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Items: 1 to 50 of 52

1.

Super refractory status epilepticus in Lafora disease interrupted by vagus nerve stimulation: A case report.

Mostacci B, Bisulli F, Muccioli L, Minardi I, Bandini M, Licchetta L, Zucchelli M, Leta C, Michelucci R, Zanello M, Tinuper P.

Brain Stimul. 2019 Aug 20. pii: S1935-861X(19)30354-7. doi: 10.1016/j.brs.2019.08.008. [Epub ahead of print] No abstract available.

PMID:
31471204
2.

An Italian multicentre study of perampanel in progressive myoclonus epilepsies.

Canafoglia L, Barbella G, Ferlazzo E, Striano P, Magaudda A, d'Orsi G, Martino T, Avolio C, Aguglia U, Sueri C, Giuliano L, Sofia V, Zibordi F, Ragona F, Freri E, Costa C, Nardi Cesarini E, Fanella M, Rossi Sebastiano D, Riguzzi P, Gambardella A, Di Bonaventura C, Michelucci R, Granata T, Bisulli F, Licchetta L, Tinuper P, Beccaria F, Visani E, Franceschetti S.

Epilepsy Res. 2019 Oct;156:106191. doi: 10.1016/j.eplepsyres.2019.106191. Epub 2019 Aug 16.

PMID:
31446282
3.

Treatment with metformin in twelve patients with Lafora disease.

Bisulli F, Muccioli L, d'Orsi G, Canafoglia L, Freri E, Licchetta L, Mostacci B, Riguzzi P, Pondrelli F, Avolio C, Martino T, Michelucci R, Tinuper P.

Orphanet J Rare Dis. 2019 Jun 21;14(1):149. doi: 10.1186/s13023-019-1132-3.

4.

Clinical Features and Pathophysiology of Disorders of Arousal in Adults: A Window Into the Sleeping Brain.

Baldini T, Loddo G, Sessagesimi E, Mignani F, Cirignotta F, Mondini S, Licchetta L, Bisulli F, Tinuper P, Provini F.

Front Neurol. 2019 May 17;10:526. doi: 10.3389/fneur.2019.00526. eCollection 2019.

5.

SCN1A mutations in focal epilepsy with auditory features: widening the spectrum of GEFS plus.

Bisulli F, Licchetta L, Baldassari S, Muccioli L, Marconi C, Cantalupo G, Myers C, Menghi V, Minardi R, Caporali L, Marini C, Guerrini R, Mefford HC, Tinuper P, Pippucci T.

Epileptic Disord. 2019 Apr 1;21(2):185-191. doi: 10.1684/epd.2019.1046.

PMID:
30977726
6.

Contribution of ultrarare variants in mTOR pathway genes to sporadic focal epilepsies.

Pippucci T, Licchetta L, Baldassari S, Marconi C, De Luise M, Myers C, Nardi E, Provini F, Cameli C, Minardi R, Bacchelli E, Giordano L, Crichiutti G, d'Orsi G, Seri M, Gasparre G, Mefford HC, Tinuper P, Bisulli F; Collaborative Group of Italian League Against Epilepsy (LICE) Genetic Commission.

Ann Clin Transl Neurol. 2019 Feb 25;6(3):475-485. doi: 10.1002/acn3.722. eCollection 2019 Mar.

7.

Juvenile absence epilepsy relapsing as recurrent absence status, mimicking transient global amnesia, in an elderly patient.

Muccioli L, Licchetta L, Stipa C, Tinuper P, Bisulli F.

Epileptic Disord. 2018 Dec 1;20(6):557-561. doi: 10.1684/epd.2018.1016.

PMID:
30530409
8.

Cortical myoclonic tremor induced by fixation-off sensitivity: An unusual cause of insomnia.

Licchetta L, Bisulli F, Ferri L, Cantalupo G, Alvisi L, Vignatelli L, Loddo G, Provini F, Tinuper P.

