Charlotte Mouraux

Liege, WAL, Belgium

Last Updated: 09/26/2026

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Found 14 publications

The diagnosis of rare movement disorders in 2026. Phenotyping, genomics, brain imag-ing, a three-part work

The diagnosis of rare movement disorders in 2026. Phenotyping, genomics, brain imag-ing, a three-part work

Journal: Revue medicale de Liege

Published: January 15, 2026

Genetic and therapeutic insights in musician's dystonia: a single-centre case series and narrative review.

Genetic and therapeutic insights in musician's dystonia: a single-centre case series and narrative review.

Journal: Acta neurologica Belgica

Published: October 28, 2025

Homozygous Pathogenic MYH3 Variants Associated With Arthrogryposis and Lingual Dystonia.

Homozygous Pathogenic MYH3 Variants Associated With Arthrogryposis and Lingual Dystonia.

Journal: Tremor and other hyperkinetic movements (New York, N.Y.)

Published: July 17, 2025

Expanding the clinical spectrum of RAB3A: from cerebellar ataxia to spastic paraplegia.

Expanding the clinical spectrum of RAB3A: from cerebellar ataxia to spastic paraplegia.

Journal: Brain : a journal of neurology

Published: June 02, 2025

Association between CACNA1A and ATP1A2 Variants are Responsible for Severe Neurodevelopmental Disorder.

Association between CACNA1A and ATP1A2 Variants are Responsible for Severe Neurodevelopmental Disorder.

Journal: Neuropediatrics

Published: December 12, 2024

Deletion of the THAP1 Gene Is Responsible for Typical DYT-THAP1.

Deletion of the THAP1 Gene Is Responsible for Typical DYT-THAP1.

Journal: Movement disorders clinical practice

Published: September 10, 2024

Epidemiological report and diagnostic approach used in the neuromuscular population of Liege, Belgium.

Epidemiological report and diagnostic approach used in the neuromuscular population of Liege, Belgium.

Journal: Orphanet journal of rare diseases

Published: July 12, 2024

Spinal Muscular Atrophy Treatment in Patients Identified by Newborn Screening-A Systematic Review.

Spinal Muscular Atrophy Treatment in Patients Identified by Newborn Screening-A Systematic Review.

Journal: Genes

Published: May 25, 2023

Late Diagnosis of 18p Syndrome with Movement Disorders by Whole Exome Sequencing Read-Depth Based Algorithm.

Late Diagnosis of 18p Syndrome with Movement Disorders by Whole Exome Sequencing Read-Depth Based Algorithm.

Journal: Movement disorders clinical practice

Published: December 07, 2022

Effort during prolonged wakefulness is associated with performance to attentional and executive tasks but not with cortical excitability in late-middle-aged healthy individuals.

Effort during prolonged wakefulness is associated with performance to attentional and executive tasks but not with cortical excitability in late-middle-aged healthy individuals.

Journal: Neuropsychology

Published: November 10, 2022

Genetic risk for insomnia is associated with objective sleep measures in young and healthy good sleepers.

Genetic risk for insomnia is associated with objective sleep measures in young and healthy good sleepers.

Journal: Neurobiology of disease

Published: June 24, 2022

Assessing the carbonisation temperatures recorded by ancient charcoals for δ13C-based palaeoclimate reconstruction.

Assessing the carbonisation temperatures recorded by ancient charcoals for δ13C-based palaeoclimate reconstruction.

Journal: Scientific reports

Published: January 07, 2022

Showing 1-12 of 14

Last Updated: 09/26/2026