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
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
Authors:
Bolino, A
Muglia, M
Conforti, FL
LeGuern, E
Salih, MAM
Georgiou, DM
Christodoulou, K
Hausmanowa-Petrusewicz, I
Mandich, P
Schenone, A
Gambardella, A
Bono, F
Quattrone, A
Devoto, M
Monaco, AP
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