De P. Mariani
Sao Paulo, SP 05403000, Brazil
Last Updated: 09/26/2026
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Found 9 publications
Integrated Clinical-Genetic-Pathological Analysis Expands the Phenotypic and Molecular Spectrum of PPNAD Across Carney Complex and Isolated Forms.
Journal: European journal of endocrinology
Published: April 15, 2026
Low Protein Expression of both ATRX and ZNRF3 as Novel Negative Prognostic Markers of Adult Adrenocortical Carcinoma.
Journal: International journal of molecular sciences
Published: November 24, 2020
Sterol O-Acyl Transferase 1 as a Prognostic Marker of Adrenocortical Carcinoma.
Journal: Cancers
Published: December 24, 2019
Allelic Variants of ARMC5 in Patients With Adrenal Incidentalomas and in Patients With Cushing's Syndrome Associated With Bilateral Adrenal Nodules.
Journal: Frontiers in endocrinology
Published: October 04, 2019
The Role of gsp Mutations on the Development of Adrenocortical Tumors and Adrenal Hyperplasia.
Journal: Frontiers in endocrinology
Published: May 03, 2016
Whole-exome sequencing in obsessive-compulsive disorder identifies rare mutations in immunological and neurodevelopmental pathways.
Journal: Translational psychiatry
Published: February 19, 2015
High 18F-FDG uptake in PMAH correlated with normal expression of Glut1, HK1, HK2, and HK3.
Journal: Acta radiologica (Stockholm, Sweden : 1987)
Published: August 27, 2014
ARMC5 mutations are a frequent cause of primary macronodular adrenal Hyperplasia.
Journal: The Journal of clinical endocrinology and metabolism
Published: April 09, 2014
Amplification of the insulin-like growth factor 1 receptor gene is a rare event in adrenocortical adenocarcinomas: searching for potential mechanisms of overexpression.
Journal: BioMed research international
Published: March 27, 2014
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Last Updated: 09/26/2026