메뉴 건너뛰기




Volumn 51, Issue 2, 1998, Pages 493-498

Unusual EEG pattern linked to chromosome 3p in a family with idiopathic generalized epilepsy

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 3P; CLINICAL ARTICLE; DELTA RHYTHM; ELECTROENCEPHALOGRAM; FEMALE; GENE MAPPING; GENERALIZED EPILEPSY; HUMAN; ITALY; MALE; PRIORITY JOURNAL;

EID: 0031723313     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.51.2.493     Document Type: Article
Times cited : (19)

References (32)
  • 1
    • 0001383694 scopus 로고
    • Action potentials of the brain in normal persons and in normal states of cerebral activity
    • Chicago
    • Davis H, Davis PA. Action potentials of the brain in normal persons and in normal states of cerebral activity. Arch Neurol Psychiatry (Chicago) 1936;36:1214-1224.
    • (1936) Arch Neurol Psychiatry , vol.36 , pp. 1214-1224
    • Davis, H.1    Davis, P.A.2
  • 3
    • 0007673374 scopus 로고
    • Genetics of convulsive disorders. II Genetic of electroencephalographic studies in centrencephalic epilepsy
    • Metrakos K, Metrakos JD. Genetics of convulsive disorders. II Genetic of electroencephalographic studies in centrencephalic epilepsy. Neurology 1961;11:474-483.
    • (1961) Neurology , vol.11 , pp. 474-483
    • Metrakos, K.1    Metrakos, J.D.2
  • 4
    • 0000887416 scopus 로고
    • Multifactorial inheritance of generalized and focal epilepsy
    • Anderson VE, Hauser WA, Penry JK, Sing CF, eds. New York: Raven Press
    • Andermann E. Multifactorial inheritance of generalized and focal epilepsy. In: Anderson VE, Hauser WA, Penry JK, Sing CF, eds. Genetic basis of the epilepsies. New York: Raven Press, 1982:355-374.
    • (1982) Genetic Basis of the Epilepsies , pp. 355-374
    • Andermann, E.1
  • 5
    • 0242501889 scopus 로고
    • Genetic aspects of the epilepsies
    • Sakai T, Tsuboi T, eds. Tokyo: Igaku-Shoin
    • Andermann E. Genetic aspects of the epilepsies. In: Sakai T, Tsuboi T, eds. Genetic aspects of human behavior. Tokyo: Igaku-Shoin, 1985:129-145.
    • (1985) Genetic Aspects of Human Behavior , pp. 129-145
    • Andermann, E.1
  • 6
    • 0026841987 scopus 로고
    • Evidence for multiple gene loci in the expression of the common generalized epilepsies
    • Greenberg DA, Durner M, Delgado-Escueta AV. Evidence for multiple gene loci in the expression of the common generalized epilepsies. Neurology 1992;42(suppl 5):56-62.
    • (1992) Neurology , vol.42 , Issue.5 SUPPL. , pp. 56-62
    • Greenberg, D.A.1    Durner, M.2    Delgado-Escueta, A.V.3
  • 9
    • 0002989368 scopus 로고
    • Genetic risk in offsprings of epileptic parents
    • Beck-Mannagetta G, Anderson VE, Doose H, Janz D, eds. Berlin-Heidelberg: Springer-Verlag
    • Tsuboi T. Genetic risk in offsprings of epileptic parents. In: Beck-Mannagetta G, Anderson VE, Doose H, Janz D, eds. Genetics of the epilepsies. Berlin-Heidelberg: Springer-Verlag, 1989:119-126.
    • (1989) Genetics of the Epilepsies , pp. 119-126
    • Tsuboi, T.1
  • 10
    • 0004963360 scopus 로고
    • Morbid risk for seizures in offsprings of patients with epilepsy
    • Beck-Mannagetta G, Anderson VE, Doose H, Janz D, eds. Berlin-Heidelberg: Springer-Verlag
    • Beck-Mannagetta G, Janz D, Hoffmaister U. Morbid risk for seizures in offsprings of patients with epilepsy. In: Beck-Mannagetta G, Anderson VE, Doose H, Janz D, eds. Genetics of the epilepsies. Berlin-Heidelberg: Springer-Verlag, 1989: 127-145.
    • (1989) Genetics of the Epilepsies , pp. 127-145
    • Beck-Mannagetta, G.1    Janz, D.2    Hoffmaister, U.3
  • 11
    • 0027525688 scopus 로고
    • Concordance of clinical forms of epilepsy in families with several affected members
