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
Brainstem auditory evoked potentials in alternating hemiplegia: ictal vs interictal assessment in one case.,
, Clinical EEG (electroencephalography), 1990 Jan, Volume 21, Issue 1, p.51-4, (1990)
Abstract
Contractions in the second polyA tract of ARX are rare, non-pathogenic polymorphisms.,
, American journal of medical genetics. Part A, 2010 Dec 10, (2010)
Abstract
Double-blind placebo-controlled trial of flunarizine as add-on therapy in refractory childhood epilepsy.,
, Brain & development, 1991 Jul, Volume 13, Issue 4, p.217-22, (1991)
Abstract
Dysgraphia as a Mild Expression of Dystonia in Children with Absence Epilepsy.,
, PloS one, 2015, Volume 10, Issue 7, p.e0130883, (2015)
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 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
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
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
Occipitotemporal seizures with ictus emeticus induced by intermittent photic stimulation.,
, Neurology, 1994 Feb, Volume 44, Issue 2, p.253-9, (1994)
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
[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