Search Results - "Piane, E"
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1
Limited chronic focal encephalitis : Another variant of Rasmussen syndrome?
Published in Neurology (29-01-2008)“…To describe a more limited and less malignant form of Rasmussen encephalitis (RE). Three subjects (all women; 37, 31, and 32 years of age) developed childhood…”
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2
MRI evidence of mesial temporal sclerosis in sporadic benign temporal lobe epilepsy
Published in Neurology (28-02-2006)“…To determine whether there is MRI-detectable mesial temporal sclerosis (MTS) in patients with sporadic benign temporal lobe epilepsy (BTLE). Brain MRIs were…”
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3
Clinical and epidemiological aspects of epilepsy in the elderly
Published in BMC geriatrics (19-05-2010)Get full text
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4
Posterior Reversible Encephalopathy Syndrome in late postpartum eclampsia
Published in Clinica terapeutica (01-01-2015)“…Posterior Reversible Encephalopathy Syndrome (PRES) is a neurological complication associated with several medical conditions and it has been described in…”
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5
Chorea induced by non-ketotic hyperglycaemia: a case report
Published in Neurological sciences (01-10-2005)“…We describe an 81-year-old woman presenting with sudden onset of generalised chorea. She was unaware of suffering from diabetes. Laboratory screening revealed…”
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6
Suggestive evidence for linkage to chromosome 13qter for autosomal dominant type 1 porencephaly
Published in Neurology (11-05-2004)“…A large three-generation family with autosomal dominant type 1 porencephaly from southern Italy was studied. A high rate of miscarriages was observed. Of the…”
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7
Silent Celiac Disease in Patients with Childhood Localization‐Related Epilepsies
Published in Epilepsia (Copenhagen) (01-09-2001)“…Purpose: To evaluate how many patients with a clinical picture of idiopathic childhood localization‐related epilepsies may also have silent celiac disease…”
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The Problematic Issue of Kufs Disease Diagnosis as Performed on Rectal Biopsies: A Case Report
Published in Ultrastructural pathology (2004)“…Kufs disease, the late-onset form of a group of neurodegenerative disorders, known as the neuronal ceroid-lipofuscinoses, is characterized by…”
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9
Idiopathic generalized epilepsies with versive or circling seizures
Published in Acta neurologica Scandinavica (01-04-1999)“…Objectives – To describe the electroclinical features of the idiopathic generalized epilepsies (IGEs) with versive or circling seizures. Methods – Sixteen…”
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10
Interhemispheric threshold differences in idiopathic generalized epilepsies with versive or circling seizures determined with focal magnetic transcranial stimulation
Published in Epilepsy research (01-06-2000)“…The interhemispheric difference of the motor-cortical threshold (IDMT) was studied with focal magnetic transcranial stimulation (TCS) in ten patients with…”
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11
Emotion‐Induced Myoclonic Absence‐Like Seizures in a Patient with Inv‐Dup(15) Syndrome: A Clinical, EEG, and Molecular Genetic Study
Published in Epilepsia (Copenhagen) (01-09-1999)“…We have described a clinical EEG and molecular genetic study of a 9‐year‐old boy with inv‐dup(15) syndrome in whom seizures were induced by emotionally…”
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12
Risk factors for unprovoked epileptic seizures in multiple sclerosis: a systematic review and meta-analysis
Published in Neurological sciences (01-03-2017)“…The role of different factors in influencing the risk of seizures during multiple sclerosis (MS) is not known. To perform a systematic review and meta-analysis…”
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13
Chlorpromazine versus sleep deprivation in activation of EEG in adult-onset partial epilepsy
Published in Journal of neurology (01-10-1994)“…We prospectively compared the activating effect of chlorpromazine (CHLP, 50 mg, i.m.) versus sleep deprivation (SD) in 41 patients with a clinical diagnosis of…”
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14
Disappearance of periodic sharp wave complexes in Creutzfeldt-Jakob disease
Published in Neurophysiologie clinique (01-09-1997)“…Periodic sharp wave complexes (PSWC) are sensitive and specific of Creutzfeldt-Jakob disease (CJD). Once they have emerged, PSWC may exceptionally disappear in…”
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15
Spontaneous remission of childhood epilepsy in two patients with focal extraopercular cortical dysplasia
Published in Brain & development (Tokyo. 1979) (01-09-1997)“…Childhood-onset partial epilepsy caused by focal cortical dysplastic lesions (FCDLs) is often severe. A few patients reported with a favorable outcome had a…”
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16
Ictal hemodynamic changes in late-onset rasmussen encephalitis
Published in Annals of neurology (01-02-2006)Get full text
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17
Familial temporal lobe epilepsy: Autosomal dominant inheritance in a large pedigree from Southern Italy
Published in Epilepsy research (01-02-2000)“…To further elucidate the inheritance pattern and range of phenotypic manifestations of benign familial temporal lobe epilepsy (FTLE), we report a large family…”
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18
Usefulness of latero-orbital electrodes in detecting interictal epileptiform activity – a study of 60 patients with complex partial seizures
Published in Electroencephalography and clinical neurophysiology (01-08-1998)“…Objectives: The use of latero-orbital (Lo) electrodes is a routine practice in any EEG laboratory to evaluate eye motion, but there are no data about their…”
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19
The Problematic Issue of Kufs Disease Diagnosis as Performed on Rectal Biopsies: A Case Report
Published in Ultrastructural pathology (2004)“…Kufs disease, the late-onset form of a group of neurodegenerative disorders, known as the neuronal ceroid-lipofuscinoses, is characterized by intraneuronal…”
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20
Mild non-lesional temporal lobe epilepsy. A common, unrecognized disorder with onset in adulthood
Published in Canadian journal of neurological sciences (01-11-1998)“…To compare mild vs. severe non-lesional temporal lobe epilepsy (TLE). Data from 104 consecutive patients with non-lesional TLE were reviewed. Seventy-three of…”
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