Claudio Zucca
IRCCS Eugenio Medea(IT)
Publications by Year
Research Areas
Epilepsy research and treatment, Genetics and Neurodevelopmental Disorders, Pharmacological Effects and Toxicity Studies, EEG and Brain-Computer Interfaces, Functional Brain Connectivity Studies
Most-Cited Works
- → De novo mutations in ATP1A3 cause alternating hemiplegia of childhood(2012)418 cited
- → Molecular Mechanisms Generating and Stabilizing Terminal 22q13 Deletions in 44 Subjects with Phelan/McDermid Syndrome(2011)229 cited
- → Familial perisylvian polymicrogyria: A new familial syndrome of cortical maldevelopment(2000)159 cited
- → A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation(2004)152 cited
- → A novel mutation in the ATP1A2 gene causes alternating hemiplegia of childhood(2004)128 cited
- → Genotype–phenotype relationship in three cases with overlapping 19p13.12 microdeletions(2010)123 cited