Michaelle Corpechot
Paris, France
Last Updated: 09/26/2026
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Found 8 publications
SCN2A variants are associated with familial and sporadic hemiplegic migraine.
Journal: Brain : a journal of neurology
Published: June 20, 2025
Exome Sequencing of Fetuses With Intracranial Hemorrhage Unravels Novel Causative Genes and an Extreme Genetic Heterogeneity.
Journal: Prenatal diagnosis
Published: September 09, 2024
Xq28 copy number gain causing moyamoya disease and a novel moyamoya syndrome.
Journal: Journal of medical genetics
Published: August 23, 2019
Clinical and Molecular Features of 5 European Multigenerational Families With Moyamoya Angiopathy.
Journal: Stroke
Published: March 26, 2019
Moyamoya angiopathy in PHACE syndrome not associated with RNF213 variants.
Journal: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
Published: January 09, 2019
Showing 1-8 of 8
Last Updated: 09/26/2026