-
1
-
-
85051688984
-
-
Recommendation No. R(90) 3 on Prenatal Genetic Screening, Prenatal Genetic Diagnosis and Associated Genetic Counseling
-
Council of Europe. Recommendation No. R(90) 3 on Prenatal Genetic Screening, Prenatal Genetic Diagnosis and Associated Genetic Counseling, 1990.
-
(1990)
-
-
-
5
-
-
0011684559
-
-
The Hague: Health Council of the Netherlands
-
Health Council of the Netherlands. Heredity: Science and Society. The Hague: Health Council of the Netherlands, 1989.
-
(1989)
Heredity: Science and Society
-
-
-
6
-
-
79251546164
-
-
London: Br Med J Publishing Group
-
Medical Ethics Today. The BMA's Handbook of Ethics and Law. London: Br Med J Publishing Group, 2004.
-
(2004)
The BMA's Handbook of Ethics and Law
-
-
-
8
-
-
33646063036
-
Legal aspects of prenatal testing for lateonset neurological diseases
-
Evers-Kiebooms G, Zoetewij MW, Harper PS, eds, Oxford: BIOS
-
Nys H, Roemo Casabona CM, Desmet C. Legal aspects of prenatal testing for lateonset neurological diseases. In: Evers-Kiebooms G, Zoetewij MW, Harper PS, eds. Prenatal Testing for Late-onset Neurogenetic Disease. Oxford: BIOS, 2002:83-106.
-
(2002)
Prenatal Testing for Late-onset Neurogenetic Disease
, pp. 83-106
-
-
Nys, H.1
Roemo Casabona, C.M.2
Desmet, C.3
-
9
-
-
85051691526
-
-
Letter to Parliament, dated March 4, in Dutch
-
Minister of Public Health of the Netherlands. Prenatal Diagnosis. Letter to Parliament, dated March 4, 1996 (in Dutch).
-
(1996)
Prenatal Diagnosis
-
-
-
10
-
-
0345623341
-
Ethical aspects of prenatal testing and preimplantation genetic diagnosis for late-onset neurogenetic disease: the case of Huntington's disease
-
Evers-Kiebooms G, Zoetewij MW, Harper PS, eds, Oxford: BIOS
-
De Wert GM. Ethical aspects of prenatal testing and preimplantation genetic diagnosis for late-onset neurogenetic disease: the case of Huntington's disease. In: Evers-Kiebooms G, Zoetewij MW, Harper PS, eds. Prenatal Testing for Late-onset Neurogenetic Disease. Oxford: BIOS, 2002:129-158.
-
(2002)
Prenatal Testing for Late-onset Neurogenetic Disease
, pp. 129-158
-
-
De Wert, G.M.1
-
11
-
-
0027163675
-
Five year study of prenatal testing for Huntington's disease: demand, attitudes, and psychological assessment
-
Adam S, Wiggins S, Whyte P, et al. Five year study of prenatal testing for Huntington's disease: demand, attitudes, and psychological assessment. J Med Genet 1993; 30(7):549-556.
-
(1993)
J Med Genet
, vol.30
, Issue.7
, pp. 549-556
-
-
Adam, S.1
Wiggins, S.2
Whyte, P.3
-
12
-
-
0035036935
-
Prenatal testing for Huntington's disease: experience within the UK 1994-1998
-
Simpson SA, Harper PS. Prenatal testing for Huntington's disease: experience within the UK 1994-1998. J Med Genet 2001; 38(5):333-335.
-
(2001)
J Med Genet
, vol.38
, Issue.5
, pp. 333-335
-
-
Simpson, S.A.1
Harper, P.S.2
-
13
-
-
0028031125
-
Guidelines for the molecular genetics predictive test in Huntington's disease
-
International Huntington Association and World Federation of Neurology. Guidelines for the molecular genetics predictive test in Huntington's disease. Neurology 1994; 44(8):1533-1536.
-
(1994)
Neurology
, vol.44
, Issue.8
, pp. 1533-1536
-
-
-
14
-
-
0037425827
-
Prenatal diagnosis requests for Huntington's disease when the father is at risk and does not want to know his genetic status: clinical, legal, and ethical viewpoints
-
Tassicker R, Savulescu J, Skene L, Marshall P, Fitzgerald L, Delatycki MB. Prenatal diagnosis requests for Huntington's disease when the father is at risk and does not want to know his genetic status: clinical, legal, and ethical viewpoints. Br Med J 2003; 326(7384):331-333.
-
(2003)
Br Med J
, vol.326
, Issue.7384
, pp. 331-333
-
-
Tassicker, R.1
Savulescu, J.2
Skene, L.3
Marshall, P.4
Fitzgerald, L.5
Delatycki, M.B.6
-
15
-
-
0034096611
-
Clinical geneticists' attitudes and practice towards testing for breast cancer susceptibility genes
-
Lucassen AM, Houlston RS. Clinical geneticists' attitudes and practice towards testing for breast cancer susceptibility genes. J Med Genet 2000; 37(2):157-160.
-
(2000)
J Med Genet
, vol.37
, Issue.2
, pp. 157-160
-
-
Lucassen, A.M.1
Houlston, R.S.2
-
16
-
-
85051689639
-
-
(in Dutch). Utrecht: Royal Dutch Society of Physicians
-
Royal Dutch Society of Physicians. Doctors and Genes (in Dutch). Utrecht: Royal Dutch Society of Physicians, 1997.
-
(1997)
Doctors and Genes
-
-
-
17
-
-
0037014823
-
Prenatale diagnostiek naar de erfelijke aanleg voor mamma-/ovariumcarcinoom-een standpuntbepaling
-
Cobben JM, Broecker AHJT, Leschot NJ. Prenatale diagnostiek naar de erfelijke aanleg voor mamma-/ovariumcarcinoom-een standpuntbepaling. Ned Tijdschr Geneeskd 2002; 146:1461-1465.
