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Items: 1 to 50 of 57

1.

Clinical spectrum of STX1B-related epileptic disorders.

Wolking S, May P, Mei D, Møller RS, Balestrini S, Helbig KL, Altuzarra CD, Chatron N, Kaiwar C, Stöhr K, Widdess-Walsh P, Mendelsohn BA, Numis A, Cilio MR, Van Paesschen W, Svendsen LL, Oates S, Hughes E, Goyal S, Brown K, Sifuentes Saenz M, Dorn T, Muhle H, Pagnamenta AT, Vavoulis DV, Knight SJL, Taylor JC, Canevini MP, Darra F, Gavrilova RH, Powis Z, Tang S, Marquetand J, Armstrong M, McHale D, Klee EW, Kluger GJ, Lowenstein DH, Weckhuysen S, Pal DK, Helbig I, Guerrini R, Thomas RH, Rees MI, Lesca G, Sisodiya SM, Weber YG, Lal D, Marini C, Lerche H, Schubert J.

Neurology. 2019 Feb 8. pii: 10.1212/WNL.0000000000007089. doi: 10.1212/WNL.0000000000007089. [Epub ahead of print]

PMID:
30737342
2.

Defining the electroclinical phenotype and outcome of PCDH19-related epilepsy: A multicenter study.

Trivisano M, Pietrafusa N, Terracciano A, Marini C, Mei D, Darra F, Accorsi P, Battaglia D, Caffi L, Canevini MP, Cappelletti S, Cesaroni E, de Palma L, Costa P, Cusmai R, Giordano L, Ferrari A, Freri E, Fusco L, Granata T, Martino T, Mastrangelo M, Bova SM, Parmeggiani L, Ragona F, Sicca F, Striano P, Specchio LM, Tondo I, Zambrelli E, Zamponi N, Zanus C, Boniver C, Vecchi M, Avolio C, Dalla Bernardina B, Bertini E, Guerrini R, Vigevano F, Specchio N.

Epilepsia. 2018 Dec;59(12):2260-2271. doi: 10.1111/epi.14600. Epub 2018 Nov 19.

PMID:
30451291
3.

Diaper changing-induced reflex seizures in CDKL5-related epilepsy.

Solazzi R, Fiorini E, Parrini E, Darra F, Dalla Bernardina B, Cantalupo G.

Epileptic Disord. 2018 Oct 1;20(5):428-433. doi: 10.1684/epd.2018.0999.

PMID:
30378547
4.

The phenotype of SCN8A developmental and epileptic encephalopathy.

Gardella E, Marini C, Trivisano M, Fitzgerald MP, Alber M, Howell KB, Darra F, Siliquini S, Bölsterli BK, Masnada S, Pichiecchio A, Johannesen KM, Jepsen B, Fontana E, Anibaldi G, Russo S, Cogliati F, Montomoli M, Specchio N, Rubboli G, Veggiotti P, Beniczky S, Wolff M, Helbig I, Vigevano F, Scheffer IE, Guerrini R, Møller RS.

Neurology. 2018 Sep 18;91(12):e1112-e1124. doi: 10.1212/WNL.0000000000006199. Epub 2018 Aug 31.

PMID:
30171078
5.

Early Treatment with Quinidine in 2 Patients with Epilepsy of Infancy with Migrating Focal Seizures (EIMFS) Due to Gain-of-Function KCNT1 Mutations: Functional Studies, Clinical Responses, and Critical Issues for Personalized Therapy.

Dilena R, DiFrancesco JC, Soldovieri MV, Giacobbe A, Ambrosino P, Mosca I, Galli MA, Guez S, Fumagalli M, Miceli F, Cattaneo D, Darra F, Gennaro E, Zara F, Striano P, Castellotti B, Gellera C, Varesio C, Veggiotti P, Taglialatela M.

Neurotherapeutics. 2018 Oct;15(4):1112-1126. doi: 10.1007/s13311-018-0657-9.

PMID:
30112700
6.

Chiari 1 Malformation in a Child with Febrile Seizures, Parasomnias, and Sleep Apnea Syndrome.

Zaffanello M, Darra F, Lo Barco T, Sala F, Gasperi E, Piacentini G.

Case Rep Pediatr. 2017;2017:8189790. doi: 10.1155/2017/8189790. Epub 2017 Dec 17.

7.