Neurology. 2018 Dec 4;91(23):1061-1063. doi: 10.1212/WNL.0000000000006620. Epub 2018 Nov 9. No abstract available.

PMID:
30413630
9.

Nocturnal motor behaviors with unexpected EEG and brain MRI findings.

Baldini T, Loddo G, Mignani F, Licchetta L, Bisulli F, Tinuper P, Provini F.

Sleep Med. 2018 Dec;52:116-117. doi: 10.1016/j.sleep.2018.08.017. Epub 2018 Sep 6. No abstract available.

PMID:
30308451
10.

Correction: The landscape of epilepsy-related GATOR1 variants.

Baldassari S, Picard F, Verbeek NE, van Kempen M, Brilstra EH, Lesca G, Conti V, Guerrini R, Bisulli F, Licchetta L, Pippucci T, Tinuper P, Hirsch E, de Saint Martin A, Chelly J, Rudolf G, Chipaux M, Ferrand-Sorbets S, Dorfmüller G, Sisodiya S, Balestrini S, Schoeler N, Hernandez-Hernandez L, Krithika S, Oegema R, Hagebeuk E, Gunning B, Deckers C, Berghuis B, Wegner I, Niks EH, Jansen FE, Braun K, de Jong D, Rubboli G, Talvik I, Sander V, Uldall P, Jacquemont ML, Nava C, Leguern E, Julia S, Gambardella A, d'Orsi G, Crichiutti G, Faivre L, Darmency V, Benova B, Krsek P, Biraben A, Lebre AS, Jennesson M, Sattar S, Marchal C, NordliJr DR, Lindstrom K, Striano P, Lomax LB, Kiss C, Bartolomei F, Lepine AF, Schoonjans AS, Stouffs K, Jansen A, Panagiotakaki E, Ricard-Mousnier B, Thevenon J, de Bellescize J, Catenoix H, Dorn T, Zenker M, Müller-Schlüter K, Brandt C, Krey I, Polster T, Wolff M, Balci M, Rostasy K, Achaz G, Zacher P, Becher T, Cloppenborg T, Yuskaitis CJ, Weckhuysen S, Poduri A, Lemke JR, Møller RS, Baulac S.

Genet Med. 2019 Aug;21(8):1896. doi: 10.1038/s41436-018-0325-9.

PMID:
30262923
11.

Estrogen-related seizure exacerbation following hormone therapy for assisted reproduction in women with epilepsy.

Mostacci B, Esposto R, Lello S, Bisulli F, Licchetta L, Tinuper P.

Seizure. 2018 Oct;61:200-202. doi: 10.1016/j.seizure.2018.08.024. Epub 2018 Aug 30.

PMID:
30199820
12.

Correction to: The landscape of epilepsy-related GATOR1 variants.

Baldassari S, Picard F, Verbeek NE, van Kempen M, Brilstra EH, Lesca G, Conti V, Guerrini R, Bisulli F, Licchetta L, Pippucci T, Tinuper P, Hirsch E, Martin AS, Chelly J, Rudolf G, Chipaux M, Ferrand-Sorbets S, Dorfmüller G, Sisodiya S, Balestrini S, Schoeler N, Hernandez-Hernandez L, Krithika S, Oegema R, Hagebeuk E, Gunning B, Deckers C, Berghuis B, Wegner I, Niks E, Jansen F, Braun K, Jong D, Rubboli G, Talvik I, Sander V, Uldall P, Jacquemont ML, Nava C, Leguern E, Julia S, Gambardella A, d'Orsi G, Crichiutti G, Faivre L, Darmency V, Benova B, Krsek P, Biraben A, Lebre AS, Jennesson M, Sattar S, Marchal C, NordliJr DR, Lindstrom K, Striano P, Lomax LB, Kiss C, Bartolomei F, Lepine AF, Schoonjans AS, Stouffs K, Jansen A, Panagiotakaki E, Ricard-Mousnier B, Thevenon J, Bellescize J, Catenoix H, Dorn T, Zenker M, Müller-Schlüter K, Brandt C, Krey I, Polster T, Wolff M, Balci M, Rostasy K, Achaz G, Zacher P, Becher T, Cloppenborg T, Yuskaitis CJ, Weckhuysen S, Poduri A, Lemke JR, Møller RS, Baulac S.

