Marcello Villanova
Bologna, Italy
Last Updated: 09/26/2026
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Found 10 publications
Reducing Body Myopathy in Female Patients With FHL1 Variants Showing Rapid and Severe Evolution Mimicking Inflammatory Myopathy: A Case Series.
Journal: Neurology. Genetics
Published: October 10, 2025
Clinical and functional characterization of a long survivor congenital titinopathy patient with a novel metatranscript-only titin variant.
Journal: Acta neuropathologica communications
Published: February 06, 2023
Respiratory muscle involvement in HNRNPDL LGMD D3 muscular dystrophy: an extensive clinical description of the first Italian patient.
Journal: Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology
Published: May 18, 2020
A new congenital multicore titinopathy associated with fast myosin heavy chain deficiency.
Journal: Annals of clinical and translational neurology
Published: December 10, 2019
Airway clearance techniques in neuromuscular disorders: A state of the art review.
Journal: Respiratory medicine
Published: November 15, 2017
New Survival Target for Duchenne Muscular Dystrophy.
Journal: American journal of physical medicine & rehabilitation
Published: January 19, 2017
Allogeneic mesenchymal stem cell therapy outcomes for three patients with spinal muscular atrophy type 1.
Journal: American journal of physical medicine & rehabilitation
Published: April 18, 2015
Prevalence of congenital muscular dystrophy in Italy: a population study.
Journal: Neurology
Published: February 06, 2015
Duchenne muscular dystrophy: life prolongation by noninvasive ventilatory support.
Journal: American journal of physical medicine & rehabilitation
Published: April 19, 2014
Duchenne muscular dystrophy and epilepsy.
Journal: Neuromuscular disorders : NMD
Published: August 28, 2012
Showing 1-10 of 10
Last Updated: 09/26/2026