I. Candiano

A Novel Exon 1 Mutation in a Patient with Atypical Lafora Progressive Myoclonus Epilepsy Seen as Childhood‐onset Cognitive Deficit

A. Quattrone, A. Gambardella, M. Zappia, 2004, Epilepsia.

NACP-REP1 polymorphism is not involved in Parkinson's disease: a case-control study in a population sample from southern Italy

A. Quattrone, P. Spadafora, G. Nicoletti, 2003, Neuroscience Letters.

Further evidence of genetic heterogeneity in families with autosomal dominant nocturnal frontal lobe epilepsy

A. Quattrone, A. Gambardella, A. Labate, 2007, Epilepsy Research.

Chronic bilateral subthalamic deep brain stimulation in a patient with homozygous deletion in the Parkin gene

M. Scerrati, L. Passamonti, L. Provinciali, 2004, Movement disorders : official journal of the Movement Disorder Society.

Myocardial 123metaiodobenzylguanidine uptake in genetic Parkinson's disease

G. Savettieri, M. D’Amelio, A. Quattrone, 2008, Movement disorders : official journal of the Movement Disorder Society.

FRAXE intermediate alleles are associated with Parkinson’s disease

A. Quattrone, G. Arabia, M. Zappia, 2004, Neuroscience Letters.

Lack of association between ubiquitin carboxy-terminal hydrolase L1 gene polymorphism and PD

G. Savettieri, A. Quattrone, G. Nicoletti, 2001, Neurology.