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529 results

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Page 1
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: liguori r. Neurology. 2008 Mar 4;70(10):762-70. doi: 10.1212/01.wnl.0000295505.74234.d0. Epub 2008 Jan 23. Neurology. 2008. PMID: 18216301
Leber's hereditary optic neuropathy (LHON/11778) with myoclonus: report of two cases.
Carelli V, Valentino ML, Liguori R, Meletti S, Vetrugno R, Provini F, Mancardi GL, Bandini F, Baruzzi A, Montagna P. Carelli V, et al. Among authors: liguori r. J Neurol Neurosurg Psychiatry. 2001 Dec;71(6):813-6. doi: 10.1136/jnnp.71.6.813. J Neurol Neurosurg Psychiatry. 2001. PMID: 11723211 Free PMC article.
Functional MRI study in a case of Charles Bonnet syndrome related to LHON.
Vacchiano V, Tonon C, Mitolo M, Evangelisti S, Carbonelli M, Liguori R, Lodi R, Carelli V, La Morgia C. Vacchiano V, et al. Among authors: liguori r. BMC Neurol. 2019 Dec 30;19(1):350. doi: 10.1186/s12883-019-1579-9. BMC Neurol. 2019. PMID: 31888524 Free PMC article.
Focal myoclonus and propriospinal propagation.
Vetrugno R, Provini F, Plazzi G, Valentino ML, Liguori R, Lugaresi E, Montagna P. Vetrugno R, et al. Among authors: liguori r. Clin Neurophysiol. 2000 Dec;111(12):2175-9. doi: 10.1016/s1388-2457(00)00471-5. Clin Neurophysiol. 2000. PMID: 11090769
Loss of temporal retinal nerve fibers in Parkinson disease: a mitochondrial pattern?
La Morgia C, Barboni P, Rizzo G, Carbonelli M, Savini G, Scaglione C, Capellari S, Bonazza S, Giannoccaro MP, Calandra-Buonaura G, Liguori R, Cortelli P, Martinelli P, Baruzzi A, Carelli V. La Morgia C, et al. Among authors: liguori r. Eur J Neurol. 2013 Jan;20(1):198-201. doi: 10.1111/j.1468-1331.2012.03701.x. Epub 2012 Mar 21. Eur J Neurol. 2013. PMID: 22436028
529 results