Publications
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Early and effective treatment of KCNQ2 encephalopathy.,
, Epilepsia, 2015 May, Volume 56, Issue 5, p.685-91, (2015)
Abstract
Mutations of protocadherin 19 in female epilepsy (PCDH19-FE) lead to allopregnanolone deficiency.,
, Human molecular genetics, 2015 Jun 29, (2015)
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)
Bilateral periventricular nodular heterotopia with mental retardation and syndactyly in boys: a new X-linked mental retardation syndrome.,
, Neurology, 1997 Oct, Volume 49, Issue 4, p.1042-7, (1997)
Abstract
Early-onset benign occipital seizure susceptibility syndrome.,
, Epilepsia, 1997 Mar, Volume 38, Issue 3, p.285-93, (1997)
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
Epileptic negative myoclonus.,
, Neurology, 1993 Jun, Volume 43, Issue 6, p.1078-83, (1993)
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