Victor Morel
Marseille, France
Last Updated: 09/26/2026
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Found 10 publications
Eating behaviour phenotype in the MYT1L-related neurodevelopmental disorder: a deep phenotyping study using standardized questionnaires.
Journal: Orphanet journal of rare diseases
Published: July 21, 2026
Intense myocardial uptake in a patient with fabry disease-a new cause of false positive of bone scintigraphy mimicking cardiac amyloidosis.
Journal: European heart journal. Cardiovascular Imaging
Published: December 29, 2025
Limb Girdle Muscular Dystrophy Associated With TRIM32 Variants: A National Cohort Study.
Journal: Muscle & nerve
Published: September 08, 2025
Phenotype, genotype and prognosis of apical hypertrophic cardiomyopathies: a French multicentric cohort.
Journal: European heart journal. Cardiovascular Imaging
Published: August 20, 2025
Anterior megalophthalmos associated with CPAMD8 mutation: a case report.
Journal: Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus
Published: May 28, 2025
Corrigendum: Exome sequencing data reanalysis of 200 hypertrophic cardiomyopathy patients: the HYPERGEN French cohort 5 years after the initial analysis.
Journal: Frontiers in medicine
Published: March 17, 2025
Exome sequencing data reanalysis of 200 hypertrophic cardiomyopathy patients: the HYPERGEN French cohort 5 years after the initial analysis.
Journal: Frontiers in medicine
Published: August 14, 2024
HINT1 neuropathy: Expanding the genotype and phenotype spectrum.
Journal: Clinical genetics
Published: June 02, 2022
Progenitor mast cells and tryptase in Q fever.
Journal: Comparative immunology, microbiology and infectious diseases
Published: February 15, 2018
Showing 1-10 of 10
Last Updated: 09/26/2026