Valentina Marchiani
Bologna, Italy
Last Updated: 09/26/2026
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Found 8 publications
Diverse faces of GNAO1: mild forms in epilepsy and autism.
Journal: Journal of neurology
Published: March 30, 2024
Focal nonconvulsive status epilepticus in children: clinical and electroencephalographic features in 38 patients.
Journal: Epilepsy & behavior : E&B
Published: November 30, 2020
Red Flags for early referral of people with symptoms suggestive of narcolepsy: a report from a national multidisciplinary panel.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: August 11, 2018
Pyridoxine-dependent epilepsies: an observational study on clinical, diagnostic, therapeutic and prognostic features in a pediatric cohort.
Journal: Metabolic brain disease
Published: October 01, 2017
Cytogenetic and molecular characterization of a recombinant X chromosome in a family with a severe neurologic phenotype and macular degeneration.
Journal: Molecular cytogenetics
Published: May 11, 2015
A mutation in PAK3 with a dual molecular effect deregulates the RAS/MAPK pathway and drives an X-linked syndromic phenotype.
Journal: Human molecular genetics
Published: February 22, 2014
Case report of pyruvate dehydrogenase deficiency with unusual increase of fats during ketogenic diet treatment.
Journal: Journal of child neurology
Published: March 02, 2012
Showing 1-8 of 8
Last Updated: 09/26/2026