Bisulli F - Search Results

1

Is Focal Cortical Dysplasia/Epilepsy Caused by Somatic MTOR Mutations Always a Unilateral Disorder?

Guerrini R, Cavallin M, Pippucci T, Rosati A, Bisulli F, Dimartino P, Barba C, Garbelli R, Buccoliero AM, Tassi L, Conti V. Guerrini R, et al. Among authors: bisulli f. Neurol Genet. 2020 Dec 8;7(1):e540. doi: 10.1212/NXG.0000000000000540. eCollection 2021 Feb. Neurol Genet. 2020. PMID: 33542949 Free PMC article. Review.

2

Efficacy of lamotrigine add-on therapy in severe partial epilepsy in adults with drop seizures and secondary bilateral synchrony on EEG.

Bisulli F, Baruzzi A, Rosati A, Riva R, Avoni P, Cerullo A, Tinuper P. Bisulli F, et al. Epileptic Disord. 2001 Sep;3(3):151-6. Epileptic Disord. 2001. PMID: 11679308 Free article. Clinical Trial.

3

Autosomal dominant early-onset cortical myoclonus, photic-induced myoclonus, and epilepsy in a large pedigree.

Gardella E, Tinuper P, Marini C, Guerrini R, Parrini E, Bisulli F, Liguori R, Montagna P, Lugaresi E. Gardella E, et al. Among authors: bisulli f. Epilepsia. 2006 Oct;47(10):1643-9. doi: 10.1111/j.1528-1167.2006.00636.x. Epilepsia. 2006. PMID: 17054686 Free article.

4

Semiological study of ictal affective behaviour in epilepsy and mental retardation limited to females (EFMR).

Antelmi E, Mastrangelo M, Bisulli F, Spaccini L, Stipa C, Mostacci B, Mei D, Guerrini R, Tinuper P. Antelmi E, et al. Among authors: bisulli f. Epileptic Disord. 2012 Sep;14(3):304-9. doi: 10.1684/epd.2012.0526. Epileptic Disord. 2012. PMID: 22932693 Free article.

5

A novel pedigree with familial cortical myoclonic tremor and epilepsy (FCMTE): clinical characterization, refinement of the FCMTE2 locus, and confirmation of a founder haplotype.

Licchetta L, Pippucci T, Bisulli F, Cantalupo G, Magini P, Alvisi L, Baldassari S, Martinelli P, Naldi I, Vanni N, Liguori R, Seri M, Tinuper P. Licchetta L, et al. Among authors: bisulli f. Epilepsia. 2013 Jul;54(7):1298-306. doi: 10.1111/epi.12216. Epub 2013 May 11. Epilepsia. 2013. PMID: 23663087 Free article.

6

Nocturnal frontal lobe epilepsy.

Nobili L, Proserpio P, Combi R, Provini F, Plazzi G, Bisulli F, Tassi L, Tinuper P. Nobili L, et al. Among authors: bisulli f. Curr Neurol Neurosci Rep. 2014 Feb;14(2):424. doi: 10.1007/s11910-013-0424-6. Curr Neurol Neurosci Rep. 2014. PMID: 24395520 Free article. Review.

7

Autosomal dominant partial epilepsy with auditory features: a new locus on chromosome 19q13.11-q13.31.

Bisulli F, Naldi I, Baldassari S, Magini P, Licchetta L, Castegnaro G, Fabbri M, Stipa C, Ferrari S, Seri M, Gonçalves Silva GE, Tinuper P, Pippucci T. Bisulli F, et al. Epilepsia. 2014 Jun;55(6):841-8. doi: 10.1111/epi.12560. Epub 2014 Mar 1. Epilepsia. 2014. PMID: 24579982 Free article.

8

LGI1 microdeletions are not a frequent cause of partial epilepsy with auditory features (PEAF).

Magini P, Bisulli F, Baldassari S, Stipa C, Naldi I, Licchetta L, Menghi V, Tinuper P, Seri M, Pippucci T. Magini P, et al. Among authors: bisulli f. Epilepsy Res. 2014 Jul;108(5):972-7. doi: 10.1016/j.eplepsyres.2014.03.005. Epub 2014 Mar 26. Epilepsy Res. 2014. PMID: 24721199

9

Auditory aura in nocturnal frontal lobe epilepsy: a red flag to suspect an extra-frontal epileptogenic zone.

Ferri L, Bisulli F, Nobili L, Tassi L, Licchetta L, Mostacci B, Stipa C, Mainieri G, Bernabè G, Provini F, Tinuper P. Ferri L, et al. Among authors: bisulli f. Sleep Med. 2014 Nov;15(11):1417-23. doi: 10.1016/j.sleep.2014.06.019. Epub 2014 Aug 15. Sleep Med. 2014. PMID: 25224073 Free PMC article.

10

PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsy.

Hildebrand MS, Tankard R, Gazina EV, Damiano JA, Lawrence KM, Dahl HH, Regan BM, Shearer AE, Smith RJ, Marini C, Guerrini R, Labate A, Gambardella A, Tinuper P, Lichetta L, Baldassari S, Bisulli F, Pippucci T, Scheffer IE, Reid CA, Petrou S, Bahlo M, Berkovic SF. Hildebrand MS, et al. Among authors: bisulli f. Ann Clin Transl Neurol. 2015 Aug;2(8):821-30. doi: 10.1002/acn3.224. Epub 2015 Jul 3. Ann Clin Transl Neurol. 2015. PMID: 26339676 Free PMC article.

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