Bruno Ragazzon
Paris, 75014, France
Last Updated: 09/26/2026
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Found 54 publications
The Proteome of Bilateral Macronodular Adrenocortical Disease (BMAD) Shows Different Profiles Correlating with the Genetic Causes and Reveals Specific Dysregulation of RNA Polymerase II and Cholesterol Biosynthesis Enzymes.
Journal: Endocrine pathology
Published: November 17, 2025
PRKACA constitutional duplication: a specific cause of primary pigmented nodular adrenocortical disease.
Journal: European journal of endocrinology
Published: August 19, 2025
Unexpected discrepancies between steroid intra-tissular content in adrenal tumors and clinical diagnosis of steroid excess.
Journal: European journal of endocrinology
Published: February 12, 2025
Letter Re: Germline NGS targeted analysis in adult patients with sporadic adrenocortical carcinoma.
Journal: European journal of cancer (Oxford, England : 1990)
Published: December 04, 2024
The mutational landscape of ARMC5 in Primary Bilateral Macronodular Adrenal Hyperplasia: an update.
Journal: Orphanet journal of rare diseases
Published: October 07, 2024
Impact of steroid differentiation on tumor microenvironment revealed by single-nucleus atlas of adrenal tumors.
Journal: Nature communications
Published: October 01, 2024
KDM1A genetic alterations, a rare cause of primary bilateral macronodular adrenal hyperplasia, strongly associated with food-dependent Cushing's syndrome: results of its systematic germline screening in 301 index cases and genotype/phenotype correlation.
Journal: European journal of endocrinology
Published: September 07, 2024
PDE11A Is a Phenotype Modulator of Primary Bilateral Macronodular Adrenal Hyperplasia: Results of a 334-Patient Series.
Journal: The Journal of clinical endocrinology and metabolism
Published: August 21, 2024
Somatic Molecular Heterogeneity in Bilateral Macronodular Adrenocortical Disease (BMAD) Differs Among the Pathological Subgroups.
Journal: Endocrine pathology
Published: August 12, 2024
Impact of Morphology in the Genotype and Phenotype Correlation of Bilateral Macronodular Adrenocortical Disease (BMAD): A Series of Clinicopathologically Well-Characterized 35 Cases.
Journal: Endocrine pathology
Published: January 12, 2023
Tumor suppressor gene ARMC5 controls adrenal redox state through NRF1 turnover.
Journal: Endocrine-related cancer
Published: August 02, 2022
Primary bilateral macronodular adrenal hyperplasia: definitely a genetic disease.
Journal: Nature reviews. Endocrinology
Published: June 30, 2022
Last Updated: 09/26/2026