Publications
Early clinical and EEG features of infantile spasms in Down syndrome.,
, Epilepsia, 1996 Oct, Volume 37, Issue 10, p.977-82, (1996)
Abstract
Early Diagnosis and Monitoring of Neurodegenerative Langerhans Cell Histiocytosis.,
, PloS one, 2015, Volume 10, Issue 7, p.e0131635, (2015)
Abstract
Early-onset benign occipital seizure susceptibility syndrome.,
, Epilepsia, 1997 Mar, Volume 38, Issue 3, p.285-93, (1997)
Abstract
Effect of alcohol on action myoclonus in Lance-Adams syndrome and progressive myoclonus epilepsy.,
, Movement disorders : official journal of the Movement Disorder Society, 1992, Volume 7, Issue 1, p.92, (1992)
Effect of delta-opioid receptor agonist deltorphin on circulating concentrations of luteinizing hormone and follicle stimulating hormone in healthy fertile women.,
, Human reproduction (Oxford, England), 1998 May, Volume 13, Issue 5, p.1159-62, (1998)
Abstract
Epilepsy and focal gyral anomalies detected by MRI: electroclinico-morphological correlations and follow-up.,
, Developmental medicine and child neurology, 1992 Aug, Volume 34, Issue 8, p.706-18, (1992)
Abstract
Epilepsy, antiepileptic drugs, and malformations in children of women with epilepsy: a French prospective cohort study.,
, Neurology, 1992 Apr, Volume 42, Issue 4 Suppl 5, p.75-82, (1992)
Abstract
Epileptic negative myoclonus.,
, Neurology, 1993 Jun, Volume 43, Issue 6, p.1078-83, (1993)
Abstract
The epileptic spectrum in the congenital bilateral perisylvian syndrome. CBPS Multicenter Collaborative Study.,
, Neurology, 1994 Mar, Volume 44, Issue 3 Pt 1, p.379-85, (1994)
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
Human doublecortin (DCX) and the homologous gene in mouse encode a putative Ca2+-dependent signaling protein which is mutated in human X-linked neuronal migration defects.,
, Human molecular genetics, 1998 Aug, Volume 7, Issue 8, p.1327-32, (1998)
Abstract
Identification and characterization of three calmodulin binding sites of the skeletal muscle ryanodine receptor.,
, Biochemistry, 1994 Aug 9, Volume 33, Issue 31, p.9078-84, (1994)
Abstract
Identification of a duplication of Xq28 associated with bilateral periventricular nodular heterotopia.,
, American journal of human genetics, 1997 Aug, Volume 61, Issue 2, p.379-87, (1997)
Abstract
Idiopathic photosensitive occipital lobe epilepsy.,
, Epilepsia, 1995 Sep, Volume 36, Issue 9, p.883-91, (1995)
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)
Infantile spasms: an early epileptic manifestation in some patients with the congenital bilateral perisylvian syndrome.,
, Journal of child neurology, 1994 Oct, Volume 9, Issue 4, p.420-3, (1994)
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
Ketamine in refractory convulsive status epilepticus in children avoids endotracheal intubation.,
, Epilepsy & behavior : E&B, 2015 Jul 16, (2015)
Abstract
Lamotrigine and seizure aggravation in severe myoclonic epilepsy.,
, Epilepsia, 1998 May, Volume 39, Issue 5, p.508-12, (1998)
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