7 results on '"Scuderi, C."'
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2. POMT1 and POMT2 mutations in CMD patients: A multicentric Italian study
3. DUCHENNE MUSCULAR DYSTROPHY - GENETICS: P.213The DMD Italian network: reporting 2127 genetic diagnoses of referred dystrophinopathies, reflections and impact on care and personalized therapies
4. C.P.3.02 Expanding the clinical spectrum of POMT1 and POMT2 phenotype: A multicentric study in the Italian population
5. M.P.1.11 Homoplasmic point mutations in mitochondrial tRNA genes in patients with encephalomyopathy
6. M.P.1.05 The COII/tRNALys intergenic 9-bp deletion in mtDNA: A new possible cause of sensorineural hearing loss?
7. 6522 POSTER EGFR mutations and response to TKIs therapy in NSCLC patients pre-treated with chemotherapy.
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