FERNANDO SCAGLIA to Neuromuscular Diseases
This is a "connection" page, showing publications FERNANDO SCAGLIA has written about Neuromuscular Diseases.
Connection Strength
0.570
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Early-onset severe neuromuscular phenotype associated with compound heterozygosity for OPA1 mutations. Mol Genet Metab. 2011 Aug; 103(4):383-7.
Score: 0.349
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Clinical spectrum, morbidity, and mortality in 113 pediatric patients with mitochondrial disease. Pediatrics. 2004 Oct; 114(4):925-31.
Score: 0.221