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Volumn 28, Issue 5, 1998, Pages 293-299

Chromosome fragile sites in mentally retarded males: Increased incidence with seizures and diphenylhydantoin therapy

Author keywords

[No Author keywords available]

Indexed keywords

PHENYTOIN;

EID: 0031684591     PISSN: 00917370     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (2)

References (18)
  • 2
    • 0028237277 scopus 로고
    • Cytogenetic studies in children on long-term anticonvulsant therapy
    • Kitsiou-Tzeli S, Galla-Voumvouraki A, Tsezou A, et al. Cytogenetic studies in children on long-term anticonvulsant therapy. Acta Pædiat 1994;83:672-3.
    • (1994) Acta Pædiat , vol.83 , pp. 672-673
    • Kitsiou-Tzeli, S.1    Galla-Voumvouraki, A.2    Tsezou, A.3
  • 3
    • 0016772929 scopus 로고
    • Cytogenetic testing in antiepileptic drugs in human patients
    • Bartsch HD. Cytogenetic testing in antiepileptic drugs in human patients. Mutation Res 1975;29: 279-81.
    • (1975) Mutation Res , vol.29 , pp. 279-281
    • Bartsch, H.D.1
  • 4
    • 0023067168 scopus 로고
    • Mutagenic risk in epileptic patients before and after anticonvulsant therapy
    • Goyle S, Maurya AK, Rout UK, et al. Mutagenic risk in epileptic patients before and after anticonvulsant therapy. Epilepsia 1987;28:81-6.
    • (1987) Epilepsia , vol.28 , pp. 81-86
    • Goyle, S.1    Maurya, A.K.2    Rout, U.K.3
  • 5
    • 0019948887 scopus 로고
    • Increased sister chromatid exchanges in epileptic children during long-term therapy with phenytoin
    • Habedank M, Esser KJ, Brull D, et al. Increased sister chromatid exchanges in epileptic children during long-term therapy with phenytoin. Human Genet 1982;61:71-2.
    • (1982) Human Genet , vol.61 , pp. 71-72
    • Habedank, M.1    Esser, K.J.2    Brull, D.3
  • 6
    • 0028074843 scopus 로고
    • Sister-chromatid exchange in epileptic patients on anticonvulsant therapy
    • Sardas S, Ada M, Karakaya AE, et al. Sister-chromatid exchange in epileptic patients on anticonvulsant therapy. Mutation Res 1994;313:21-4.
    • (1994) Mutation Res , vol.313 , pp. 21-24
    • Sardas, S.1    Ada, M.2    Karakaya, A.E.3
  • 7
    • 3543053159 scopus 로고
    • The meaning of seizures, paroxysmal activity and hypereactivity in subjects with Fragile X syndrome
    • Snowmass, Co., June 16-20
    • Musumeci SA. The meaning of seizures, paroxysmal activity and hypereactivity in subjects with Fragile X syndrome. 1992 International Fragile X Conference Proceedings. Snowmass, Co., June 16-20, 1992.
    • (1992) 1992 International Fragile X Conference Proceedings
    • Musumeci, S.A.1
  • 8
    • 0025153456 scopus 로고
    • Chromosome lesions which could be interpreted as "fragile sites" on the distal end of Xq
    • Butler MG, Allen AG, Haynes JL, et al. Chromosome lesions which could be interpreted as "fragile sites" on the distal end of Xq. Amer J Human Genet 1990;37: 250-3.
    • (1990) Amer J Human Genet , vol.37 , pp. 250-253
    • Butler, M.G.1    Allen, A.G.2    Haynes, J.L.3
  • 9
    • 3543091787 scopus 로고
    • Cytogenetic and other chromosomal abnormalities
    • DeLisi LE, Ross AL, White BJ, et al. Cytogenetic and other chromosomal abnormalities. Schizophrenia Res 1988;1:277-81.
    • (1988) Schizophrenia Res , vol.1 , pp. 277-281
    • DeLisi, L.E.1    Ross, A.L.2    White, B.J.3
  • 11
    • 0026520331 scopus 로고
    • Chromosome fragility and psychopathology in obligate female carriers of the fragile X-chromosome
    • Freund LS, Reiss AL, Hagerman R, et al. Chromosome fragility and psychopathology in obligate female carriers of the fragile X-chromosome. Arch Gen Psychiatry 1992;49:54-60.
    • (1992) Arch Gen Psychiatry , vol.49 , pp. 54-60
    • Freund, L.S.1    Reiss, A.L.2    Hagerman, R.3
  • 12
    • 0025060399 scopus 로고
    • No significant relationship between age and frequency of chromosome lesions in mentally retarded individuals with or without the fragile X syndrome
    • Butler MG. No significant relationship between age and frequency of chromosome lesions in mentally retarded individuals with or without the fragile X syndrome. Human Genet 1990;84:216-7.
    • (1990) Human Genet , vol.84 , pp. 216-217
    • Butler, M.G.1
  • 13
    • 0023618109 scopus 로고
    • Sister chromatid exchange analysis in the Prader-Labhart-Willi syndrome
    • Butler MG, Jenkins BB. Sister chromatid exchange analysis in the Prader-Labhart-Willi syndrome. Amer J Med Genet 1987;28:821-7.
    • (1987) Amer J Med Genet , vol.28 , pp. 821-827
    • Butler, M.G.1    Jenkins, B.B.2
  • 14
    • 0024349301 scopus 로고
    • Analysis of chromosome breakage in the Prader-Labhart-Willi syndrome
    • Butler MG, Jenkins BB. Analysis of chromosome breakage in the Prader-Labhart-Willi syndrome. Amer J Med Genet 1989;2:514-9.
    • (1989) Amer J Med Genet , vol.2 , pp. 514-519
    • Butler, M.G.1    Jenkins, B.B.2
  • 15
    • 0028264049 scopus 로고
    • Is Rett syndrome a chromosome breakage syndrome?
    • Telvi L, Leboyer M, Chirou C, et al. Is Rett syndrome a chromosome breakage syndrome? Amer J Med Genet 1994;5:602-5.
    • (1994) Amer J Med Genet , vol.5 , pp. 602-605
    • Telvi, L.1    Leboyer, M.2    Chirou, C.3
  • 16
    • 0029964332 scopus 로고    scopus 로고
    • Increased expression of aphidocolin-induced common fragile sites in Tourette syndrome
    • Geriche GS, Simonie I, Cloete E, et al. Increased expression of aphidocolin-induced common fragile sites in Tourette syndrome. Amer J Med Genet 1996; 67:25-30.
    • (1996) Amer J Med Genet , vol.67 , pp. 25-30
    • Geriche, G.S.1    Simonie, I.2    Cloete, E.3
  • 17
    • 0019411446 scopus 로고
    • Sister chromatid exchange (SCE) and structural chromosome aberration in mutagenicity testing
    • Gebhart E. Sister chromatid exchange (SCE) and structural chromosome aberration in mutagenicity testing. Human Genet 1981;58:235-54.
    • (1981) Human Genet , vol.58 , pp. 235-254
    • Gebhart, E.1
  • 18
    • 0019425762 scopus 로고
    • Chromosomal investigations in epileptic children during long-term therapy with phenytoin or primidone
    • Esser KJ, Kotlarek F, Habedank M, et al. Chromosomal investigations in epileptic children during long-term therapy with phenytoin or primidone. Human Genet 1981;56:345-8.
    • (1981) Human Genet , vol.56 , pp. 345-348
    • Esser, K.J.1    Kotlarek, F.2    Habedank, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.