Genet Med. 2019 Jul;21(7):1671. doi: 10.1038/s41436-018-0284-1.

PMID:
30158694
13.

The landscape of epilepsy-related GATOR1 variants.

Baldassari S, Picard F, Verbeek NE, van Kempen M, Brilstra EH, Lesca G, Conti V, Guerrini R, Bisulli F, Licchetta L, Pippucci T, Tinuper P, Hirsch E, de Saint Martin A, Chelly J, Rudolf G, Chipaux M, Ferrand-Sorbets S, Dorfmüller G, Sisodiya S, Balestrini S, Schoeler N, Hernandez-Hernandez L, Krithika S, Oegema R, Hagebeuk E, Gunning B, Deckers C, Berghuis B, Wegner I, Niks E, Jansen FE, Braun K, de Jong D, Rubboli G, Talvik I, Sander V, Uldall P, Jacquemont ML, Nava C, Leguern E, Julia S, Gambardella A, d'Orsi G, Crichiutti G, Faivre L, Darmency V, Benova B, Krsek P, Biraben A, Lebre AS, Jennesson M, Sattar S, Marchal C, Nordli DR Jr, Lindstrom K, Striano P, Lomax LB, Kiss C, Bartolomei F, Lepine AF, Schoonjans AS, Stouffs K, Jansen A, Panagiotakaki E, Ricard-Mousnier B, Thevenon J, de Bellescize J, Catenoix H, Dorn T, Zenker M, Müller-Schlüter K, Brandt C, Krey I, Polster T, Wolff M, Balci M, Rostasy K, Achaz G, Zacher P, Becher T, Cloppenborg T, Yuskaitis CJ, Weckhuysen S, Poduri A, Lemke JR, Møller RS, Baulac S.

Genet Med. 2019 Feb;21(2):398-408. doi: 10.1038/s41436-018-0060-2. Epub 2018 Aug 10. Erratum in: Genet Med. 2018 Aug 29;:. Genet Med. 2018 Sep 27;:.

14.

Profile of neuropsychological impairment in Sleep-related Hypermotor Epilepsy.

Licchetta L, Poda R, Vignatelli L, Pippucci T, Zenesini C, Menghi V, Mostacci B, Baldassari S, Provini F, Tinuper P, Bisulli F.

Sleep Med. 2018 Aug;48:8-15. doi: 10.1016/j.sleep.2018.03.027. Epub 2018 Apr 30.

PMID:
29843024
15.

Epilepsy with auditory features: Long-term outcome and predictors of terminal remission.

Bisulli F, Menghi V, Vignatelli L, Licchetta L, Zenesini C, Stipa C, Morigi F, Gizzi M, Avoni P, Provini F, Mostacci B, d'Orsi G, Pippucci T, Muccioli L, Tinuper P.

Epilepsia. 2018 Apr;59(4):834-843. doi: 10.1111/epi.14033. Epub 2018 Feb 21.

16.

Phenotype variability of GLUT1 deficiency syndrome: Description of a case series with novel SLC2A1 gene mutations.

Di Vito L, Licchetta L, Pippucci T, Baldassari S, Stipa C, Mostacci B, Alvisi L, Tinuper P, Bisulli F.

Epilepsy Behav. 2018 Feb;79:169-173. doi: 10.1016/j.yebeh.2017.12.012. Epub 2018 Jan 4. No abstract available.

PMID:
29306089
17.

Specific motor patterns of arousal disorders in adults: a video-polysomnographic analysis of 184 episodes.

Loddo G, Sessagesimi E, Mignani F, Cirignotta F, Mondini S, Licchetta L, Bisulli F, Tinuper P, Provini F.

Sleep Med. 2018 Jan;41:102-109. doi: 10.1016/j.sleep.2017.08.019. Epub 2017 Oct 7.

