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Détail de l'auteur
Auteur P. GIOVANARDI ROSSI |
Documents disponibles écrits par cet auteur (2)
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Migraine and benign epilepsy with Rolandic spikes in childhood: a case-control study / Margherita SANTUCCI in Developmental Medicine & Child Neurology, 27-1 (February 1985)
[article]
Titre : Migraine and benign epilepsy with Rolandic spikes in childhood: a case-control study Type de document : Texte imprimé et/ou numérique Auteurs : Margherita SANTUCCI, Auteur ; P. GIOVANARDI ROSSI, Auteur ; G. AMBROSETTO, Auteur ; T. SACQUEGNA, Auteur ; R. D'ALESSANDRO, Auteur Année de publication : 1985 Article en page(s) : p.60-62 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=586
in Developmental Medicine & Child Neurology > 27-1 (February 1985) . - p.60-62[article] Migraine and benign epilepsy with Rolandic spikes in childhood: a case-control study [Texte imprimé et/ou numérique] / Margherita SANTUCCI, Auteur ; P. GIOVANARDI ROSSI, Auteur ; G. AMBROSETTO, Auteur ; T. SACQUEGNA, Auteur ; R. D'ALESSANDRO, Auteur . - 1985 . - p.60-62.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 27-1 (February 1985) . - p.60-62
Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=586 Periodic spasms: an unclassified type of epileptic seizure in childhood / Giuseppe GOBBI in Developmental Medicine & Child Neurology, 29-6 (December 1987)
[article]
Titre : Periodic spasms: an unclassified type of epileptic seizure in childhood Type de document : Texte imprimé et/ou numérique Auteurs : Giuseppe GOBBI, Auteur ; P. GIOVANARDI ROSSI, Auteur ; Licia BRUNO, Auteur ; Antonella PINI, Auteur ; Carlo Alberto TASSINARI, Auteur Année de publication : 1987 Article en page(s) : p.766-775 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Seven boys aged between 14 months and 13 years with focal or multifocal partial epilepsy had very unusual seizures, characterized by series of periodic bilateral spasms. These consisted of a brief, complex movement of slight to severe intensity, mainly involving the axial muscles, with raising of the shoulders, adversion of the eyes and head, often with rictus-type facial grimaces and occasional stretching of the legs and emission of a guttural sound. The ictal EEG showed a pattern of periodic complexes, characterized by a slow wave with superimposed fast activity. This form of epileptic seizure is resistant to treatment and is found only in patients affected by a brain disease consisting of a fixed or progressive encephalopathy. These observations document the existence of a rare form of seizure or epileptic event, not yet included in the International Classification of epileptic seizures and clinically relevant because of its diagnostic and prognostic implications. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=631
in Developmental Medicine & Child Neurology > 29-6 (December 1987) . - p.766-775[article] Periodic spasms: an unclassified type of epileptic seizure in childhood [Texte imprimé et/ou numérique] / Giuseppe GOBBI, Auteur ; P. GIOVANARDI ROSSI, Auteur ; Licia BRUNO, Auteur ; Antonella PINI, Auteur ; Carlo Alberto TASSINARI, Auteur . - 1987 . - p.766-775.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 29-6 (December 1987) . - p.766-775
Index. décimale : PER Périodiques Résumé : Seven boys aged between 14 months and 13 years with focal or multifocal partial epilepsy had very unusual seizures, characterized by series of periodic bilateral spasms. These consisted of a brief, complex movement of slight to severe intensity, mainly involving the axial muscles, with raising of the shoulders, adversion of the eyes and head, often with rictus-type facial grimaces and occasional stretching of the legs and emission of a guttural sound. The ictal EEG showed a pattern of periodic complexes, characterized by a slow wave with superimposed fast activity. This form of epileptic seizure is resistant to treatment and is found only in patients affected by a brain disease consisting of a fixed or progressive encephalopathy. These observations document the existence of a rare form of seizure or epileptic event, not yet included in the International Classification of epileptic seizures and clinically relevant because of its diagnostic and prognostic implications. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=631