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Volumn 88, Issue 3, 2015, Pages 220-223

Low utilization of prenatal and pre-implantation genetic diagnosis in Huntington disease - risk discounting in preventive genetics

Author keywords

Huntington disease; PGD; Prenatal diagnosis; Reproductive options

Indexed keywords

HUNTINGTIN;

EID: 84938876807     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/cge.12523     Document Type: Article
Times cited : (10)

References (15)
  • 2
    • 34249950821 scopus 로고    scopus 로고
    • Decision-making about reproductive choices among individuals at-risk for Huntington's disease
    • Klitzman R, Thorne D, Williamson J, Chung W, Marder K. Decision-making about reproductive choices among individuals at-risk for Huntington's disease. J Genet Couns 2007: 16 (3): 347-362.
    • (2007) J Genet Couns , vol.16 , Issue.3 , pp. 347-362
    • Klitzman, R.1    Thorne, D.2    Williamson, J.3    Chung, W.4    Marder, K.5
  • 3
    • 0029912923 scopus 로고    scopus 로고
    • Preimplantation genetic testing for Huntington disease and certain other dominantly inherited disorders
    • Schulman JD, Black SH, Handyside A, Nance WE. Preimplantation genetic testing for Huntington disease and certain other dominantly inherited disorders. Clin Genet 1996: 49 (2): 57-58.
    • (1996) Clin Genet , vol.49 , Issue.2 , pp. 57-58
    • Schulman, J.D.1    Black, S.H.2    Handyside, A.3    Nance, W.E.4
  • 4
    • 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 (6): 462-475.
    • (2003) Clin Genet , vol.63 , Issue.6 , pp. 462-475
    • Creighton, S.1    Almqvist, E.W.2    MacGregor, D.3
  • 5
    • 0032412865 scopus 로고    scopus 로고
    • Non-disclosure preimplantation genetic diagnosis for Huntington's disease: practical and ethical dilemmas
    • Braude PR, De Wert GM, Evers-Kiebooms G, Pettigrew RA, Geraedts JP. Non-disclosure preimplantation genetic diagnosis for Huntington's disease: practical and ethical dilemmas. Prenat Diagn 1998: 18 (13): 1422-1426.
    • (1998) Prenat Diagn , vol.18 , Issue.13 , pp. 1422-1426
    • Braude, P.R.1    De Wert, G.M.2    Evers-Kiebooms, G.3    Pettigrew, R.A.4    Geraedts, J.P.5
  • 6
    • 84876814569 scopus 로고    scopus 로고
    • Reproductive options for prospective parents in families with Huntington's disease: clinical, psychological and ethical reflections
    • de Die-Smulders CE, de Wert GM, Liebaers I, Tibben A, Evers-Kiebooms G. Reproductive options for prospective parents in families with Huntington's disease: clinical, psychological and ethical reflections. Hum Reprod Update 2013: 19 (3): 304-315.
    • (2013) Hum Reprod Update , vol.19 , Issue.3 , pp. 304-315
    • de Die-Smulders, C.E.1    de Wert, G.M.2    Liebaers, I.3    Tibben, A.4    Evers-Kiebooms, G.5
  • 7
    • 77955923867 scopus 로고    scopus 로고
    • Conceptualizing couples' decision making in PGD: emerging cognitive, emotional, and moral dimensions
    • Hershberger PE, Pierce PF. Conceptualizing couples' decision making in PGD: emerging cognitive, emotional, and moral dimensions. Patient Educ Couns 2010: 81 (1): 53-62.
    • (2010) Patient Educ Couns , vol.81 , Issue.1 , pp. 53-62
    • Hershberger, P.E.1    Pierce, P.F.2
  • 8
    • 84864749266 scopus 로고    scopus 로고
    • The incidence and prevalence of Huntington's disease: a systematic review and meta-analysis
    • Pringsheim T, Wiltshire K, Day L, Dykeman J, Steeves T, Jette N. The incidence and prevalence of Huntington's disease: a systematic review and meta-analysis. Mov Disord 2012: 27 (9): 1083-1091.
