Ignazio G. Arena
Messina, Italy
Last Updated: 09/26/2026
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Found 9 publications
Non-invasive biomarkers for diagnosis and monitoring of primary mitochondrial diseases.
Journal: Journal of neurology
Published: February 08, 2026
Myopathy and ataxia related to impaired mitochondrial function in mevalonate kinase deficiency.
Journal: Orphanet journal of rare diseases
Published: February 28, 2025
Management of presymptomatic juvenile patients with late-onset Pompe disease (LOPD).
Journal: Neuromuscular disorders : NMD
Published: September 30, 2024
Pseudodominance in RFC1-Spectrum Disorder.
Journal: Cerebellum (London, England)
Published: August 14, 2024
Primary mitochondrial myopathy: 12-month follow-up results of an Italian cohort.
Journal: Journal of neurology
Published: June 08, 2022
Case Report: Rare Homozygous RNASEH1 Mutations Associated With Adult-Onset Mitochondrial Encephalomyopathy and Multiple Mitochondrial DNA Deletions.
Journal: Frontiers in genetics
Published: March 28, 2022
Molecular Genetics Overview of Primary Mitochondrial Myopathies.
Journal: Journal of clinical medicine
Published: December 08, 2021
Pediatric adverse reactions to antiseizure medications - An analysis of data from the Italian spontaneous reporting system (2001-2019).
Journal: Epilepsy & behavior : E&B
Published: February 04, 2021
Showing 1-9 of 9
Last Updated: 09/26/2026