275 related articles for article (PubMed ID: 24116895)
1. Epilepsy in ring 14 syndrome: a clinical and EEG study of 22 patients.
Giovannini S; Marangio L; Fusco C; Scarano A; Frattini D; Della Giustina E; Zollino M; Neri G; Gobbi G
Epilepsia; 2013 Dec; 54(12):2204-13. PubMed ID: 24116895
[TBL] [Abstract][Full Text] [Related]
2. Epileptic and nonepileptic features in patients with early onset epileptic encephalopathy and STXBP1 mutations.
Milh M; Villeneuve N; Chouchane M; Kaminska A; Laroche C; Barthez MA; Gitiaux C; Bartoli C; Borges-Correia A; Cacciagli P; Mignon-Ravix C; Cuberos H; Chabrol B; Villard L
Epilepsia; 2011 Oct; 52(10):1828-34. PubMed ID: 21770924
[TBL] [Abstract][Full Text] [Related]
3. Ring chromosome 20 syndrome: electroclinical description of six patients and review of the literature.
Elens I; Vanrykel K; De Waele L; Jansen K; Segeren M; Van Paesschen W; Ceulemans B; Boel M; Frijns JP; Buyse G; Lagae L
Epilepsy Behav; 2012 Apr; 23(4):409-14. PubMed ID: 22424860
[TBL] [Abstract][Full Text] [Related]
4. Infantile epileptic encephalopathy with late-onset spasms: report of 19 patients.
Auvin S; Lamblin MD; Pandit F; Vallée L; Bouvet-Mourcia A
Epilepsia; 2010 Jul; 51(7):1290-6. PubMed ID: 20345938
[TBL] [Abstract][Full Text] [Related]
5. Early pattern of epilepsy in the ring chromosome 20 syndrome.
Ville D; Kaminska A; Bahi-Buisson N; Biraben A; Plouin P; Telvi L; Dulac O; Chiron C
Epilepsia; 2006 Mar; 47(3):543-9. PubMed ID: 16529619
[TBL] [Abstract][Full Text] [Related]
6. Atypical benign partial epilepsy/pseudo-Lennox syndrome.
Hahn A
Epileptic Disord; 2000; 2 Suppl 1():S11-7. PubMed ID: 11231218
[TBL] [Abstract][Full Text] [Related]
7. Panayiotopoulos syndrome: a benign childhood autonomic epilepsy frequently imitating encephalitis, syncope, migraine, sleep disorder, or gastroenteritis.
Covanis A
Pediatrics; 2006 Oct; 118(4):e1237-43. PubMed ID: 16950946
[TBL] [Abstract][Full Text] [Related]
8. Late onset epileptic spasms is frequent in MECP2 gene duplication: electroclinical features and long-term follow-up of 8 epilepsy patients.
Caumes R; Boespflug-Tanguy O; Villeneuve N; Lambert L; Delanoe C; Leheup B; Bahi-Buisson N; Auvin S
Eur J Paediatr Neurol; 2014 Jul; 18(4):475-81. PubMed ID: 24703762
[TBL] [Abstract][Full Text] [Related]
9. Epilepsy in ring 14 chromosome syndrome.
Specchio N; Trivisano M; Serino D; Cappelletti S; Carotenuto A; Claps D; Marras CE; Fusco L; Elia M; Vigevano F
Epilepsy Behav; 2012 Dec; 25(4):585-92. PubMed ID: 23159383
[TBL] [Abstract][Full Text] [Related]
10. 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. PubMed ID: 22578097
[TBL] [Abstract][Full Text] [Related]
11. 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. PubMed ID: 27816898
[TBL] [Abstract][Full Text] [Related]
12. [Ring chromosome 20: a distinctive syndrome identifiable by electroclinical diagnosis].
Gonzalez-Delgado M; Salas J; Hernando I; Calleja S; Hernandez C
Neurologia; 2004 May; 19(4):215-9. PubMed ID: 15131740
[TBL] [Abstract][Full Text] [Related]
13. 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. PubMed ID: 22946748
[TBL] [Abstract][Full Text] [Related]
14. Epilepsy in Aicardi-Goutières syndrome.
Ramantani G; Maillard LG; Bast T; Husain RA; Niggemann P; Kohlhase J; Hertzberg C; Ungerath K; Innes MA; Walkenhorst H; Bevot A; von Stülpnagel C; Thomas K; Niemann F; Ergun MA; Tacke U; Häusler M; Ikonomidou C; Korinthenberg R; Lee-Kirsch MA
Eur J Paediatr Neurol; 2014 Jan; 18(1):30-7. PubMed ID: 24011626
[TBL] [Abstract][Full Text] [Related]
15. [Epilepsy in three children with Wolf-Hirschhorn syndrome].
Kaciński M; Kostyk E; Kruczek A; Skowronek-Bała B
Przegl Lek; 2005; 62(11):1298-301. PubMed ID: 16512625
[TBL] [Abstract][Full Text] [Related]
16. Spectrum of epilepsy in terminal 1p36 deletion syndrome.
Bahi-Buisson N; Guttierrez-Delicado E; Soufflet C; Rio M; Daire VC; Lacombe D; Héron D; Verloes A; Zuberi S; Burglen L; Afenjar A; Moutard ML; Edery P; Novelli A; Bernardini L; Dulac O; Nabbout R; Plouin P; Battaglia A
Epilepsia; 2008 Mar; 49(3):509-15. PubMed ID: 18031548
[TBL] [Abstract][Full Text] [Related]
17. Myoclonic astatic epilepsy: an age-dependent epileptic syndrome with favorable seizure outcome but variable cognitive evolution.
Trivisano M; Specchio N; Cappelletti S; Di Ciommo V; Claps D; Specchio LM; Vigevano F; Fusco L
Epilepsy Res; 2011 Nov; 97(1-2):133-41. PubMed ID: 21873030
[TBL] [Abstract][Full Text] [Related]
18. [A case of epilepsy with ring chromosome 20 syndrome].
Tanaka A; Ohtake M; Yoshimi T; Suzuki T; Abe I; Iwasaki H; Sue H; Kaito K
Rinsho Byori; 2012 Sep; 60(9):847-52. PubMed ID: 23157113
[TBL] [Abstract][Full Text] [Related]
19. Cryptogenic late-onset epileptic spasms: an overlooked syndrome of early childhood?
Eisermann MM; Ville D; Soufflet C; Plouin P; Chiron C; Dulac O; Kaminska A
Epilepsia; 2006 Jun; 47(6):1035-42. PubMed ID: 16822250
[TBL] [Abstract][Full Text] [Related]
20. Benign infantile focal epilepsy with midline spikes and waves during sleep: a new epileptic syndrome or a variant of benign focal epilepsy?
Flesler S; Sakr D; Cersósimo R; Caraballo R
Epileptic Disord; 2010 Sep; 12(3):205-11. PubMed ID: 20822975
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
