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Journal of Cellular and Molecular Medicine
|
July 26, 2022
MicroRNAs as serum biomarkers in Becker muscular dystrophy
Delia Gagliardi, Mafalda Rizzuti, Roberta Brusa, et al.
Frontiers in Neurology
|
July 15, 2021
Early Findings in Neonatal Cases of <i>RYR1</i>-Related Congenital Myopathies
Eleonora Mauri, Daniela Piga, Alessandra Govoni, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie
|
June 6, 2026
Integrated electrophysiological, cellular, and pharmacological profiling reveals variant-specific mechanisms in SCN4A-related myotonia
Anthony Frosio, Serena Calamaio, Serena Pagliarani, et al.
Pharmacological Research
|
February 7, 2012
Nitric oxide donor and non steroidal anti inflammatory drugs as a therapy for muscular dystrophies: evidence from a safety study with pilot efficacy measures in adult dystrophic patients
Maria Grazia D'Angelo, Sandra Gandossini, Filippo Martinelli Boneschi, et al.
Muscle & Nerve
|
July 23, 2021
Impact of COVID-19 on the quality of life of patients with neuromuscular disorders in the Lombardy area, Italy
Delia Gagliardi, Gianluca Costamagna, Elena Abati, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
December 13, 2023
Proposal of a new clinical protocol for evaluating fatigability in adult SMA patients
Giulia Ricci, Francesca Torri, Alessandra Govoni, et al.
International Journal of Molecular Sciences
|
March 29, 2023
Extracellular Matrix Disorganization and Sarcolemmal Alterations in COL6-Related Myopathy Patients with New Variants of COL6 Genes
Simona Zanotti, Francesca Magri, Sabrina Salani, et al.
Neuromuscular Disorders : NMD
|
May 16, 2018
A new case of limb girdle muscular dystrophy 2G in a Greek patient, founder effect and review of the literature
Roberta Brusa, Francesca Magri, Dimitra Papadimitriou, et al.
BMC Neurology
|
June 12, 2026
Late-onset severe axonal polyneuropathy in mut0 methylmalonic acidemia after liver-kidney transplantation: a genotype-informed case report
Mariapia Griffo, Francesca Magri, Francesca Furlan, et al.
Skeletal Muscle
|
September 29, 2022
Megaconial congenital muscular dystrophy due to novel CHKB variants: a case report and literature review
Francesca Magri, Sara Antognozzi, Michela Ripolone, et al.
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Search research articles
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Showing results (111-120 of 174) with videos related to
Sort By:
Page
of 18
Journal of Cellular and Molecular Medicine
|
July 26, 2022
MicroRNAs as serum biomarkers in Becker muscular dystrophy
Delia Gagliardi, Mafalda Rizzuti, Roberta Brusa, et al.
Frontiers in Neurology
|
July 15, 2021
Early Findings in Neonatal Cases of <i>RYR1</i>-Related Congenital Myopathies
Eleonora Mauri, Daniela Piga, Alessandra Govoni, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie
|
June 6, 2026
Integrated electrophysiological, cellular, and pharmacological profiling reveals variant-specific mechanisms in SCN4A-related myotonia
Anthony Frosio, Serena Calamaio, Serena Pagliarani, et al.
Pharmacological Research
|
February 7, 2012
Nitric oxide donor and non steroidal anti inflammatory drugs as a therapy for muscular dystrophies: evidence from a safety study with pilot efficacy measures in adult dystrophic patients
Maria Grazia D'Angelo, Sandra Gandossini, Filippo Martinelli Boneschi, et al.
Muscle & Nerve
|
July 23, 2021
Impact of COVID-19 on the quality of life of patients with neuromuscular disorders in the Lombardy area, Italy
Delia Gagliardi, Gianluca Costamagna, Elena Abati, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
December 13, 2023
Proposal of a new clinical protocol for evaluating fatigability in adult SMA patients
Giulia Ricci, Francesca Torri, Alessandra Govoni, et al.
International Journal of Molecular Sciences
|
March 29, 2023
Extracellular Matrix Disorganization and Sarcolemmal Alterations in COL6-Related Myopathy Patients with New Variants of COL6 Genes
Simona Zanotti, Francesca Magri, Sabrina Salani, et al.
Neuromuscular Disorders : NMD
|
May 16, 2018
A new case of limb girdle muscular dystrophy 2G in a Greek patient, founder effect and review of the literature
Roberta Brusa, Francesca Magri, Dimitra Papadimitriou, et al.
BMC Neurology
|
June 12, 2026
Late-onset severe axonal polyneuropathy in mut0 methylmalonic acidemia after liver-kidney transplantation: a genotype-informed case report
Mariapia Griffo, Francesca Magri, Francesca Furlan, et al.
Skeletal Muscle
|
September 29, 2022
Megaconial congenital muscular dystrophy due to novel CHKB variants: a case report and literature review
Francesca Magri, Sara Antognozzi, Michela Ripolone, et al.
Page
of 18