Maurizio Moggio

Milan, 20122, Italy

Last Updated: 09/26/2026

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Found 133 publications

Skeletal muscle in spinal muscular atrophy: Critical insights from pathogenesis to therapeutic strategies.

Skeletal muscle in spinal muscular atrophy: Critical insights from pathogenesis to therapeutic strategies.

Journal: Neurobiology of disease

Published: January 17, 2026

Beyond motor neurons: peripheral TDP-43 pathology in skeletal muscle and intramuscular nerves in amyotrophic lateral sclerosis.

Beyond motor neurons: peripheral TDP-43 pathology in skeletal muscle and intramuscular nerves in amyotrophic lateral sclerosis.

Journal: Brain communications

Published: January 13, 2026

Age-progressive stratification of Becker muscular dystrophy patients: a focus on muscle biopsy fibrosis, inflammation and capillary network.

Age-progressive stratification of Becker muscular dystrophy patients: a focus on muscle biopsy fibrosis, inflammation and capillary network.

Journal: Life sciences

Published: February 12, 2025

Artificial intelligence as a ploy to delve into the intricate link between genetics and mitochondria in patients with MASLD.

Artificial intelligence as a ploy to delve into the intricate link between genetics and mitochondria in patients with MASLD.

Journal: JHEP reports : innovation in hepatology

Published: November 08, 2024

The Profiling of 179 miRNA Expression in Serum from Limb Girdle Muscular Dystrophy Patients and Healthy Controls.

The Profiling of 179 miRNA Expression in Serum from Limb Girdle Muscular Dystrophy Patients and Healthy Controls.

Journal: International journal of molecular sciences

Published: October 24, 2023

Lafora Disease: A Case Report and Evolving Treatment Advancements.

Lafora Disease: A Case Report and Evolving Treatment Advancements.

Journal: Brain sciences

Published: October 18, 2023

Prominent muscle involvement in a familial form of mitochondrial disease due to a COA8 variant.

Prominent muscle involvement in a familial form of mitochondrial disease due to a COA8 variant.

Journal: Frontiers in genetics

Published: August 16, 2023

Characterization of Skeletal Muscle Biopsy and Derived Myoblasts in a Patient Carrying Arg14del Mutation in Phospholamban Gene.

Characterization of Skeletal Muscle Biopsy and Derived Myoblasts in a Patient Carrying Arg14del Mutation in Phospholamban Gene.

Journal: Cells

Published: March 16, 2023

Distribution of Exonic Variants in Glycogen Synthesis and Catabolism Genes in Late Onset Pompe Disease (LOPD).

Distribution of Exonic Variants in Glycogen Synthesis and Catabolism Genes in Late Onset Pompe Disease (LOPD).

Journal: Current issues in molecular biology

Published: March 02, 2023

MERRF Mutation A8344G in a Four-Generation Family without Central Nervous System Involvement: Clinical and Molecular Characterization.

MERRF Mutation A8344G in a Four-Generation Family without Central Nervous System Involvement: Clinical and Molecular Characterization.

Journal: Journal of personalized medicine

Published: December 09, 2022

Using Cluster Analysis to Overcome the Limits of Traditional Phenotype-Genotype Correlations: The Example of RYR1-Related Myopathies.

Using Cluster Analysis to Overcome the Limits of Traditional Phenotype-Genotype Correlations: The Example of RYR1-Related Myopathies.

Journal: Genes

Published: November 25, 2022

NEB mutations disrupt the super-relaxed state of myosin and remodel the muscle metabolic proteome in nemaline myopathy.

NEB mutations disrupt the super-relaxed state of myosin and remodel the muscle metabolic proteome in nemaline myopathy.

Journal: Acta neuropathologica communications

Published: October 28, 2022

Showing 1-12 of 133

Last Updated: 09/26/2026