Publications by authors named "Valerio Melas"

Purpose: To study for the first time the incidence of adult-onset CNS tumors in Southern Sardinia, Italy.

Methods: Clinical records of patients > 18 years old who were diagnosed with primary CNS tumors during 2016-2019 in the study area were reviewed. Meningiomas, cranial/paraspinal nerve tumors, lymphomas, and pituitary tumors were excluded.

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C9orf72 mutation (C9) is a common genetic cause of frontotemporal dementia and amyotrophic lateral sclerosis. C9 clinical phenotype is heterogeneous and epilepsy has been recently described in few cases. We report a 47-year-old patient who developed reflex reading epilepsy (RRE) at the age of 19.

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