Search Results - "DI BARTOLO, R. M"

Occipital intermittent rhythmic delta activity only following eye closure in atypical CNS Salmonellosis by Buoni, S., Zannolli, R., Di Bartolo, R.M., Macucci, F., Migliorini, L., Sansoni, R., Cellesi, C.

“…A statement recently published on the base of a large retrospective analysis, report that the occipital intermittent rhythmic delta activity (OIRDA) “is…”
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Atypical BECTS and homocystinuria by BUONI, S, DI BARTOLO, R. M, MOLINELLI, M, PALMERI, S, ZANNOLLI, R

“…Reported is an association of atypical benign childhood epilepsy with centrotemporal spikes (BECTS) and homocystinuria in three apparently healthy children…”
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Efficacy and safety of topiramate in infants according to epilepsy syndromes by Grosso, S., Galimberti, D., Farnetani, M.A., Cioni, M., Mostardini, R., Vivarelli, R., Di Bartolo, R.M., Bernardoni, E., Berardi, R., Morgese, G., Balestri, P.

“…Studies of the efficacy of topiramate (TPM) in infants and young children are few. Here we report an open, prospective, and pragmatic study of effectiveness of…”
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Chromosome 18 aberrations and epilepsy: A review by Grosso, S., Pucci, L., Di Bartolo, R.M., Gobbi, G., Bartalini, G., Anichini, C., Scarinci, R., Balestri, M., Farnetani, M.A., Cioni, M., Morgese, G., Balestri, P.

“…Epilepsy is commonly observed in patients with chromosomal aberrations. We evaluated epilepsy and electroencephalographic (EEG) features in a group of patients…”
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Oxcarbazepine and atypical evolution of benign idiopathic focal epilepsy of childhood by Grosso, S., Balestri, M., Di Bartolo, R. M., Corbini, L., Vatti, G., Curatolo, P., Balestri, P.

“…Patients that have benign epilepsy with centrotemporal spikes (BECTS) may occasionally experience an atypical development in their course when treated with…”
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18q‐ syndrome and ectodermal dysplasia syndrome: Description of a child and his family by Zannolli, R., Pierluigi, M., Pucci, L., Lagrasta, N., Gasparre, O., Matera, M.R., Di Bartolo, R.M., Mazzei, M.A., Sacco, P., Miracco, C., de Santi, M.M., Aitiani, P., Cavani, S., Pellegrini, L., Fimiani, M., Alessandrini, C., Galluzzi, P., Livi, W., Gonnelli, S., Terrosi‐Vagnoli, P., Zappella, M., Morgese, G.

“…The 18q‐ syndrome [MIM #601808] is a terminal deletion of the long arm of chromosome 18. The most common deletion extends from region q21 to qter. We report…”
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Childhood Absence Epilepsy: Evolution and Prognostic Factors by Grosso, Salvatore, Galimberti, Daniela, Vezzosi, Piero, Farnetani, Mariangela, Di Bartolo, Rosanna Maria, Bazzotti, Simone, Morgese, Guido, Balestri, Paolo

“…Purpose: To evaluate how diagnostic criteria influence remission rates for patients with childhood absence epilepsy (CAE) and to assess clinical and EEG…”
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Segregation analysis in typical absence epilepsy by Buoni, S, Grosso, S, Di Cosmo, G, Di Bartolo, R M, Di Marco, V, Fois, A

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Cerebral glucose metabolism in neurofibromatosis type 1 assessed with [18F]-2-fluoro-2-deoxy-D-glucose and PET by Balestri, P, Lucignani, G, Fois, A, Magliani, L, Calistri, L, Grana, C, Di Bartolo, R M, Perani, D, Fazio, F

“…Cerebral PET with [18F]-2-fluoro-2-deoxy-D-glucose has been performed in four patients with neurofibromatosis type 1 (NF1) to assess the relation between…”
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Association of Chiari I malformation, mental retardation, speech delay, and epilepsy: a specific disorder? by Grosso, S, Scattolini, R, Paolo, G, Di Bartolo, R M, Morgese, G, Balestri, P