Electroclinical findings and long-term outcomes in epileptic patients with inv dup (15).

Matricardi S, Darra F, Spalice A, Basti C, Fontana E, Dalla Bernardina B, Elia M, Giordano L, Accorsi P, Cusmai R, De Liso P, Romeo A, Ragona F, Granata T, Concolino D, Carotenuto M, Pavone P, Pruna D, Striano P, Savasta S, Verrotti A.

Acta Neurol Scand. 2018 Jun;137(6):575-581. doi: 10.1111/ane.12902. Epub 2018 Jan 23.

PMID:
29363096
8.

The ketogenic diet in patients with myoclonic status in non-progressive encephalopathy.

Caraballo R, Darra F, Reyes G, Armeno M, Cresta A, Mestre G, Bernardina BD.

Seizure. 2017 Oct;51:1-5. doi: 10.1016/j.seizure.2017.07.002. Epub 2017 Jul 11.

9.

Neuroimaging Changes in Menkes Disease, Part 1.

Manara R, D'Agata L, Rocco MC, Cusmai R, Freri E, Pinelli L, Darra F, Procopio E, Mardari R, Zanus C, Di Rosa G, Soddu C, Severino M, Ermani M, Longo D, Sartori S; Menkes Working Group in the Italian Neuroimaging Network for Rare Diseases.

AJNR Am J Neuroradiol. 2017 Oct;38(10):1850-1857. doi: 10.3174/ajnr.A5186. Epub 2017 May 11. Review.

10.

Neuroimaging Changes in Menkes Disease, Part 2.

Manara R, Rocco MC, D'agata L, Cusmai R, Freri E, Giordano L, Darra F, Procopio E, Toldo I, Peruzzi C, Vittorini R, Spalice A, Fusco C, Nosadini M, Longo D, Sartori S; Menkes Working Group in the Italian Neuroimaging Network for Rare Diseases.

AJNR Am J Neuroradiol. 2017 Oct;38(10):1858-1865. doi: 10.3174/ajnr.A5192. Epub 2017 May 11. Review.

11.

EEG findings during "paroxysmal hemiplegia" in a patient with GLUT1-deficiency.

Pellegrin S, Cantalupo G, Opri R, Dalla Bernardina B, Darra F.

Eur J Paediatr Neurol. 2017 May;21(3):580-582. doi: 10.1016/j.ejpn.2017.01.002. Epub 2017 Jan 17.

PMID:
28129950
12.

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
13.

Symptomatic and presumed symptomatic focal epilepsies in childhood: An observational, prospective multicentre study.

Vecchi M, Barba C, De Carlo D, Stivala M, Guerrini R, Albamonte E, Ranalli D, Battaglia D, Lunardi G, Boniver C, Piccolo B, Pisani F, Cantalupo G, Nieddu G, Casellato S, Cappanera S, Cesaroni E, Zamponi N, Serino D, Fusco L, Iodice A, Palestra F, Giordano L, Freri E, De Giorgi I, Ragona F, Granata T, Fiocchi I, Bova SM, Mastrangelo M, Verrotti A, Matricardi S, Fontana E, Caputo D, Darra F, Dalla Bernardina B, Beccaria F, Capovilla G, Baglietto MP, Gagliardi A, Vignoli A, Canevini MP, Perissinotto E, Francione S.

Epilepsia. 2016 Nov;57(11):1808-1816. doi: 10.1111/epi.13574. Epub 2016 Oct 20.

14.

Progressive Myoclonus Epilepsy in Congenital Generalized Lipodystrophy type 2: Report of 3 cases and literature review.

Opri R, Fabrizi GM, Cantalupo G, Ferrarini M, Simonati A, Dalla Bernardina B, Darra F.

Seizure. 2016 Nov;42:1-6. doi: 10.1016/j.seizure.2016.08.008. Epub 2016 Sep 5. Review.

15.

Congenital disorders of glycosylation presenting as epileptic encephalopathy with migrating partial seizures in infancy.

Barba C, Darra F, Cusmai R, Procopio E, Dionisi Vici C, Keldermans L, Vuillaumier-Barrot S, Lefeber DJ, Guerrini R; CDG Group.

Dev Med Child Neurol. 2016 Oct;58(10):1085-91. doi: 10.1111/dmcn.13141. Epub 2016 May 13.

16.

