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Volumn 80, Issue 6, 2011, Pages 586-590

Huntington's disease in Greece: The experience of 14 years

Author keywords

Epidemiology; Greece; Huntington's disease; Neurogenetic; Population

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; ATN1 GENE; CAG REPEAT; CHILD; CLINICAL FEATURE; CONTROLLED STUDY; DENTATORUBROPALLIDOLUYSIAN ATROPHY; FALSE POSITIVE RESULT; FAMILY HISTORY; FEMALE; GENE; GENETIC COUNSELING; GENETIC ISOLATION BY DISTANCE; GENETIC RISK; GREECE; HUMAN; HUNTINGTON CHOREA; MAJOR CLINICAL STUDY; MALE; MOLECULAR DIAGNOSIS; PREDICTIVE VALUE; PRIORITY JOURNAL; PROSPECTIVE STUDY; SCHOOL CHILD;

EID: 80054886149     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/j.1399-0004.2010.01603.x     Document Type: Article
Times cited : (38)

References (19)
  • 2
    • 0027275819 scopus 로고
    • A new polymerase chain reaction (PCR) assay for the trinucleotide repeat that is unstable and expanded on Huntington's disease chromosomes.
    • Warner JP, Barron LH, Brock DJ. A new polymerase chain reaction (PCR) assay for the trinucleotide repeat that is unstable and expanded on Huntington's disease chromosomes. Mol Cell Probes 1993: 7: 235-239.
    • (1993) Mol Cell Probes , vol.7 , pp. 235-239
    • Warner, J.P.1    Barron, L.H.2    Brock, D.J.3
  • 3
    • 0031782911 scopus 로고    scopus 로고
    • Simple nonisotopic assays for detection of (CAG)n repeats expansions associated with seven neurodegenerative disorders.
    • Vuillaume I, Schraen S, Rousseaux J, Sablonnière B. Simple nonisotopic assays for detection of (CAG)n repeats expansions associated with seven neurodegenerative disorders. Diagn Mol Pathol 1998: 7: 174-179.
    • (1998) Diagn Mol Pathol , vol.7 , pp. 174-179
    • Vuillaume, I.1    Schraen, S.2    Rousseaux, J.3    Sablonnière, B.4
  • 4
    • 0021260868 scopus 로고
    • Huntington disease: genetics and epidemiology.
    • Conneally PM. Huntington disease: genetics and epidemiology. Am J Hum Genet 1984: 36: 506-526.
    • (1984) Am J Hum Genet , vol.36 , pp. 506-526
    • Conneally, P.M.1
  • 5
    • 0033546889 scopus 로고    scopus 로고
    • DNA analysis of Huntington's disease: five years of experience in Germany, Austria, and Switzerland.
    • Laccone F, Engel U, Holinski-Feder E et al. DNA analysis of Huntington's disease: five years of experience in Germany, Austria, and Switzerland. Neurology 1999: 53: 801-806.
    • (1999) Neurology , vol.53 , pp. 801-806
    • Laccone, F.1    Engel, U.2    Holinski-Feder, E.3
  • 6
    • 0034780024 scopus 로고    scopus 로고
    • High incidence rate and absent family histories in one quarter of patients newly diagnosed with Huntington disease in British Columbia.
    • Almqvist EW, Elterman DS, MacLeod PM, Hayden MR. High incidence rate and absent family histories in one quarter of patients newly diagnosed with Huntington disease in British Columbia. Clin Genet 2001: 60: 198-205.
    • (2001) Clin Genet , vol.60 , pp. 198-205
    • Almqvist, E.W.1    Elterman, D.S.2    MacLeod, P.M.3    Hayden, M.R.4
  • 7
    • 10744224655 scopus 로고    scopus 로고
    • Molecular diagnosis of Huntington disease in Portugal: implications for genetic counselling and clinical practice.
    • Costa Mdo C, Magalhães P, Ferreirinha F et al. Molecular diagnosis of Huntington disease in Portugal: implications for genetic counselling and clinical practice. Eur J Hum Genet 2003: 11: 872-878.
    • (2003) Eur J Hum Genet , vol.11 , pp. 872-878
    • Costa Mdo, C.1    Magalhães, P.2    Ferreirinha, F.3
  • 8
    • 0027240431 scopus 로고
    • Trinucleotide repeat length instability and age of onset in Huntington's disease.
    • Duyao M, Ambrose C, Myers R et al. Trinucleotide repeat length instability and age of onset in Huntington's disease. Nat Genet 1993: 4: 387-392.
    • (1993) Nat Genet , vol.4 , pp. 387-392
