106 related articles for article (PubMed ID: 10510981)
21. Genetic localization of the familial adult myoclonic epilepsy (FAME) gene to chromosome 8q24.
Plaster NM; Uyama E; Uchino M; Ikeda T; Flanigan KM; Kondo I; Ptácek LJ
Neurology; 1999 Oct; 53(6):1180-3. PubMed ID: 10522869
[TBL] [Abstract][Full Text] [Related]
22. Replication analysis of a putative susceptibility locus (EGI) for idiopathic generalized epilepsy on chromosome 8q24.
Sander T; Kretz R; Schulz H; Sailer U; Bauer G; Scaramelli A; Epplen JT; Riess O; Janz D
Epilepsia; 1998 Jul; 39(7):715-20. PubMed ID: 9670899
[TBL] [Abstract][Full Text] [Related]
23. Human glutamate pyruvate transaminase (GPT): localization to 8q24.3, cDNA and genomic sequences, and polymorphic sites.
Sohocki MM; Sullivan LS; Harrison WR; Sodergren EJ; Elder FF; Weinstock G; Tanase S; Daiger SP
Genomics; 1997 Mar; 40(2):247-52. PubMed ID: 9119391
[TBL] [Abstract][Full Text] [Related]
24. Looking for epilepsy genes: clinical and molecular genetic studies.
Delgado-Escueta AV; White R; Greenberg DA; Treiman LJ
Adv Neurol; 1986; 44():77-95. PubMed ID: 3010682
[TBL] [Abstract][Full Text] [Related]
25. Mapping of genes predisposing to idiopathic generalized epilepsy.
Zara F; Bianchi A; Avanzini G; Di Donato S; Castellotti B; Patel PI; Pandolfo M
Hum Mol Genet; 1995 Jul; 4(7):1201-7. PubMed ID: 8528209
[TBL] [Abstract][Full Text] [Related]
26. Genetic architecture of idiopathic generalized epilepsy: clinical genetic analysis of 55 multiplex families.
Marini C; Scheffer IE; Crossland KM; Grinton BE; Phillips FL; McMahon JM; Turner SJ; Dean JT; Kivity S; Mazarib A; Neufeld MY; Korczyn AD; Harkin LA; Dibbens LM; Wallace RH; Mulley JC; Berkovic SF
Epilepsia; 2004 May; 45(5):467-78. PubMed ID: 15101828
[TBL] [Abstract][Full Text] [Related]
27. Absence of linkage to 8q24 in a European family with familial adult myoclonic epilepsy (FAME).
Labauge P; Amer LO; Simonetta-Moreau M; Attané F; Tannier C; Clanet M; Castelnovo G; An-Gourfinkel I; Agid Y; Brice A; Ducros A; LeGuern E
Neurology; 2002 Mar; 58(6):941-4. PubMed ID: 11914412
[TBL] [Abstract][Full Text] [Related]
28. Familial form of typical childhood absence epilepsy in a consanguineous context.
Abouda H; Hizem Y; Gargouri A; Depienne C; Bouteiller D; Riant F; Tournier-Lasserve E; Gourfinkel-An I; LeGuern E; Gouider R
Epilepsia; 2010 Sep; 51(9):1889-93. PubMed ID: 20561025
[TBL] [Abstract][Full Text] [Related]
29. Mutation screening of the chromosome 8q24.3-human activity-regulated cytoskeleton-associated gene (ARC) in idiopathic generalized epilepsy.
Haug K; Kremerskothen J; Hallmann K; Sander T; Dullinger J; Rau B; Beyenburg S; Lentze MJ; Barnekow A; Elger CE; Propping P; Heils A
Mol Cell Probes; 2000 Aug; 14(4):255-60. PubMed ID: 10970730
[TBL] [Abstract][Full Text] [Related]
30. Genome-wide linkage scan of epilepsy-related photoparoxysmal electroencephalographic response: evidence for linkage on chromosomes 7q32 and 16p13.
Pinto D; Westland B; de Haan GJ; Rudolf G; da Silva BM; Hirsch E; Lindhout D; Trenité DG; Koeleman BP
Hum Mol Genet; 2005 Jan; 14(1):171-8. PubMed ID: 15548544
[TBL] [Abstract][Full Text] [Related]
31. Statistical recombinant mapping in extended high-risk Utah pedigrees narrows the 8q24 prostate cancer locus to 2.0 Mb.
