Quentin H. Thomas

Dijon, 21000, France

Last Updated: 09/26/2026

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Found 41 publications

Ion Transport through Permselective Nanochannels of 2D-Covalent Organic Frameworks: Insights from Nonequilibrium Atomistic MD Simulations.

Ion Transport through Permselective Nanochannels of 2D-Covalent Organic Frameworks: Insights from Nonequilibrium Atomistic MD Simulations.

Journal: The journal of physical chemistry. B

Published: May 26, 2026

Charge state-dependent ion condensation near conjugated polymer backbones.

Charge state-dependent ion condensation near conjugated polymer backbones.

Journal: Materials horizons

Published: November 26, 2025

Cognitive Decline, Neurologic Involvement, and Neonatal Crisis in ABCC9-Related Intellectual Disability and Myopathy Syndrome.

Cognitive Decline, Neurologic Involvement, and Neonatal Crisis in ABCC9-Related Intellectual Disability and Myopathy Syndrome.

Journal: Neurology. Genetics

Published: October 06, 2025

Systematic Genetic Assessment in Young Patients With Cryptogenic Stroke: The ES-EASY project.

Systematic Genetic Assessment in Young Patients With Cryptogenic Stroke: The ES-EASY project.

Journal: Stroke

Published: September 19, 2025

Past, present, and future of genomic technologies in cerebellar ataxias.

Past, present, and future of genomic technologies in cerebellar ataxias.

Journal: Journal of neurology

Published: July 03, 2025

Mild and late onset forms of type I 3-methylglutaconic aciduria presenting as isolated cerebellar ataxia without leukodystrophy: case reports and phenotype expansion.

Mild and late onset forms of type I 3-methylglutaconic aciduria presenting as isolated cerebellar ataxia without leukodystrophy: case reports and phenotype expansion.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: June 11, 2025

French guidelines for the diagnosis and management of pure hereditary spastic paraplegia.

French guidelines for the diagnosis and management of pure hereditary spastic paraplegia.

Journal: Revue neurologique

Published: March 26, 2025

Neuropathy in GAA-FGF14 Late-Onset Cerebellar Ataxia (SCA27B): Prevalence and Characteristics.

Neuropathy in GAA-FGF14 Late-Onset Cerebellar Ataxia (SCA27B): Prevalence and Characteristics.

Journal: European journal of neurology

Published: March 10, 2025

Further phenotypical delineation of DLG3-related neurodevelopmental disorders.

Further phenotypical delineation of DLG3-related neurodevelopmental disorders.

Journal: European journal of human genetics : EJHG

Published: February 10, 2025

Age doesn't matter: Very late-onset Niemann-Pick type C disease presenting as a PSP Richardson syndrome mimic.

Age doesn't matter: Very late-onset Niemann-Pick type C disease presenting as a PSP Richardson syndrome mimic.

Journal: Parkinsonism & related disorders

Published: December 27, 2024

The Frequencies of Different Inborn Errors of Metabolism in Adult Metabolic Centres: 10 Years Later, Another Report From the SSIEM Adult Metabolic Physicians Group.

The Frequencies of Different Inborn Errors of Metabolism in Adult Metabolic Centres: 10 Years Later, Another Report From the SSIEM Adult Metabolic Physicians Group.

Journal: Journal of inherited metabolic disease

Published: November 12, 2024

Compound Heterozygous WARS2 Variants Including a Hypomorphic Allele Cause a Milder Phenotype of Complex Dopa Responsive Dystonia: Case Report and Review of the Literature.

Compound Heterozygous WARS2 Variants Including a Hypomorphic Allele Cause a Milder Phenotype of Complex Dopa Responsive Dystonia: Case Report and Review of the Literature.

Journal: Cerebellum (London, England)

Published: July 24, 2024

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Last Updated: 09/26/2026