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Results:
1-18
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Results: 18
Authors:
Musso, M
Balestra, P
Bellone, E
Cassandrini, D
Di Maria, E
Doria, LL
Grandis, M
Mancardi, G
Schenone, A
Levi, G
Ajmar, F
Mandich, P
Citation: M. Musso et al., The D355V mutation decreases EGR2 binding to an element within the Cx32 promoter, NEUROBIOL D, 8(4), 2001, pp. 700-706
Authors:
Saverino, A
Solaro, C
Capello, E
Trompetto, C
Abbruzzese, G
Schenone, A
Citation: A. Saverino et al., Tremor associated with benign IgM paraproteinaemic neuropathy successfullytreated with gabapentin, MOVEMENT D, 16(5), 2001, pp. 967-968
Authors:
Nobbio, L
Mancardi, G
Grandis, M
Levi, G
Surer, U
Nave, KA
Windebank, AJ
Abbruzzese, M
Schenone, A
Citation: L. Nobbio et al., PMP22 transgenic dorsal root ganglia cultures show myelin abnormalities similar to those of human CMT1A, ANN NEUROL, 50(1), 2001, pp. 47-55
Authors:
Grandis, M
Nobbio, L
Abbruzzese, M
Banchi, L
Minuto, F
Barreca, A
Garrone, S
Mancardi, GL
Schenone, A
Citation: M. Grandis et al., Insulin treatment enhances expression of IGF-I in sural nerves of diabeticpatients, MUSCLE NERV, 24(5), 2001, pp. 622-629
Authors:
Capello, E
Roccatagliata, L
Schenone, A
Gazzola, P
Inglese, M
Abbruzzese, M
Mancardi, GL
Citation: E. Capello et al., Acute axonal form of Guillain-Barre syndrome in a multiple sclerosis patient: chance association or linked disorders?, EUR J NEUR, 7(2), 2000, pp. 223-225
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:
Solaro, C
Schenone, A
Di Sapio, A
Pradotto, L
Mancardi, GL
Primavera, A
Mauro, A
Citation: C. Solaro et al., An Italian family with Ala-47 transthyretin mutation associated with cardiomyopathy and polyneuropathy, NEUROMUSC D, 10(1), 2000, pp. 52-55
Authors:
Zunino, A
Viaggi, S
Ottaggio, L
Fronza, G
Schenone, A
Roncella, S
Abbondandolo, A
Citation: A. Zunino et al., Chromosomal aberrations evaluated by CGH, FISH and GTG-banding in a case of AIDS-related Burkitt's lymphoma, HAEMATOLOG, 85(3), 2000, pp. 250-255
Authors:
Nardone, A
Tarantola, J
Miscio, G
Pisano, F
Schenone, A
Schieppati, M
Citation: A. Nardone et al., Loss of large-diameter spindle afferent fibres is not detrimental to the control of body sway during upright stance: evidence from neuropathy, EXP BRAIN R, 135(2), 2000, pp. 155-162
Authors:
Masulli, F
Schenone, A
Massone, AM
Citation: F. Masulli et al., Fuzzy clustering methods for the segmentation of multimodal medical images, STUD FUZZ S, 41, 2000, pp. 335-350
Authors:
Schenone, A
Mancardi, GL
Citation: A. Schenone et Gl. Mancardi, Molecular basis of inherited neuropathies, CURR OP NEU, 12(5), 1999, pp. 603-616
Authors:
Masulli, F
Schenone, A
Citation: F. Masulli et A. Schenone, A fuzzy clustering based segmentation system as support to diagnosis in medical imaging, ARTIF INT M, 16(2), 1999, pp. 129-147
Authors:
Mandich, P
Mancardi, GL
Varese, A
Soriani, S
Di Maria, E
Bellone, E
Bado, M
Gross, L
Windebank, AJ
Ajmar, F
Schenone, A
Citation: P. Mandich et al., Congenital hypomyelination due to myelin protein zero Q215X mutation, ANN NEUROL, 45(5), 1999, pp. 676-678
Authors:
Marinelli, L
Cammarata, S
Nobbio, L
Schenone, A
Zaccheo, D
Angelini, G
Tabaton, M
Citation: L. Marinelli et al., Tyrosine kinase A-nerve growth factor receptor is antigenically present indystrophic neurites from a variety of conditions but not in Alzheimer's disease, NEUROSCI L, 273(1), 1999, pp. 67-71
Exclusion of the ninjurin gene as a candidate for hereditary sensory neuropathies type I and type II
Authors:
Mandich, P
Bellone, E
Di Maria, E
Pigullo, S
Pizzuti, A
Schenone, A
Soriani, S
Varese, A
Windebank, AJ
Ajmar, F
Citation: P. Mandich et al., Exclusion of the ninjurin gene as a candidate for hereditary sensory neuropathies type I and type II, AM J MED G, 83(5), 1999, pp. 409-410
Authors:
Penco, S
Schenone, A
Bordo, D
Bolognesi, M
Abbruzzese, M
Bugiani, O
Ajmar, F
Garre, C
Citation: S. Penco et al., A SOD1 gene mutation in a patient with slowly progressing familial ALS, NEUROLOGY, 53(2), 1999, pp. 404-406
Authors:
Tredici, G
Braga, M
Nicolini, G
Miloso, M
Marmiroli, P
Schenone, A
Nobbio, L
Frattola, L
Cavaletti, G
Citation: G. Tredici et al., Effect of recombinant human nerve growth factor on cisplatin neurotoxicityin rats, EXP NEUROL, 159(2), 1999, pp. 551-558
Authors:
Bolino, A
Seri, M
Caroli, F
Eubanks, J
Srinivasan, J
Mandich, P
Schenone, A
Quattrone, A
Romeo, G
Catterall, WA
Devoto, M
Citation: A. Bolino et al., Exclusion of the SCN2B gene as candidate for CMT4B, EUR J HUM G, 6(6), 1998, pp. 629-634
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