    • Italian League against Epilepsy Genetics Collaborative Group. Concordance of clinical forms of epilepsy in families with several affected members. Epilepsia 1993;34:819-826.
    • (1993) Epilepsia , vol.34 , pp. 819-826
  • 12
    • 0015139734 scopus 로고
    • Essential isochronic epilepsy in MZ twin pairs
    • Roma
    • Gedda L, Tatarelli L. Essential isochronic epilepsy in MZ twin pairs. Acta Genet Med Gemellol (Roma) 1971;20:380-383.
    • (1971) Acta Genet Med Gemellol , vol.20 , pp. 380-383
    • Gedda, L.1    Tatarelli, L.2
  • 14
    • 0023197659 scopus 로고
    • Interdependence of different genetic EEG patterns in siblings of epileptic patients
    • Baier WK, Doose H. Interdependence of different genetic EEG patterns in siblings of epileptic patients. Electroencephalogr Clin Neurophysiol 1987;66:483-488.
    • (1987) Electroencephalogr Clin Neurophysiol , vol.66 , pp. 483-488
    • Baier, W.K.1    Doose, H.2
  • 15
    • 0026310770 scopus 로고
    • The use and role of EEG in the genetic analysis of epilepsy
    • Anderson VE, et al., eds. New York: Elsevier
    • Pedley TA. The use and role of EEG in the genetic analysis of epilepsy. In: Anderson VE, et al., eds. Genetic strategies in epilepsy research. New York: Elsevier, 1991:31-44.
    • (1991) Genetic Strategies in Epilepsy Research , pp. 31-44
    • Pedley, T.A.1
  • 16
    • 0028872907 scopus 로고
    • A 1.5 Mb submicroscopic deletion in 17p11.2-p12 is frequently observed in Italian families with hereditary neuropathy with liability to pressure palsies
    • Lorenzetti D, Pareyson D, Sghirlanzoni A, et al. A 1.5 Mb submicroscopic deletion in 17p11.2-p12 is frequently observed in Italian families with hereditary neuropathy with liability to pressure palsies. Am J Hum Genet 1995;56:91-98.
    • (1995) Am J Hum Genet , vol.56 , pp. 91-98
    • Lorenzetti, D.1    Pareyson, D.2    Sghirlanzoni, A.3
  • 18
    • 0028231090 scopus 로고
    • The 1993-94 Genethon human genetic linkage map
    • Gyapay G, Morisette J, Vignal A, et al. The 1993-94 Genethon human genetic linkage map. Nature Genet 1994;7:246-339.
    • (1994) Nature Genet , vol.7 , pp. 246-339
    • Gyapay, G.1    Morisette, J.2    Vignal, A.3
  • 19
    • 0027479304 scopus 로고
    • Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12
    • Tournier-Lasserve E, Joutel A, Melki J, et al. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12. Nature Genet 1993;3:256-259.
    • (1993) Nature Genet , vol.3 , pp. 256-259
    • Tournier-Lasserve, E.1    Joutel, A.2    Melki, J.3
  • 20
    • 0021850103 scopus 로고
    • Multilocus linkage analysis in humans: Detection of linkage and estimation of recombination
    • Lathrop GM, Laouel JM, Julier C, Ott J. Multilocus linkage analysis in humans: detection of linkage and estimation of recombination. Am J Hum Genet 1985;47:926-934.
    • (1985) Am J Hum Genet , vol.47 , pp. 926-934
    • Lathrop, G.M.1    Laouel, J.M.2    Julier, C.3    Ott, J.4
  • 23
    • 0024317220 scopus 로고
    • Proposal for revised classification of epilepsies and epileptic syndromes
    • Commission on Classification and Terminology of the International League Against Epilepsy. Proposal for revised classification of epilepsies and epileptic syndromes. Epilepsia 1989; 30:389-399.
    • (1989) Epilepsia , vol.30 , pp. 389-399
  • 24
    • 0028877463 scopus 로고
    • Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results
    • Lander ES, Kruglyak L. Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nature Genet 1995;11:241-247.
    • (1995) Nature Genet , vol.11 , pp. 241-247
    • Lander, E.S.1    Kruglyak, L.2
  • 25
    • 0015699587 scopus 로고
    • On the genetics of the primary generalized epilepsy with sporadic myoclonias of impulsive petit mal type
