Sghirlanzoni A - Search Results

1

Conduction velocities in Charcot-Marie-Tooth polyneuropathy type 1.

Pareyson D, Sghirlanzoni A. Pareyson D, et al. Among authors: sghirlanzoni a. Neurology. 1994 Nov;44(11):2216. doi: 10.1212/wnl.44.11.2216. Neurology. 1994. PMID: 7969998 No abstract available.

2

Gene dosage effects in hereditary peripheral neuropathy. Expression of peripheral myelin protein 22 in Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies nerve biopsies.

Gabriel JM, Erne B, Pareyson D, Sghirlanzoni A, Taroni F, Steck AJ. Gabriel JM, et al. Among authors: sghirlanzoni a. Neurology. 1997 Dec;49(6):1635-40. doi: 10.1212/wnl.49.6.1635. Neurology. 1997. PMID: 9409359

3

Charcot-Marie-Tooth disease type 2 and P0 gene mutations.

Pareyson D, Sghirlanzoni A, Bolti S, Ciano C, Fallica E, Mora M, Taroni F. Pareyson D, et al. Among authors: sghirlanzoni a. Neurology. 1999 Mar 23;52(5):1110-1. doi: 10.1212/wnl.52.5.1106-f. Neurology. 1999. PMID: 10102454 No abstract available.

4

17p11.2 duplication is a common finding in sporadic cases of Charcot-Marie-Tooth type 1.

Mancardi GL, Uccelli A, Bellone E, Sghirlanzoni A, Mandich P, Pareyson D, Schenone A, Abbruzzese M, Ajmar F. Mancardi GL, et al. Among authors: sghirlanzoni a. Eur Neurol. 1994;34(3):135-9. doi: 10.1159/000117026. Eur Neurol. 1994. PMID: 8033938

5

Neurophysiological diagnosis of acquired sensory ganglionopathies.

Lauria G, Pareyson D, Sghirlanzoni A. Lauria G, et al. Among authors: sghirlanzoni a. Eur Neurol. 2003;50(3):146-52. doi: 10.1159/000073055. Eur Neurol. 2003. PMID: 14530620

6

Phenotypic heterogeneity in hereditary neuropathy with liability to pressure palsies associated with chromosome 17p11.2-12 deletion.

Pareyson D, Scaioli V, Taroni F, Botti S, Lorenzetti D, Solari A, Ciano C, Sghirlanzoni A. Pareyson D, et al. Among authors: sghirlanzoni a. Neurology. 1996 Apr;46(4):1133-7. doi: 10.1212/wnl.46.4.1133. Neurology. 1996. PMID: 8780105

7

Heterozygous null mutation in the P0 gene associated with mild Charcot-Marie-Tooth disease.

Pareyson D, Menichella D, Botti S, Sghirlanzoni A, Fallica E, Mora M, Ciano C, Shy ME, Taroni F. Pareyson D, et al. Among authors: sghirlanzoni a. Ann N Y Acad Sci. 1999 Sep 14;883:477-80. Ann N Y Acad Sci. 1999. PMID: 10586278 No abstract available.

8

Cranial nerve involvement in CMT disease type 1 due to early growth response 2 gene mutation.

Pareyson D, Taroni F, Botti S, Morbin M, Baratta S, Lauria G, Ciano C, Sghirlanzoni A. Pareyson D, et al. Among authors: sghirlanzoni a. Neurology. 2000 Apr 25;54(8):1696-8. doi: 10.1212/wnl.54.8.1696. Neurology. 2000. PMID: 10762521 Free article.

9

Chronic cryptogenic sensory polyneuropathy.

Lauria G, Pareyson D, Sghirlanzoni A. Lauria G, et al. Among authors: sghirlanzoni a. Arch Neurol. 2000 May;57(5):759-60. Arch Neurol. 2000. PMID: 10815150 Free article. No abstract available.

10

HMSN III phenotype due to homozygous expression of a dominant HMSN II gene.

Sghirlanzoni A, Pareyson D, Balestrini MR, Bellone E, Berta E, Ciano C, Mandich P, Marazzi R. Sghirlanzoni A, et al. Neurology. 1992 Nov;42(11):2201-4. doi: 10.1212/wnl.42.11.2201. Neurology. 1992. PMID: 1436537

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