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REFERENCES

  • 1
    Sander JWAS. The epidemiology and prognosis of typical absence seizures. In: DuncanJS, PanayiotopoulosCP, eds. Typical absences and related epileptic syndromes. London : Churchill Communications, 1995: 13544.
  • 2
    Panayiotopoulos CP. Typical absence seizures and their treatment. Arch Dis Child 1999;81: 3515.
  • 3
    Loiseau J, Loiseau P, Guyot M, et al. Survey of seizure disorders in the French southwest, I: incidence of epileptic syndromes. Epilepsia 1990;31: 3916.
  • 4
    Buoni S, Grosso S, Di Cosmo G, et al. Segregation analysis in typical absence epilepsy. J Child Neurol 1998;13: 8993.
  • 5
    Berkovic SF, Howell RA, Hay DA, et al. Epilepsies in twins: genetics of the major epilepsy syndromes. Ann Neurol 1998;43: 43545.
  • 6
    Crunelli V, Leresche N. Childhood absence epilepsy: genes, channels, neurons and networks. Nat Rev Neurosci 2002;3: 37182.
  • 7
    Fong GC, Shah PU, Gee MN, et al. Childhood absence epilepsy with tonic-clonic seizures and electroencephalogram 3-4-Hz spike and multispike-slow wave complexes: linkage to chromosome 8q24. Am J Hum Genet 1998;63: 111729.
  • 8
    Sugimoto Y, Morita R, Amano K, et al. Childhood absence epilepsy in 8q24: refinement of candidate region and construction of physical map. Genomics 2000;68: 26472.
  • 9
    Feucht M, Fuchs K, Pichlbauer E, et al. Possible association between childhood absence epilepsy and the gene encoding GABRB3. Biol Psychiatry 1999;46: 9971002.
  • 10
    Ptacek LJ, Fu YH. Channelopathies: episodic disorders of the nervous system. Epilepsia 2001;42: 3543.
  • 11
    Noebels JL. Single locus mutations in mice expressing generalized spike-wave absence epilepsies. Ital J Neurol Sci 1995;16: 10711.
  • 12
    Burgess DL, Noebels JL. Single gene defects in mice: the role of voltage-dependent calcium channels in absence models. Epilepsy Res 1999;36: 11122.
  • 13
    Coenen AM, Drinkenburg WH, Inoue M, et al. Genetic models of absence epilepsy, with emphasis on the WAG/Rij strain of rats. Epilepsy Res 1992;12: 7586.
  • 14
    Danober L, Deransart C, Depaulis A, et al. Pathophysiological mechanisms of genetic absence epilepsy in the rat. Prog Neurobiol 1998;55: 2757.
  • 15
    Marescaux C, Vergnes M. Genetic absence epilepsy in rats from Strasbourg (GAERS). Ital J Neurol Sci 1995;16: 1138.
  • 16
    Meeren HK, Pijn JP, Van Luijtelaar EL, et al. Cortical focus drives widespread corticothalamic networks during spontaneous absence seizures in rats. J Neurosci 2002;22: 148095.
  • 17
    Van Luijtelaar ELJM, Coenen AML. Two types of electrocortical paroxysms in an inbred strain of rats. Neurosci Lett 1986;70: 3937.
  • 18
    Midzianovskaia IS, Kuznetsova GD, Coenen AM, et al. Electrophysiological and pharmacological characteristics of two types of spike-wave discharges in WAG/Rij rats. Brain Res 2001;911: 6270.
  • 19
    Inoue M, Peeters BW, Van Luijtelaar EL, et al. Spontaneous occurrence of spike-wave discharges in five inbred strains of rats. Physiol Behav 1990;48: 199201.
  • 20
    Peeters BW, Kerbusch JM, Van Luijtelaar EL, et al. Genetics of absence epilepsy in rats. Behav Genet 1990;20: 45360.
  • 21
    Peeters BW, Kerbusch JM, Coenen AM, et al. Genetics of spike-wave discharges in the electroencephalogram (EEG) of the WAG/Rij inbred rat strain: a classical mendelian crossbreeding study. Behav Genet 1992;22: 3618.
  • 22
    Vadasz C, Carpi D, Jando G, et al. Genetic threshold hypothesis of neocortical spike-and-wave discharges in the rat: an animal model of petit mal epilepsy. Am J Med Genet 1995;60: 5563.
  • 23
    Paxinos G, Watson C. The rat brain in stereotaxoc coordinates. London : Academic Press, 1997.
  • 24
    Bihoreau MT, Gauguier D, Kato N, et al. A linkage map of the rat genome derived from three F2 crosses. Genome Res 1997;7: 43440.
  • 25
    Bihoreau MT, Sebag-Montefiore L, Godfrey RF, et al. A high resolution consensus linkage map of the rat integrating radiation hybrid and genetic maps. Genomics 2001;75: 5769.
