CATALOGO DEI PRODOTTI DELLA RICERCA

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Titolo Data di pubblicazione Autore(i) File
DNA fragmentation in normal development of the human central nervous system: A morphological study during corticogenesis 1-gen-1997 Simonati, Alessandro; T., Rosso; Rizzuto, Nicolo'
Botulinum toxin treatment of muscle cramps: a clinical and neurophysiological study 1-gen-1997 Bertolasi, L.; Priori, A.; Tomelleri, G.; Bongiovanni, L. G.; Fincati, E.; Simonati, A.; De Grandis, D.; Rizzuto, N.
Ponto-cerebellar hypoplasia with dystonia: Clinico-pathological findings in a sporadic case 1-gen-1997 Simonati, Alessandro; DALLA BERNARDINA, Bernardo; R., Colombari; Rizzuto, Nicolo'
Clinical and pathological correlations in Charcot-Marie-Tooth neuropathy type 1A with the 17p11.2p12 duplication: a cross-sectional morphometric and immunohistochemical study in twenty cases 1-gen-1998 Fabrizi, Gian Maria; Simonati, Alessandro; Morbin, M.; Cavallaro, T.; Taioli, Federica; Benedetti, M. D.; Edomi, P.; Rizzuto, Nicolo'
High-field-magnetic resonance imaging of the developing human brain from the 10th to the 16th week of gestational age 1-gen-1998 Sbarbati, Andrea; Marzola, Pasquina; Simonati, Alessandro; Nicolato, Elena; Osculati, Francesco
Coeliac disease associated with peripheral neuropathy in a child: A case report 1-gen-1998 Simonati, Alessandro; P. A., Battistella; G., Guariso; M., Clementi; Rizzuto, Nicolo'
Mechanisms of corticogenesis: cell proliferation and death in the developing human central nervous system 1-gen-1999 Simonati, Alessandro; Tosati, C.; Piazzola, E.; Rizzuto, Nicolo'
Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a point mutation of peripheral myelin protein-22 1-gen-1999 Fabrizi, Gian Maria; Cavallaro, T.; Taioli, Federica; Orrico, D.; Morbin, M.; Simonati, Alessandro; Rizzuto, Nicolo'
Neuroaxonal dystrophy with dystonia and pallidal involvement 1-gen-1999 Simonati, A.; Trevisan, C.; Salviati, A.; Rizzuto, N.
Cell proliferation and death: morphological evidence during corticogenesis in the developing human brain 1-gen-1999 Simonati, Alessandro; C., Tosati; T., Rosso; E., Piazzola; Rizzuto, Nicolo'
Novel mutation of the P0 extracellular domain causes a Dejerine-Sottas syndrome 1-gen-1999 Fabrizi, Gian Maria; Cavallaro, T.; Morbin, M.; Simonati, Alessandro; Taioli, Federica; Rizzuto, Nicolo'
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22 1-gen-1999 Simonati, Alessandro; Fabrizi, Gian Maria; Pasquinelli, A.; Taioli, Federica; Cavallaro, T.; Morbin, M.; Marcon, G.; Papini, M.; Rizzuto, Nicolo'
Congenital hypomyelination neuropathy with a novel mutation of PMP22 1-gen-2000 Rigatelli, F.; Fabrizi, Gian Maria; Simonati, Alessandro; Cavallaro, Tiziana; Ferrarini, Moreno; Taioli, Federica; Mostacciuolo, M. L.; Rizzuto, Nicolo'
A CLN2 gene nonsense mutation is associated with severe caudate atrophy and dystonia in LINCL 1-gen-2000 Simonati, Alessandro; Santorum, E.; Tessa, A.; Polo, A.; Simonetti, F.; DALLA BERNARDINA, Bernardo; Santorelli, F. M.; Rizzuto, Nicolo'
A novel nonsense mutation (Q509X) in three Italian Late infantile neuronal ceroid-lipofuscinosis children 1-gen-2000 A., Tessa; Simonati, Alessandro; A., Tavoni; E., Bertini; F. M., Santorelli
Neuronal ceroid lipofuscinoses: pathological features of bioptic specimens from 28 patients 1-gen-2000 Simonati, Alessandro; Rizzuto, Nicolo'
Focally folded myelin in Charcot-Marie-Tooth neuropathy type 1B with Ser49Leu in the myelin protein zero 1-gen-2000 Fabrizi, Gm; Taioli, F; Cavallaro, T; Rigatelli, F; Simonati, A; Mariani, G; Perrone, P; Rizzuto, N
PMP22 related congenital hypomyelination neuropathy 1-gen-2001 Fabrizi, Gian Maria; Simonati, Alessandro; Taioli, Federica; Cavallaro, T.; Ferrarini, Moreno; Mostacciuolo, M. L.; Rizzuto, Nicolo'
Dejerine-Sottas neuropathy with multiple nerve roots enlargement and hypomyelination associated with a missense mutation of the transmembrane domain of MPZ/P0 1-gen-2002 Simonati, Alessandro; Fabrizi, Gian Maria; Taioli, Federica; Polo, A.; Cerini, Roberto; Rizzuto, Nicolo'
The K-C1 cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosum 1-gen-2002 Howard, H. C.; Mount, D. B.; Rochefort, D.; Byun, N.; Dupré, N.; Lu, J.; Fan, X.; Song, L.; Rivière, J. B.; Prévost, C.; Horst, J.; Simonati, Alessandro; Lemcke, B.; Welch, R.; England, R.; Zhan, F. Q.; Mercado, A.; Siesser, W. B.; George A. L., Jr; Mcdonald, M. P.; Bouchard, J. P.; Mathieu, J.; Delpire, E.; Rouleau, G. A.
Mostrati risultati da 41 a 60 di 162
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