Pareyson D - Search Results

1

Subclinical leukodystrophy and infertility in a man with a novel homozygous CLCN2 mutation.

Di Bella D, Pareyson D, Savoiardo M, Farina L, Ciano C, Caldarazzo S, Sagnelli A, Bonato S, Nava S, Bresolin N, Tedeschi G, Taroni F, Salsano E. Di Bella D, et al. Among authors: pareyson d. Neurology. 2014 Sep 23;83(13):1217-8. doi: 10.1212/WNL.0000000000000812. Epub 2014 Aug 15. Neurology. 2014. PMID: 25128180 Free article. No abstract available.

2

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

3

The effects of wallerian degeneration of the optic radiations demonstrated by MRI.

Savoiardo M, Pareyson D, Grisoli M, Forester M, D'Incerti L, Farina L. Savoiardo M, et al. Among authors: d incerti l, pareyson d. Neuroradiology. 1992;34(4):323-5. doi: 10.1007/BF00588192. Neuroradiology. 1992. PMID: 1528444

4

Combined central and peripheral acute demyelination.

Pareyson D, Ciano C, Fiacchino F, Gemma M, Savoiardo M, Sghirlanzoni A. Pareyson D, et al. Ital J Neurol Sci. 1993 Jan;14(1):83-6. doi: 10.1007/BF02339047. Ital J Neurol Sci. 1993. PMID: 8386146

5

Spinal epidural abscess complicating tuberculous spondylitis.

Pareyson D, Savoiardo M, D'Incerti L, Sghirlanzoni A. Pareyson D, et al. Among authors: d incerti l. Ital J Neurol Sci. 1995 Jun;16(5):321-5. doi: 10.1007/BF02249108. Ital J Neurol Sci. 1995. PMID: 8537221

6

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. Ital J Neurol Sci. 1995 Oct;16(7):467-71. doi: 10.1007/BF02229324. Ital J Neurol Sci. 1995. PMID: 8749704

7

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

8

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

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

9

Very late onset Friedreich's ataxia without cardiomyopathy is associated with limited GAA expansion in the X25 gene.

Gellera C, Pareyson D, Castellotti B, Mazzucchelli F, Zappacosta B, Pandolfo M, Di Donato S. Gellera C, et al. Among authors: pareyson d. Neurology. 1997 Oct;49(4):1153-5. doi: 10.1212/wnl.49.4.1153. Neurology. 1997. PMID: 9339708

10

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

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

329 results

Search Page

Filters