Spinal muscular atrophy associated with progressive myoclonic epilepsy: A rare condition caused by mutations in ASAH1.

Rubboli G, Veggiotti P, Pini A, Berardinelli A, Cantalupo G, Bertini E, Tiziano FD, D'Amico A, Piazza E, Abiusi E, Fiori S, Pasini E, Darra F, Gobbi G, Michelucci R.

Epilepsia. 2015 May;56(5):692-8. doi: 10.1111/epi.12977. Epub 2015 Apr 3.

17.

Optimizing the molecular diagnosis of CDKL5 gene-related epileptic encephalopathy in boys.

Mei D, Darra F, Barba C, Marini C, Fontana E, Chiti L, Parrini E, Dalla Bernardina B, Guerrini R.

Epilepsia. 2014 Nov;55(11):1748-53. doi: 10.1111/epi.12803. Epub 2014 Sep 29.

18.

Epilepsy in Menkes disease: an electroclinical long-term study of 28 patients.

Verrotti A, Cusmai R, Darra F, Martelli P, Accorsi P, Bergamo S, Bevivino E, Coppola G, Freri E, Grosso S, Matricardi S, Parisi P, Sartori S, Spalice A, Specchio N, Carelli A, Zini D, Dalla Bernardina B, Giordano L.

Epilepsy Res. 2014 Nov;108(9):1597-603. doi: 10.1016/j.eplepsyres.2014.08.006. Epub 2014 Aug 30.

PMID:
25218893
19.

Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome.

Romani M, Micalizzi A, Kraoua I, Dotti MT, Cavallin M, Sztriha L, Ruta R, Mancini F, Mazza T, Castellana S, Hanene B, Carluccio MA, Darra F, Máté A, Zimmermann A, Gouider-Khouja N, Valente EM.

Orphanet J Rare Dis. 2014 May 5;9:72. doi: 10.1186/1750-1172-9-72.

20.

Epilepsy-related brain networks in ring chromosome 20 syndrome: an EEG-fMRI study.

Vaudano AE, Ruggieri A, Vignoli A, Avanzini P, Benuzzi F, Gessaroli G, Nichelli PF, Darra F, Cantalupo G, Mastrangelo M, Dalla Bernardina B, Canevini MP, Meletti S.

Epilepsia. 2014 Mar;55(3):403-13. doi: 10.1111/epi.12539. Epub 2014 Jan 31.

21.

Early onset absence epilepsy with onset in the first year of life: a multicenter cohort study.

Giordano L, Vignoli A, Cusmai R, Parisi P, Mastrangelo M, Coppola G, Cordelli DM, Accorsi P, Milito G, Darra F, Pruna D, Belcastro V, Verrotti A, Striano P.

Epilepsia. 2013 Oct;54 Suppl 7:66-9. doi: 10.1111/epi.12311.

22.

Clinical dissection of early onset absence epilepsy in children and prognostic implications.

Agostinelli S, Accorsi P, Beccaria F, Belcastro V, Canevini MP, Capovilla G, Cappanera S, Dalla Bernardina B, Darra F, Del Gaudio L, Elia M, Falsaperla R, Giordano L, Gobbi G, Minetti C, Nicita F, Parisi P, Pavone P, Pezzella M, Sesta M, Spalice A, Striano S, Tozzi E, Traverso M, Vari S, Vignoli A, Zamponi N, Zara F, Striano P, Verrotti A; SINP (Società Italiana Neurologia Pediatrica) Collaborative Working Group.

Epilepsia. 2013 Oct;54(10):1761-70. doi: 10.1111/epi.12341. Epub 2013 Aug 27.

23.

Low frequency mu-like activity characterizes cortical rhythms in epilepsy due to ring chromosome 20.

Avanzini P, Vaudano AE, Vignoli A, Ruggieri A, Benuzzi F, Darra F, Mastrangelo M, Dalla Bernardina B, Nichelli PF, Canevini MP, Meletti S.

Clin Neurophysiol. 2014 Feb;125(2):239-49. doi: 10.1016/j.clinph.2013.07.009. Epub 2013 Aug 19.

PMID:
23968845
24.

Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly.

