Giulia Coarelli

Paris, 75013, France

Last Updated: 09/26/2026

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Found 74 publications

Biallelic ATG9B Variants Define a Novel Autophagy-Related Neurodevelopmental Disorder with Cerebellar Ataxia.

Biallelic ATG9B Variants Define a Novel Autophagy-Related Neurodevelopmental Disorder with Cerebellar Ataxia.

Journal: Genes
Published: April 17, 2026

Spatial analysis of paraneoplastic cerebellar degeneration in ovarian cancer with anti-Yo syndrome and SCA1.

Spatial analysis of paraneoplastic cerebellar degeneration in ovarian cancer with anti-Yo syndrome and SCA1.

Journal: Journal of neurology
Published: March 01, 2026

Cerebellar cognitive-affective syndrome in Friedreich Ataxia.

Cerebellar cognitive-affective syndrome in Friedreich Ataxia.

Journal: Journal of neurology
Published: January 15, 2026

Sequence Variants in Small CAG Repeat Expansions of the HTT Gene and Disease Onset and Progression in Huntington Disease.

Sequence Variants in Small CAG Repeat Expansions of the HTT Gene and Disease Onset and Progression in Huntington Disease.

Journal: Neurology
Published: December 19, 2025

Early and Progressive Spinal Cord Atrophy in Spinocerebellar Ataxia Type 1.

Early and Progressive Spinal Cord Atrophy in Spinocerebellar Ataxia Type 1.

Journal: Movement disorders : official journal of the Movement Disorder Society
Published: December 09, 2025

A Severity-Agnostic Atrophy Pattern in Spinocerebellar Ataxia Type 3: Volumetrics from ENIGMA-Ataxia.

A Severity-Agnostic Atrophy Pattern in Spinocerebellar Ataxia Type 3: Volumetrics from ENIGMA-Ataxia.

Journal: Movement disorders : official journal of the Movement Disorder Society
Published: October 31, 2025

Prevalence, Severity, and Progression of Cerebellar Cognitive-Affective Syndrome in Patients With Spinocerebellar Ataxias.

Prevalence, Severity, and Progression of Cerebellar Cognitive-Affective Syndrome in Patients With Spinocerebellar Ataxias.

Journal: Neurology
Published: August 20, 2025

Best Oculomotor Endpoints for Clinical Trials in Hereditary Ataxias: A Systematic Review and Consensus by the Ataxia Global Initiative Working Group on Digital‑Motor Biomarkers.

Best Oculomotor Endpoints for Clinical Trials in Hereditary Ataxias: A Systematic Review and Consensus by the Ataxia Global Initiative Working Group on Digital‑Motor Biomarkers.

Journal: Cerebellum (London, England)
Published: August 05, 2025

Digenic inheritance of mutations in SPG7 and AFG3L2 causes motor neuron and cerebellar disorders.

Digenic inheritance of mutations in SPG7 and AFG3L2 causes motor neuron and cerebellar disorders.

Journal: BMC medicine
Published: July 29, 2025

Quantifying Placebo Effects in Hereditary Ataxia Trials: A Meta-Analysis of Scale for the Assessment and Rating of Ataxia (SARA) Score Changes.

Quantifying Placebo Effects in Hereditary Ataxia Trials: A Meta-Analysis of Scale for the Assessment and Rating of Ataxia (SARA) Score Changes.

Journal: Movement disorders : official journal of the Movement Disorder Society
Published: July 29, 2025

Brain atrophy staging in spinocerebellar ataxia type 3 for clinical prognosis and trial enrichment.

Brain atrophy staging in spinocerebellar ataxia type 3 for clinical prognosis and trial enrichment.

Journal: EBioMedicine
Published: June 30, 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
Showing 1-12 of 74

Last Updated: 09/26/2026