adrenocortical disease and familial gene mutation].
Ran H et al.
Zhonghua Nei Ke Za Zhi, 2014
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