Canafoglia L - Search Results

1

Epileptic syndrome with myoclonus as manifestation of adult-onset CblC deficiency.

Di Giacomo R, Salsano E, Deleo F, Pastori C, Didato G, Stabile A, Ferrario R, Giovagnoli AR, Benzoni C, Sarro L, Visani E, Canafoglia L. Di Giacomo R, et al. Among authors: canafoglia l. J Neurol. 2022 Sep;269(9):5173-5178. doi: 10.1007/s00415-022-11129-4. Epub 2022 Apr 11. J Neurol. 2022. PMID: 35403876 No abstract available.

2

Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals.

Montanucci L, Lewis-Smith D, Collins RL, Niestroj LM, Parthasarathy S, Xian J, Ganesan S, Macnee M, Brünger T, Thomas RH, Talkowski M; Epi25 Collaborative; Helbig I, Leu C, Lal D. Montanucci L, et al. Nat Commun. 2023 Jul 20;14(1):4392. doi: 10.1038/s41467-023-39539-6. Nat Commun. 2023. PMID: 37474567 Free PMC article.

3

GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture.

International League Against Epilepsy Consortium on Complex Epilepsies. International League Against Epilepsy Consortium on Complex Epilepsies. Nat Genet. 2023 Sep;55(9):1471-1482. doi: 10.1038/s41588-023-01485-w. Epub 2023 Aug 31. Nat Genet. 2023. PMID: 37653029 Free PMC article.

4

Epileptic phenotypes associated with mitochondrial disorders.

Canafoglia L, Franceschetti S, Antozzi C, Carrara F, Farina L, Granata T, Lamantea E, Savoiardo M, Uziel G, Villani F, Zeviani M, Avanzini G. Canafoglia L, et al. Neurology. 2001 May 22;56(10):1340-6. doi: 10.1212/wnl.56.10.1340. Neurology. 2001. PMID: 11376185

5

Movement-activated myoclonus in genetically defined progressive myoclonic epilepsies: EEG-EMG relationship estimated using autoregressive models.

Panzica F, Canafoglia L, Franceschetti S, Binelli S, Ciano C, Visani E, Avanzini G. Panzica F, et al. Among authors: canafoglia l. Clin Neurophysiol. 2003 Jun;114(6):1041-52. doi: 10.1016/s1388-2457(03)00066-x. Clin Neurophysiol. 2003. PMID: 12804673

6

Rhythmic cortical myoclonus in a case of HIV-related encephalopathy.

Canafoglia L, Panzica F, Franceschetti S, Carriero MR, Ciano C, Scaioli V, Chiapparini L, Visani E, Avanzini G. Canafoglia L, et al. Mov Disord. 2003 Dec;18(12):1533-8. doi: 10.1002/mds.10584. Mov Disord. 2003. PMID: 14673894

7

Sensorimotor cortex excitability in Unverricht-Lundborg disease and Lafora body disease.

Canafoglia L, Ciano C, Panzica F, Scaioli V, Zucca C, Agazzi P, Visani E, Avanzini G, Franceschetti S. Canafoglia L, et al. Neurology. 2004 Dec 28;63(12):2309-15. doi: 10.1212/01.wnl.0000147475.71345.aa. Neurology. 2004. PMID: 15623692

8

FVEPs in Creutzfeldt-Jacob disease: waveforms and interaction with the periodic EEG pattern assessed by single sweep analysis.

Visani E, Agazzi P, Scaioli V, Giaccone G, Binelli S, Canafoglia L, Panzica F, Tagliavini F, Bugiani O, Avanzini G, Franceschetti S. Visani E, et al. Among authors: canafoglia l. Clin Neurophysiol. 2005 Apr;116(4):895-904. doi: 10.1016/j.clinph.2004.11.019. Epub 2005 Jan 13. Clin Neurophysiol. 2005. PMID: 15792899

9

Movement-related desynchronization-synchronization (ERD/ERS) in patients with Unverricht-Lundborg disease.

Visani E, Agazzi P, Canafoglia L, Panzica F, Ciano C, Scaioli V, Avanzini G, Franceschetti S. Visani E, et al. Among authors: canafoglia l. Neuroimage. 2006 Oct 15;33(1):161-8. doi: 10.1016/j.neuroimage.2006.06.036. Epub 2006 Aug 10. Neuroimage. 2006. PMID: 16904345

10

High-frequency rhythmic cortical myoclonus in a long-surviving patient with nonketotic hypergylcemia.

Mastrangelo M, Canafoglia L, Franceschetti S, Oppezzo C, Mosca F, Menni F, Parini R, Ciano C, Scaioli V, Panzica F. Mastrangelo M, et al. Among authors: canafoglia l. J Child Neurol. 2008 Mar;23(3):321-4. doi: 10.1177/0883073807308699. Epub 2008 Jan 8. J Child Neurol. 2008. PMID: 18182648

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