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2. Beyond spinal muscular atrophy with lower extremity dominance: cerebellar hypoplasia associated with a novel mutation in BICD2. (April 2016)

4. Early‐onset absence epilepsy: SLC2A1 gene analysis and treatment evolution. Issue 5 (30th September 2012)

5. Functional characterization of the c.462delA mutation in the NDUFS4 subunit gene of mitochondrial complex I. (11th September 2013)

6. MYH7-related myopathies: clinical, histopathological and imaging findings in a cohort of Italian patients. Issue 1 (December 2016)