Poirier K, Lebrun N, Broix L, Tian G, Saillour Y, Boscheron C, Parrini E, Valence S, Pierre BS, Oger M, Lacombe D, Geneviève D, Fontana E, Darra F, Cances C, Barth M, Bonneau D, Bernadina BD, N'guyen S, Gitiaux C, Parent P, des Portes V, Pedespan JM, Legrez V, Castelnau-Ptakine L, Nitschke P, Hieu T, Masson C, Zelenika D, Andrieux A, Francis F, Guerrini R, Cowan NJ, Bahi-Buisson N, Chelly J.

Nat Genet. 2013 Jun;45(6):639-47. doi: 10.1038/ng.2613. Epub 2013 Apr 21. Erratum in: Nat Genet. 2013 Aug;45(8):962.

25.

Epilepsy with myoclonic atonic seizures: an electroclinical study of 69 patients.

Caraballo RH, Chamorro N, Darra F, Fortini S, Arroyo H.

Pediatr Neurol. 2013 May;48(5):355-62. doi: 10.1016/j.pediatrneurol.2012.12.022.

PMID:
23583052
26.

Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significance.

Zara F, Specchio N, Striano P, Robbiano A, Gennaro E, Paravidino R, Vanni N, Beccaria F, Capovilla G, Bianchi A, Caffi L, Cardilli V, Darra F, Bernardina BD, Fusco L, Gaggero R, Giordano L, Guerrini R, Incorpora G, Mastrangelo M, Spaccini L, Laverda AM, Vecchi M, Vanadia F, Veggiotti P, Viri M, Occhi G, Budetta M, Taglialatela M, Coviello DA, Vigevano F, Minetti C.

Epilepsia. 2013 Mar;54(3):425-36. doi: 10.1111/epi.12089. Epub 2013 Jan 29.

27.

Early-onset absence epilepsy: SLC2A1 gene analysis and treatment evolution.

Agostinelli S, Traverso M, Accorsi P, Beccaria F, Belcastro V, Capovilla G, Cappanera S, Coppola A, Dalla Bernardina B, Darra F, Ferretti M, Elia M, Galeone D, Giordano L, Gobbi G, Nicita F, Parisi P, Pezzella M, Spalice A, Striano S, Tozzi E, Vignoli A, Minetti C, Zara F, Striano P, Verrotti A.

Eur J Neurol. 2013 May;20(5):856-9. doi: 10.1111/j.1468-1331.2012.03871.x. Epub 2012 Sep 30.

28.

Somatic mosaicism of PCDH19 mutation in a family with low-penetrance EFMR.

Terracciano A, Specchio N, Darra F, Sferra A, Bernardina BD, Vigevano F, Bertini E.

Neurogenetics. 2012 Nov;13(4):341-5. doi: 10.1007/s10048-012-0342-9. Epub 2012 Sep 6.

PMID:
22949144
29.

Focal seizures with affective symptoms are a major feature of PCDH19 gene-related epilepsy.

Marini C, Darra F, Specchio N, Mei D, Terracciano A, Parmeggiani L, Ferrari A, Sicca F, Mastrangelo M, Spaccini L, Canopoli ML, Cesaroni E, Zamponi N, Caffi L, Ricciardelli P, Grosso S, Pisano T, Canevini MP, Granata T, Accorsi P, Battaglia D, Cusmai R, Vigevano F, Dalla Bernardina B, Guerrini R.

Epilepsia. 2012 Dec;53(12):2111-9. doi: 10.1111/j.1528-1167.2012.03649.x. Epub 2012 Sep 4.

30.

Individually tailored extratemporal epilepsy surgery in children: anatomo-electro-clinical features and outcome predictors in a population of 53 cases.

Liava A, Francione S, Tassi L, Lo Russo G, Cossu M, Mai R, Darra F, Fontana E, Dalla Bernardina B.

Epilepsy Behav. 2012 Sep;25(1):68-80. doi: 10.1016/j.yebeh.2012.05.008. Epub 2012 Aug 17.

PMID:
22902651
31.

Electroclinical pattern in MECP2 duplication syndrome: eight new reported cases and review of literature.

Vignoli A, Borgatti R, Peron A, Zucca C, Ballarati L, Bonaglia C, Bellini M, Giordano L, Romaniello R, Bedeschi MF, Epifanio R, Russo S, Caselli R, Giardino D, Darra F, La Briola F, Banderali G, Canevini MP.

Epilepsia. 2012 Jul;53(7):1146-55. doi: 10.1111/j.1528-1167.2012.03501.x. Epub 2012 May 11. Review.