Camp NJ; Farnham JM; Allen-Brady K; Cannon-Albright LA
Prostate; 2007 Sep; 67(13):1456-64. PubMed ID: 17654497
[TBL] [Abstract][Full Text] [Related]
32. Positional candidate approach for the gene responsible for benign adult familial myoclonic epilepsy.
Sano A; Mikami M; Nakamura M; Ueno S; Tanabe H; Kaneko S
Epilepsia; 2002; 43 Suppl 9():26-31. PubMed ID: 12383276
[TBL] [Abstract][Full Text] [Related]
33. Common subtypes of idiopathic generalized epilepsies: lack of linkage to D20S19 close to candidate loci (EBN1, EEGV1) on chromosome 20.
Sander T; Hildmann T; Wienker TF; Ramel C; Beck-Mannagetta G; Bianchi A; Sailer U; Berek K; Bauer G; Neitzel H; Schmitz B; Durner M; Johnson KJ; Janz D
Am J Med Genet; 1996 Feb; 67(1):31-9. PubMed ID: 8678111
[TBL] [Abstract][Full Text] [Related]
34. Fine Mapping of a Dravet Syndrome Modifier Locus on Mouse Chromosome 5 and Candidate Gene Analysis by RNA-Seq.
Hawkins NA; Zachwieja NJ; Miller AR; Anderson LL; Kearney JA
PLoS Genet; 2016 Oct; 12(10):e1006398. PubMed ID: 27768696
[TBL] [Abstract][Full Text] [Related]
35. Carboxypeptidase A6 gene (CPA6) mutations in a recessive familial form of febrile seizures and temporal lobe epilepsy and in sporadic temporal lobe epilepsy.
Salzmann A; Guipponi M; Lyons PJ; Fricker LD; Sapio M; Lambercy C; Buresi C; Ouled Amar Bencheikh B; Lahjouji F; Ouazzani R; Crespel A; Chaigne D; Malafosse A
Hum Mutat; 2012 Jan; 33(1):124-35. PubMed ID: 21922598
[TBL] [Abstract][Full Text] [Related]
36. An association analysis at 2q36 reveals a new candidate susceptibility gene for juvenile absence epilepsy and/or absence seizures associated with generalized tonic-clonic seizures.
Yalçin O; Baykan B; Ağan K; Yapici Z; Yalçin D; Dizdarer G; Türkdoğan D; Ozkara C; Unalp A; Uludüz D; Gül G; Kuşcu D; Ayta S; Tutkavul K; Comu S; Tatli B; Meral C; Bebek N; Cağlayan SH
Epilepsia; 2011 May; 52(5):975-83. PubMed ID: 21320115
[TBL] [Abstract][Full Text] [Related]
37. Genes for epilepsy mapped in the mouse.
Rise ML; Frankel WN; Coffin JM; Seyfried TN
Science; 1991 Aug; 253(5020):669-73. PubMed ID: 1871601
[TBL] [Abstract][Full Text] [Related]
38. Do idiopathic generalized epilepsies share a common susceptibility gene?
Janz D; Beck-Mannagetta G; Sander T
Neurology; 1992 Apr; 42(4 Suppl 5):48-55. PubMed ID: 1574176
[TBL] [Abstract][Full Text] [Related]
39. Case-control study and transmission/disequilibrium tests of the genes encoding GABRA5 and GABRB3 in a Chinese population affected by childhood absence epilepsy.
Lü JJ; Zhang YH; Pan H; Chen YC; Liu XY; Jiang YW; Bao XH; Shen Y; Wu HS; Xu KM; Wu XR
Chin Med J (Engl); 2004 Oct; 117(10):1497-501. PubMed ID: 15498372
[TBL] [Abstract][Full Text] [Related]
40. Chromosomal localization of the human and mouse hyaluronan synthase genes.
Spicer AP; Seldin MF; Olsen AS; Brown N; Wells DE; Doggett NA; Itano N; Kimata K; Inazawa J; McDonald JA
Genomics; 1997 May; 41(3):493-7. PubMed ID: 9169154
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
