Franco Taroni

Head

Fondazione IRCCS Istituto Neurologico Carlo Besta

Italy

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About

Franco Taroni is the Head at Fondazione IRCCS Istituto Neurologico Carlo Besta in Italy. His research focuses on neurodegenerative disorders, genetic neuropathies, and drug repurposing for neurodegenerative conditions. Recent publications include studies on KIF1C pathogenic variants, Charcot-Marie-Tooth disease, and pediatric-onset epilepsies.

Articles (10)

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2025

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2024

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2024

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2024

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2024

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2024

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2024

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2023

Collaborators (12)

Vincent Huin

Associate professor

Université de Lille

FRANCE

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richard dobson

King’s College London

UNITED KINGDOM

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Daniela Di Bella

Fondazione IRCCS Istituto Neurologico Carlo Besta

ITALY

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Elena Rossini

Sapienza University of Rome

ITALY

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Charles Curtis

King’s College London

UNITED KINGDOM

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Viviana Pensato

Fondazione IRCCS Istituto Neurologico Carlo Besta

ITALY

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Mariarita Galbiati

Associate Professor

Università degli Studi di Torino

ITALY

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Chiara Pisciotta

Fondazione IRCCS Istituto Neurologico Carlo Besta

ITALY

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Eleonora Cavalca

Collaboratore professionale di ricerca sanitaria

Fondazione IRCCS Istituto Neurologico Carlo Besta

ITALY

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Massimo Russo

Prof.

University of Messina

ITALY

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Raymond Chung

King’s College London

UNITED KINGDOM

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Gita Ramdharry

Honorary Associate Professor

UCL Institute of Neurology, University College London

UNITED KINGDOM

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Franco Taroni

Research Interests

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Articles (10)

Teaching NeuroImage: Distinctive White Matter Abnormalities in KIF1C Pathogenic Variants

Phenotypic spectrum of myelin protein zero-related neuropathies: a large cohort study from five mutation clusters across Italy

Role of the repeat expansion size in predicting age of onset and severity in RFC1 disease

Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data

Altered molecular and cellular mechanisms in KIF5A-associated neurodegenerative or neurodevelopmental disorders

A familial form of Charcot-Marie-Tooth disease (type 2d) caused by a previously unreported variant in <i>GARS1</i>.

Paroxysmal Non-Kinesigenic Dyskinesias Associated with Biallelic POLG Variants: A Case Report.

Next-generation sequencing in pediatric-onset epilepsies: Analysis with target panels and personalized therapeutic approach.

Phenotypic Spectrum and Natural History of Gillespie Syndrome. An Updated Literature Review with 2 New Cases.

Genetic analysis and natural history of Charcot-Marie-Tooth disease CMTX1 due to GJB1 variants.

Collaborators (12)

Vincent Huin

richard dobson

Daniela Di Bella

Elena Rossini

Charles Curtis

Viviana Pensato

Mariarita Galbiati

Chiara Pisciotta

Eleonora Cavalca

Massimo Russo

Raymond Chung

Gita Ramdharry

Make your next move.

Franco Taroni

Research Interests

Explore related searches

Contact this professor

About

Articles (10)

Teaching NeuroImage: Distinctive White Matter Abnormalities in KIF1C Pathogenic Variants

Phenotypic spectrum of myelin protein zero-related neuropathies: a large cohort study from five mutation clusters across Italy

Role of the repeat expansion size in predicting age of onset and severity in RFC1 disease

Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data

Altered molecular and cellular mechanisms in KIF5A-associated neurodegenerative or neurodevelopmental disorders

A familial form of Charcot-Marie-Tooth disease (type 2d) caused by a previously unreported variant in &lt;i&gt;GARS1&lt;/i&gt;.

Paroxysmal Non-Kinesigenic Dyskinesias Associated with Biallelic POLG Variants: A Case Report.

Next-generation sequencing in pediatric-onset epilepsies: Analysis with target panels and personalized therapeutic approach.

Phenotypic Spectrum and Natural History of Gillespie Syndrome. An Updated Literature Review with 2 New Cases.

Genetic analysis and natural history of Charcot-Marie-Tooth disease CMTX1 due to GJB1 variants.

Collaborators (12)

Vincent Huin

richard dobson

Daniela Di Bella

Elena Rossini

Charles Curtis

Viviana Pensato

Mariarita Galbiati

Chiara Pisciotta

Eleonora Cavalca

Massimo Russo

Raymond Chung

Gita Ramdharry

Make your next move.

A familial form of Charcot-Marie-Tooth disease (type 2d) caused by a previously unreported variant in <i>GARS1</i>.