Caterina Mariotti

Fondazione IRCCS Istituto Neurologico Carlo Besta

Italy

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Articles (10)

Year:

2023

Year:

2023

Year:

2021

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2021

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2021

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2021

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2021

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2021

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2021

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2020

Collaborators (12)

federica rachele danti

Fondazione IRCCS Istituto Neurologico Carlo Besta

ITALY

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Alessandra Solari

Head, MD

Fondazione IRCCS Istituto Neurologico Carlo Besta

ITALY

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Fabrizio Tagliavini

Fondazione IRCCS Istituto Neurologico Carlo Besta

ITALY

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Anna Castaldo

Fondazione IRCCS Istituto Neurologico Carlo Besta

ITALY

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Rizzo Elena

Fondazione IRCCS Istituto Neurologico Carlo Besta

ITALY

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Antonio Emanuele Elia

Fondazione IRCCS Istituto Neurologico Carlo Besta

ITALY

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LUCIANO MERLINI

University of Bologna

ITALY

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luca giani

Istituti Clinici Scientifici Maugeri SpA IRCCS Lumezzane

ITALY

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Alessia Mongelli

Fondazione IRCCS Istituto Neurologico Carlo Besta

ITALY

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David R. Lynch

UNITED STATES

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Marinella De Salvatore

Fondazione IRCCS Istituto Neurologico Carlo Besta

ITALY

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Anna Rita Giovagnoli

Fondazione IRCCS Istituto Neurologico Carlo Besta

ITALY

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Caterina Mariotti

Research Interests

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Articles (10)

Italian cross-cultural adaptation of the patient-reported outcome measure of ataxia

Efficacy of Omaveloxolone in Friedreich's Ataxia: Delayed‐Start Analysis of the MOXIe Extension

Utility of the Parkinson's disease-Cognitive Rating Scale for the screening of global cognitive status in Huntington's disease (vol 267, pg 1527, 2020)

Progression characteristics of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS): a 4-year cohort study.

Neuro-telehealth for fragile patients in a tertiary referral neurological institute during the COVID-19 pandemic in Milan, Lombardy.

Missing the pathological expansion in Huntington disease: de novo c.51C>G variant on the expanded allele causing intrafamilial allele dropout

Expanding the Spectrum of AP5Z1-Related Hereditary Spastic Paraplegia (HSP-SPG48): A Multicenter Study on a Rare Disease

Safety and Efficacy of Omaveloxolone in Friedreich Ataxia (MOXIe Study)

The European Reference Network for Rare Neurological Diseases

Next-generation sequencing application to investigate skeletal muscle channelopathies in a large cohort of Italian patients.

Collaborators (12)

federica rachele danti

Alessandra Solari

Fabrizio Tagliavini

Anna Castaldo

Rizzo Elena

Antonio Emanuele Elia

LUCIANO MERLINI

luca giani

Alessia Mongelli

David R. Lynch

Marinella De Salvatore

Anna Rita Giovagnoli

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