  • 26
    Wilder SP, Bihoreau MT, Argoud K, et al. Integration of the rat recombination and EST maps in the rat genomic sequence and comparative mapping analysis with the mouse genome. Genome Res 2004;14: 75865.
  • 27
    Watanabe TK, Bihoreau MT, McCarthy LC, et al. A map of the rat genome containing 5,203 markers: 4,700 microsatellites and 605 genes in a rat, mouse and human comparative map. Nat Genet 1999;2: 2736.
  • 28
    Stam P, Van Ooijen JW. JoinMap version 2.0: Software for the calculation of genetic linkage maps: centre for Plant Breeding and Reproduction Research. Wageningen, The Netherlands : 1995.
  • 29
    Lander ES, Green P, Abrahamson J, et al. MAPMAKER: an interactive computer package for constructing primary genetic linkage maps of experimental and natural populations. Genomics 1987;1: 17481.
  • 30
    Churchill GA, Doerge RW. Empirical threshold values for quantitative trait mapping. Genetics 1994;138: 96371.
  • 31
    Doerge RW, Churchill GA. Permutation tests for multiple loci affecting a quantitative character. Genetics 1996;142: 28594.
  • 32
    Rudolf G, Bihoreau MT, Godfrey R, et al. Polygenic control of idiopathic generalized epilepsy phenotypes in the genetic absences rats from Strasbourg (GAERS). Epilepsia 2004;45: 18.
  • 33
    Coenen AM, Blezer EH, Van Luijtelaar EL. Effects of the GABA-uptake inhibitor tiagabine on electroencephalogram, spike-wave discharges and behaviour of rats. Epilepsy Res 1995;21: 8994.
  • 34
    Inoue M, Ates N, Vossen JM, et al. Effects of the neuroleptanalgesic fentanyl-fluanisone (Hypnorm) on spike-wave discharges in epileptic rats. Pharmacol Biochem Behav 1994;48: 54751.
  • 35
    Deransart C, Riban V, Le B, et al. Dopamine in the striatum modulates seizures in a genetic model of absence epilepsy in the rat. Neuroscience 2000;100: 33544.
  • 36
    De Bruin NM, Van Luijtelaar EL, Jansen SJ, et al. Dopamine characteristics in different rat genotypes: the relation to absence epilepsy. Neurosci Res 2000;38: 16573.
  • 37
    Van Luijtelaar EL, Dirksen R, Vree TB, et al. Effects of acute and chronic cocaine administration on EEG and behaviour in intact and castrated male and intact and ovariectomized female rats. Brain Res Bull 1996;40: 4350.
  • 38
    Coenen AM, Van Luijtelaar EL. The WAG/Rij rat model for absence epilepsy: age and sex factors. Epilepsy Res 1987;1: 297301.
  • 39
    Buzsaki G, Bickford RG, Armstrong DM, et al. Electric activity in the neocortex of freely moving young and aged rats. Neuroscience 1988;26: 735744.
  • 40
    Radek RJ, Curzon P, Decker MW. Characterization of high voltage spindles and spatial memory in young, mature and aged rats. Brain Res Bull 1994;33: 1838.
  • 41
    Willoughby JO, Mackenzie L. Nonconvulsive electrocorticographic paroxysms (absence epilepsy) in rat strains. Lab Anim Sci 1992;42: 5514.
  • 42
    Moyanova S, Kortenska L, Kirov R. High-voltage electroencephalogram spindles in rats, aging and 5-HT2 antagonism. Brain Res 1998;786: 5563.
  • 43
    Kopito RR, Lee BS, Simmons DM, et al. Regulation of intracellular pH by a neuronal homolog of the erythrocyte anion exchanger. Cell 1989;59: 92737.
  • 44
    Arai M, Prystowsky MB, Cohen JA. Expression of the T-lymphocyte activation gene, F5, by mature neurons. J Neurosci Res 1992;33: 5277.
  • 45
    Cox GA, Lutz CM, Yang CL, et al. Sodium/hydrogen exchanger gene defect in slow-wave epilepsy mutant mice. Cell 1997;91: 13948.
  • 46
    Waymire KG, Mahuren JD, Jaje JM, et al. Mice lacking tissue non-specific alkaline phosphatase die from seizures due to defective metabolism of vitamin B-6. Nat Genet 1995;11: 4551.
  • 47
    Ferraro TN, Golden GT, Smith GG, et al. Mapping loci for pentylenetetrazol-induced seizure susceptibility in mice. J Neurosci 1999;19: 67339.
  • 48
    Sander T, Schulz H, Saar K, et al. Genome search for susceptibility loci of common idiopathic generalised epilepsies. Hum Mol Genet 2000;12: 146572.
  • 49
    Lander E, Kruglyak L. Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat Genet 1995;11: 2417.