-
(2002)
Ned Tijdschr Geneeskd
, vol.146
, pp. 1461-1465
-
-
Cobben, J.M.1
Broecker, A.H.J.T.2
Leschot, N.J.3
-
18
-
-
0035913275
-
Breast cancer after prophylactic bilateral mastectomy in women with a BRCA1 or BRCA2 mutation
-
Meijers-Heijboer H, van Geel B, van Putten WL, et al. Breast cancer after prophylactic bilateral mastectomy in women with a BRCA1 or BRCA2 mutation. N Engl J Med 2001; 345(3):159-164.
-
(2001)
N Engl J Med
, vol.345
, Issue.3
, pp. 159-164
-
-
Meijers-Heijboer, H.1
van Geel, B.2
van Putten, W.L.3
-
19
-
-
0028346992
-
Multiple pregnancy induction and selective fetal reduction in high genetic risk couples
-
Brambati B, Formigli L, Mori M, Tului L. Multiple pregnancy induction and selective fetal reduction in high genetic risk couples. Hum Reprod 1994; 9(4):746-749.
-
(1994)
Hum Reprod
, vol.9
, Issue.4
, pp. 746-749
-
-
Brambati, B.1
Formigli, L.2
Mori, M.3
Tului, L.4
-
20
-
-
18544396194
-
International, collaborative experience of 1789 patients having multifetal pregnancy reduction: a plateauing of risks and outcomes
-
Evans MI, Dommergues M, Wapner RJ, et al. International, collaborative experience of 1789 patients having multifetal pregnancy reduction: a plateauing of risks and outcomes. J Soc Gynecol Investig 1996; 3(1):23-26.
-
(1996)
J Soc Gynecol Investig
, vol.3
, Issue.1
, pp. 23-26
-
-
Evans, M.I.1
Dommergues, M.2
Wapner, R.J.3
-
21
-
-
0012367161
-
-
London: Nuffield Council on Bioethics
-
Nuffield Council on Bioethics. Genetics and Human Behaviour. London: Nuffield Council on Bioethics, 2002.
-
(2002)
Genetics and Human Behaviour
-
-
-
22
-
-
0031605860
-
Choosing the sexual orientation of children
-
Stein E. Choosing the sexual orientation of children. Bioethics 1998; 12(1):1-24.
-
(1998)
Bioethics
, vol.12
, Issue.1
, pp. 1-24
-
-
Stein, E.1
-
23
-
-
0031607064
-
The use of reproductive technologies in selecting the sexual orientation, the race, and the sex of children
-
Ten CL. The use of reproductive technologies in selecting the sexual orientation, the race, and the sex of children. Bioethics 1998; 12(1):45-48.
-
(1998)
Bioethics
, vol.12
, Issue.1
, pp. 45-48
-
-
Ten, C.L.1
-
24
-
-
85051691433
-
Prenatal testing and selection; proceed with caution
-
Galjaard H, Noor LHW, eds, New Developments and Ethical Dilemmas. Amsterdam:Royal Netherlands Academy of Sciences
-
De Wert GM. Prenatal testing and selection; proceed with caution. In: Galjaard H, Noor LHW, eds. Prenatal Testing. New Developments and Ethical Dilemmas. Amsterdam:Royal Netherlands Academy of Sciences, 2003:61-68.
-
(2003)
Prenatal Testing
, pp. 61-68
-
-
De Wert, G.M.1
-
26
-
-
85051689564
-
-
Embryo Protection Act (Germany; BGBI.I S.2746)
-
Embryo Protection Act (Germany; BGBI.I S.2746). 1990.
-
(1990)
-
-
-
27
-
-
85051689833
-
-
Law on Medically Assisted Reproduction (Italy)
-
Law on Medically Assisted Reproduction (Italy). 2004.
-
(2004)
-
-
-
28
-
-
85051689622
-
-
Genetische Diagnostik vor und während der Schwangerschaft
-
Nationaler Ethikrat. Stellungnahme. Genetische Diagnostik vor und während der Schwangerschaft, 2003.
-
(2003)
Stellungnahme
-
-
-
29
-
-
85051691162
-
-
Loi relative au don et à utilisation des elements et produits du corps humain, à l'assistance medicale à la procreation et au diagnostic prenatal (L94-654), Revisee 2004 (L2004-800)
-
Loi relative au don et à utilisation des elements et produits du corps humain, à l'assistance medicale à la procreation et au diagnostic prenatal (L94-654), Revisee 2004 (L2004-800), 2004.
-
(2004)
-
-
-
32
-
-
0037181166
-
Preimplantation diagnosis for early-onset Alzheimer disease caused by V717L mutation
-
Verlinsky Y, Rechitsky S, Verlinsky O, Masciangelo C, Lederer K, Kuliev A. Preimplantation diagnosis for early-onset Alzheimer disease caused by V717L mutation. J Am Med Assoc 2002; 287(8):1018-1021.
-
(2002)
J Am Med Assoc
, vol.287
, Issue.8
, pp. 1018-1021
-
-
Verlinsky, Y.1
Rechitsky, S.2
Verlinsky, O.3
Masciangelo, C.4
Lederer, K.5
Kuliev, A.6
-
33
-
-
85051690468
-
-
UK
-
Human Fertilisation and Embryology Act. 1990, UK.
-
(1990)
-
-
-
36
-
-
0029912923
-
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
-
37
-
-
0032412865
-
Nondisclosure preimplantation genetic diagnosis for Huntington's disease: practical and ethical dilemmas
-
Braude PR, De Wert GM, Evers-Kiebooms G, Pettigrew RA, Geraedts JP. Nondisclosure 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
-
38
-
-
0037342089
-
Taskforce 5:preimplantation genetic diagnosis
-
Shenfield F, Pennings G, Devroey P, Sureau C, Tarlatzis B, Cohen J. Taskforce 5:preimplantation genetic diagnosis. Hum Reprod 2003; 18(3):649-651.
-
(2003)
Hum Reprod
, vol.18
, Issue.3
, pp. 649-651
-
-
Shenfield, F.1
Pennings, G.2
Devroey, P.3
Sureau, C.4
Tarlatzis, B.5
Cohen, J.6
-
39
-
-
28544446962
-
Preimplantation genetic diagnosis: the ethics of ''intermediate'' cases
-
De Wert GM. Preimplantation genetic diagnosis: the ethics of ''intermediate'' cases. Hum Reprod 2005; 20(12): 3261-3266.
