192 related articles for article (PubMed ID: 19723564)
1. Neuroimaging and neurogenetics of epilepsy in humans.
Siniatchkin M; Koepp M
Neuroscience; 2009 Nov; 164(1):164-73. PubMed ID: 19723564
[TBL] [Abstract][Full Text] [Related]
2. Genes and mutations in idiopathic epilepsy.
Steinlein OK
Am J Med Genet; 2001; 106(2):139-45. PubMed ID: 11579434
[TBL] [Abstract][Full Text] [Related]
3. [Genetic background of epilepsies].
Kelemen A; Szucs A; Rásonyi G; Janszky J; Holló A; Halász P
Ideggyogy Sz; 2004 May; 57(5-6):141-51. PubMed ID: 15264690
[TBL] [Abstract][Full Text] [Related]
4. Genetics of idiopathic epilepsies.
Hirose S; Mitsudome A; Okada M; Kaneko S;
Epilepsia; 2005; 46 Suppl 1():38-43. PubMed ID: 15816978
[TBL] [Abstract][Full Text] [Related]
5. [Genetic approach to the pathogeneses of epilepsy].
Hirose S
Rinsho Shinkeigaku; 2004 Nov; 44(11):975-8. PubMed ID: 15651347
[TBL] [Abstract][Full Text] [Related]
6. [Molecular defects may cause epilepsy. New discoveries can provide better possibilities for directional diagnostics and treatment].
Brismar T
Lakartidningen; 2000 Nov; 97(45):5102-6. PubMed ID: 11116887
[TBL] [Abstract][Full Text] [Related]
7. Familial severe myoclonic epilepsy of infancy: truncation of Nav1.1 and genetic heterogeneity.
Gennaro E; Veggiotti P; Malacarne M; Madia F; Cecconi M; Cardinali S; Cassetti A; Cecconi I; Bertini E; Bianchi A; Gobbi G; Zara F
Epileptic Disord; 2003 Mar; 5(1):21-5. PubMed ID: 12773292
[TBL] [Abstract][Full Text] [Related]
8. Severe epilepsy syndromes of early childhood: the link between genetics and pathophysiology with a focus on SCN1A mutations.
Stafstrom CE
J Child Neurol; 2009 Aug; 24(8 Suppl):15S-23S. PubMed ID: 19666879
[TBL] [Abstract][Full Text] [Related]
9. Sacred disease secrets revealed: the genetics of human epilepsy.
Turnbull J; Lohi H; Kearney JA; Rouleau GA; Delgado-Escueta AV; Meisler MH; Cossette P; Minassian BA
Hum Mol Genet; 2005 Oct; 14 Spec No. 2():2491-2500. PubMed ID: 16278970
[TBL] [Abstract][Full Text] [Related]
10. Sodium and potassium channel dysfunctions in rare and common idiopathic epilepsy syndromes.
Hahn A; Neubauer BA
Brain Dev; 2009 Aug; 31(7):515-20. PubMed ID: 19464834
[TBL] [Abstract][Full Text] [Related]
11. Cryptogenic epileptic syndromes related to SCN1A: twelve novel mutations identified.
Zucca C; Redaelli F; Epifanio R; Zanotta N; Romeo A; Lodi M; Veggiotti P; Airoldi G; Panzeri C; Romaniello R; De Polo G; Bonanni P; Cardinali S; Baschirotto C; Martorell L; Borgatti R; Bresolin N; Bassi MT
Arch Neurol; 2008 Apr; 65(4):489-94. PubMed ID: 18413471
[TBL] [Abstract][Full Text] [Related]
12. How do mutant Nav1.1 sodium channels cause epilepsy?
Ragsdale DS
Brain Res Rev; 2008 Jun; 58(1):149-59. PubMed ID: 18342948
[TBL] [Abstract][Full Text] [Related]
13. Genes associated with idiopathic epilepsies: a current overview.
Lu Y; Wang X
Neurol Res; 2009 Mar; 31(2):135-43. PubMed ID: 19298753
[TBL] [Abstract][Full Text] [Related]
14. Gene defects in idiopathic epilepsy.
Steinlein OK
Rev Neurol (Paris); 1999 Jul; 155(6-7):450-3. PubMed ID: 10472657
[TBL] [Abstract][Full Text] [Related]
15. Molecular analysis of the A322D mutation in the GABA receptor alpha-subunit causing juvenile myoclonic epilepsy.
Krampfl K; Maljevic S; Cossette P; Ziegler E; Rouleau GA; Lerche H; Bufler J
Eur J Neurosci; 2005 Jul; 22(1):10-20. PubMed ID: 16029191
[TBL] [Abstract][Full Text] [Related]
16. [Ion channel dysfunction in pathogenesis of idiopathic epilepsies].
Różycka A; Dorszewska J; Jagodziński PP
Neurol Neurochir Pol; 2011; 45(1):42-56. PubMed ID: 21384293
[TBL] [Abstract][Full Text] [Related]
17. Epilepsy with a de novo missense mutation in the sodium channel a1 subunit: a case report.
Stefanaki E; Aggelakou V; Orfanou M; Kokori E; Boutoufianakis S
Acta Paediatr; 2006 Dec; 95(12):1703-6. PubMed ID: 17129991
[TBL] [Abstract][Full Text] [Related]
18. Ion channels and epilepsy.
Lerche H; Jurkat-Rott K; Lehmann-Horn F
Am J Med Genet; 2001; 106(2):146-59. PubMed ID: 11579435
[TBL] [Abstract][Full Text] [Related]
19. Genetic basis of autosomal dominant nocturnal frontal lobe epilepsy.
Rózycka A; Trzeciak WH
J Appl Genet; 2003; 44(2):197-207. PubMed ID: 12773798
[TBL] [Abstract][Full Text] [Related]
20. Clinical correlations of mutations in the SCN1A gene: from febrile seizures to severe myoclonic epilepsy in infancy.
Ceulemans BP; Claes LR; Lagae LG
Pediatr Neurol; 2004 Apr; 30(4):236-43. PubMed ID: 15087100
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
