Taroni F - Search Results

1

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: taroni f. Neurology. 1997 Dec;49(6):1635-40. doi: 10.1212/wnl.49.6.1635. Neurology. 1997. PMID: 9409359

2

Kennedy's disease: clinical and molecular study of two Italian families.

Pareyson D, Castellotti B, Botti S, Defanti CA, Gellera C, Taroni F, Sghirlanzoni A. Pareyson D, et al. Among authors: taroni f. Ital J Neurol Sci. 1995 Oct;16(7):467-71. doi: 10.1007/BF02229324. Ital J Neurol Sci. 1995. PMID: 8749704

3

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: taroni f. Neurology. 1996 Apr;46(4):1133-7. doi: 10.1212/wnl.46.4.1133. Neurology. 1996. PMID: 8780105

4

Deletion of the PMP22 gene and hereditary neuropathy with liability to pressure palsies.

Pareyson D, Taroni F. Pareyson D, et al. Among authors: taroni f. Curr Opin Neurol. 1996 Oct;9(5):348-54. doi: 10.1097/00019052-199610000-00006. Curr Opin Neurol. 1996. PMID: 8894410 Review.

5

PMP22 frameshift mutation and hereditary neuropathy with liability to pressure palsies.

Pareyson D, Botti S, Sghirlanzoni A, Taroni F. Pareyson D, et al. Among authors: taroni f. Neurology. 1997 Nov;49(5):1478-9. doi: 10.1212/wnl.49.5.1478. Neurology. 1997. PMID: 9371959 No abstract available.

6

Facial nerve is liable to pressure palsy.

Poloni TE, Merlo IM, Alfonsi E, Marinou-Aktipi K, Botti S, Arrigo A, Taroni F, Ceroni M. Poloni TE, et al. Among authors: taroni f. Neurology. 1998 Jul;51(1):320-2. doi: 10.1212/wnl.51.1.320. Neurology. 1998. PMID: 9674839 No abstract available.

7

Detection of hereditary neuropathy with liability to pressure palsies among patients with acute painless mononeuropathy or plexopathy.

Pareyson D, Solari A, Taroni F, Botti S, Fallica E, Scaioli V, Ciano C, Sghirlanzoni A. Pareyson D, et al. Among authors: taroni f. Muscle Nerve. 1998 Dec;21(12):1686-91. doi: 10.1002/(sici)1097-4598(199812)21:12<1686::aid-mus10>3.0.co;2-z. Muscle Nerve. 1998. PMID: 9843070

8

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: taroni f. Neurology. 1999 Mar 23;52(5):1110-1. doi: 10.1212/wnl.52.5.1106-f. Neurology. 1999. PMID: 10102454 No abstract available.

9

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: taroni f. Ann N Y Acad Sci. 1999 Sep 14;883:477-80. Ann N Y Acad Sci. 1999. PMID: 10586278 No abstract available.

10

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: taroni f. Neurology. 2000 Apr 25;54(8):1696-8. doi: 10.1212/wnl.54.8.1696. Neurology. 2000. PMID: 10762521 Free article.

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