-
(2005)
Hum Reprod
, vol.20
, Issue.12
, pp. 3261-3266
-
-
De Wert, G.M.1
-
40
-
-
0042524363
-
Evolving ethics in medically assisted reproduction
-
Pennings G, de Wert G. Evolving ethics in medically assisted reproduction. Hum Reprod Update 2003; 9(4):397-404.
-
(2003)
Hum Reprod Update
, vol.9
, Issue.4
, pp. 397-404
-
-
Pennings, G.1
de Wert, G.2
-
41
-
-
0006296115
-
Parity for donation of bone marrow
-
Blank RH, Bonnicksen AL, eds, New York:Columbia University Press
-
KearneyW, Caplan AC. Parity for donation of bone marrow. In: Blank RH, Bonnicksen AL, eds. Emerging Issues in Biomedical Policy. An Annual Review Vol. 1. New York:Columbia University Press, 1992:262-285.
-
(1992)
Emerging Issues in Biomedical Policy. An Annual Review
, vol.1
, pp. 262-285
-
-
Kearney, W.1
Caplan, A.C.2
-
43
-
-
85051689089
-
-
Directorate of Legal Affairs, Strasbourg
-
Council of Europe. Convention on Human Rights and Biomedicine. Directorate of Legal Affairs, Strasbourg, 1996.
-
(1996)
Convention on Human Rights and Biomedicine
-
-
-
45
-
-
0042579712
-
-
The Hague:Health Council of the Netherlands
-
Health Council of the Netherlands. Sex Selection for Non-medical Reasons. The Hague:Health Council of the Netherlands, 1995.
-
(1995)
Sex Selection for Non-medical Reasons
-
-
-
47
-
-
3543087138
-
-
A Report on the HFEA's 2002-2003 Review of Sex Selection Including Discussion of Legislative and Regulatory Options. London: HFEA
-
Human Fertilisation and Embryology Authority. Sex Selection: Options for Regulation. A Report on the HFEA's 2002-2003 Review of Sex Selection Including Discussion of Legislative and Regulatory Options. London: HFEA, 2003.
-
(2003)
Sex Selection: Options for Regulation
-
-
-
48
-
-
1642299818
-
The presumption in favour of liberty: a comment on the HFEA's public consultation on sex selection
-
Dahl E. The presumption in favour of liberty: a comment on the HFEA's public consultation on sex selection. Reprod Biomed Online 2004; 8(3):266-267.
-
(2004)
Reprod Biomed Online
, vol.8
, Issue.3
, pp. 266-267
-
-
Dahl, E.1
-
49
-
-
0030281202
-
Ethics of sex selection for family balancing
-
Pennings G. Ethics of sex selection for family balancing.HumReprod 1996; 11:2339-2345.
-
(1996)
HumReprod
, vol.11
, pp. 2339-2345
-
-
Pennings, G.1
-
50
-
-
1642340538
-
Gender variety as a valid choice: a comment on the HFEA response to Edgar Dahl's ''The presumption in favour of liberty''
-
Robertson JA. Gender variety as a valid choice: a comment on the HFEA response to Edgar Dahl's ''The presumption in favour of liberty''. Reprod Biomed Online 2004; 8(3):270-271.
-
(2004)
Reprod Biomed Online
, vol.8
, Issue.3
, pp. 270-271
-
-
Robertson, J.A.1
-
51
-
-
0141891304
-
Preimplantation genetic diagnosis as a novel source of embryos for stem cell research
-
Pickering SJ, Braude PR, Patel M, et al. Preimplantation genetic diagnosis as a novel source of embryos for stem cell research. Reprod Biomed Online 2003; 7(3):353-364.
-
(2003)
Reprod Biomed Online
, vol.7
, Issue.3
, pp. 353-364
-
-
Pickering, S.J.1
Braude, P.R.2
Patel, M.3
-
52
-
-
0037386324
-
Human embryonic stem cells: research, ethics and policy
-
de Wert G, Mummery C. Human embryonic stem cells: research, ethics and policy. Hum Reprod 2003; 18(4):672-682.
-
(2003)
Hum Reprod
, vol.18
, Issue.4
, pp. 672-682
-
-
de Wert, G.1
Mummery, C.2
-
54
-
-
0004160185
-
-
Ethical Issues. London: Nuffield Council on Bioethics
-
Nuffield Council on Bioethics. Genetic Screening. Ethical Issues. London: Nuffield Council on Bioethics, 1993.
-
(1993)
Genetic Screening
-
-
-
55
-
-
0005057964
-
-
The Hague: Health Council of The Netherlands
-
Health Council of the Netherlands. Genetic Screening. The Hague: Health Council of The Netherlands, 1994.
-
(1994)
Genetic Screening
-
-
-
56
-
-
0032088112
-
Genetic screening and ethics: European perspectives
-
Chadwick R, ten Have HA, Husted J, et al. Genetic screening and ethics: European perspectives. J Med Philos 1998; 23(3):255-273.
-
(1998)
J Med Philos
, vol.23
, Issue.3
, pp. 255-273
-
-
Chadwick, R.1
ten Have, H.A.2
Husted, J.3
-
57
-
-
1342324899
-
Population genetic screening programmes:principles, techniques, practices, and policies
-
Godard B, ten Kate LP, Evers-Kiebooms G, Ayme S. Population genetic screening programmes:principles, techniques, practices, and policies. Eur J Hum Genet 2003; 11(Suppl 2):S49-S87.
-
(2003)
Eur J Hum Genet
, vol.11
, pp. S49-S87
-
-
Godard, B.1
ten Kate, L.P.2
Evers-Kiebooms, G.3
Ayme, S.4
-
58
-
-
85051690397
-
De maatschappelijke effecten van genetisch onderzoek. Over misbruik, keuzemogelijkheden en verplichtingen
-
Van Wijnen AC. De maatschappelijke effecten van genetisch onderzoek. Over misbruik, keuzemogelijkheden en verplichtingen. Medisch Contact 1995; 50:1192-1195.
