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Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: a novel mutation in the SPG11 gene and further evidence for genetic heterogeneity.
Pippucci T, Panza E, Pompilii E, Donadio V, Borreca A, Babalini C, Patrono C, Zuntini R, Kawarai T, Bernardi G, Liguori R, Romeo G, Montagna P, Orlacchio A, Seri M. Pippucci T, et al. Among authors: montagna p. Eur J Neurol. 2009 Jan;16(1):121-6. doi: 10.1111/j.1468-1331.2008.02367.x. Eur J Neurol. 2009. PMID: 19087158
Palmaris brevis spasm: an occupational syndrome.
Liguori R, Donadio V, Di Stasi V, Cianchi C, Montagna P. Liguori R, et al. Among authors: montagna p. Neurology. 2003 May 27;60(10):1705-7. doi: 10.1212/01.wnl.0000064165.70159.93. Neurology. 2003. PMID: 12771275
Acquired neuromyotonia after bone marrow transplantation.
Liguori R, Vincent A, Avoni P, Valentino ML, D'Alessandro R, Zaccaria A, Bandini G, Montagna P. Liguori R, et al. Among authors: montagna p. Neurology. 2000 Mar 28;54(6):1390-1. doi: 10.1212/wnl.54.6.1390. Neurology. 2000. PMID: 10746621 No abstract available.
Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus.
La Morgia C, Achilli A, Iommarini L, Barboni P, Pala M, Olivieri A, Zanna C, Vidoni S, Tonon C, Lodi R, Vetrugno R, Mostacci B, Liguori R, Carroccia R, Montagna P, Rugolo M, Torroni A, Carelli V. La Morgia C, et al. Among authors: montagna p. Neurology. 2008 Mar 4;70(10):762-70. doi: 10.1212/01.wnl.0000295505.74234.d0. Epub 2008 Jan 23. Neurology. 2008. PMID: 18216301
Development of a disability scale for myotonic dystrophy type 1.
Contardi S, Pizza F, Falzone F, D'Alessandro R, Avoni P, Di Stasi V, Montagna P, Liguori R. Contardi S, et al. Among authors: montagna p. Acta Neurol Scand. 2012 Jun;125(6):431-8. doi: 10.1111/j.1600-0404.2011.01587.x. Epub 2011 Sep 8. Acta Neurol Scand. 2012. PMID: 21902674
801 results