Pareyson D - Search Results

1

Hereditary neuropathy with liability to pressure palsies.

Attarian S, Fatehi F, Rajabally YA, Pareyson D. Attarian S, et al. Among authors: pareyson d. J Neurol. 2020 Aug;267(8):2198-2206. doi: 10.1007/s00415-019-09319-8. Epub 2019 Apr 15. J Neurol. 2020. PMID: 30989370 Review.

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: pareyson d. J Neurol. 1992 Jul;239(6):317-21. doi: 10.1007/BF00867587. J Neurol. 1992. PMID: 1324984

3

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. Among authors: pareyson d. Neurology. 1992 Nov;42(11):2201-4. doi: 10.1212/wnl.42.11.2201. Neurology. 1992. PMID: 1436537

4

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. Among authors: pareyson d. 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.

5

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: pareyson d. Ital J Neurol Sci. 1990 Oct;11(5):471-9. doi: 10.1007/BF02336567. Ital J Neurol Sci. 1990. PMID: 2272782

6

Recurrent familial neuropathy due to liability to pressure palsies.

Marazzi R, Pareyson D, Scaioli V, Corbo M, Boiardi A, Chiodelli G, Sghirlanzoni A. Marazzi R, et al. Among authors: pareyson d. Ital J Neurol Sci. 1988 Aug;9(4):355-63. doi: 10.1007/BF02333999. Ital J Neurol Sci. 1988. PMID: 3220711

7

A 1.5-Mb deletion in 17p11.2-p12 is frequently observed in Italian families with hereditary neuropathy with liability to pressure palsies.

Lorenzetti D, Pareyson D, Sghirlanzoni A, Roa BB, Abbas NE, Pandolfo M, Di Donato S, Lupski JR. Lorenzetti D, et al. Among authors: pareyson d. Am J Hum Genet. 1995 Jan;56(1):91-8. Am J Hum Genet. 1995. PMID: 7825607 Free PMC article.

8

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: pareyson d. Eur Neurol. 1994;34(3):135-9. doi: 10.1159/000117026. Eur Neurol. 1994. PMID: 8033938

9

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

10

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

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

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