Rizzuto N - Search Results

1

Central-peripheral sensory axonopathy in a juvenile case of Alpers-Huttenlocher disease.

Simonati A, Filosto M, Tomelleri G, Savio C, Tonin P, Polo A, Rizzuto N. Simonati A, et al. Among authors: rizzuto n. J Neurol. 2003 Jun;250(6):702-6. doi: 10.1007/s00415-003-1065-5. J Neurol. 2003. PMID: 12796833

2

Features of cell death in brain and liver, the target tissues of progressive neuronal degeneration of childhood with liver disease (Alpers-Huttenlocher disease).

Simonati A, Filosto M, Savio C, Tomelleri G, Tonin P, Dalla Bernardina B, Rizzuto N. Simonati A, et al. Among authors: rizzuto n. Acta Neuropathol. 2003 Jul;106(1):57-65. doi: 10.1007/s00401-003-0698-x. Epub 2003 Apr 30. Acta Neuropathol. 2003. PMID: 12721699

3

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

4

Reversible upper limb muscle weakness with selective loss of thick filaments.

Vattemi G, Tonin P, Filosto M, Savio C, Rizzuto N, Tomelleri G. Vattemi G, et al. Among authors: rizzuto n. Neurology. 2003 Sep 23;61(6):863-4. doi: 10.1212/wnl.61.6.863. Neurology. 2003. PMID: 14504344 No abstract available.

5

The role of muscle biopsy in investigating isolated muscle pain.

Filosto M, Tonin P, Vattemi G, Bertolasi L, Simonati A, Rizzuto N, Tomelleri G. Filosto M, et al. Among authors: rizzuto n. Neurology. 2007 Jan 16;68(3):181-6. doi: 10.1212/01.wnl.0000252252.29532.cc. Neurology. 2007. PMID: 17224570

6

Hepato-cerebral syndrome: genetic and pathological studies in an infant with a dGK mutation.

Filosto M, Mancuso M, Tomelleri G, Rizzuto N, Dalla Bernardina B, DiMauro S, Simonati A. Filosto M, et al. Among authors: rizzuto n. Acta Neuropathol. 2004 Aug;108(2):168-71. doi: 10.1007/s00401-004-0872-9. Epub 2004 May 19. Acta Neuropathol. 2004. PMID: 15150663

7

SERCA1 and calsequestrin storage myopathy: a new surplus protein myopathy.

Tomelleri G, Palmucci L, Tonin P, Mongini T, Marini M, L'erario R, Rizzuto N, Vattemi G. Tomelleri G, et al. Among authors: rizzuto n. Brain. 2006 Aug;129(Pt 8):2085-92. doi: 10.1093/brain/awl128. Epub 2006 May 19. Brain. 2006. PMID: 16714317

8

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

9

Motor neuron disease with pyramidal tract dysfunction involves the cortical generators of the early somatosensory evoked potential to tibial nerve stimulation.

Zanette G, Tinazzi M, Polo A, Rizzuto N. Zanette G, et al. Among authors: rizzuto n. Neurology. 1996 Oct;47(4):932-8. doi: 10.1212/wnl.47.4.932. Neurology. 1996. PMID: 8857722

10

Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a point mutation of peripheral myelin protein-22.

Fabrizi GM, Cavallaro T, Taioli F, Orrico D, Morbin M, Simonati A, Rizzuto N. Fabrizi GM, et al. Among authors: rizzuto n. Neurology. 1999 Sep 11;53(4):846-51. doi: 10.1212/wnl.53.4.846. Neurology. 1999. PMID: 10489052

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