-
(1995)
Medisch Contact
, vol.50
, pp. 1192-1195
-
-
Van Wijnen, A.C.1
-
62
-
-
0032084128
-
The meaning of the act: reflections on the expressive force of reproductive decision making and policies
-
Nelson JL. The meaning of the act: reflections on the expressive force of reproductive decision making and policies. Kennedy Inst Ethics J 1998; 8(2):165-182.
-
(1998)
Kennedy Inst Ethics J
, vol.8
, Issue.2
, pp. 165-182
-
-
Nelson, J.L.1
-
63
-
-
0032706588
-
Prenatal diagnosis and selective abortion: a challenge to practice and policy
-
Asch A. Prenatal diagnosis and selective abortion: a challenge to practice and policy. Am J Public Health 1999; 89(11):1649-1657.
-
(1999)
Am J Public Health
, vol.89
, Issue.11
, pp. 1649-1657
-
-
Asch, A.1
-
64
-
-
0345106410
-
The perfect baby: introduction
-
Chadwick R, ed, London: Routledge
-
Chadwick R. The perfect baby: introduction. In: Chadwick R, ed. Ethics, Reproduction and Genetic Control. London: Routledge; 1987,:93-135.
-
(1987)
Ethics, Reproduction and Genetic Control
, pp. 93-135
-
-
Chadwick, R.1
-
65
-
-
85051691113
-
Prenatale diagnostiek. De morele bezwaren gewogen
-
Den Hartogh GA. Prenatale diagnostiek. De morele bezwaren gewogen. Medisch Contact 1997; 52:1591-1594.
-
(1997)
Medisch Contact
, vol.52
, pp. 1591-1594
-
-
Den Hartogh, G.A.1
-
66
-
-
0033016804
-
Screening for cystic fibrosis
-
Murray J, Cuckle H, Taylor G, Littlewood J, Hewison J. Screening for cystic fibrosis. Health Technol Assess 1999; 3(8):1-104.
-
(1999)
Health Technol Assess
, vol.3
, Issue.8
, pp. 1-104
-
-
Murray, J.1
Cuckle, H.2
Taylor, G.3
Littlewood, J.4
Hewison, J.5
-
67
-
-
85051690866
-
Erfelijkheidsonderzoek en ethiek: een gordiaanse knoop
-
De Wert GM. Erfelijkheidsonderzoek en ethiek: een gordiaanse knoop. Wijsgerig perspectief 2000; 40(2000):150-156.
-
(2000)
Wijsgerig perspectief
, vol.40
, Issue.2000
, pp. 150-156
-
-
De Wert, G.M.1
-
69
-
-
0031087198
-
Genetic dilemmas and the child's right to an open future
-
Davis DS. Genetic dilemmas and the child's right to an open future. Hastings Center Report 1997; 27(2):7-15.
-
(1997)
Hastings Center Report
, vol.27
, Issue.2
, pp. 7-15
-
-
Davis, D.S.1
-
70
-
-
0004785579
-
Prenatal genetic screening. Paradigms and perspectives
-
Harper PS, Clarke AJ, eds, Abingdon: Bios Scientific Publishers
-
Clarke AJ. Prenatal genetic screening. Paradigms and perspectives. In: Harper PS, Clarke AJ, eds. Genetics, Society, and Clinical Practice. Abingdon: Bios Scientific Publishers, 1997.
-
(1997)
Genetics, Society, and Clinical Practice
-
-
Clarke, A.J.1
-
73
-
-
0022650629
-
Randomised controlled trial of genetic amniocentesis in 4606 low-risk women
-
Tabor A, Philip J, Madsen M, Bang J, Obel EB, Norgaard-Pedersen B. Randomised controlled trial of genetic amniocentesis in 4606 low-risk women. Lancet 1986; 1(8493):1287-1293.
-
(1986)
Lancet
, vol.1
, Issue.8493
, pp. 1287-1293
-
-
Tabor, A.1
Philip, J.2
Madsen, M.3
Bang, J.4
Obel, E.B.5
Norgaard-Pedersen, B.6
-
74
-
-
0031395671
-
Antenatal screening for Down's syndrome
-
Wald NJ, Kennard A, Hackshaw A, McGuire A. Antenatal screening for Down's syndrome. J Med Screen 1997; 4(4):181-246.
-
(1997)
J Med Screen
, vol.4
, Issue.4
, pp. 181-246
-
-
Wald, N.J.1
Kennard, A.2
Hackshaw, A.3
McGuire, A.4
-
75
-
-
0032883373
-
Termination rates after prenatal diagnosis of Down syndrome, spina bifida, anencephaly, and Turner and Klinefelter syndromes:a systematic literature review. European Concerted Action: DADA (Decisionmaking After the Diagnosis of a fetal Abnormality)
-
Mansfield C, Hopfer S, Marteau TM. Termination rates after prenatal diagnosis of Down syndrome, spina bifida, anencephaly, and Turner and Klinefelter syndromes:a systematic literature review. European Concerted Action: DADA (Decisionmaking After the Diagnosis of a fetal Abnormality). Prenat Diagn 1999; 19(9):808-812.
-
(1999)
Prenat Diagn
, vol.19
, Issue.9
, pp. 808-812
-
-
Mansfield, C.1
Hopfer, S.2
Marteau, T.M.3
-
76
-
-
0033795010
-
Women's knowledge of and attitudes to first and second trimester screening for Down's syndrome
-
Mulvey S, Wallace EM. Women's knowledge of and attitudes to first and second trimester screening for Down's syndrome. Br J Obstet Gynaecol 2000; 107(10):1302-1305.
