• Disturbances of cortical development
• Ependymal abnormalities in lissencephaly/pachygyria
• Epileptogenic brain malformations: clinical presentation, malformative patterns and indications for genetic testing
• Epileptogenic brain malformations: clinical presentation, malformative patterns and indications for genetic testing
• Interrelationship of genetics and prenatal injury in the genesis of malformations of cortical development
• Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats
• Lissencephaly in an epilepsy cohort: Molecular, radiological and clinical aspects
• Microdeletions of chromosome 17p13 as a cause of isolated lissencephaly
• Neuropathological aspects of infantile spasms
• Role of cytoskeletal abnormalities in the neuropathology and pathophysiology of type I lissencephaly