Volpi N - Search Results

1

A new mutation in DNM2 gene in a large Italian family.

Lopergolo D, Bocci S, Pinto AM, Valentino F, Doddato G, Ginanneschi F, Volpi N, Renieri A, Giannini F. Lopergolo D, et al. Among authors: volpi n. Neurol Sci. 2021 Jun;42(6):2509-2513. doi: 10.1007/s10072-020-04972-8. Epub 2021 Jan 18. Neurol Sci. 2021. PMID: 33459893

2

FACL4, encoding fatty acid-CoA ligase 4, is mutated in nonspecific X-linked mental retardation.

Meloni I, Muscettola M, Raynaud M, Longo I, Bruttini M, Moizard MP, Gomot M, Chelly J, des Portes V, Fryns JP, Ropers HH, Magi B, Bellan C, Volpi N, Yntema HG, Lewis SE, Schaffer JE, Renieri A. Meloni I, et al. Among authors: volpi n. Nat Genet. 2002 Apr;30(4):436-40. doi: 10.1038/ng857. Epub 2002 Mar 11. Nat Genet. 2002. PMID: 11889465

3

Hereditary neuronal intranuclear inclusion disease with autonomic failure and cerebellar degeneration.

Zannolli R, Gilman S, Rossi S, Volpi N, Bernini A, Galluzzi P, Galimberti D, Pucci L, D'Ambrosio A, Morgese G, Giannini F. Zannolli R, et al. Among authors: volpi n. Arch Neurol. 2002 Aug;59(8):1319-26. doi: 10.1001/archneur.59.8.1319. Arch Neurol. 2002. PMID: 12164731

4

Thalidomide-induced neuropathy: a ganglionopathy?

Giannini F, Volpi N, Rossi S, Passero S, Fimiani M, Cerase A. Giannini F, et al. Among authors: volpi n. Neurology. 2003 Mar 11;60(5):877-8. doi: 10.1212/01.wnl.0000049462.03800.b1. Neurology. 2003. PMID: 12629253 No abstract available.

5

Uncommon findings in idiopathic hypertrophic cranial pachymeningitis.

Rossi S, Giannini F, Cerase A, Bartalini S, Tripodi S, Volpi N, Vatti G, Passero S, Galluzzi P, Ulivelli M. Rossi S, et al. Among authors: volpi n. J Neurol. 2004 May;251(5):548-55. doi: 10.1007/s00415-004-0362-y. J Neurol. 2004. PMID: 15164187

6

D90A-SOD1 mutation in ALS: The first report of heterozygous Italian patients and unusual findings.

Giannini F, Battistini S, Mancuso M, Greco G, Ricci C, Volpi N, Del Corona A, Piazza S, Siciliano G. Giannini F, et al. Among authors: volpi n. Amyotroph Lateral Scler. 2010;11(1-2):216-9. doi: 10.3109/17482960902721642. Amyotroph Lateral Scler. 2010. PMID: 20184519

7

Progressive mitochondrial myopathy, deafness, and sporadic seizures associated with a novel mutation in the mitochondrial tRNASer(AGY) gene.

Cardaioli E, Malfatti E, Da Pozzo P, Gallus GN, Carluccio MA, Rufa A, Volpi N, Dotti MT, Federico A. Cardaioli E, et al. Among authors: volpi n. J Neurol Sci. 2011 Apr 15;303(1-2):142-5. doi: 10.1016/j.jns.2010.12.020. Epub 2011 Jan 22. J Neurol Sci. 2011. PMID: 21257182

8

Antiangiogenic VEGF isoform in inflammatory myopathies.

Volpi N, Pecorelli A, Lorenzoni P, Di Lazzaro F, Belmonte G, Aglianò M, Cantarini L, Giannini F, Grasso G, Valacchi G. Volpi N, et al. Mediators Inflamm. 2013;2013:219313. doi: 10.1155/2013/219313. Epub 2013 Jun 12. Mediators Inflamm. 2013. PMID: 23840094 Free PMC article.

9

Rhabdomyolysis in an elderly multitreated patient: multiple drug interactions after statin withdrawal.

Ginanneschi F, Volpi N, Giannini F, Rocchi R, Donati D, Aglianò M, Lorenzoni P, Rossi A. Ginanneschi F, et al. Among authors: volpi n. J Neurol Sci. 2014 Jan 15;336(1-2):284-7. doi: 10.1016/j.jns.2013.10.040. Epub 2013 Nov 6. J Neurol Sci. 2014. PMID: 24252882

10

SCN11A variant as possible pain generator in sensory axonal neuropathy.

Ginanneschi F, Rubegni A, Moro F, Volpi N, Santorelli FM, Rossi A. Ginanneschi F, et al. Among authors: volpi n. Neurol Sci. 2019 Jun;40(6):1295-1297. doi: 10.1007/s10072-019-3703-4. Epub 2019 Jan 8. Neurol Sci. 2019. PMID: 30623267 No abstract available.

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