-
(2000)
Br J Obstet Gynaecol
, vol.107
, Issue.10
, pp. 1302-1305
-
-
Mulvey, S.1
Wallace, E.M.2
-
77
-
-
0033797165
-
How women deal with the results of serum screening for Down syndrome in the second trimester of pregnancy
-
Weinans MJ, Huijssoon AM, Tymstra T, Gerrits MC, Beekhuis JR, Mantingh A. How women deal with the results of serum screening for Down syndrome in the second trimester of pregnancy. Prenat Diagn 2000; 20(9):705-708.
-
(2000)
Prenat Diagn
, vol.20
, Issue.9
, pp. 705-708
-
-
Weinans, M.J.1
Huijssoon, A.M.2
Tymstra, T.3
Gerrits, M.C.4
Beekhuis, J.R.5
Mantingh, A.6
-
78
-
-
0035990138
-
Womens' preference in Down syndrome screening
-
de Graaf IM, Tijmstra T, Bleker OP, van Lith JM. Womens' preference in Down syndrome screening. Prenat Diagn 2002; 22(7):624-629.
-
(2002)
Prenat Diagn
, vol.22
, Issue.7
, pp. 624-629
-
-
de Graaf, I.M.1
Tijmstra, T.2
Bleker, O.P.3
van Lith, J.M.4
-
79
-
-
4944267089
-
Antenatal screening for Down's syndrome
-
Alfirevic Z, Neilson JP. Antenatal screening for Down's syndrome. Br Med J 2004; 329(7470):811-812.
-
(2004)
Br Med J
, vol.329
, Issue.7470
, pp. 811-812
-
-
Alfirevic, Z.1
Neilson, J.P.2
-
81
-
-
7944223347
-
Multi-marker serum screening for chromosomal abnormalities
-
Milunsky A, ed, Baltimore, MD: Johns Hopkins University Press
-
Cuckle H, Arbuzova S. Multi-marker serum screening for chromosomal abnormalities. In: Milunsky A, ed. Genetic Disorders and the Fetus. Diagnosis, Prevention, and Treatment. Baltimore, MD: Johns Hopkins University Press, 2004.
-
(2004)
Genetic Disorders and the Fetus. Diagnosis, Prevention, and Treatment
-
-
Cuckle, H.1
Arbuzova, S.2
-
84
-
-
0033781072
-
Dépistage prénatal de la trisomie 21 par marquers sériques maternels: de l'information à la prise de décision des femmes enceintes
-
Seror V, Costet N, Ayme S. Dépistage prénatal de la trisomie 21 par marquers sériques maternels: de l'information à la prise de décision des femmes enceintes. J Gynecol Obstet Biol Reprod (Paris) 2000; 29(5):492-500.
-
(2000)
J Gynecol Obstet Biol Reprod (Paris)
, vol.29
, Issue.5
, pp. 492-500
-
-
Seror, V.1
Costet, N.2
Ayme, S.3
-
85
-
-
4544322158
-
Psychosocial aspects of genetic screening of pregnant women and newborns: a systematic review
-
Green JM, Hewison J, Bekker HL, Bryant LD, Cuckle HS. Psychosocial aspects of genetic screening of pregnant women and newborns: a systematic review. Health Technol Assess 2004; 8(33):iii, ix-iii, 109.
-
(2004)
Health Technol Assess
, vol.8
, Issue.33
-
-
Green, J.M.1
Hewison, J.2
Bekker, H.L.3
Bryant, L.D.4
Cuckle, H.S.5
-
86
-
-
0036401547
-
Informed choice to undergo prenatal screening: a comparison of two hospitals conducting testing either as part of a routine visit or requiring a separate visit
-
Dormandy E, Hooper R, Michie S, Marteau TM. Informed choice to undergo prenatal screening: a comparison of two hospitals conducting testing either as part of a routine visit or requiring a separate visit. J Med Screen 2002; 9(3):109-114.
-
(2002)
J Med Screen
, vol.9
, Issue.3
, pp. 109-114
-
-
Dormandy, E.1
Hooper, R.2
Michie, S.3
Marteau, T.M.4
-
87
-
-
0023875348
-
Two models of implementing informed consent
-
Lidz CW, Appelbaum PS, Meisel A. Two models of implementing informed consent. Arch Intern Med 1988; 148(6):1385-1389.
-
(1988)
Arch Intern Med
, vol.148
, Issue.6
, pp. 1385-1389
-
-
Lidz, C.W.1
Appelbaum, P.S.2
Meisel, A.3
-
88
-
-
0029298503
-
Risk, autonomy, and responsibility. Informed consent for prenatal testing
-
Press N, Browner CH. Risk, autonomy, and responsibility. Informed consent for prenatal testing. Hastings Cent Rep 1995; 25:S9-S12.
-
(1995)
Hastings Cent Rep
, vol.25
, pp. S9-S12
-
-
Press, N.1
Browner, C.H.2
-
89
-
-
0031014578
-
Counselling implications of chromosomal abnormalities other than trisomy 21 detected through a maternal serum screening programme
-
Sheridan E, Williams J, Caine A, Morgan R, Mason G, Mueller RF. Counselling implications of chromosomal abnormalities other than trisomy 21 detected through a maternal serum screening programme. Br J Obstet Gynaecol 1997; 104(1):42-45.
-
(1997)
Br J Obstet Gynaecol
, vol.104
, Issue.1
, pp. 42-45
-
-
Sheridan, E.1
Williams, J.2
Caine, A.3
Morgan, R.4
Mason, G.5
Mueller, R.F.6
-
90
-
-
84927098863
-
Prenatale diagnostiek en selectieve abortus. Enkele ethische overwegingen
-
ten Have HA, ed, Deventer: Kluwer
-
De Wert GM. Prenatale diagnostiek en selectieve abortus. Enkele ethische overwegingen. In: ten Have HA, ed. Ethiek en recht in de gezondheidszorg. Deventer: Kluwer, 1990:121-153.
-
(1990)
Ethiek en recht in de gezondheidszorg
, pp. 121-153
-
-
De Wert, G.M.1
-
91
-
-
19944407550
-
Rapid prenatal diagnosis of common chromosome aneuploidies by QF-PC. Assessment on 18,000 consecutive clinical samples
-
Cirigliano V, Voglino G, Canadas MP, et al. Rapid prenatal diagnosis of common chromosome aneuploidies by QF-PC. Assessment on 18,000 consecutive clinical samples. Mol Hum Reprod 2004; 10(11):839-846.