PMID:
29174185
18.

A stereo EEG study in a patient with sleep-related hypermotor epilepsy due to DEPDC5 mutation.

Ferri L, Bisulli F, Mai R, Licchetta L, Leta C, Nobili L, Mostacci B, Pippucci T, Tinuper P.

Seizure. 2017 Dec;53:51-54. doi: 10.1016/j.seizure.2017.10.022. Epub 2017 Nov 4.

19.

Proton MR Spectroscopy in Patients With Sleep-Related Hypermotor Epilepsy (SHE): Evidence of Altered Cingulate Cortex Metabolism.

Naldi I, Bisulli F, Testa C, Rizzo G, Ferri L, Gramegna LL, Licchetta L, Lodi R, Tonon C, Tinuper P.

Sleep. 2017 Sep 1;40(9). doi: 10.1093/sleep/zsx115.

PMID:
28934527
20.

Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K+ channel properties.

Oliver KL, Franceschetti S, Milligan CJ, Muona M, Mandelstam SA, Canafoglia L, Boguszewska-Chachulska AM, Korczyn AD, Bisulli F, Di Bonaventura C, Ragona F, Michelucci R, Ben-Zeev B, Straussberg R, Panzica F, Massano J, Friedman D, Crespel A, Engelsen BA, Andermann F, Andermann E, Spodar K, Lasek-Bal A, Riguzzi P, Pasini E, Tinuper P, Licchetta L, Gardella E, Lindenau M, Wulf A, Møller RS, Benninger F, Afawi Z, Rubboli G, Reid CA, Maljevic S, Lerche H, Lehesjoki AE, Petrou S, Berkovic SF.

Ann Neurol. 2017 May;81(5):677-689. doi: 10.1002/ana.24929.

PMID:
28380698
21.

Prevalence of Sleep-Related Hypermotor Epilepsy-Formerly Named Nocturnal Frontal Lobe Epilepsy-in the Adult Population of the Emilia-Romagna Region, Italy.

Vignatelli L, Bisulli F, Giovannini G, Licchetta L, Naldi I, Mostacci B, Rubboli G, Provini F, Tinuper P, Meletti S.

Sleep. 2017 Feb 1;40(2). doi: 10.1093/sleep/zsw041. No abstract available.

PMID:
28364515
22.

Incidence of sudden unexpected death in epilepsy in sleep-related hypermotor epilepsy, formerly named nocturnal frontal lobe epilepsy.

Mostacci B, Bisulli F, Vignatelli L, Licchetta L, Di Vito L, Rinaldi C, Trippi I, Ferri L, Plazzi G, Provini F, Tinuper P.

Sleep Med. 2017 Jan;29:98. doi: 10.1016/j.sleep.2016.09.005. Epub 2016 Oct 29. No abstract available.

PMID:
27915205
23.

Sleep-related hypermotor epilepsy: Long-term outcome in a large cohort.

Licchetta L, Bisulli F, Vignatelli L, Zenesini C, Di Vito L, Mostacci B, Rinaldi C, Trippi I, Naldi I, Plazzi G, Provini F, Tinuper P.

Neurology. 2017 Jan 3;88(1):70-77. doi: 10.1212/WNL.0000000000003459. Epub 2016 Nov 23.

24.

Epilepsy in ring chromosome 20 syndrome.

Vignoli A, Bisulli F, Darra F, Mastrangelo M, Barba C, Giordano L, Turner K, Zambrelli E, Chiesa V, Bova S, Fiocchi I, Peron A, Naldi I, Milito G, Licchetta L, Tinuper P, Guerrini R, Dalla Bernardina B, Canevini MP.

Epilepsy Res. 2016 Dec;128:83-93. doi: 10.1016/j.eplepsyres.2016.10.004. Epub 2016 Oct 24.

PMID:
27816898
25.

Identity by descent fine mapping of familial adult myoclonus epilepsy (FAME) to 2p11.2-2q11.2.

