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Citation: A. Gambardella et al., Juvenile Huntington's disease presenting as progressive myoclonic epilepsy, NEUROLOGY, 57(4), 2001, pp. 708-711

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

Authors: Oliveri, RL Muglia, M De Stefano, N Mazzei, R Labate, A Conforti, FL Patitucci, A Gabriele, AL Tagarelli, G Magariello, A Zappia, M Gambardella, A Federico, A Quattrone, A

Citation: Rl. Oliveri et al., A novel mutation in the Notch3 gene in an Italian family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy - Genetic and magnetic resonance spectroscopic findings, ARCH NEUROL, 58(9), 2001, pp. 1418-1422

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Citation: A. Bolino et al., Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2, NAT GENET, 25(1), 2000, pp. 17-19

Authors: Bolino, A Levy, ER Muglia, M Conforti, FL LeGuern, E Salih, MAM Georgiou, DM Hausmanowa-Petrusewicz, I Mandich, P Gambardella, A Quattrone, A Devoto, M Monaco, AP

Citation: A. Bolino et al., Genetic refinement and physical mapping of the CMT4B gene on chromosome 11q22, GENOMICS, 63(2), 2000, pp. 271-278

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