-
(2004)
Mol Hum Reprod
, vol.10
, Issue.11
, pp. 839-846
-
-
Cirigliano, V.1
Voglino, G.2
Canadas, M.P.3
-
93
-
-
0034596381
-
[Sensitive and specific screening for detection of spina bifida by echography in the second trimester; systematic review and meta-analysis]
-
Vos JM, Offringa M, Bilardo CM, Lijmer JG, Barth PG. [Sensitive and specific screening for detection of spina bifida by echography in the second trimester; systematic review and meta-analysis]. Ned Tijdschr Geneeskd 2000; 144(36):1736-1741.
-
(2000)
Ned Tijdschr Geneeskd
, vol.144
, Issue.36
, pp. 1736-1741
-
-
Vos, J.M.1
Offringa, M.2
Bilardo, C.M.3
Lijmer, J.G.4
Barth, P.G.5
-
94
-
-
0030997185
-
Perception of information, expectations and experiences among women and their partners attending a secondtrimester routine ultrasound scan
-
Eurenius K, Axelsson O, Gallstedt-Fransson I, Sjoden PO. Perception of information, expectations and experiences among women and their partners attending a secondtrimester routine ultrasound scan. Ultrasound Obstet Gynecol 1997; 9(2):86-90.
-
(1997)
Ultrasound Obstet Gynecol
, vol.9
, Issue.2
, pp. 86-90
-
-
Eurenius, K.1
Axelsson, O.2
Gallstedt-Fransson, I.3
Sjoden, P.O.4
-
95
-
-
0032841573
-
Prenatal tests: how are women deciding?
-
Michie S, Smith D, Marteau TM. Prenatal tests: how are women deciding? Prenat Diagn 1999; 19(8):743-748.
-
(1999)
Prenat Diagn
, vol.19
, Issue.8
, pp. 743-748
-
-
Michie, S.1
Smith, D.2
Marteau, T.M.3
-
97
-
-
0031021070
-
Carrier testing in the fragile X syndrome: attitudes and opinions of obligate carriers
-
McConkie-Rosell A, Spiridigliozzi GA, Iafolla T, Tarleton J, Lachiewicz AM. Carrier testing in the fragile X syndrome: attitudes and opinions of obligate carriers. Am J Med Genet 1997; 68(1):62-69.
-
(1997)
Am J Med Genet
, vol.68
, Issue.1
, pp. 62-69
-
-
McConkie-Rosell, A.1
Spiridigliozzi, G.A.2
Iafolla, T.3
Tarleton, J.4
Lachiewicz, A.M.5
-
98
-
-
0026006411
-
Couple screening for cystic fibrosis
-
Wald NJ. Couple screening for cystic fibrosis. Lancet 1991; 338(8778):1318-1319.
-
(1991)
Lancet
, vol.338
, Issue.8778
, pp. 1318-1319
-
-
Wald, N.J.1
-
99
-
-
0028836712
-
Antenatal screening for carriers of cystic fibrosis: randomised trial of stepwise v couple screening
-
Miedzybrodzka ZH, Hall MH, Mollison J, et al. Antenatal screening for carriers of cystic fibrosis: randomised trial of stepwise v couple screening. Br Med J 1995; 310(6976):353-357.
-
(1995)
Br Med J
, vol.310
, Issue.6976
, pp. 353-357
-
-
Miedzybrodzka, Z.H.1
Hall, M.H.2
Mollison, J.3
-
100
-
-
0028935321
-
Stepwise or couple antenatal carrier screening for cystic fibrosis: Women's preferences and willingness to pay
-
Miedzybrodzka Z, Semper J, Shackley P, Abdalla M, Donaldson C. Stepwise or couple antenatal carrier screening for cystic fibrosis: Women's preferences and willingness to pay. J Med Genet 1995; 32(4):282-283.
-
(1995)
J Med Genet
, vol.32
, Issue.4
, pp. 282-283
-
-
Miedzybrodzka, Z.1
Semper, J.2
Shackley, P.3
Abdalla, M.4
Donaldson, C.5
-
101
-
-
0036583279
-
Preconceptional couple screening for cystic fibrosis carrier status: couples prefer full disclosure of test results
-
Henneman L, ten Kate LP. Preconceptional couple screening for cystic fibrosis carrier status: couples prefer full disclosure of test results. J Med Genet 2002; 39(5):E26.
-
(2002)
J Med Genet
, vol.39
, Issue.5
, pp. E26
-
-
Henneman, L.1
ten Kate, L.P.2
-
102
-
-
0030904547
-
Risk perception after CF carrier testing and impact of the test result on reproductive decision making
-
Denayer L, Welkenhuysen M, Evers-Kiebooms G, Cassiman JJ, Van den Berghe H. Risk perception after CF carrier testing and impact of the test result on reproductive decision making. Am J Med Genet 1997; 69(4):422-428.
-
(1997)
Am J Med Genet
, vol.69
, Issue.4
, pp. 422-428
-
-
Denayer, L.1
Welkenhuysen, M.2
Evers-Kiebooms, G.3
Cassiman, J.J.4
Van den Berghe, H.5
-
103
-
-
0034791365
-
Participation in preconceptional carrier couple screening: characteristics, attitudes, and knowledge of both partners
-
Henneman L, Bramsen I, van der Ploeg HM, et al. Participation in preconceptional carrier couple screening: characteristics, attitudes, and knowledge of both partners. J Med Genet 2001; 38(10):695-703.
-
(2001)
J Med Genet
, vol.38
, Issue.10
, pp. 695-703
-
-
Henneman, L.1
Bramsen, I.2
van der Ploeg, H.M.3
-
105
-
-
0032836920
-
Antenatal and neonatal haemoglobinopathy screening in the UK: review and economic analysis
-
Zeuner D, Ades AE, Karnon J, Brown J, Dezateux C, Anionwu EN. Antenatal and neonatal haemoglobinopathy screening in the UK: review and economic analysis. Health Technol Assess 1999; 3(11):1-186.
