Publications
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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)
Mutations of protocadherin 19 in female epilepsy (PCDH19-FE) lead to allopregnanolone deficiency.,
, Human molecular genetics, 2015 Jun 29, (2015)
Abstract
Neurological findings and seizure outcome in children with bilateral opercular macrogyric-like changes detected by MRI.,
, Developmental medicine and child neurology, 1992 Aug, Volume 34, Issue 8, p.694-705, (1992)
Abstract
Reflex seizures are frequent in patients with Down syndrome and epilepsy.,
, Epilepsia, 1990 Jul-Aug, Volume 31, Issue 4, p.406-17, (1990)
Abstract
X-linked malformations of neuronal migration.,
, Neurology, 1996 Aug, Volume 47, Issue 2, p.331-9, (1996)
Abstract
[Contribution of ambulatory EEG recording (Medilog 9000) in a population of epileptics].,
, Neurophysiologie clinique = Clinical neurophysiology, 1989 Jun, Volume 19, Issue 3, p.219-30, (1989)
Abstract
[Partial trisomy of the long arm of chromosome 6. A clinical case].,
, Minerva pediatrica, 1993 Dec, Volume 45, Issue 12, p.517-21, (1993)
Abstract
[The evolution of epilepsy in the most common genetic forms with mental retardation (Down's syndrome and the fragile X syndrome)].,
, La Pediatria medica e chirurgica : Medical and surgical pediatrics, 1993 May-Jun, Volume 15 Suppl 1, p.19-22, (1993)
Abstract