Publications
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[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
[Psychopathological risk in children with early onset of partial epilepsy].,
, Minerva pediatrica, 1995 May, Volume 47, Issue 5, p.193-7, (1995)
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
[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
Trisomy 12p syndrome: a chromosomal disorder associated with generalized 3-Hz spike and wave discharges.,
, Epilepsia, 1990 Sep-Oct, Volume 31, Issue 5, p.557-66, (1990)
Abstract
Reversible pseudoatrophy of the brain and mental deterioration associated with valproate treatment.,
, Epilepsia, 1998 Jan, Volume 39, Issue 1, p.27-32, (1998)
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
Periventricular nodular heterotopia in Smith-Magenis syndrome.,
, American journal of medical genetics. Part A, 2014 Dec, Volume 164A, Issue 12, p.3142-7, (2014)
Abstract
Paroxysmal tonic upgaze of childhood with ataxia: a benign transient dystonia with autosomal dominant inheritance.,
, Brain & development, 1998 Mar, Volume 20, Issue 2, p.116-8, (1998)
Abstract
Panic attacks mistaken for relapse of epilepsy.,
, Epilepsia, 1995 Jan, Volume 36, Issue 1, p.48-51, (1995)
Abstract
Occipitotemporal seizures with ictus emeticus induced by intermittent photic stimulation.,
, Neurology, 1994 Feb, Volume 44, Issue 2, p.253-9, (1994)
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
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
Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brain.,
, Human molecular genetics, 1997 Apr, Volume 6, Issue 4, p.555-62, (1997)
Abstract
Lamotrigine and seizure aggravation in severe myoclonic epilepsy.,
, Epilepsia, 1998 May, Volume 39, Issue 5, p.508-12, (1998)
Abstract
The influence of dosage, age, and comedication on steady state plasma lamotrigine concentrations in epileptic children: a prospective study with preliminary assessment of correlations with clinical response.,
, Therapeutic drug monitoring, 1997 Jun, Volume 19, Issue 3, p.252-60, (1997)
Abstract
Induction of partial seizures by visual stimulation. Clinical and electroencephalographic features and evoked potential studies.,
, Advances in neurology, 1998, Volume 75, p.159-78, (1998)
Idiopathic photosensitive occipital lobe epilepsy.,
, Epilepsia, 1995 Sep, Volume 36, Issue 9, p.883-91, (1995)
Abstract
Familial periventricular nodular heterotopia, epilepsy and Melnick-Needles Syndrome caused by a single FLNA mutation with combined gain-of-function and loss-of-function effects.,
, Journal of medical genetics, 2015 Jun, Volume 52, Issue 6, p.405-12, (2015)
Abstract