-
(1999)
Health Technol Assess
, vol.3
, Issue.11
, pp. 1-186
-
-
Zeuner, D.1
Ades, A.E.2
Karnon, J.3
Brown, J.4
Dezateux, C.5
Anionwu, E.N.6
-
106
-
-
0036075767
-
Race, ethnicity, and genomics: social classifications as proxies of biological heterogeneity
-
Foster MW, Sharp RR. Race, ethnicity, and genomics: social classifications as proxies of biological heterogeneity. Genome Res 2002; 12(6):844-850.
-
(2002)
Genome Res
, vol.12
, Issue.6
, pp. 844-850
-
-
Foster, M.W.1
Sharp, R.R.2
-
107
-
-
17744403039
-
Screening for sickle cell disease and thalassaemia: a systematic review with supplementary research
-
Davies SC, Cronin E, Gill M, Greengross P, Hickman M, Normand C. Screening for sickle cell disease and thalassaemia: a systematic review with supplementary research. Health Technol Assess 2000; 4(3):1-99.
-
(2000)
Health Technol Assess
, vol.4
, Issue.3
, pp. 1-99
-
-
Davies, S.C.1
Cronin, E.2
Gill, M.3
Greengross, P.4
Hickman, M.5
Normand, C.6
-
108
-
-
0030883157
-
Audit of process of antenatal screening for sickle cell disorders at a north London hospital
-
Neuenschwander H, Modell B. Audit of process of antenatal screening for sickle cell disorders at a north London hospital. Br Med J 1997; 315(7111):784-785.
-
(1997)
Br Med J
, vol.315
, Issue.7111
, pp. 784-785
-
-
Neuenschwander, H.1
Modell, B.2
-
109
-
-
1042278815
-
Screening approach for fragile X syndrome
-
Delatycki MB, Sheffield LJ, Wake S, Cohen J. Screening approach for fragile X syndrome. Prenat Diagn 2004; 24(1):67-68.
-
(2004)
Prenat Diagn
, vol.24
, Issue.1
, pp. 67-68
-
-
Delatycki, M.B.1
Sheffield, L.J.2
Wake, S.3
Cohen, J.4
-
110
-
-
85044702643
-
Screening for fragile X syndrome: a literature review and modelling study
-
Song FJ, Barton P, Sleightholme V, Yao GL, Fry-Smith A. Screening for fragile X syndrome: a literature review and modelling study. Health Technol Assess 2003; 7(16):1-106.
-
(2003)
Health Technol Assess
, vol.7
, Issue.16
, pp. 1-106
-
-
Song, F.J.1
Barton, P.2
Sleightholme, V.3
Yao, G.L.4
Fry-Smith, A.5
-
111
-
-
0037196891
-
Screening op dragerschap van het fragiele-X-syndroom; ethische verkenning
-
de Jong A, de Wert G. Screening op dragerschap van het fragiele-X-syndroom; ethische verkenning. Ned Tijdschr Geneeskd 2002; 146(13):611-615.
-
(2002)
Ned Tijdschr Geneeskd
, vol.146
, Issue.13
, pp. 611-615
-
-
de Jong, A.1
de Wert, G.2
-
112
-
-
2342635196
-
The fragile-X premutation: a maturing perspective
-
Hagerman PJ, Hagerman RJ. The fragile-X premutation: a maturing perspective. Am J Hum Genet 2004; 74(5):805-816.
-
(2004)
Am J Hum Genet
, vol.74
, Issue.5
, pp. 805-816
-
-
Hagerman, P.J.1
Hagerman, R.J.2
-
113
-
-
0037395258
-
A new approach to antenatal screening for fragile X syndrome
-
Wald NJ, Morris JK. A new approach to antenatal screening for fragile X syndrome. Prenat Diagn 2003; 23(4):345-351.
-
(2003)
Prenat Diagn
, vol.23
, Issue.4
, pp. 345-351
-
-
Wald, N.J.1
Morris, J.K.2
-
114
-
-
0035684463
-
First-trimester fetal sex determination in maternal serum using real-time PCR
-
Costa JM, Benachi A, Gautier E, Jouannic JM, Ernault P, Dumez Y. First-trimester fetal sex determination in maternal serum using real-time PCR. Prenat Diagn 2001; 21(12):1070-1074.
-
(2001)
Prenat Diagn
, vol.21
, Issue.12
, pp. 1070-1074
-
-
Costa, J.M.1
Benachi, A.2
Gautier, E.3
Jouannic, J.M.4
Ernault, P.5
Dumez, Y.6
-
115
-
-
85051689363
-
Ethical implications of early non-invasive fetal sex determination
-
Rijnders RJ, ed, Thesis, Utrecht University, Utrecht
-
Rijnders RJ, Christiaens GC, Van der Smagt J, De Haas M, Van der Schoot CE, Ralston AS. Ethical implications of early non-invasive fetal sex determination. In: Rijnders RJ, ed. Cell-free Fetal DNA in Maternal Plasma. Thesis, Utrecht University, Utrecht, 2003:111-124.
-
(2003)
Cell-free Fetal DNA in Maternal Plasma
, pp. 111-124
-
-
Rijnders, R.J.1
Christiaens, G.C.2
Van der Smagt, J.3
De Haas, M.4
Van der Schoot, C.E.5
Ralston, A.S.6
-
116
-
-
0033906467
-
Screening for fragile X syndrome in women of reproductive age
-
Pesso R, Berkenstadt M, Cuckle H, et al. Screening for fragile X syndrome in women of reproductive age. Prenat Diagn 2000; 20(8):611-614.
-
(2000)
Prenat Diagn
, vol.20
, Issue.8
, pp. 611-614
-
-
Pesso, R.1
Berkenstadt, M.2
Cuckle, H.3
-
117
-
-
2442724489
-
Feasibility and acceptance of screening for fragile X mutations in low-risk pregnancies
-
Ryynanen M, Heinonen S, Makkonen M, Kajanoja E, Mannermaa A, Pertti K. Feasibility and acceptance of screening for fragile X mutations in low-risk pregnancies. Eur J Hum Genet 1999; 7(2):212-216.
