Original articles
- 
																							
	
	
Congenital myopathy associated with a novel mutation in MEGF10 gene, myofibrillar alteration and progressive course
 - 
																							
	
	
Peripheral circulation disturbances in two consecutive children with spinal muscular atrophy and literature review
 - 
																							
	
	
The role of BAG3 in dilated cardiomyopathy and its association with Charcot-Marie-Tooth disease type 2
 - 
																							
	
	
Impact of the COVID-19 pandemic on neuromuscular rehabilitation setting. Part 2: patients and families’ views on the received health care during the pandemic
 - 
																							
	
	
Muscle quantitative MRI in adult SMA patients on nusinersen treatment: a longitudinal study
 - 
																							
	
	
Cardiac disorders worsen the final outcome in myasthenic crisis undergoing non-invasive mechanical ventilation: a retrospective 20-year study from a single center
 - 
																							
	
	
Experience with telemedicine in neuromuscular clinic during COVID-19 pandemic
 - 
																							
	
	
Frailties and critical issues in neuromuscular diseases highlighted by SARS-CoV-2 pandemic: how many patients are still “invisible”?
 - 
																							
	
	
Ambulatory Duchenne muscular dystrophy children: cross-sectional correlation between function, quantitative muscle ultrasound and MRI
 - 
																							
	
	
Xp21 contiguous gene deletion syndrome presenting as Duchenne muscular dystrophy and glycerol kinase deficiency associated with intellectual disability: case report and review literature
 - 
																							
	
	
VCP-related myopathy: a case series and a review of literature
 - 
																							
	
	
Telemedicine applied to neuromuscular disorders: focus on the COVID-19 pandemic era
 
					Previous
				
			31-42 of 42