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1. Cell environment shapes TDP-43 function with implications in neuronal and muscle disease

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

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

6. Safety and efficacy of avalglucosidase alfa versus alglucosidase alfa in patients with late-onset Pompe disease (COMET): a phase 3, randomised, multicentre trial

7. Mitochondria: Muscle Morphology

9. A 5-year clinical follow-up study from the Italian National Registry for FSHD

11. Lafora Disease: A Case Report and Evolving Treatment Advancements

14. Impairments in contractility and cytoskeletal organisation cause nuclear defects in nemaline myopathy

15. Value of structured reporting in neuromuscular disorders

16. Assessing the Role of Anti rh-GAA in Modulating Response to ERT in a Late-Onset Pompe Disease Cohort from the Italian GSDII Study Group

17. Muscle pain in mitochondrial diseases: a picture from the Italian network

18. Large genotype–phenotype study in carriers of D4Z4 borderline alleles provides guidance for facioscapulohumeral muscular dystrophy diagnosis

20. Diagnosis of Duchenne Muscular Dystrophy in Italy in the last decade: Critical issues and areas for improvements

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

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

24. Histological effects of givinostat in boys with Duchenne muscular dystrophy

25. “Mitochondrial neuropathies”: A survey from the large cohort of the Italian Network

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

29. A Schematic Approach to Defining the Prevalence of COL VI Variants in Five Years of Next-Generation Sequencing

31. Immunofluorescence signal intensity measurements as a semi-quantitative tool to assess sarcoglycan complex expression in muscle biopsy

32. Vaccination recommendations for patients with neuromuscular disease

33. The clinical spectrum of CASQ1-related myopathy

36. New Mutations in NEB Gene Discovered by Targeted Next-Generation Sequencing in Nemaline Myopathy Italian Patients

37. A novel clinical tool to classify facioscapulohumeral muscular dystrophy phenotypes

38. Cell environment shapes TDP-43 function with implications in neuronal and muscle disease

39. Antisense Morpholino-Based In Vitro Correction of a Pseudoexon-Generating Variant in the SGCB Gene

43. Redefining phenotypes associated with mitochondrial DNA single deletion

48. Genetic defects are common in myopathies with tubular aggregates

49. Safety and efficacy of avalglucosidase alfa versus alglucosidase alfa in patients with late-onset Pompe disease (COMET): a phase 3, randomised, multicentre trial

50. Polymorphism in exercise genes and respiratory function in late-onset Pompe disease

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