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Elisabetta Bucci

Showing results (21-30 of 30) with videos related to

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Journal of the Neurological Sciences|June 3, 2019
Reply to the letter entitled "Predictors of respiratory impairment in patients with myotonic dystrophy type 1"Salvatore Rossi, Giacomo Della Marca, Martina Ricci, et al.
Journal of the Neurological Sciences|February 25, 2019
Prevalence and predictor factors of respiratory impairment in a large cohort of patients with Myotonic Dystrophy type 1 (DM1): A retrospective, cross sectional studySalvatore Rossi, Giacomo Della Marca, Martina Ricci, et al.
European Journal of Neurology|November 9, 2021
Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trialsMatteo Garibaldi, Tommaso Nicoletti, Elisabetta Bucci, et al.
Journal of Neurology|August 20, 2020
A 5-year clinical follow-up study from the Italian National Registry for FSHDLiliana Vercelli, Fabiano Mele, Lucia Ruggiero, et al.
BMC Musculoskeletal Disorders|January 5, 2024
Physical activity practiced at a young age is associated with a less severe subsequent clinical presentation in facioscapulohumeral muscular dystrophyCinzia Bettio, Federico Banchelli, Valentina Salsi, et al.
JAMA Network Open|May 2, 2020
Phenotypic Variability Among Patients With D4Z4 Reduced Allele Facioscapulohumeral Muscular DystrophyLucia Ruggiero, Fabiano Mele, Fiore Manganelli, et al.
Journal of Neurology|April 30, 2016
A novel clinical tool to classify facioscapulohumeral muscular dystrophy phenotypesGiulia Ricci, Lucia Ruggiero, Liliana Vercelli, et al.
BMJ Open|January 7, 2016
Clinical expression of facioscapulohumeral muscular dystrophy in carriers of 1-3 D4Z4 reduced alleles: experience of the FSHD Italian National RegistryAna Nikolic, Giulia Ricci, Francesco Sera, et al.
Scientific Reports|December 11, 2020
Large genotype-phenotype study in carriers of D4Z4 borderline alleles provides guidance for facioscapulohumeral muscular dystrophy diagnosisGiulia Ricci, Fabiano Mele, Monica Govi, et al.
Brain : a Journal of Neurology|September 14, 2013
Large scale genotype-phenotype analyses indicate that novel prognostic tools are required for families with facioscapulohumeral muscular dystrophyGiulia Ricci, Isabella Scionti, Francesco Sera, et al.
Pageof 3

Showing results (21-30 of 30) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
Journal of the Neurological Sciences|June 3, 2019
Reply to the letter entitled "Predictors of respiratory impairment in patients with myotonic dystrophy type 1"Salvatore Rossi, Giacomo Della Marca, Martina Ricci, et al.
Journal of the Neurological Sciences|February 25, 2019
Prevalence and predictor factors of respiratory impairment in a large cohort of patients with Myotonic Dystrophy type 1 (DM1): A retrospective, cross sectional studySalvatore Rossi, Giacomo Della Marca, Martina Ricci, et al.
European Journal of Neurology|November 9, 2021
Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trialsMatteo Garibaldi, Tommaso Nicoletti, Elisabetta Bucci, et al.
Journal of Neurology|August 20, 2020
A 5-year clinical follow-up study from the Italian National Registry for FSHDLiliana Vercelli, Fabiano Mele, Lucia Ruggiero, et al.
BMC Musculoskeletal Disorders|January 5, 2024
Physical activity practiced at a young age is associated with a less severe subsequent clinical presentation in facioscapulohumeral muscular dystrophyCinzia Bettio, Federico Banchelli, Valentina Salsi, et al.
JAMA Network Open|May 2, 2020
Phenotypic Variability Among Patients With D4Z4 Reduced Allele Facioscapulohumeral Muscular DystrophyLucia Ruggiero, Fabiano Mele, Fiore Manganelli, et al.
Journal of Neurology|April 30, 2016
A novel clinical tool to classify facioscapulohumeral muscular dystrophy phenotypesGiulia Ricci, Lucia Ruggiero, Liliana Vercelli, et al.
BMJ Open|January 7, 2016
Clinical expression of facioscapulohumeral muscular dystrophy in carriers of 1-3 D4Z4 reduced alleles: experience of the FSHD Italian National RegistryAna Nikolic, Giulia Ricci, Francesco Sera, et al.
Scientific Reports|December 11, 2020
Large genotype-phenotype study in carriers of D4Z4 borderline alleles provides guidance for facioscapulohumeral muscular dystrophy diagnosisGiulia Ricci, Fabiano Mele, Monica Govi, et al.
Brain : a Journal of Neurology|September 14, 2013
Large scale genotype-phenotype analyses indicate that novel prognostic tools are required for families with facioscapulohumeral muscular dystrophyGiulia Ricci, Isabella Scionti, Francesco Sera, et al.
Pageof 3