Giovanni Provenzano

Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern Italy.

Compound heterozygosity in DJ-1 gene non-coding portion related to parkinsonism.

Novel human pathological mutations. Gene symbol: SCN1A. Disease: severe myoclonic epilepsy of infancy.

Electroclinical characterization of epileptic seizures in leucine-rich, glioma-inactivated 1-deficient mice.

Lack of association between G-protein coupled receptor kinase 5 gene and Parkinson's disease.

Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson's disease in southern Italy.

Mutation analysis of the PINK1 gene in Southern Italian patients with early- and late-onset parkinsonism.

The role of GABAergic system in neurodevelopmental disorders: a focus on autism and epilepsy.

Mutant mouse models of autism spectrum disorders.

Kainic acid-induced seizures modulate Akt (SER473) phosphorylation in the hippocampus of dopamine D2 receptor knockout mice.

Loss of GABAergic neurons in the hippocampus and cerebral cortex of Engrailed-2 null mutant mice: implications for autism spectrum disorders.

Transcriptome profiling in engrailed-2 mutant mice reveals common molecular pathways associated with autism spectrum disorders.

GH Dysfunction in Engrailed-2 Knockout Mice, a Model for Autism Spectrum Disorders.

Hippocampal dysregulation of neurofibromin-dependent pathways is associated with impaired spatial learning in engrailed 2 knock-out mice.