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Results: 1-9 |
Results: 9
Juvenile Huntington's disease presenting as progressive myoclonic epilepsy
Authors: Gambardella, A Muglia, M Labate, A Magariello, A Gabriele, AL Mazzei, R Pirritano, D Conforti, FL Patitucci, A Valentino, P Zappia, M Quattrone, A
Citation: A. Gambardella et al., Juvenile Huntington's disease presenting as progressive myoclonic epilepsy, NEUROLOGY, 57(4), 2001, pp. 708-711
Cerebral venous thrombosis and isolated intracranial hypertension without papilledema in CDH
Authors: Quattrone, A Bono, F Oliveri, RL Gambardella, A Pirritano, D Labate, A Lucisano, A Valentino, P Zappia, M Aguglia, U Lavano, A Fera, F Pardatscher, K
Citation: A. Quattrone et al., Cerebral venous thrombosis and isolated intracranial hypertension without papilledema in CDH, NEUROLOGY, 57(1), 2001, pp. 31-36
Clinical and genetic study of a large Charcot-Marie-Tooth type 2A family from southern Italy
Authors: Muglia, M Zappia, M Timmerman, V Valentino, P Gabriele, AL Conforti, FL De Jonghe, P Ragno, M Mazzei, R Sabatelli, M Nicoletti, G Patitucci, AM Oliveri, RL Bono, F Gambardella, A Quattrone, A
Citation: M. Muglia et al., Clinical and genetic study of a large Charcot-Marie-Tooth type 2A family from southern Italy, NEUROLOGY, 56(1), 2001, pp. 100-103
Silent celiac disease in patients with childhood localization-related epilepsies
Authors: Labate, A Gambardella, A Messina, D Tammaro, S Le Piane, E Pirritano, D Cosco, C Doldo, P Mazzei, R Oliveri, RL Bosco, D Zappia, M Valentino, P Aguglia, U Quattrone, A
Citation: A. Labate et al., Silent celiac disease in patients with childhood localization-related epilepsies, EPILEPSIA, 42(9), 2001, pp. 1153-1155
Calf pseudohypertrophy in a patient with double neurogenic pathology
Authors: Donato, G Valentino, P Santucci, M Amorosi, A Pittelli, M Maltese, L Volpentesta, G Lavano, A Chirchiglia, D Iannello, AN Ferraro, G Signorelli, CD
Citation: G. Donato et al., Calf pseudohypertrophy in a patient with double neurogenic pathology, CLIN NEUR, 19(3), 2000, pp. 142-144
Vitamin E deficiency due to chylomicron retention disease in Marinesco-Sjogren syndrome
Authors: Aguglia, U Annesi, G Pasquinelli, G Spadafora, P Gambardella, A Annesi, F Pasqua, AA Cavalcanti, F Crescibene, L Bagala, A Bone, F Oliveri, RL Valentino, P Zappia, M Quattrone, A
Citation: U. Aguglia et al., Vitamin E deficiency due to chylomicron retention disease in Marinesco-Sjogren syndrome, ANN NEUROL, 47(2), 2000, pp. 260-264
A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps tochromosome 1
Authors: Gambardella, A Annesi, G De Fusco, M Patrignani, A Aguglia, U Annesi, F Pasqua, AA Spadafora, P Oliveri, RL Valentino, P Zappia, M Ballabio, A Casari, G Quattrone, A
Citation: A. Gambardella et al., A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps tochromosome 1, NEUROLOGY, 55(10), 2000, pp. 1467-1471
Hyperekplexia in a patient with a brainstem vascular anomaly
Authors: Gambardella, A Valentino, P Annesi, G Oliveri, RL Bono, F Mazzei, RL Conforti, FL Aguglia, U Zappia, M Pardatscher, K Quattrone, A
Citation: A. Gambardella et al., Hyperekplexia in a patient with a brainstem vascular anomaly, ACT NEUR SC, 99(4), 1999, pp. 255-259
APOE and risk of cognitive impairment in multiple sclerosis
Authors: Oliveri, RL Cittadella, R Sibilia, G Manna, I Valentino, P Gambardella, A Aguglia, U Zappia, M Romeo, N Andreoli, V Bono, F Caracciolo, M Quattrone, A
Citation: Rl. Oliveri et al., APOE and risk of cognitive impairment in multiple sclerosis, ACT NEUR SC, 100(5), 1999, pp. 290-295
Risultati: 1-9 |