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You searched for: Author/Creator Cocozza, S.

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2. The complex phenotype of spinocerebellar ataxia type 48 in eight unrelated Italian families. (1st November 2019)

3. Diffuse brain connectivity changes in Charcot–Marie–Tooth type 1a patients: a resting‐state functional magnetic resonance imaging study. (20th October 2020)

4. Identification of C12orf4 as a gene for autosomal recessive intellectual disability. Issue 1 (12th July 2016)

5. Grey:white matter ratio at diagnosis and the risk of 10‐year multiple sclerosis progression. (1st November 2016)