Search Results - "Hercent, Agathe"
-
1
Detection of Nine Oncogenes Amplification in Lung and Colorectal Cancer Formalin-Fixed Paraffin-Embedded Tissue Samples using Combined Next-Generation Sequencing-Based Script and Digital Droplet Polymerase Chain Reaction
Published in Cancer control (01-01-2023)“…Introduction Gene copy number variations have theranostic impact and require reliable methods for their identification. We aimed to evaluate the reliability of…”
Get full text
Journal Article -
2
Clinical vs. molecular diagnosis of Gorlin syndrome: relevance of diagnostic criteria depends on the age of the patients
Published in Clinical and experimental dermatology (20-05-2024)“…Abstract Background Gorlin syndrome (GS) is an autosomal dominant disorder characterized by a predisposition to basal cell carcinoma and developmental defects…”
Get full text
Journal Article -
3
Pancreatic Neuroendocrine Tumors in French VHL Mutation Carriers
Published in The journal of clinical endocrinology and metabolism (06-05-2024)“…Abstract Context Von Hippel-Lindau disease (VHL) is a rare, autosomal-dominant hereditary cancer-predisposition syndrome caused by germline pathogenic variants…”
Get full text
Journal Article -
4
Borderline Hepatocellular Adenomas: A Practical Diagnostic Approach Based on Pathologic and Molecular Features
Published in Modern pathology (01-09-2023)“…Borderline hepatocellular adenomas (BL-HCA) are characterized by focal architectural/cytologic atypia and reticulin loss, features that are insufficient for a…”
Get full text
Journal Article -
5
Clinical versus molecular diagnosis of Gorlin syndrome: Relevance of diagnostic criteria depends on the age of patients
Published in Clinical and experimental dermatology (20-05-2024)“…Gorlin Syndrome (GS) is an autosomal dominant disorder characterised by a predisposition to basal cell carcinoma and developmental defects, and caused by…”
Get full text
Journal Article -
6
Pancreatic neuroendocrine tumors in French VHL mutation carriers: a multicentric retrospective study
Published in The journal of clinical endocrinology and metabolism (06-05-2024)“…Von Hippel-Lindau disease (VHL) is a rare autosomal dominant hereditary cancer-predisposition syndrome caused by germline pathogenic variants (PV) in VHL gene…”
Get full text
Journal Article