Henden L, Freytag S, Afawi Z, Baldassari S, Berkovic SF, Bisulli F, Canafoglia L, Casari G, Crompton DE, Depienne C, Gecz J, Guerrini R, Helbig I, Hirsch E, Keren B, Klein KM, Labauge P, LeGuern E, Licchetta L, Mei D, Nava C, Pippucci T, Rudolf G, Scheffer IE, Striano P, Tinuper P, Zara F, Corbett M, Bahlo M.

Hum Genet. 2016 Oct;135(10):1117-25. doi: 10.1007/s00439-016-1700-8. Epub 2016 Jul 1.

PMID:
27368338
26.

GATOR1 complex: the common genetic actor in focal epilepsies.

Baldassari S, Licchetta L, Tinuper P, Bisulli F, Pippucci T.

J Med Genet. 2016 Aug;53(8):503-10. doi: 10.1136/jmedgenet-2016-103883. Epub 2016 May 19. Review.

PMID:
27208208
27.

Definition and diagnostic criteria of sleep-related hypermotor epilepsy.

Tinuper P, Bisulli F, Cross JH, Hesdorffer D, Kahane P, Nobili L, Provini F, Scheffer IE, Tassi L, Vignatelli L, Bassetti C, Cirignotta F, Derry C, Gambardella A, Guerrini R, Halasz P, Licchetta L, Mahowald M, Manni R, Marini C, Mostacci B, Naldi I, Parrino L, Picard F, Pugliatti M, Ryvlin P, Vigevano F, Zucconi M, Berkovic S, Ottman R.

Neurology. 2016 May 10;86(19):1834-42. doi: 10.1212/WNL.0000000000002666. Epub 2016 Apr 15. Review.

28.

Epilepsy with auditory features: A heterogeneous clinico-molecular disease.

Pippucci T, Licchetta L, Baldassari S, Palombo F, Menghi V, D'Aurizio R, Leta C, Stipa C, Boero G, d'Orsi G, Magi A, Scheffer I, Seri M, Tinuper P, Bisulli F.

Neurol Genet. 2015 May 14;1(1):e5. doi: 10.1212/NXG.0000000000000005. eCollection 2015 Jun.

29.

DEPDC5 mutations in epilepsy with auditory features.

Bisulli F, Licchetta L, Baldassari S, Pippucci T, Tinuper P.

Epilepsia. 2016 Feb;57(2):335. doi: 10.1111/epi.13233. No abstract available.

30.

Psychiatric comorbidities in patients from seven families with autosomal dominant cortical tremor, myoclonus, and epilepsy.

Coppola A, Caccavale C, Santulli L, Balestrini S, Cagnetti C, Licchetta L, Esposito M, Bisulli F, Tinuper P, Provinciali L, Minetti C, Zara F, Striano P, Striano S.

Epilepsy Behav. 2016 Mar;56:38-43. doi: 10.1016/j.yebeh.2015.12.038. Epub 2016 Jan 29.

PMID:
26827300
31.

Behçet disease presenting with movement disorders and antibasal ganglia antibodies.

Rizzo G, Licchetta L, Scaglione C, Buttiglione M, Capellari S, Martinelli P, Martino D.

Autoimmun Rev. 2016 Mar;15(3):287-8. doi: 10.1016/j.autrev.2015.11.011. Epub 2015 Nov 27. No abstract available.

PMID:
26640160
32.

Mutations in the mammalian target of rapamycin pathway regulators NPRL2 and NPRL3 cause focal epilepsy.

Ricos MG, Hodgson BL, Pippucci T, Saidin A, Ong YS, Heron SE, Licchetta L, Bisulli F, Bayly MA, Hughes J, Baldassari S, Palombo F; Epilepsy Electroclinical Study Group, Santucci M, Meletti S, Berkovic SF, Rubboli G, Thomas PQ, Scheffer IE, Tinuper P, Geoghegan J, Schreiber AW, Dibbens LM.

Ann Neurol. 2016 Jan;79(1):120-31. doi: 10.1002/ana.24547. Epub 2015 Dec 12.

