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Neuromuscular Disorders : NMD
|
November 13, 2025
Novel missense variants associated with GNE myopathy
Johanna Ranta-Aho, Viviana Cetrangolo, Luca Bello, et al.
Blood Advances
|
September 21, 2021
Ablation of collagen VI leads to the release of platelets with altered function
Vittorio Abbonante, Cristian Gruppi, Monica Battiston, et al.
Acta Neuropathologica Communications
|
May 24, 2025
Evaluation of aggrephagy markers in myofibrillar myopathies
Eliana Iannibelli, Alessandra Ruggieri, Antonello Maruotti, et al.
Children (Basel, Switzerland)
|
May 16, 2023
Upper Limb Changes in DMD Patients Amenable to Skipping Exons 44, 45, 51 and 53: A 24-Month Study
Claudia Brogna, Marika Pane, Giorgia Coratti, et al.
American Journal of Human Genetics
|
October 18, 2016
Association Study of Exon Variants in the NF-κB and TGFβ Pathways Identifies CD40 as a Modifier of Duchenne Muscular Dystrophy
Luca Bello, Kevin M Flanigan, Robert B Weiss, et al.
Plos One
|
October 30, 2015
Genetic Modifiers of Duchenne Muscular Dystrophy and Dilated Cardiomyopathy
Andrea Barp, Luca Bello, Luisa Politano, et al.
HGG Advances
|
January 20, 2022
RNA-seq in DMD urinary stem cells recognized muscle-related transcription signatures and addressed the identification of atypical mutations by whole-genome sequencing
Maria S Falzarano, Andrea Grilli, Silvia Zia, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
February 1, 2025
Transition of patients with Duchenne muscular dystrophy from paediatric to adult care: An international Delphi consensus study
Diana Castro, Thomas Sejersen, Luca Bello, et al.
Journal of Neurology
|
September 27, 2019
European muscle MRI study in limb girdle muscular dystrophy type R1/2A (LGMDR1/LGMD2A)
Andrea Barp, Pascal Laforet, Luca Bello, et al.
European Journal of Human Genetics : EJHG
|
January 4, 2020
TCTEX1D1 is a genetic modifier of disease progression in Duchenne muscular dystrophy
Pietro Spitali, Irina Zaharieva, Stefan Bohringer, et al.
Page
of 15
Search research articles
Search
Showing results (81-90 of 144) with videos related to
Sort By:
Page
of 15
Neuromuscular Disorders : NMD
|
November 13, 2025
Novel missense variants associated with GNE myopathy
Johanna Ranta-Aho, Viviana Cetrangolo, Luca Bello, et al.
Blood Advances
|
September 21, 2021
Ablation of collagen VI leads to the release of platelets with altered function
Vittorio Abbonante, Cristian Gruppi, Monica Battiston, et al.
Acta Neuropathologica Communications
|
May 24, 2025
Evaluation of aggrephagy markers in myofibrillar myopathies
Eliana Iannibelli, Alessandra Ruggieri, Antonello Maruotti, et al.
Children (Basel, Switzerland)
|
May 16, 2023
Upper Limb Changes in DMD Patients Amenable to Skipping Exons 44, 45, 51 and 53: A 24-Month Study
Claudia Brogna, Marika Pane, Giorgia Coratti, et al.
American Journal of Human Genetics
|
October 18, 2016
Association Study of Exon Variants in the NF-κB and TGFβ Pathways Identifies CD40 as a Modifier of Duchenne Muscular Dystrophy
Luca Bello, Kevin M Flanigan, Robert B Weiss, et al.
Plos One
|
October 30, 2015
Genetic Modifiers of Duchenne Muscular Dystrophy and Dilated Cardiomyopathy
Andrea Barp, Luca Bello, Luisa Politano, et al.
HGG Advances
|
January 20, 2022
RNA-seq in DMD urinary stem cells recognized muscle-related transcription signatures and addressed the identification of atypical mutations by whole-genome sequencing
Maria S Falzarano, Andrea Grilli, Silvia Zia, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
February 1, 2025
Transition of patients with Duchenne muscular dystrophy from paediatric to adult care: An international Delphi consensus study
Diana Castro, Thomas Sejersen, Luca Bello, et al.
Journal of Neurology
|
September 27, 2019
European muscle MRI study in limb girdle muscular dystrophy type R1/2A (LGMDR1/LGMD2A)
Andrea Barp, Pascal Laforet, Luca Bello, et al.
European Journal of Human Genetics : EJHG
|
January 4, 2020
TCTEX1D1 is a genetic modifier of disease progression in Duchenne muscular dystrophy
Pietro Spitali, Irina Zaharieva, Stefan Bohringer, et al.
Page
of 15