Publications
Filters: First Letter Of Title is M [Clear All Filters]
Myoclonic absence-like seizures and chromosome abnormality syndromes.,
, Epilepsia, 1998 Jun, Volume 39, Issue 6, p.660-3, (1998)
Abstract
Mutations of protocadherin 19 in female epilepsy (PCDH19-FE) lead to allopregnanolone deficiency.,
, Human molecular genetics, 2015 Jun 29, (2015)
Abstract
Mitochondrial respiratory chain defects in skin fibroblasts from patients with Dravet syndrome.,
, Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2015 Jul 14, (2015)