PMID:
26505888
33.

A novel mutation af Cln3 associated with delayed-classic juvenile ceroid lipofuscinois and autophagic vacuolar myopathy.

Licchetta L, Bisulli F, Fietz M, Valentino ML, Morbin M, Mostacci B, Oliver KL, Berkovic SF, Tinuper P.

Eur J Med Genet. 2015 Oct;58(10):540-4. doi: 10.1016/j.ejmg.2015.09.002. Epub 2015 Sep 7.

PMID:
26360874
34.

Response to the letter "New avenues to prevent sudden unexpected death in nocturnal frontal lobe epilepsy: follow the route established by omega-3 polyunsaturated fatty acids".

Mostacci B, Bisulli F, Vignatelli L, Licchetta L, Di Vito L, Rinaldi C, Trippi I, Ferri L, Plazzi G, Provini F, Tinuper P.

Sleep Med. 2015 Aug;16(8):1022-3. doi: 10.1016/j.sleep.2015.04.017. Epub 2015 May 27. No abstract available.

PMID:
26116948
35.

Incidence of sudden unexpected death in nocturnal frontal lobe epilepsy: a cohort study.

Mostacci B, Bisulli F, Vignatelli L, Licchetta L, Di Vito L, Rinaldi C, Trippi I, Ferri L, Plazzi G, Provini F, Tinuper P.

Sleep Med. 2015 Feb;16(2):232-6. doi: 10.1016/j.sleep.2014.09.019. Epub 2014 Dec 16.

36.

Prevalence of nocturnal frontal lobe epilepsy in the adult population of Bologna and Modena, Emilia-Romagna region, Italy.

Vignatelli L, Bisulli F, Giovannini G, Licchetta L, Naldi I, Mostacci B, Rubboli G, Provini F, Tinuper P, Meletti S.

Sleep. 2015 Mar 1;38(3):479-85. doi: 10.5665/sleep.4514.

37.

A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy.

Muona M, Berkovic SF, Dibbens LM, Oliver KL, Maljevic S, Bayly MA, Joensuu T, Canafoglia L, Franceschetti S, Michelucci R, Markkinen S, Heron SE, Hildebrand MS, Andermann E, Andermann F, Gambardella A, Tinuper P, Licchetta L, Scheffer IE, Criscuolo C, Filla A, Ferlazzo E, Ahmad J, Ahmad A, Baykan B, Said E, Topcu M, Riguzzi P, King MD, Ozkara C, Andrade DM, Engelsen BA, Crespel A, Lindenau M, Lohmann E, Saletti V, Massano J, Privitera M, Espay AJ, Kauffmann B, Duchowny M, Møller RS, Straussberg R, Afawi Z, Ben-Zeev B, Samocha KE, Daly MJ, Petrou S, Lerche H, Palotie A, Lehesjoki AE.

Nat Genet. 2015 Jan;47(1):39-46. doi: 10.1038/ng.3144. Epub 2014 Nov 17.

38.

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.

Sleep Med. 2014 Nov;15(11):1417-23. doi: 10.1016/j.sleep.2014.06.019. Epub 2014 Aug 15.

39.

Limbic encephalitis with anti-GAD antibodies and Thomsen myotonia: a casual or causal association?

Licchetta L, Bisulli F, Naldi I, Mainieri G, Tinuper P.

Epileptic Disord. 2014 Sep;16(3):362-5. doi: 10.1684/epd.2014.0668.

40.

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.

Epilepsy Res. 2014 Jul;108(5):972-7. doi: 10.1016/j.eplepsyres.2014.03.005. Epub 2014 Mar 26.

PMID:
24721199
41.

Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformations.

Scheffer IE, Heron SE, Regan BM, Mandelstam S, Crompton DE, Hodgson BL, Licchetta L, Provini F, Bisulli F, Vadlamudi L, Gecz J, Connelly A, Tinuper P, Ricos MG, Berkovic SF, Dibbens LM.

