Search Results - "Piane, E"

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  1. 1

    Limited chronic focal encephalitis : Another variant of Rasmussen syndrome? by GAMBARDELLA, A, ANDERMANN, F, SHORVON, S, LE PIANE, E, AGUGLIA, U

    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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    MRI evidence of mesial temporal sclerosis in sporadic benign temporal lobe epilepsy by LABATE, A, VENTURA, P, AGUGLIA, U, QUATTRONE, A, GAMBARDELLA, A, LE PIANE, E, COLOSIMO, E, LEGGIO, U, AMBROSIO, R, CONDINO, F, MESSINA, D, LANZA, P

    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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    Posterior Reversible Encephalopathy Syndrome in late postpartum eclampsia by Pezzi, M, Le Piane, E, Giglio, A M, Pagnotta, L, Scozzafava, A, Tortorella, V, Sergi, A, Verre, M

    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. 5

    Chorea induced by non-ketotic hyperglycaemia: a case report by Branca, D, Gervasio, O, Le Piane, E, Russo, C, Aguglia, U

    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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    Suggestive evidence for linkage to chromosome 13qter for autosomal dominant type 1 porencephaly by AGUGLIA, U, GAMBARDELLA, A, BREEDVELD, G. J, OLIVERI, R. L, LE PIANE, E, MESSINA, D, QUATTRONE, A, HEUTINK, P

    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. 7

    Silent Celiac Disease in Patients with Childhood Localization‐Related Epilepsies by Labate, A., Gambardella, A., Messina, D., Tammaro, S., Le Piane, E., Pirritano, D., Cosco, C., Doldo, P., Mazzei, R., Oliveri, R. L., Bosco, D., Zappia, M., Valentino, P., Aguglia, U., Quattrone, A.

    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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  8. 8

    The Problematic Issue of Kufs Disease Diagnosis as Performed on Rectal Biopsies: A Case Report by Pasquinelli, G., Cenacchi, G., Piane, E. Le, Russo, C., Aguglia, U.

    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. 9

    Idiopathic generalized epilepsies with versive or circling seizures by Aguglia, U., Gambardella, A., Piane, E. Le, Messina, D., Russo, C., Oliveri, R. L., Zappia, M., Quattrone, A.

    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. 10

    Interhemispheric threshold differences in idiopathic generalized epilepsies with versive or circling seizures determined with focal magnetic transcranial stimulation by Aguglia, U., Gambardella, A., Quartarone, A., Girlanda, P., Le Piane, E., Messina, D., Oliveri, R.L., Zappia, M., Quattrone, A.

    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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    Emotion‐Induced Myoclonic Absence‐Like Seizures in a Patient with Inv‐Dup(15) Syndrome: A Clinical, EEG, and Molecular Genetic Study by Aguglia, Umberto, Piane, Emilio, Gambardella, Antonio, Messina, Demetrio, Russo, Concetta, Sirchia, Silvia Maria, Porta, Giovanni, Quattrone, Aldo

    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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    Risk factors for unprovoked epileptic seizures in multiple sclerosis: a systematic review and meta-analysis by Gasparini, Sara, Ferlazzo, Edoardo, Ascoli, Michele, Sueri, Chiara, Cianci, Vittoria, Russo, Concetta, Pisani, Laura Rosa, Striano, Pasquale, Elia, Maurizio, Beghi, Ettore, Colica, Carmela, Aguglia, Umberto

    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. 13

    Chlorpromazine versus sleep deprivation in activation of EEG in adult-onset partial epilepsy by AGUGLIA, U, GAMBARDELLA, A, LE PIANE, E, DE SARRO, G. B, ZAPPIA, M, QUATTRONE, A

    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. 14

    Disappearance of periodic sharp wave complexes in Creutzfeldt-Jakob disease by Aguglia, U, Gambardella, A, Le Piane, E, Messina, D, Farnarier, G, Oliveri, RL, Zappia, M, Quattrone, A

    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. 15

    Spontaneous remission of childhood epilepsy in two patients with focal extraopercular cortical dysplasia by Gambardella, Antonio, Le Piane, Emilio, Oliveri, R. Luciano, Zappia, Mario, Pardatscher, Kurth, Quattrone, Aldo, Aguglia, Umberto

    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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    Familial temporal lobe epilepsy: Autosomal dominant inheritance in a large pedigree from Southern Italy by Gambardella, Antonio, Messina, Demetrio, Le Piane, Emilio, Oliveri, R.Luciano, Annesi, Grazia, Zappia, Mario, Andermann, Eva, Quattrone, Aldo, Aguglia, Umberto

    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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    The Problematic Issue of Kufs Disease Diagnosis as Performed on Rectal Biopsies: A Case Report by Pasquinelli, G., Cenacchi, G., Piane, E. Le, Russo, C., Aguglia, U.

    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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    Journal Article
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    Mild non-lesional temporal lobe epilepsy. A common, unrecognized disorder with onset in adulthood by Aguglia, U, Gambardella, A, Le Piane, E, Messina, D, Oliveri, R L, Russo, C, Zappia, M, Quattrone, A

    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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