32.

Molecular mechanisms generating and stabilizing terminal 22q13 deletions in 44 subjects with Phelan/McDermid syndrome.

Bonaglia MC, Giorda R, Beri S, De Agostini C, Novara F, Fichera M, Grillo L, Galesi O, Vetro A, Ciccone R, Bonati MT, Giglio S, Guerrini R, Osimani S, Marelli S, Zucca C, Grasso R, Borgatti R, Mani E, Motta C, Molteni M, Romano C, Greco D, Reitano S, Baroncini A, Lapi E, Cecconi A, Arrigo G, Patricelli MG, Pantaleoni C, D'Arrigo S, Riva D, Sciacca F, Dalla Bernardina B, Zoccante L, Darra F, Termine C, Maserati E, Bigoni S, Priolo E, Bottani A, Gimelli S, Bena F, Brusco A, di Gregorio E, Bagnasco I, Giussani U, Nitsch L, Politi P, Martinez-Frias ML, Martínez-Fernández ML, Martínez Guardia N, Bremer A, Anderlid BM, Zuffardi O.

PLoS Genet. 2011 Jul;7(7):e1002173. doi: 10.1371/journal.pgen.1002173. Epub 2011 Jul 14.

33.

Pathogenic role of the X-linked cyclin-dependent kinase-like 5 and aristaless-related homeobox genes in epileptic encephalopathy of unknown etiology with onset in the first year of life.

Sartori S, Polli R, Bettella E, Rossato S, Andreoli W, Vecchi M, Giordano L, Accorsi P, Di Rosa G, Toldo I, Zamponi N, Darra F, Dalla Bernardina B, Perilongo G, Boniver C, Murgia A.

J Child Neurol. 2011 Jun;26(6):683-91. doi: 10.1177/0883073810387827. Epub 2011 Apr 11.

PMID:
21482751
34.

Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutations.

Specchio N, Marini C, Terracciano A, Mei D, Trivisano M, Sicca F, Fusco L, Cusmai R, Darra F, Bernardina BD, Bertini E, Guerrini R, Vigevano F.

Epilepsia. 2011 Jul;52(7):1251-7. doi: 10.1111/j.1528-1167.2011.03063.x. Epub 2011 Apr 11.

35.

A multicenter, randomized, placebo-controlled trial of levetiracetam in children and adolescents with newly diagnosed absence epilepsy.

Fattore C, Boniver C, Capovilla G, Cerminara C, Citterio A, Coppola G, Costa P, Darra F, Vecchi M, Perucca E.

Epilepsia. 2011 Apr;52(4):802-9. doi: 10.1111/j.1528-1167.2010.02976.x. Epub 2011 Feb 14.

36.

Absence seizures in the first 3 years of life: an electroclinical study of 46 cases.

Caraballo RH, Darra F, Fontana E, Garcia R, Monese E, Dalla Bernardina B.

Epilepsia. 2011 Feb;52(2):393-400. doi: 10.1111/j.1528-1167.2010.02926.x. Epub 2011 Jan 26.

37.

Cognitive development in Dravet syndrome: a retrospective, multicenter study of 26 patients.

Ragona F, Granata T, Dalla Bernardina B, Offredi F, Darra F, Battaglia D, Morbi M, Brazzo D, Cappelletti S, Chieffo D, De Giorgi I, Fontana E, Freri E, Marini C, Toraldo A, Specchio N, Veggiotti P, Vigevano F, Guerrini R, Guzzetta F, Dravet C.

Epilepsia. 2011 Feb;52(2):386-92. doi: 10.1111/j.1528-1167.2010.02925.x. Epub 2011 Jan 26.

38.

Familial Ohtahara syndrome due to a novel ARX gene mutation.

Giordano L, Sartori S, Russo S, Accorsi P, Galli J, Tiberti A, Bettella E, Marchi M, Vignoli A, Darra F, Murgia A, Bernardina BD.

Am J Med Genet A. 2010 Dec;152A(12):3133-7. doi: 10.1002/ajmg.a.33701.

39.

Electroclinical findings in four patients with karyotype 47,XYY.

Torniero C, Bernardina BD, Fontana E, Darra F, Danesino C, Elia M.

