Publications
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Angelman syndrome: correlations between epilepsy phenotypes and genotypes.,
, Annals of neurology, 1998 Apr, Volume 43, Issue 4, p.485-93, (1998)
Abstract
Band heterotopia: correlation of outcome with magnetic resonance imaging parameters.,
, Annals of neurology, 1994 Oct, Volume 36, Issue 4, p.609-17, (1994)
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Bilateral parasagittal parietooccipital polymicrogyria and epilepsy.,
, Annals of neurology, 1997 Jan, Volume 41, Issue 1, p.65-73, (1997)
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Bilateral periventricular nodular heterotopia with mental retardation and frontonasal malformation.,
, Neurology, 1998 Aug, Volume 51, Issue 2, p.499-503, (1998)
Abstract
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
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
Compulsive somatosensory self-stimulation inducing epileptic seizures.,
, Epilepsia, 1992 May-Jun, Volume 33, Issue 3, p.509-16, (1992)
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Continuous focal spikes during REM sleep in a case of acquired aphasia (Landau-Kleffner syndrome).,
, Sleep, 1992 Oct, Volume 15, Issue 5, p.454-60, (1992)
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Cortical myoclonus in Angelman syndrome.,
, Annals of neurology, 1996 Jul, Volume 40, Issue 1, p.39-48, (1996)
Abstract
Early clinical and EEG features of infantile spasms in Down syndrome.,
, Epilepsia, 1996 Oct, Volume 37, Issue 10, p.977-82, (1996)
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Early Diagnosis and Monitoring of Neurodegenerative Langerhans Cell Histiocytosis.,
, PloS one, 2015, Volume 10, Issue 7, p.e0131635, (2015)
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)
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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
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 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)
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