193 related articles for article (PubMed ID: 26216793)
1. DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy.
Striano P; Serioli E; Santulli L; Manna I; Labate A; Dazzo E; Pasini E; Gambardella A; Michelucci R; Striano S; Nobile C
Epilepsia; 2015 Oct; 56(10):e168-71. PubMed ID: 26216793
[TBL] [Abstract][Full Text] [Related]
2. Familial mesial temporal lobe epilepsy (FMTLE) : a clinical and genetic study of 15 Italian families.
Striano P; Gambardella A; Coppola A; Di Bonaventura C; Bovo G; Diani E; Boaretto F; Egeo G; Ciampa C; Labate A; Testoni S; Passarelli D; Manna I; Sferro C; Aguglia U; Caranci F; Giallonardo AT; Striano S; Nobile C; Michelucci R
J Neurol; 2008 Jan; 255(1):16-23. PubMed ID: 18004642
[TBL] [Abstract][Full Text] [Related]
3. Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations.
Michelucci R; Pasini E; Malacrida S; Striano P; Bonaventura CD; Pulitano P; Bisulli F; Egeo G; Santulli L; Sofia V; Gambardella A; Elia M; de Falco A; Neve Al; Banfi P; Coppola G; Avoni P; Binelli S; Boniver C; Pisano T; Marchini M; Dazzo E; Fanciulli M; Bartolini Y; Riguzzi P; Volpi L; de Falco FA; Giallonardo AT; Mecarelli O; Striano S; Tinuper P; Nobile C
Epilepsia; 2013 Jul; 54(7):1288-97. PubMed ID: 23621105
[TBL] [Abstract][Full Text] [Related]
4. 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. PubMed ID: 23542697
[TBL] [Abstract][Full Text] [Related]
5. Autosomal dominant lateral temporal epilepsy (ADLTE): novel structural and single-nucleotide LGI1 mutations in families with predominant visual auras.
Dazzo E; Santulli L; Posar A; Fattouch J; Conti S; Lodén-van Straaten M; Mijalkovic J; De Bortoli M; Rosa M; Millino C; Pacchioni B; Di Bonaventura C; Giallonardo AT; Striano S; Striano P; Parmeggiani A; Nobile C
Epilepsy Res; 2015 Feb; 110():132-8. PubMed ID: 25616465
[TBL] [Abstract][Full Text] [Related]
6. DEPDC5 mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsy.
Picard F; Makrythanasis P; Navarro V; Ishida S; de Bellescize J; Ville D; Weckhuysen S; Fosselle E; Suls A; De Jonghe P; Vasselon Raina M; Lesca G; Depienne C; An-Gourfinkel I; Vlaicu M; Baulac M; Mundwiller E; Couarch P; Combi R; Ferini-Strambi L; Gambardella A; Antonarakis SE; Leguern E; Steinlein O; Baulac S
Neurology; 2014 Jun; 82(23):2101-6. PubMed ID: 24814846
[TBL] [Abstract][Full Text] [Related]
7. What is the impact of a novel DEPDC5 variant on an infant with focal epilepsy: a case report.
Gu C; Lu X; Ma J; Pu L; Zhi X; Shu J; Li D; Cai C
BMC Pediatr; 2022 Jul; 22(1):459. PubMed ID: 35907814
[TBL] [Abstract][Full Text] [Related]
8. Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3.
Hedera P; Blair MA; Andermann E; Andermann F; D'Agostino D; Taylor KA; Chahine L; Pandolfo M; Bradford Y; Haines JL; Abou-Khalil B
Neurology; 2007 Jun; 68(24):2107-12. PubMed ID: 17377072
[TBL] [Abstract][Full Text] [Related]
9. Genetics advances in autosomal dominant focal epilepsies: focus on DEPDC5.
Baulac S
Prog Brain Res; 2014; 213():123-39. PubMed ID: 25194487
[TBL] [Abstract][Full Text] [Related]
10. DEPDC5 mutations in familial and sporadic focal epilepsy.
Tsai MH; Chan CK; Chang YC; Yu YT; Chuang ST; Fan WL; Li SC; Fu TY; Chang WN; Liou CW; Chuang YC; Ng CC; Hwang DY; Lim KS
Clin Genet; 2017 Oct; 92(4):397-404. PubMed ID: 28170089
[TBL] [Abstract][Full Text] [Related]
11. Magnetoencephalogram-assisted diagnosis of familial focal epilepsy with variable foci in a Chinese family with a novel DEPDC5 mutation.