Brain Dev. 2011 May;33(5):384-9. doi: 10.1016/j.braindev.2010.07.010. Epub 2010 Sep 16.

PMID:
20817432
40.

Refining the phenotype associated with MEF2C haploinsufficiency.

Novara F, Beri S, Giorda R, Ortibus E, Nageshappa S, Darra F, Dalla Bernardina B, Zuffardi O, Van Esch H.

Clin Genet. 2010 Nov;78(5):471-7. doi: 10.1111/j.1399-0004.2010.01413.x.

PMID:
20412115
41.

Ring chromosome 20 syndrome: a link between epilepsy onset and neuropsychological impairment in three children.

Vignoli A, Canevini MP, Darra F, La Selva L, Fiorini E, Piazzini A, Lazzarotto F, Zucca C, Dalla Bernardina B.

Epilepsia. 2009 Nov;50(11):2420-7. doi: 10.1111/j.1528-1167.2009.02176.x. Epub 2009 Jul 2.

42.

A study of 63 cases with eyelid myoclonia with or without absences: type of seizure or an epileptic syndrome?

Caraballo RH, Fontana E, Darra F, Chacon S, Ross N, Fiorini E, Fejerman N, Dalla Bernardina B.

Seizure. 2009 Jul;18(6):440-5. doi: 10.1016/j.seizure.2009.04.004. Epub 2009 May 5.

43.

Childhood absence epilepsy and electroencephalographic focal abnormalities with or without clinical manifestations.

Caraballo RH, Fontana E, Darra F, Bongiorni L, Fiorini E, Cersosimo R, Fejerman N, Bernardinab BD.

Seizure. 2008 Oct;17(7):617-24. doi: 10.1016/j.seizure.2008.03.009.

44.

Different clinical and immunological presentation of ataxia-telangiectasia within the same family.

Soresina A, Meini A, Lougaris V, Cattaneo G, Pellegrino S, Piane M, Darra F, Plebani A.

Neuropediatrics. 2008 Feb;39(1):43-5. doi: 10.1055/s-2008-1076736.

PMID:
18504682
45.

Migrating focal seizures in infancy: analysis of the electroclinical patterns in 17 patients.

Caraballo RH, Fontana E, Darra F, Cassar L, Negrini F, Fiorini E, Arroyo H, Ferraro S, Fejerman N, Dalla Bernardina B.

J Child Neurol. 2008 May;23(5):497-506. doi: 10.1177/0883073807309771. Epub 2008 Jan 29.

PMID:
18230844
46.

Uncombable hair syndrome, mental retardation, single palmar crease and arched palate in a patient with neurofibromatosis type I.

Schena D, Germi L, Zamperetti MR, Darra F, Giacopuzzi S, Girolomoni G.

Pediatr Dermatol. 2007 Sep-Oct;24(5):E73-5.

PMID:
17958786
47.

Scotosensitive and photosensitive myoclonic seizures in an infant with trisomy 13.

Torniero C, Zuffardi O, Darra F, Dalla Bernardina B.

Epilepsia. 2007 Nov;48(11):2177-80. Epub 2007 Jul 28.

48.

Brain MRI findings in severe myoclonic epilepsy in infancy and genotype-phenotype correlations.

Striano P, Mancardi MM, Biancheri R, Madia F, Gennaro E, Paravidino R, Beccaria F, Capovilla G, Dalla Bernardina B, Darra F, Elia M, Giordano L, Gobbi G, Granata T, Ragona F, Guerrini R, Marini C, Mei D, Longaretti F, Romeo A, Siri L, Specchio N, Vigevano F, Striano S, Tortora F, Rossi A, Minetti C, Dravet C, Gaggero R, Zara F.

Epilepsia. 2007 Jun;48(6):1092-6. Epub 2007 Mar 22.

49.

Benign myoclonic epilepsy in infancy (BMEI): a longitudinal electroclinical study of 22 cases.

Darra F, Fiorini E, Zoccante L, Mastella L, Torniero C, Cortese S, Meneghello L, Fontana E, Bernardina BD.

Epilepsia. 2006;47 Suppl 5:31-5.

50.

Temporal lobe epilepsy in children: electroclinical study of 77 cases.

Fontana E, Negrini F, Francione S, Mai R, Osanni E, Menna E, Offredi F, Darra F, Bernardina BD.

Epilepsia. 2006;47 Suppl 5:26-30.

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