8 results on '"Gallano, Pia"'
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2. Distal myopathy due to digenic inheritance of TIA1 and SQSTM1 variants in two unrelated Spanish patients
3. A novel phenotype of AChR-deficiency syndrome with predominant facial and distal weakness resulting from the inclusion of an evolutionary alternatively-spliced exon in CHRNA1
4. Muscle imaging in muscle dystrophies produced by mutations in the EMD and LMNA genes
5. Phenotypic variability in a Spanish family with a Caveolin-3 mutation
6. A new homozygous missense variant in LMOD3 gene causing mild nemaline myopathy with prominent facial weakness
7. Evidence-Based Consensus and Systematic Review on Reducing the Time to Diagnosis of Duchenne Muscular Dystrophy
8. Dysferlinopathy masquerading as a refractory polymyositis
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