Corrado I. Angelini

Padova, Italy

Last Updated: 09/26/2026

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Found 213 publications

Hereditary spastic paraplegia: from decades of therapy to future innovations.

Hereditary spastic paraplegia: from decades of therapy to future innovations.

Journal: Therapeutic advances in neurological disorders

Published: August 01, 2025

Health-Related Quality-of-Life Outcomes in Patients with Recessive and Dominant LGMD: A Comparative Cross-Sectional Study.

Health-Related Quality-of-Life Outcomes in Patients with Recessive and Dominant LGMD: A Comparative Cross-Sectional Study.

Journal: Muscles (Basel, Switzerland)

Published: June 27, 2025

Case Report: Pathogenic PNPLA2 variants and nonsense-mediated mRNA decay result in an early-onset neutral lipid storage disease with myopathy.

Case Report: Pathogenic PNPLA2 variants and nonsense-mediated mRNA decay result in an early-onset neutral lipid storage disease with myopathy.

Journal: Frontiers in genetics

Published: June 06, 2025

EAN 2024 Guideline on the Diagnostic Approach to Oligo/Asymptomatic HyperCKemia.

EAN 2024 Guideline on the Diagnostic Approach to Oligo/Asymptomatic HyperCKemia.

Journal: European journal of neurology

Published: April 17, 2025

Treatabolome for finely targeting muscle pathology in LGMD.

Treatabolome for finely targeting muscle pathology in LGMD.

Journal: Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology

Published: February 07, 2025

What Are the Normal Serum Creatine Kinase Values for Skeletal Muscle? A Worldwide Systematic Review.

What Are the Normal Serum Creatine Kinase Values for Skeletal Muscle? A Worldwide Systematic Review.

Journal: European journal of neurology

Published: February 04, 2025

Disease spectrum and long-term prognosis of patients with BAG3-associated neuromuscular diseases in Europe.

Disease spectrum and long-term prognosis of patients with BAG3-associated neuromuscular diseases in Europe.

Journal: Brain : a journal of neurology

Published: January 27, 2025

Clinical, Histopathologic, and Genetic Features of Patients With Myofibrillary and Distal Myopathies: Experience From the Italian Network.

Clinical, Histopathologic, and Genetic Features of Patients With Myofibrillary and Distal Myopathies: Experience From the Italian Network.

Journal: Neurology

Published: August 05, 2024

Editorial: Sleep disorders in neuromuscular diseases: treatable conditions: the evolving scenario of sleep in neuromuscular disorders.

Editorial: Sleep disorders in neuromuscular diseases: treatable conditions: the evolving scenario of sleep in neuromuscular disorders.

Journal: Frontiers in neurology

Published: June 13, 2024

E-Health & Innovation to Overcome Barriers in Neuromuscular Diseases. Report from the 3rd eNMD Congress: Pisa, Italy, 29-30 October 2021: Remote Monitoring: New Solutions for New Avenues in Neuromuscular Disorders.

E-Health & Innovation to Overcome Barriers in Neuromuscular Diseases. Report from the 3rd eNMD Congress: Pisa, Italy, 29-30 October 2021: Remote Monitoring: New Solutions for New Avenues in Neuromuscular Disorders.

Journal: Journal of neuromuscular diseases

Published: May 10, 2024

The Multifaceted Cause of Lipid Storage Myopathies, Genetics, and Treatment.

The Multifaceted Cause of Lipid Storage Myopathies, Genetics, and Treatment.

Journal: Frontiers in bioscience (Scholar edition)

Published: March 21, 2024

Editorial: Development of the precision diagnostics and treatment for duchenne/becker muscular dystrophy.

Editorial: Development of the precision diagnostics and treatment for duchenne/becker muscular dystrophy.

Journal: Frontiers in neurology

Published: March 06, 2024

Showing 1-12 of 213

Last Updated: 09/26/2026