Ann Neurol. 2014 May;75(5):782-7. doi: 10.1002/ana.24126. Epub 2014 Apr 14.

PMID:
24585383
42.

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.

Epilepsia. 2014 Jun;55(6):841-8. doi: 10.1111/epi.12560. Epub 2014 Mar 1.

43.

Tailored surgery for drug-resistant epilepsy due to temporal pole encephalocele and microdysgenesis.

Giulioni M, Licchetta L, Bisulli F, Rubboli G, Mostacci B, Marucci G, Martinoni M, Ferri L, Volpi L, Calbucci F, Baruzzi A, Tinuper P.

Seizure. 2014 Feb;23(2):164-6. doi: 10.1016/j.seizure.2013.10.005. Epub 2013 Oct 17. No abstract available.

44.

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.

Epilepsia. 2013 Jul;54(7):1298-306. doi: 10.1111/epi.12216. Epub 2013 May 11. Erratum in: Epilepsia. 2013 Sep;54(9):1709.

45.

Mutations in DEPDC5 cause familial focal epilepsy with variable foci.

Dibbens LM, de Vries B, Donatello S, Heron SE, Hodgson BL, Chintawar S, Crompton DE, Hughes JN, Bellows ST, Klein KM, Callenbach PM, Corbett MA, Gardner AE, Kivity S, Iona X, Regan BM, Weller CM, Crimmins D, O'Brien TJ, Guerrero-López R, Mulley JC, Dubeau F, Licchetta L, Bisulli F, Cossette P, Thomas PQ, Gecz J, Serratosa J, Brouwer OF, Andermann F, Andermann E, van den Maagdenberg AM, Pandolfo M, Berkovic SF, Scheffer IE.

Nat Genet. 2013 May;45(5):546-51. doi: 10.1038/ng.2599. Epub 2013 Mar 31.

PMID:
23542697
46.

Tobacco habits in nocturnal frontal lobe epilepsy.

Naldi I, Bisulli F, Vignatelli L, Licchetta L, Pittau F, Di Vito L, Mostacci B, Menghi V, Provini F, Montagna P, Tinuper P.

Epilepsy Behav. 2013 Jan;26(1):114-7. doi: 10.1016/j.yebeh.2012.10.014. Epub 2012 Dec 12.

PMID:
23246147
47.

Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy.

Heron SE, Smith KR, Bahlo M, Nobili L, Kahana E, Licchetta L, Oliver KL, Mazarib A, Afawi Z, Korczyn A, Plazzi G, Petrou S, Berkovic SF, Scheffer IE, Dibbens LM.

Nat Genet. 2012 Nov;44(11):1188-90. doi: 10.1038/ng.2440. Epub 2012 Oct 21.

PMID:
23086396
48.

Ictal characteristics of psychogenic nonepileptic seizures: what we have learned from video/EEG recordings--a literature review.

Mostacci B, Bisulli F, Alvisi L, Licchetta L, Baruzzi A, Tinuper P.

Epilepsy Behav. 2011 Oct;22(2):144-53. doi: 10.1016/j.yebeh.2011.07.003. Review.

PMID:
21856237
49.

Epilepsy in coeliac disease: not just a matter of calcifications.

Licchetta L, Bisulli F, Di Vito L, La Morgia C, Naldi I, Volta U, Tinuper P.

Neurol Sci. 2011 Dec;32(6):1069-74. doi: 10.1007/s10072-011-0629-x. Epub 2011 Jun 1.

PMID:
21630037
50.

Relationship between adverse effects of antiepileptic drugs, number of coprescribed drugs, and drug load in a large cohort of consecutive patients with drug-refractory epilepsy.

Canevini MP, De Sarro G, Galimberti CA, Gatti G, Licchetta L, Malerba A, Muscas G, La Neve A, Striano P, Perucca E; SOPHIE Study Group.

Epilepsia. 2010 May;51(5):797-804. doi: 10.1111/j.1528-1167.2010.02520.x. Epub 2010 Apr 20.

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