Publications
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Bilateral parasagittal parietooccipital polymicrogyria and epilepsy.,
, Annals of neurology, 1997 Jan, Volume 41, Issue 1, p.65-73, (1997)
Abstract
Congenital bilateral perisylvian syndrome: study of 31 patients. The CBPS Multicenter Collaborative Study.,
, Lancet (London, England), 1993 Mar 6, Volume 341, Issue 8845, p.608-12, (1993)
Abstract
Early and effective treatment of KCNQ2 encephalopathy.,
, Epilepsia, 2015 May, Volume 56, Issue 5, p.685-91, (2015)
Abstract
Early Diagnosis and Monitoring of Neurodegenerative Langerhans Cell Histiocytosis.,
, PloS one, 2015, Volume 10, Issue 7, p.e0131635, (2015)
Abstract
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
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
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
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
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
Myoclonic absence-like seizures and chromosome abnormality syndromes.,
, Epilepsia, 1998 Jun, Volume 39, Issue 6, p.660-3, (1998)
Abstract
Sequential occurrence of benign partial epilepsy and childhood absence epilepsy in three patients.,
, Brain & development, 1996 May-Jun, Volume 18, Issue 3, p.212-5, (1996)
Abstract
X-linked malformations of neuronal migration.,
, Neurology, 1996 Aug, Volume 47, Issue 2, p.331-9, (1996)
Abstract