Publications
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Mutations of protocadherin 19 in female epilepsy (PCDH19-FE) lead to allopregnanolone deficiency.,
, Human molecular genetics, 2015 Jun 29, (2015)
Abstract
Ketamine in refractory convulsive status epilepticus in children avoids endotracheal intubation.,
, Epilepsy & behavior : E&B, 2015 Jul 16, (2015)
Abstract
Angelman syndrome: correlations between epilepsy phenotypes and genotypes.,
, Annals of neurology, 1998 Apr, Volume 43, Issue 4, p.485-93, (1998)
Abstract
Early-onset benign occipital seizure susceptibility syndrome.,
, Epilepsia, 1997 Mar, Volume 38, Issue 3, p.285-93, (1997)
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
Early clinical and EEG features of infantile spasms in Down syndrome.,
, Epilepsia, 1996 Oct, Volume 37, Issue 10, p.977-82, (1996)
Abstract
Cortical myoclonus in Angelman syndrome.,
, Annals of neurology, 1996 Jul, Volume 40, Issue 1, p.39-48, (1996)
Abstract
X-linked malformations of neuronal migration.,
, Neurology, 1996 Aug, Volume 47, Issue 2, p.331-9, (1996)
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
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
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
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