    • Tsuboi T, Christian W. On the genetics of the primary generalized epilepsy with sporadic myoclonias of impulsive petit mal type. Humangenetik 1977;19:155-182.
    • (1977) Humangenetik , vol.19 , pp. 155-182
    • Tsuboi, T.1    Christian, W.2
  • 26
    • 0023712810 scopus 로고
    • Juvenile myoclonic epilepsy (JME) may be linked to the BF and HLA loci on human chromosome 6
    • Greenberg DA, Delgado-Escueta VA, Widelitz H. Juvenile myoclonic epilepsy (JME) may be linked to the BF and HLA loci on human chromosome 6. Am J Med Genet 1988;31:185-192.
    • (1988) Am J Med Genet , vol.31 , pp. 185-192
    • Greenberg, D.A.1    Delgado-Escueta, V.A.2    Widelitz, H.3
  • 27
    • 0026057715 scopus 로고
    • Confirmation of linkage between juvenile myoclonic epilepsy locus and the HLA region on chromosome 6p
    • Weissbecker KA, Durner M, Janz D. Confirmation of linkage between juvenile myoclonic epilepsy locus and the HLA region on chromosome 6p. Am J Med Genet 1991;38:32-36.
    • (1991) Am J Med Genet , vol.38 , pp. 32-36
    • Weissbecker, K.A.1    Durner, M.2    Janz, D.3
  • 28
    • 0029013275 scopus 로고
    • Juvenile myoclonic epilepsy locus in chromosome 6p21.1-p11: Linkage to convulsions and electroencephalography trait
    • Liu AW, Delgado-Escueta AV, Serratosa JM, et al. Juvenile myoclonic epilepsy locus in chromosome 6p21.1-p11: linkage to convulsions and electroencephalography trait. Am J Hum Genet 1995;57:368-381.
    • (1995) Am J Hum Genet , vol.57 , pp. 368-381
    • Liu, A.W.1    Delgado-Escueta, A.V.2    Serratosa, J.M.3
  • 29
    • 0029041041 scopus 로고
    • The genetics of idiopathic generalized epilepsies of adolescent onset: Differences between juvenile myoclonic epilepsy and epilepsy with random grand mal and with awakening grand mal
    • Greenberg DA, Durner M, Resor S, et al. The genetics of idiopathic generalized epilepsies of adolescent onset: differences between juvenile myoclonic epilepsy and epilepsy with random grand mal and with awakening grand mal. Neurology 1995;45:942-946.
    • (1995) Neurology , vol.45 , pp. 942-946
    • Greenberg, D.A.1    Durner, M.2    Resor, S.3
  • 30
    • 0026706497 scopus 로고
    • Assignment of the gene encoding the alpha 1 subunit of the neuroendocrine/ brain-type calcium channel (CACNL1A2) to human chromosome 3, band p14.3
    • Seino S, Yamada Y, Espinosa R III, et al. Assignment of the gene encoding the alpha 1 subunit of the neuroendocrine/ brain-type calcium channel (CACNL1A2) to human chromosome 3, band p14.3. Genomics 1992;13:1375-1377.
    • (1992) Genomics , vol.13 , pp. 1375-1377
    • Seino, S.1    Yamada, Y.2    Espinosa R. III3
  • 31
    • 0031228095 scopus 로고    scopus 로고
    • 2+ channel gene in familial hemiplegic migraine and migraine with and without aura. Dutch Migraine Genetics Research Group
    • 2+ channel gene in familial hemiplegic migraine and migraine with and without aura. Dutch Migraine Genetics Research Group. Headache 1997;37:479-485.
    • (1997) Headache , vol.37 , pp. 479-485
    • Ophoff, R.A.1    Terwindt, G.M.2    Vergouwe, M.N.3
  • 32
    • 0031064169 scopus 로고    scopus 로고
    • Mutations in the CACNL1A4 calcium channel gene are associated with seizures, cerebellar degeneration, and ataxia in tottering and leaner mutant mice
    • Doyle J, Ren X, Lennon G, Stubbs L. Mutations in the CACNL1A4 calcium channel gene are associated with seizures, cerebellar degeneration, and ataxia in tottering and leaner mutant mice. Mamm Genome 1997;8:113-120.
    • (1997) Mamm Genome , vol.8 , pp. 113-120
    • Doyle, J.1    Ren, X.2    Lennon, G.3    Stubbs, L.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.