Rizzuto N - Search Results

1

Neuroaxonal dystrophy with dystonia and pallidal involvement.

Simonati A, Trevisan C, Salviati A, Rizzuto N. Simonati A, et al. Among authors: rizzuto n. Neuropediatrics. 1999 Jun;30(3):151-4. doi: 10.1055/s-2007-973482. Neuropediatrics. 1999. PMID: 10480212

2

Coeliac disease associated with peripheral neuropathy in a child: a case report.

Simonati A, Battistella PA, Guariso G, Clementi M, Rizzuto N. Simonati A, et al. Among authors: rizzuto n. Neuropediatrics. 1998 Jun;29(3):155-8. doi: 10.1055/s-2007-973553. Neuropediatrics. 1998. PMID: 9706627

3

A CLN2 gene nonsense mutation is associated with severe caudate atrophy and dystonia in LINCL.

Simonati A, Santorum E, Tessa A, Polo A, Simonetti F, Bernardina BD, Santorelli FM, Rizzuto N. Simonati A, et al. Among authors: rizzuto n. Neuropediatrics. 2000 Aug;31(4):199-201. doi: 10.1055/s-2000-7453. Neuropediatrics. 2000. PMID: 11071145

4

Sensory involvement in X-linked spino-bulbar muscular atrophy (Kennedy's syndrome): an electrophysiological study.

Polo A, Teatini F, D'Anna S, Manganotti P, Salviati A, Dallapiccola B, Zanette G, Rizzuto N. Polo A, et al. Among authors: rizzuto n. J Neurol. 1996 May;243(5):388-92. doi: 10.1007/BF00868997. J Neurol. 1996. PMID: 8741078

5

Neuronal ceroid lipofuscinoses: pathological features of bioptic specimens from 28 patients.

Simonati A, Rizzuto N. Simonati A, et al. Among authors: rizzuto n. Neurol Sci. 2000;21(3 Suppl):S63-70. doi: 10.1007/s100720070042. Neurol Sci. 2000. PMID: 11073230

6

Clinical features of Kleine-Levin syndrome with localized encephalitis.

Fenzi F, Simonati A, Crosato F, Ghersini L, Rizzuto N. Fenzi F, et al. Among authors: rizzuto n. Neuropediatrics. 1993 Oct;24(5):292-5. doi: 10.1055/s-2008-1071559. Neuropediatrics. 1993. PMID: 8309520

7

Inherited neuroaxonal dystrophy in C6 deficient rabbits.

Giannini C, Monaco S, Kirschfink M, Rother KO, Lorbacher de Ruiz H, Nardelli E, Bonetti B, Salviati A, Zanette GP, Rizzuto N. Giannini C, et al. Among authors: rizzuto n. J Neuropathol Exp Neurol. 1992 Sep;51(5):514-22. doi: 10.1097/00005072-199209000-00006. J Neuropathol Exp Neurol. 1992. PMID: 1517772

8

Dejerine-Sottas neuropathy with multiple nerve roots enlargement and hypomyelination associated with a missense mutation of the transmembrane domain of MPZ/P0.

Simonati A, Fabrizi GM, Taioli F, Polo A, Cerini R, Rizzuto N. Simonati A, et al. Among authors: rizzuto n. J Neurol. 2002 Sep;249(9):1298-302. doi: 10.1007/s00415-002-0810-5. J Neurol. 2002. PMID: 12242557

9

Ponto-cerebellar hypoplasia with dystonia: clinico-pathological findings in a sporadic case.

Simonati A, Dalla Bernardina B, Colombari R, Rizzuto N. Simonati A, et al. Among authors: rizzuto n. Childs Nerv Syst. 1997 Nov-Dec;13(11-12):642-7. doi: 10.1007/s003810050161. Childs Nerv Syst. 1997. PMID: 9454987

10

Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22.

Simonati A, Fabrizi GM, Pasquinelli A, Taioli F, Cavallaro T, Morbin M, Marcon G, Papini M, Rizzuto N. Simonati A, et al. Among authors: rizzuto n. Neuromuscul Disord. 1999 Jun;9(4):257-61. doi: 10.1016/s0960-8966(99)00008-5. Neuromuscul Disord. 1999. PMID: 10399754

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