    • Duyao, M.1    Ambrose, C.2    Myers, R.3
  • 9
    • 0027261537 scopus 로고
    • Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease.
    • Snell RG, MacMillan JC, Cheadle JP et al. Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease. Nat Genet 1993: 4: 393-397.
    • (1993) Nat Genet , vol.4 , pp. 393-397
    • Snell, R.G.1    MacMillan, J.C.2    Cheadle, J.P.3
  • 10
    • 14544284039 scopus 로고    scopus 로고
    • Incidence and mutation rates of Huntington's disease in Spain: experience of 9 years of direct genetic testing.
    • Ramos-Arroyo MA, Moreno S, Valiente A. Incidence and mutation rates of Huntington's disease in Spain: experience of 9 years of direct genetic testing. J Neurol Neurosurg Psychiatry 2005: 76: 337-342.
    • (2005) J Neurol Neurosurg Psychiatry , vol.76 , pp. 337-342
    • Ramos-Arroyo, M.A.1    Moreno, S.2    Valiente, A.3
  • 11
  • 12
    • 0026684333 scopus 로고
    • The epidemiology of Huntington's disease.
    • Harper PS. The epidemiology of Huntington's disease. Hum Genet 1992: 89: 365-376.
    • (1992) Hum Genet , vol.89 , pp. 365-376
    • Harper, P.S.1
  • 13
    • 0028359603 scopus 로고
    • Incidence and prevalence of Huntington's disease in Olmsted County, Minnesota (1950 through 1989).
    • Kokmen E, Ozekmekçi FS, Beard CM, O'Brien PC, Kurland LT. Incidence and prevalence of Huntington's disease in Olmsted County, Minnesota (1950 through 1989). Arch Neurol 1994: 51: 696-698.
    • (1994) Arch Neurol , vol.51 , pp. 696-698
    • Kokmen, E.1    Ozekmekçi, F.S.2    Beard, C.M.3    O'Brien, P.C.4    Kurland, L.T.5
  • 14
    • 10744221876 scopus 로고    scopus 로고
    • Predictive, pre-natal and diagnostic genetic testing for Huntington's disease: the experience in Canada from 1987 to 2000.
    • Creighton S, Almqvist EW, MacGregor D et al. Predictive, pre-natal and diagnostic genetic testing for Huntington's disease: the experience in Canada from 1987 to 2000. Clin Genet 2003: 63: 462-475.
    • (2003) Clin Genet , vol.63 , pp. 462-475
    • Creighton, S.1    Almqvist, E.W.2    MacGregor, D.3
  • 15
    • 0033865906 scopus 로고    scopus 로고
    • Ten years of presymptomatic testing for Huntington's disease: the experience of the UK Huntington's Disease Prediction Consortium.
    • Harper PS, Lim C, Craufurd D. Ten years of presymptomatic testing for Huntington's disease: the experience of the UK Huntington's Disease Prediction Consortium. J Med Genet 2000: 37: 567-571.
    • (2000) J Med Genet , vol.37 , pp. 567-571
    • Harper, P.S.1    Lim, C.2    Craufurd, D.3
  • 17
    • 0028470671 scopus 로고
    • International Huntington Association and the World Federation of Neurology Research Group on Huntington's chorea: Guidelines for the molecular genetics predictive test in Huntington's disease.
    • International Huntington Association and the World Federation of Neurology Research Group on Huntington's chorea: Guidelines for the molecular genetics predictive test in Huntington's disease. J Med Genet 1994: 31: 555-559.
    • (1994) J Med Genet , vol.31 , pp. 555-559
  • 18
    • 8744268164 scopus 로고    scopus 로고
    • Predictive genetic testing in young people: when is it appropriate?
    • Duncan RE. Predictive genetic testing in young people: when is it appropriate? J Paediatr Child Health 2004: 40: 593-595.
    • (2004) J Paediatr Child Health , vol.40 , pp. 593-595
    • Duncan, R.E.1
  • 19
    • 0036861352 scopus 로고    scopus 로고
    • Prenatal testing for Huntington's disease: a European collaborative study.
    • Simpson SA, Zoeteweij MW, Nys K et al. Prenatal testing for Huntington's disease: a European collaborative study. Eur J Hum Genet 2002: 10: 689-693.
    • (2002) Eur J Hum Genet , vol.10 , pp. 689-693
    • Simpson, S.A.1    Zoeteweij, M.W.2    Nys, K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.