Scaioli V - Search Results

1

Novel mutations in the HSN2 gene causing hereditary sensory and autonomic neuropathy type II.

Coen K, Pareyson D, Auer-Grumbach M, Buyse G, Goemans N, Claeys KG, Verpoorten N, Laurà M, Scaioli V, Salmhofer W, Pieber TR, Nelis E, De Jonghe P, Timmerman V. Coen K, et al. Among authors: scaioli v. Neurology. 2006 Mar 14;66(5):748-51. doi: 10.1212/01.wnl.0000201191.57519.47. Neurology. 2006. PMID: 16534117

2

Peripheral nerve involvement in Churg-Strauss syndrome.

Marazzi R, Pareyson D, Boiardi A, Corbo M, Scaioli V, Sghirlanzoni A. Marazzi R, et al. Among authors: scaioli v. J Neurol. 1992 Jul;239(6):317-21. doi: 10.1007/BF00867587. J Neurol. 1992. PMID: 1324984

3

F response and somatosensory and brainstem auditory evoked potential studies in HMSN type I and II.

Scaioli V, Pareyson D, Avanzini G, Sghirlanzoni A. Scaioli V, et al. J Neurol Neurosurg Psychiatry. 1992 Nov;55(11):1027-31. doi: 10.1136/jnnp.55.11.1027. J Neurol Neurosurg Psychiatry. 1992. PMID: 1469398 Free PMC article.

4

Hereditary motor and sensory neuropathy type I and type II.

Sghirlanzoni A, Pareyson D, Scaioli V, Marazzi R, Pacini L. Sghirlanzoni A, et al. Among authors: scaioli v. Ital J Neurol Sci. 1990 Oct;11(5):471-9. doi: 10.1007/BF02336567. Ital J Neurol Sci. 1990. PMID: 2272782

5

Neurogenic muscle hypertrophy. Report of two cases.

Pareyson D, Morandi L, Scaioli V, Marazzi R, Boiardi A, Sghirlanzoni A. Pareyson D, et al. Among authors: scaioli v. J Neurol. 1989 Jul;236(5):292-5. doi: 10.1007/BF00314459. J Neurol. 1989. PMID: 2760647

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

7

Acoustic nerve in peripheral neuropathy: a BAEP study. Brainstem Auditory Evoked Potentials.

Pareyson D, Scaioli V, Berta E, Sghirlanzoni A. Pareyson D, et al. Among authors: scaioli v. Electromyogr Clin Neurophysiol. 1995 Oct;35(6):359-64. Electromyogr Clin Neurophysiol. 1995. PMID: 8785933

8

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: scaioli v. 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

9

Clinical and electrophysiological aspects of Charcot-Marie-Tooth disease.

Pareyson D, Scaioli V, Laurà M. Pareyson D, et al. Among authors: scaioli v. Neuromolecular Med. 2006;8(1-2):3-22. doi: 10.1385/nmm:8:1-2:3. Neuromolecular Med. 2006. PMID: 16775364 Review.

10

Rapid progression of late onset axonal Charcot-Marie-Tooth disease associated with a novel MPZ mutation in the extracellular domain.

Laurà M, Milani M, Morbin M, Moggio M, Ripolone M, Jann S, Scaioli V, Taroni F, Pareyson D. Laurà M, et al. Among authors: scaioli v. J Neurol Neurosurg Psychiatry. 2007 Nov;78(11):1263-6. doi: 10.1136/jnnp.2006.112276. J Neurol Neurosurg Psychiatry. 2007. PMID: 17940173 Free PMC article.

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