    • (2012) Mov Disord , vol.27 , Issue.9 , pp. 1083-1091
    • Pringsheim, T.1    Wiltshire, K.2    Day, L.3    Dykeman, J.4    Steeves, T.5    Jette, N.6
  • 9
    • 0036289444 scopus 로고    scopus 로고
    • Non-disclosing preimplantation genetic diagnosis for Huntington disease
    • Stern HJ, Harton GL, Sisson ME et al. Non-disclosing preimplantation genetic diagnosis for Huntington disease. Prenat Diagn 2002: 22 (6): 503-507.
    • (2002) Prenat Diagn , vol.22 , Issue.6 , pp. 503-507
    • Stern, H.J.1    Harton, G.L.2    Sisson, M.E.3
  • 10
    • 84859982777 scopus 로고    scopus 로고
    • The ESHRE PGD Consortium: 10 years of data collection
    • Harper JC, Wilton L, Traeger-Synodinos J et al. The ESHRE PGD Consortium: 10 years of data collection. Hum Reprod Update 2012: 18 (3): 234-247.
    • (2012) Hum Reprod Update , vol.18 , Issue.3 , pp. 234-247
    • Harper, J.C.1    Wilton, L.2    Traeger-Synodinos, J.3
  • 11
    • 84880523793 scopus 로고    scopus 로고
    • The direct medical costs of Huntington's disease by stage. A retrospective commercial and Medicaid claims data analysis
    • Divino V, Dekoven M, Warner JH et al. The direct medical costs of Huntington's disease by stage. A retrospective commercial and Medicaid claims data analysis. J Med Econ 2013: 16 (8): 1043-1050.
    • (2013) J Med Econ , vol.16 , Issue.8 , pp. 1043-1050
    • Divino, V.1    Dekoven, M.2    Warner, J.H.3
  • 12
    • 0037390446 scopus 로고    scopus 로고
    • The hereditary nonpolyposis colorectal cancer syndrome: genetics and clinical implications
    • Chung DC, Rustgi AK. The hereditary nonpolyposis colorectal cancer syndrome: genetics and clinical implications. Ann Intern Med 2003: 138 (7): 560-570.
    • (2003) Ann Intern Med , vol.138 , Issue.7 , pp. 560-570
    • Chung, D.C.1    Rustgi, A.K.2
  • 13
    • 84882750431 scopus 로고    scopus 로고
    • Uptake of genetic testing by relatives of lynch syndrome probands: a systematic review
    • Sharaf RN, Myer P, Stave CD, Diamond LC, Ladabaum U. Uptake of genetic testing by relatives of lynch syndrome probands: a systematic review. Clin Gastroenterol Hepatol 2013: 11 (9): 1093-1100.
    • (2013) Clin Gastroenterol Hepatol , vol.11 , Issue.9 , pp. 1093-1100
    • Sharaf, R.N.1    Myer, P.2    Stave, C.D.3    Diamond, L.C.4    Ladabaum, U.5
  • 14
    • 0034528209 scopus 로고    scopus 로고
    • Uptake of hereditary breast/ovarian cancer genetic testing in a French national sample of BRCA1 families. The French Cancer Genetic Network
    • Julian-Reynier C, Sobol H, Sevilla C, Nogues C, Bourret P. Uptake of hereditary breast/ovarian cancer genetic testing in a French national sample of BRCA1 families. The French Cancer Genetic Network. Psychooncology 2000: 9 (6): 504-510.
    • (2000) Psychooncology , vol.9 , Issue.6 , pp. 504-510
    • Julian-Reynier, C.1    Sobol, H.2    Sevilla, C.3    Nogues, C.4    Bourret, P.5
  • 15
    • 21244473319 scopus 로고    scopus 로고
    • Genetic uptake in BRCA-mutation families is related to emotional and behavioral communication characteristics of index patients
    • Landsbergen K, Verhaak C, Kraaimaat F, Hoogerbrugge N. Genetic uptake in BRCA-mutation families is related to emotional and behavioral communication characteristics of index patients. Fam Cancer 2005: 4 (2): 115-119.
    • (2005) Fam Cancer , vol.4 , Issue.2 , pp. 115-119
    • Landsbergen, K.1    Verhaak, C.2    Kraaimaat, F.3    Hoogerbrugge, N.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.