Li M; Huang Z; Zhang X; Duan Y; Jia Y; Ye J; Wang Y
Epileptic Disord; 2019 Jun; 21(3):289-294. PubMed ID: 31225799
[TBL] [Abstract][Full Text] [Related]
12. Involvement of GATOR complex genes in familial focal epilepsies and focal cortical dysplasia.
Weckhuysen S; Marsan E; Lambrecq V; Marchal C; Morin-Brureau M; An-Gourfinkel I; Baulac M; Fohlen M; Kallay Zetchi C; Seeck M; de la Grange P; Dermaut B; Meurs A; Thomas P; Chassoux F; Leguern E; Picard F; Baulac S
Epilepsia; 2016 Jun; 57(6):994-1003. PubMed ID: 27173016
[TBL] [Abstract][Full Text] [Related]
13. Familial Mesial Temporal Lobe Epilepsy: Clinical Spectrum and Genetic Evidence for a Polygenic Architecture.
Harris RV; Oliver KL; Perucca P; Striano P; Labate A; Riva A; Grinton BE; Reid J; Hutton J; Todaro M; O'Brien TJ; Kwan P; Sadleir LG; Mullen SA; Dazzo E; Crompton DE; Scheffer IE; Bahlo M; Nobile C; Gambardella A; Berkovic SF
Ann Neurol; 2023 Nov; 94(5):825-835. PubMed ID: 37597255
[TBL] [Abstract][Full Text] [Related]
14. Mutations of DEPDC5 cause autosomal dominant focal epilepsies.
Ishida S; Picard F; Rudolf G; Noé E; Achaz G; Thomas P; Genton P; Mundwiller E; Wolff M; Marescaux C; Miles R; Baulac M; Hirsch E; Leguern E; Baulac S
Nat Genet; 2013 May; 45(5):552-5. PubMed ID: 23542701
[TBL] [Abstract][Full Text] [Related]
15. A recurrent mutation in DEPDC5 predisposes to focal epilepsies in the French-Canadian population.
Martin C; Meloche C; Rioux MF; Nguyen DK; Carmant L; Andermann E; Gravel M; Cossette P
Clin Genet; 2014 Dec; 86(6):570-4. PubMed ID: 24283814
[TBL] [Abstract][Full Text] [Related]
16. Familial mesial temporal lobe epilepsy: a benign epilepsy syndrome showing complex inheritance.
Crompton DE; Scheffer IE; Taylor I; Cook MJ; McKelvie PA; Vears DF; Lawrence KM; McMahon JM; Grinton BE; McIntosh AM; Berkovic SF
Brain; 2010 Nov; 133(11):3221-31. PubMed ID: 20864493
[TBL] [Abstract][Full Text] [Related]
17. DEPDC5 mutation and familial focal epilepsy with variable foci: genotype and phenotype of a family.
Aberastury M; Fernández R; Córdoba M; Comas B; Peralta M; Agosta G; Kauffman M; Silva W
Epileptic Disord; 2019 Feb; 21(1):42-47. PubMed ID: 30767899
[TBL] [Abstract][Full Text] [Related]
18. Familial focal epilepsy with focal cortical dysplasia due to DEPDC5 mutations.
Baulac S; Ishida S; Marsan E; Miquel C; Biraben A; Nguyen DK; Nordli D; Cossette P; Nguyen S; Lambrecq V; Vlaicu M; Daniau M; Bielle F; Andermann E; Andermann F; Leguern E; Chassoux F; Picard F
Ann Neurol; 2015 Apr; 77(4):675-83. PubMed ID: 25623524
[TBL] [Abstract][Full Text] [Related]
19. Abnormal phonologic processing in familial lateral temporal lobe epilepsy due to a new LGI1 mutation.
Pisano T; Marini C; Brovedani P; Brizzolara D; Pruna D; Mei D; Moro F; Cianchetti C; Guerrini R
Epilepsia; 2005 Jan; 46(1):118-23. PubMed ID: 15660777
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
