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Elisabetta Bucci

Showing results (11-20 of 30) with videos related to

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Plos One|June 4, 2016
"I Know that You Know that I Know": Neural Substrates Associated with Social Cognition Deficits in DM1 PatientsLaura Serra, Mara Cercignani, Michela Bruschini, et al.
Journal of Neurology|February 1, 2025
Correction: Muscle MRI as a biomarker of disease activity and progression in myotonic dystrophy type 1: a longitudinal studyLaura Fionda, Luca Leonardi, Laura Tufano, et al.
Journal of Neurology|July 7, 2024
Muscle MRI as a biomarker of disease activity and progression in myotonic dystrophy type 1: a longitudinal studyLaura Fionda, Luca Leonardi, Laura Tufano, et al.
Journal of Neurology|January 8, 2016
Increased risk of tumor in DM1 is not related to exposure to common lifestyle risk factorsMaria Laura Ester Bianchi, Emanuele Leoncini, Marcella Masciullo, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 13, 2023
Comparison of quantitative muscle ultrasound and whole-body muscle MRI in facioscapulohumeral muscular dystrophy type 1 patientsLaura Fionda, Fiammetta Vanoli, Antonella Di Pasquale, et al.
Journal of Neurology|February 26, 2016
Erratum to: Increased risk of tumor in DM1 is not related to exposure to common lifestyle risk factorsMaria Laura Ester Bianchi, Emanuele Leoncini, Marcella Masciullo, et al.
Journal of Neurology|February 12, 2018
A 34-year longitudinal study on long-term cardiac outcomes in DM1 patients with normal ECG at baseline at an Italian clinical centreElisabetta Bucci, Marco Testa, Loretta Licchelli, et al.
Autoimmunity Reviews|February 17, 2020
Muscle involvement in myasthenia gravis: Expanding the clinical spectrum of Myasthenia-Myositis association from a large cohort of patientsMatteo Garibaldi, Laura Fionda, Fiammetta Vanoli, et al.
Neuroepidemiology|February 17, 2016
An Age-Standardized Prevalence Estimate and a Sex and Age Distribution of Myotonic Dystrophy Types 1 and 2 in the Rome Province, ItalyNicola Vanacore, Emanuele Rastelli, Giovanni Antonini, et al.
Neuromuscular Disorders : NMD|January 1, 2021
Novel ACTA1 mutation causes late-presenting nemaline myopathy with unusual dark coresMatteo Garibaldi, Fabiana Fattori, Elena Maria Pennisi, et al.
Pageof 3

Showing results (11-20 of 30) with videos related to

Sort By:
Pageof 3
Plos One|June 4, 2016
"I Know that You Know that I Know": Neural Substrates Associated with Social Cognition Deficits in DM1 PatientsLaura Serra, Mara Cercignani, Michela Bruschini, et al.
Journal of Neurology|February 1, 2025
Correction: Muscle MRI as a biomarker of disease activity and progression in myotonic dystrophy type 1: a longitudinal studyLaura Fionda, Luca Leonardi, Laura Tufano, et al.
Journal of Neurology|July 7, 2024
Muscle MRI as a biomarker of disease activity and progression in myotonic dystrophy type 1: a longitudinal studyLaura Fionda, Luca Leonardi, Laura Tufano, et al.
Journal of Neurology|January 8, 2016
Increased risk of tumor in DM1 is not related to exposure to common lifestyle risk factorsMaria Laura Ester Bianchi, Emanuele Leoncini, Marcella Masciullo, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 13, 2023
Comparison of quantitative muscle ultrasound and whole-body muscle MRI in facioscapulohumeral muscular dystrophy type 1 patientsLaura Fionda, Fiammetta Vanoli, Antonella Di Pasquale, et al.
Journal of Neurology|February 26, 2016
Erratum to: Increased risk of tumor in DM1 is not related to exposure to common lifestyle risk factorsMaria Laura Ester Bianchi, Emanuele Leoncini, Marcella Masciullo, et al.
Journal of Neurology|February 12, 2018
A 34-year longitudinal study on long-term cardiac outcomes in DM1 patients with normal ECG at baseline at an Italian clinical centreElisabetta Bucci, Marco Testa, Loretta Licchelli, et al.
Autoimmunity Reviews|February 17, 2020
Muscle involvement in myasthenia gravis: Expanding the clinical spectrum of Myasthenia-Myositis association from a large cohort of patientsMatteo Garibaldi, Laura Fionda, Fiammetta Vanoli, et al.
Neuroepidemiology|February 17, 2016
An Age-Standardized Prevalence Estimate and a Sex and Age Distribution of Myotonic Dystrophy Types 1 and 2 in the Rome Province, ItalyNicola Vanacore, Emanuele Rastelli, Giovanni Antonini, et al.
Neuromuscular Disorders : NMD|January 1, 2021
Novel ACTA1 mutation causes late-presenting nemaline myopathy with unusual dark coresMatteo Garibaldi, Fabiana Fattori, Elena Maria Pennisi, et al.
Pageof 3