David Pellerin

UCL Queen Square Institute Of Neurology
London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 76 publications

The Real Life of Ataxia Patients Without a Vertical Family History: a Twenty-year Experience in South Brazil.

The Real Life of Ataxia Patients Without a Vertical Family History: a Twenty-year Experience in South Brazil.

Journal: Cerebellum (London, England)
Published: June 08, 2026

Establishment and characterization of two human pluripotent stem cell lines from patients with ATX-FGF14/spinocerebellar ataxia 27A (SCA27A).

Establishment and characterization of two human pluripotent stem cell lines from patients with ATX-FGF14/spinocerebellar ataxia 27A (SCA27A).

Journal: Stem cell research
Published: May 19, 2026

Establishment and characterization of three human pluripotent stem cell lines from patients with spinocerebellar ataxia 27B (SCA27B).

Establishment and characterization of three human pluripotent stem cell lines from patients with spinocerebellar ataxia 27B (SCA27B).

Journal: Stem cell research
Published: May 12, 2026

Expert commentary for "Episodic cerebellar ataxia mimicking stroke - diagnostic and therapeutic lessons from SCA27B".

Expert commentary for "Episodic cerebellar ataxia mimicking stroke - diagnostic and therapeutic lessons from SCA27B".

Journal: Parkinsonism & related disorders
Published: April 14, 2026

A 5' UTR CCG expansion in TBC1D7 causes oculopharyngodistal myopathy.

A 5' UTR CCG expansion in TBC1D7 causes oculopharyngodistal myopathy.

Journal: medRxiv : the preprint server for health sciences
Published: April 10, 2026

Teaching NeuroImage: Superior Cerebellar Peduncle Tract Sign in SCA27B.

Teaching NeuroImage: Superior Cerebellar Peduncle Tract Sign in SCA27B.

Journal: Neurology
Published: March 10, 2026

Cerebellar cognitive affective syndrome (CCAS) and [18F]-FDG PET findings in spinocerebellar ataxia type SCA27B.

Cerebellar cognitive affective syndrome (CCAS) and [18F]-FDG PET findings in spinocerebellar ataxia type SCA27B.

Journal: Journal of neurology
Published: March 07, 2026

Frequency and phenotype of GAA-FGF14 disease in bilateral vestibulopathy syndromes: insights from repeat expansion carriers, including a case of co-occurrence with RFC1-related CANVAS.

Frequency and phenotype of GAA-FGF14 disease in bilateral vestibulopathy syndromes: insights from repeat expansion carriers, including a case of co-occurrence with RFC1-related CANVAS.

Journal: Journal of neurology
Published: January 21, 2026

Longitudinal progression, metrics, age-dependence, and modifiers of ataxia severity in SCA27B: a multicentre study of 219 patients.

Longitudinal progression, metrics, age-dependence, and modifiers of ataxia severity in SCA27B: a multicentre study of 219 patients.

Journal: EBioMedicine
Published: November 03, 2025

"Subthreshold" Expansions in Individuals With Otherwise-Typical Clinicoradiological Features of GAA-FGF14-Related Cerebellar Ataxia (SCA27B).

"Subthreshold" Expansions in Individuals With Otherwise-Typical Clinicoradiological Features of GAA-FGF14-Related Cerebellar Ataxia (SCA27B).

Journal: Journal of movement disorders
Published: November 01, 2025

Genotype and Age at Onset Drive Vermis Atrophy in CACNA1A- and GAA-FGF14-related Ataxias.

Genotype and Age at Onset Drive Vermis Atrophy in CACNA1A- and GAA-FGF14-related Ataxias.

Journal: Cerebellum (London, England)
Published: September 15, 2025

Identification of FGF14 GAA Expansions in Polish Patients with Undiagnosed Cerebellar Ataxia - A Preliminary Study.

Identification of FGF14 GAA Expansions in Polish Patients with Undiagnosed Cerebellar Ataxia - A Preliminary Study.

Journal: Cerebellum (London, England)
Published: September 07, 2025
Showing 1-12 of 76

Last Updated: 09/26/2026