Eudeline Alix
Lyon, France
Last Updated: 09/26/2026
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Found 24 publications
How modern imaging can change diagnoses in historical cases of constitutional bone diseases.
Journal: Archives of disease in childhood
Published: June 22, 2026
Compound heterozygous SLC12A5 variants expand the molecular and functional spectrum of KCC2-developmental and epileptic encephalopathy.
Journal: Epilepsia
Published: November 13, 2025
Histomolecular Features of a Rare Subtype of Pleomorphic Adenoma Characterised by Abundant Lymphoid Stroma and HMGA2 Rearrangements.
Journal: Head and neck pathology
Published: October 10, 2025
Molecular Relationship Between Ovarian Sertoli-Leydig Cell Tumors and Their Heterologous Elements: Emphasis on the Possible Prognostic Significance of TERT Pathogenic Variants.
Journal: The American journal of surgical pathology
Published: May 28, 2025
The MEF2D::NCOA2 Fusion Defines a Distinct Emerging Vulvovaginal Myxoid Epithelioid Tumor With Smooth Muscle Differentiation.
Journal: Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc
Published: October 10, 2024
Case report: 7p22.3 deletion and 8q24.3 duplication in a patient with epilepsy and psychomotor delay-Does both possibly act to modulate a candidate gene region for the patient's phenotype?
Journal: Frontiers in genetics
Published: October 04, 2022
Variability in CD39 and CD73 protein levels in uveal melanoma patients.
Journal: Nucleosides, nucleotides & nucleic acids
Published: February 24, 2022
Chromosomal instability in the prediction of pituitary neuroendocrine tumors prognosis.
Journal: Acta neuropathologica communications
Published: August 25, 2020
Progressive Myoclonus Epilepsy Caused by a Homozygous Splicing Variant of SLC7A6OS.
Journal: Annals of neurology
Published: July 02, 2020
SST5 expression and USP8 mutation in functioning and silent corticotroph pituitary tumors.
Journal: Endocrine connections
Published: February 17, 2020
A Case of Trisomy 13 Mosaicism Presenting with a Severe Aortic Root Dilatation and Marfanoid Habitus due to an Unpredictable Cytogenetic Mechanism.
Journal: Cytogenetic and genome research
Published: January 14, 2020
Multisystem disorders, severe developmental delay and seizures in two affected siblings, expanding the phenotype of PIGC deficiency.
Journal: European journal of medical genetics
Published: October 16, 2019
Last Updated: 09/26/2026