407 related articles for article (PubMed ID: 16302872)
21. Epidemiology of idiopathic generalized epilepsies.
Jallon P; Latour P
Epilepsia; 2005; 46 Suppl 9():10-4. PubMed ID: 16302871
[TBL] [Abstract][Full Text] [Related]
22. Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies.
Haug K; Warnstedt M; Alekov AK; Sander T; Ramírez A; Poser B; Maljevic S; Hebeisen S; Kubisch C; Rebstock J; Horvath S; Hallmann K; Dullinger JS; Rau B; Haverkamp F; Beyenburg S; Schulz H; Janz D; Giese B; Müller-Newen G; Propping P; Elger CE; Fahlke C; Lerche H; Heils A
Nat Genet; 2003 Apr; 33(4):527-32. PubMed ID: 12612585
[TBL] [Abstract][Full Text] [Related]
23. The phenotypic spectrum related to the human epilepsy susceptibility gene "EJM1".
Sander T; Hildmann T; Janz D; Wienker TF; Neitzel H; Bianchi A; Bauer G; Sailer U; Berek K; Schmitz B
Ann Neurol; 1995 Aug; 38(2):210-7. PubMed ID: 7654068
[TBL] [Abstract][Full Text] [Related]
24. A novel locus for generalized epilepsy with febrile seizures plus in French families.
Baulac S; Gourfinkel-An I; Couarch P; Depienne C; Kaminska A; Dulac O; Baulac M; LeGuern E; Nabbout R
Arch Neurol; 2008 Jul; 65(7):943-51. PubMed ID: 18625863
[TBL] [Abstract][Full Text] [Related]
25. Genetics of myoclonic and myoclonus epilepsies.
Minassian BA; Sainz J; Delgado-Escueta AV
Clin Neurosci; 1995-1996; 3(4):223-35. PubMed ID: 8891396
[TBL] [Abstract][Full Text] [Related]
26. Genetic mechanisms in idiopathic epilepsies.
Weber YG; Lerche H
Dev Med Child Neurol; 2008 Sep; 50(9):648-54. PubMed ID: 18754913
[TBL] [Abstract][Full Text] [Related]
27. Effects of Cav3.2 channel mutations linked to idiopathic generalized epilepsy.
Khosravani H; Bladen C; Parker DB; Snutch TP; McRory JE; Zamponi GW
Ann Neurol; 2005 May; 57(5):745-9. PubMed ID: 15852375
[TBL] [Abstract][Full Text] [Related]
28. KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes.
Neubauer BA; Waldegger S; Heinzinger J; Hahn A; Kurlemann G; Fiedler B; Eberhard F; Muhle H; Stephani U; Garkisch S; Eeg-Olofsson O; Müller U; Sander T
Neurology; 2008 Jul; 71(3):177-83. PubMed ID: 18625963
[TBL] [Abstract][Full Text] [Related]
29. Genome scan of idiopathic generalized epilepsy: evidence for major susceptibility gene and modifying genes influencing the seizure type.
Durner M; Keddache MA; Tomasini L; Shinnar S; Resor SR; Cohen J; Harden C; Moshe SL; Rosenbaum D; Kang H; Ballaban-Gil K; Hertz S; Labar DR; Luciano D; Wallace S; Yohai D; Klotz I; Dicker E; Greenberg DA
Ann Neurol; 2001 Mar; 49(3):328-35. PubMed ID: 11261507
[TBL] [Abstract][Full Text] [Related]
30. Extended spectrum of idiopathic generalized epilepsies associated with CACNA1H functional variants.
Heron SE; Khosravani H; Varela D; Bladen C; Williams TC; Newman MR; Scheffer IE; Berkovic SF; Mulley JC; Zamponi GW
Ann Neurol; 2007 Dec; 62(6):560-8. PubMed ID: 17696120
[TBL] [Abstract][Full Text] [Related]
31. Monogenic idiopathic epilepsies.
Gourfinkel-An I; Baulac S; Nabbout R; Ruberg M; Baulac M; Brice A; LeGuern E
Lancet Neurol; 2004 Apr; 3(4):209-18. PubMed ID: 15039033
[TBL] [Abstract][Full Text] [Related]
32. [Advances in the studies on the molecular and genetic aspects of epilepsy].
Wang X; Wang T; Yuan MX; Liu MG; Wang Q
Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2005 Jun; 27(3):388-93. PubMed ID: 16038283
[TBL] [Abstract][Full Text] [Related]
33. A de novo KCNQ2 mutation detected in non-familial benign neonatal convulsions.
Ishii A; Fukuma G; Uehara A; Miyajima T; Makita Y; Hamachi A; Yasukochi M; Inoue T; Yasumoto S; Okada M; Kaneko S; Mitsudome A; Hirose S
Brain Dev; 2009 Jan; 31(1):27-33. PubMed ID: 18640800
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. Clinical spectrum of SCN1A mutations.
Gambardella A; Marini C
Epilepsia; 2009 May; 50 Suppl 5():20-3. PubMed ID: 19469841
[TBL] [Abstract][Full Text] [Related]
36. Molecular genetics of infantile nervous system channelopathies.
Gardiner M
Early Hum Dev; 2006 Dec; 82(12):775-9. PubMed ID: 17049761
[TBL] [Abstract][Full Text] [Related]
37. Impact of our understanding of the genetic aetiology of epilepsy.
Gardiner RM
J Neurol; 2000 May; 247(5):327-34. PubMed ID: 10896263
[TBL] [Abstract][Full Text] [Related]
38. A profile of alternative RNA splicing and transcript variation of CACNA1H, a human T-channel gene candidate for idiopathic generalized epilepsies.
Zhong X; Liu JR; Kyle JW; Hanck DA; Agnew WS
Hum Mol Genet; 2006 May; 15(9):1497-512. PubMed ID: 16565161
[TBL] [Abstract][Full Text] [Related]
39. A novel inherited mutation in the voltage sensor region of SCN1A is associated with Panayiotopoulos syndrome in siblings and generalized epilepsy with febrile seizures plus.
Livingston JH; Cross JH; Mclellan A; Birch R; Zuberi SM
J Child Neurol; 2009 Apr; 24(4):503-8. PubMed ID: 19339291
[TBL] [Abstract][Full Text] [Related]
40. Advances on the genetics of mendelian idiopathic epilepsies.
Baulac S; Baulac M
Neurol Clin; 2009 Nov; 27(4):1041-1061. PubMed ID: 19853223
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]