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Results: 1-8 |
Results: 8
Absence of sleep EEG markers in fatal familial insomnia healthy carriers: a spectral analysis study
Authors: Ferrillo, F Plazzi, G Nobili, L Beelke, M De Carli, F Cortelli, P Tinuper, P Avoni, P Vandi, S Gambetti, P Lugaresi, E Montagna, P
Citation: F. Ferrillo et al., Absence of sleep EEG markers in fatal familial insomnia healthy carriers: a spectral analysis study, CLIN NEU, 112(10), 2001, pp. 1888-1892
Efficacy of lamotrigine add-on therapy in severe partial epilepsy in adults with drop seizures and secondary bilateral synchrony on EEG
Authors: Bisulli, F Baruzzi, A Rosati, A Riva, R Avoni, P Cerullo, A Tinuper, P
Citation: F. Bisulli et al., Efficacy of lamotrigine add-on therapy in severe partial epilepsy in adults with drop seizures and secondary bilateral synchrony on EEG, EPILEPT DIS, 3(3), 2001, pp. 151-156
Levodopa therapy monitoring in patients with Parkinson disease: a kinetic-dynamic approach
Authors: Contin, M Riva, R Martinelli, P Albani, F Avoni, P Baruzzi, A
Citation: M. Contin et al., Levodopa therapy monitoring in patients with Parkinson disease: a kinetic-dynamic approach, THER DRUG M, 23(6), 2001, pp. 621-629
Familial continuous motor unit activity and epilepsy
Authors: Liguori, R Avoni, P Baruzzi, A Di Stasi, V Montagna, P
Citation: R. Liguori et al., Familial continuous motor unit activity and epilepsy, MUSCLE NERV, 24(5), 2001, pp. 630-633
Dysgeusia in epileptic patients treated with lamotrigine: Report of three cases
Authors: Avoni, P Contin, M Riva, R Albani, F Liguori, R Baruzzi, A
Citation: P. Avoni et al., Dysgeusia in epileptic patients treated with lamotrigine: Report of three cases, NEUROLOGY, 57(8), 2001, pp. 1521-1521
Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability
Authors: Eunson, LH Rea, R Zuberi, SM Youroukos, S Panayiotopoulos, CP Liguori, R Avoni, P McWilliam, RC Stephenson, JBP Hanna, MG Kullmann, DM Spauschus, A
Citation: Lh. Eunson et al., Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability, ANN NEUROL, 48(4), 2000, pp. 647-656
Congenital encephalomyopathy with epilepsy, chorioretinitis, basal gangliainvolvement, and muscle minicores
Authors: Avoni, P Monari, L Carelli, V Carcangiu, R Barboni, P Donati, C Badiali, L Baruzzi, A Montagna, P
Citation: P. Avoni et al., Congenital encephalomyopathy with epilepsy, chorioretinitis, basal gangliainvolvement, and muscle minicores, ANN NEUROL, 47(3), 2000, pp. 395-399
Acquired neuromyotonia after bone marrow transplantation
Authors: Liguori, R Vincent, A Avoni, P Valentino, ML D'Alessandro, R Zaccaria, A Bandini, G Montagna, P
Citation: R. Liguori et al., Acquired neuromyotonia after bone marrow transplantation, NEUROLOGY, 54(6), 2000, pp. 1390-1391
Risultati: 1-8 |