Elia Pancheri
Verona, Italy
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 16 publications
Immune-mediated necrotizing myopathies: clinico-serological features and treatment outcomes of a large Italian cohort of patients.
Journal: Journal of neurology
Published: May 04, 2026
A novel in-frame deletion in MYOT causes an early adult onset distal myopathy.
Journal: Clinical genetics
Published: May 30, 2023
Ryanodine receptor 1 (RYR1) mutations in two patients with tubular aggregate myopathy.
Journal: The European journal of neuroscience
Published: December 24, 2021
Movement Disorders in Children with a Mitochondrial Disease: A Cross-Sectional Survey from the Nationwide Italian Collaborative Network of Mitochondrial Diseases.
Journal: Journal of clinical medicine
Published: March 27, 2021
Whole-exome sequencing in patients with protein aggregate myopathies reveals causative mutations associated with novel atypical phenotypes.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: May 04, 2020
Acetylcholine Receptor-Antibody-Positive Myasthenia Gravis Presenting with Early Atrophy and Nonfluctuating Weakness of Proximal Limb Muscles.
Journal: Journal of clinical neurology (Seoul, Korea)
Published: April 22, 2020
Amyloid myopathy: an intriguing diagnosis.
Journal: Clinical neurology and neurosurgery
Published: January 15, 2020
Mitochondrial epilepsy: a cross-sectional nationwide Italian survey.
Journal: Neurogenetics
Published: September 09, 2019
Multiple acyl-COA dehydrogenase deficiency in elderly carriers.
Journal: Journal of neurology
Published: July 26, 2019
A novel emerin gene mutation in Emery Dreifuss muscular dystrophy patient with spontaneous chordae tendinae rupture.
Journal: Clinical neurology and neurosurgery
Published: June 24, 2019
Last Updated: 09/26/2026