Elisabetta Bucci

Rome, Italy

Last Updated: 09/26/2026

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Found 28 publications

Correction: Muscle MRI as a biomarker of disease activity and progression in myotonic dystrophy type 1: a longitudinal study.

Correction: Muscle MRI as a biomarker of disease activity and progression in myotonic dystrophy type 1: a longitudinal study.

Journal: Journal of neurology

Published: February 01, 2025

Muscle MRI as a biomarker of disease activity and progression in myotonic dystrophy type 1: a longitudinal study.

Muscle MRI as a biomarker of disease activity and progression in myotonic dystrophy type 1: a longitudinal study.

Journal: Journal of neurology

Published: March 10, 2024

Physical activity practiced at a young age is associated with a less severe subsequent clinical presentation in facioscapulohumeral muscular dystrophy.

Physical activity practiced at a young age is associated with a less severe subsequent clinical presentation in facioscapulohumeral muscular dystrophy.

Journal: BMC musculoskeletal disorders

Published: May 15, 2023

Comparison of quantitative muscle ultrasound and whole-body muscle MRI in facioscapulohumeral muscular dystrophy type 1 patients.

Comparison of quantitative muscle ultrasound and whole-body muscle MRI in facioscapulohumeral muscular dystrophy type 1 patients.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: January 06, 2023

Distal upper limb involvement in myasthenia-myositis association.

Distal upper limb involvement in myasthenia-myositis association.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: July 16, 2022

Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trials.

Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trials.

Journal: European journal of neurology

Published: September 17, 2021

Gender effect on cardiac involvement in myotonic dystrophy type 1.

Gender effect on cardiac involvement in myotonic dystrophy type 1.

Journal: European journal of neurology

Published: October 12, 2020

Changes of clinical, neurophysiological and nerve ultrasound characteristics in CIDP over time: a 3-year follow-up.

Changes of clinical, neurophysiological and nerve ultrasound characteristics in CIDP over time: a 3-year follow-up.

Journal: Journal of neurology

Published: September 21, 2020

Large genotype-phenotype study in carriers of D4Z4 borderline alleles provides guidance for facioscapulohumeral muscular dystrophy diagnosis.

Large genotype-phenotype study in carriers of D4Z4 borderline alleles provides guidance for facioscapulohumeral muscular dystrophy diagnosis.

Journal: Scientific reports

Published: August 10, 2020

A 5-year clinical follow-up study from the Italian National Registry for FSHD.

A 5-year clinical follow-up study from the Italian National Registry for FSHD.

Journal: Journal of neurology

Published: July 02, 2020

Novel ACTA1 mutation causes late-presenting nemaline myopathy with unusual dark cores.

Novel ACTA1 mutation causes late-presenting nemaline myopathy with unusual dark cores.

Journal: Neuromuscular disorders : NMD

Published: May 24, 2020

Phenotypic Variability Among Patients With D4Z4 Reduced Allele Facioscapulohumeral Muscular Dystrophy.

Phenotypic Variability Among Patients With D4Z4 Reduced Allele Facioscapulohumeral Muscular Dystrophy.

Journal: JAMA network open

Published: May 02, 2020

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Last Updated: 09/26/2026