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You searched for: Author/Creator Pro, Stefano

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1. Hereditary spastic paraplegia is a novel phenotype for germline de novo ATP1A1 mutation. Issue 3 (5th December 2019)

3. A novel KCTD17 mutation is associated with childhood early-onset hyperkinetic movement disorder. (April 2019)

6. WE-112. High intellectual potential and high functioning autism: Clinical and neurophysiological features in a pediatric sample. (September 2022)

8. Acute strabismus in neurological emergencies of childhood: A retrospective, single-centre study. (May 2021)

10. Bilateral loss of cortical SEPs predict severe MRI lesions in neonatal hypoxic ischemic encephalopathy treated with hypothermia. Issue 1 (January 2018)