“…The Chiari I malformation is defined as tonsillar herniation of at least 3 to 5 mm below the foramen magnum. Although Chiari I malformation is considered to…”
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Cortical periventricular heterotopia with ectodermal dysplasia by Zannolli, R., Conversano, E., Serracca, L., Di Bartolo, R.M., Molinelli, M., Galluzzi, P., Mazzei, M.A., Terrosi-Vagnoli, P., Miracco, C., de Santi, M.M., Vatti, G., Coviello, G., Malandrini, A., Gonnelli, S., Alessandrini, C., Fimiani, M.

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Novel CNS syndrome and ectodermal dysplasia by Zannolli, R., Macucci, F., Di Bartolo, R.M., Serracca, L., Miracco, C., de Santi, M.M., Giannini, F., Malandrini, A., Galluzzi, P., De Robertis, S., Hadjistilianou, T., Perotti, R., Fimiani, M., Doldo, T., Giorgetti, R., Cavani, S., Pierluigi, M.

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Epilepsy, progressive cerebral calcifications, and coeliac disease by Fois, A, Balestri, P, Vascotto, M, Farnetani, M A, Di Bartolo, R M, Di Marco, V

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Vigabatrin treatment in children by FOIS, A, BUONI, S, DI BARTOLO, R. M, DI MARCO, V, MOSTARDINI, R

“…Sixty-nine children, aged from 2 months to 16 years and suffering from different types of drug-resistant epileptic seizures, mostly complex partial and…”
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Progressive cerebral calcifications, epilepsy, and celiac disease by Fois, A, Balestri, P, Vascotto, M, Farnetani, M A, Di Bartolo, R M, Di Marco, V, Vindigni, C

“…A case with progressive cerebral calcifications, white matter involvement, and drug-resistant epilepsy in a 9-year-old boy is described. The final diagnosis…”
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SHORT COMMUNICATION: Oxcarbazepine and atypical evolution of benign idiopathic focal epilepsy of childhood by Grosso, S, Balestri, M, Di Bartolo, RM, Corbini, L, Vatti, G, Curatolo, P, Balestri, P

“…Patients that have benign epilepsy with centrotemporal spikes (BECTS) may occasionally experience an atypical development in their course when treated with…”
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Typical absence seizures associated with localization-related epilepsy: A clinical and electroencephalographic characterization by Grosso, Salvatore, Galimberti, Daniela, Gobbi, Giuseppe, Farnetani, Mariangela, Di Bartolo, Rosanna Maria, Morgese, Guido, Balestri, Paolo

“…This paper describes the characteristics of patients with typical absence seizures associated with localization related epilepsy (LRE) and compares…”
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Electroencephalographic and Epileptic Patterns in X Chromosome Anomalies by Grosso, Salvatore, Farnetani, Mariangela A, Di Bartolo, Rosanna Maria, Berardi, Rosario, Pucci, Lucia, Mostardini, Rosa, Anichini, Cecilia, Bartalini, Gabriella, Galimberti, Daniela, Morgese, Guido, Balestri, Paolo

“…Although epilepsy and mental retardation are commonly observed in individuals with chromosomal aberrations, the identification of EEG/epileptic profiles in…”
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Celiac disease and epilepsy in pediatric patients by Fois, A, Vascotto, M, Di Bartolo, R M, Di Marco, V

“…Among 783 patients referred to our institute with different types of seizures as presenting symptom, systematic evaluation of antigliadin and antiendomysial…”
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Epilepsy and Electroencephalographic Findings in Pericentric Inversion of Chromosome 12 by Grosso, Salvatore, Pucci, Lucia, Farnetani, MariAngela, Di Bartolo, Rosanna Maria, Galimberti, Daniela, Mostardini, Rosa, Anichini, Cecilia, Balestri, Martina, Morgese, Guido, Balestri, Paolo

“…Epilepsy, together with mental retardation, represents a common manifestation of chromosomal aberrations. Specific electroencephalographic (EEG) and epileptic…”
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