Riccardo Curro

London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 35 publications

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

Motor, Extrapyramidal, and Cognitive Involvement in RFC1 Disease: A Systematic Review and Meta-Analysis.

Motor, Extrapyramidal, and Cognitive Involvement in RFC1 Disease: A Systematic Review and Meta-Analysis.

Journal: Neurology. Genetics
Published: December 02, 2025

Gene-Pseudogene Inversions as a Hidden Source of Missing Heritability.

Gene-Pseudogene Inversions as a Hidden Source of Missing Heritability.

Journal: medRxiv : the preprint server for health sciences
Published: November 24, 2025

Clinical and genetic characteristics of CANVAS patients - a single-center experience.

Clinical and genetic characteristics of CANVAS patients - a single-center experience.

Journal: Neurologia i neurochirurgia polska
Published: April 24, 2025

CGG repeat expansions in Charcot-Marie-Tooth disease: insights from the 100 000 Genomes Project.

CGG repeat expansions in Charcot-Marie-Tooth disease: insights from the 100 000 Genomes Project.

Journal: Journal of neurology, neurosurgery, and psychiatry
Published: April 24, 2025

Author Correction: A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry.

Author Correction: A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry.

Journal: Nature communications
Published: October 17, 2024

Cough Reflex Hypersensitivity in Cerebellar Ataxia with Neuropathy and Vestibular Areflexia Syndrome-associated Chronic Cough.

Cough Reflex Hypersensitivity in Cerebellar Ataxia with Neuropathy and Vestibular Areflexia Syndrome-associated Chronic Cough.

Journal: American journal of respiratory and critical care medicine
Published: August 07, 2024

Biallelic variants in ARHGAP19 cause a progressive inherited motor-predominant neuropathy.

Biallelic variants in ARHGAP19 cause a progressive inherited motor-predominant neuropathy.

Journal: The Journal of clinical investigation
Published: July 08, 2024

Genotype and phenotype spectrum of Charcot-Marie-Tooth disease due to mutations in SORD.

Genotype and phenotype spectrum of Charcot-Marie-Tooth disease due to mutations in SORD.

Journal: Brain : a journal of neurology
Published: June 08, 2024

Repeat expansions in RFC1 gene in refractory chronic cough.

Repeat expansions in RFC1 gene in refractory chronic cough.

Journal: ERJ open research
Published: June 07, 2024

Nerve ultrasound in CANVAS-spectrum disease: Reduced nerve size distinguishes genetically confirmed CANVAS from other axonal polyneuropathies.

Nerve ultrasound in CANVAS-spectrum disease: Reduced nerve size distinguishes genetically confirmed CANVAS from other axonal polyneuropathies.

Journal: Journal of the peripheral nervous system : JPNS
Published: April 25, 2024

Neurological disorders caused by novel non-coding repeat expansions: clinical features and differential diagnosis.

Neurological disorders caused by novel non-coding repeat expansions: clinical features and differential diagnosis.

Journal: The Lancet. Neurology
Published: February 03, 2024
Showing 1-12 of 35

Last Updated: 09/26/2026