-
(1999)
Eur J Hum Genet
, vol.7
, Issue.2
, pp. 212-216
-
-
Ryynanen, M.1
Heinonen, S.2
Makkonen, M.3
Kajanoja, E.4
Mannermaa, A.5
Pertti, K.6
-
118
-
-
0032740074
-
Screening for female fragile X premutation and full mutation carriers
-
Tejada MI, Duran M. Screening for female fragile X premutation and full mutation carriers. Community Genet 1999; 2(1):49-50.
-
(1999)
Community Genet
, vol.2
, Issue.1
, pp. 49-50
-
-
Tejada, M.I.1
Duran, M.2
-
119
-
-
0033843996
-
Prenatal diagnosis of fragile X syndrome and the risk of expansion of a premutation
-
Kallinen J, Heinonen S, Mannermaa A, Ryynanen M. Prenatal diagnosis of fragile X syndrome and the risk of expansion of a premutation. Clin Genet 2000; 58(2):111-115.
-
(2000)
Clin Genet
, vol.58
, Issue.2
, pp. 111-115
-
-
Kallinen, J.1
Heinonen, S.2
Mannermaa, A.3
Ryynanen, M.4
-
120
-
-
29344449120
-
Screening for fragile X syndrome
-
Murray J, Cuckle H, Taylor G, Hewison J. Screening for fragile X syndrome. Health Technol Assess 1997; 1(4):i-71.
-
(1997)
Health Technol Assess
, vol.1
, Issue.4
, pp. i-71
-
-
Murray, J.1
Cuckle, H.2
Taylor, G.3
Hewison, J.4
-
121
-
-
0035077123
-
An assessment of screening strategies for fragile X syndrome in the UK
-
Pembrey ME, Barnicoat AJ, Carmichael B, Bobrow M, Turner G. An assessment of screening strategies for fragile X syndrome in the UK. Health Technol Assess 2001; 5(7):1-95.
-
(2001)
Health Technol Assess
, vol.5
, Issue.7
, pp. 1-95
-
-
Pembrey, M.E.1
Barnicoat, A.J.2
Carmichael, B.3
Bobrow, M.4
Turner, G.5
-
124
-
-
0141946048
-
Prenatal genetic testing and the courts
-
Parens E, Asch A, eds, Washington, DC: Georgetown University Press
-
Ossorio PN. Prenatal genetic testing and the courts. In: Parens E, Asch A, eds. Prenatal testing and disability rights. Washington, DC: Georgetown University Press, 2000:308-333.
-
(2000)
Prenatal testing and disability rights
, pp. 308-333
-
-
Ossorio, P.N.1
-
125
-
-
0036613251
-
Wrongful life: the recent French Cour de Cassation decisions
-
Duguet AM. Wrongful life: the recent French Cour de Cassation decisions. Eur J Health Law 2002; 9:139-163.
-
(2002)
Eur J Health Law
, vol.9
, pp. 139-163
-
-
Duguet, A.M.1
-
126
-
-
85051689486
-
Bundesgerichtshof VI Zivilsenat
-
Bundesgerichtshof VI Zivilsenat. Fundstelle: BGHZ 1983; 86:240.
-
(1983)
Fundstelle: BGHZ
, vol.86
, pp. 240
-
-
-
129
-
-
85051689490
-
-
Royal Commission on Civil Liability and Compensation for Personal Injury. Royal Commission on Civil Liability and Compensation for Personal Injury. Civil Liability and Compensation for Personal Injury. Report, London: HSMO, Cmnd.7045-I
-
Royal Commission on Civil Liability and Compensation for Personal Injury. Royal Commission on Civil Liability and Compensation for Personal Injury. Civil Liability and Compensation for Personal Injury. Report, Vol. 1. London: HSMO, 1978:Cmnd.7045-I.
-
(1978)
, vol.1
-
-
-
130
-
-
85051691222
-
-
L'Assemblée nationale et le Sénat. LOI no. 2002-303 du 4 mars 2002 relative aux droits des malades et à la qualité du système de santé
-
L'Assemblée nationale et le Sénat. LOI no. 2002-303 du 4 mars 2002 relative aux droits des malades et à la qualité du système de santé, 2002.
-
(2002)
-
-
-
131
-
-
85051689043
-
-
Eerste Kamer, nr C03/206HR, (Accessed March 18, 2005, at
-
Hoge Raad der Nederlanden. Uitspraak 18 maart 2005. Eerste Kamer, nr C03/206HR, 2005. (Accessed March 18, 2005, at www.rechtspraak.nl.).
-
(2005)
Hoge Raad der Nederlanden. Uitspraak 18 maart 2005
-
-
-
133
-
-
1942467883
-
Recent developments in fetal medicine
-
Kumar S, O'Brien A. Recent developments in fetal medicine. Br Med J 2004; 328(7446):1002-1006.
-
(2004)
Br Med J
, vol.328
, Issue.7446
, pp. 1002-1006
-
-
Kumar, S.1
O'Brien, A.2
-
134
-
-
0032556437
-
Successful fetal surgery for spina bifida
-
Adzick NS, Sutton LN, Crombleholme TM, Flake AW. Successful fetal surgery for spina bifida. Lancet 1998; 352(9141):1675-1676.
-
(1998)
Lancet
, vol.352
, Issue.9141
, pp. 1675-1676
-
-
Adzick, N.S.1
Sutton, L.N.2
Crombleholme, T.M.3
Flake, A.W.4
-
135
-
-
0033579131
-
Fetal surgery for myelomeningocele and the incidence of shunt-dependent hydrocephalus
-
Bruner JP, Tulipan N, Paschall RL, et al. Fetal surgery for myelomeningocele and the incidence of shunt-dependent hydrocephalus. J Am Med Assoc 1999; 282(19):1819-1825.
-
(1999)
J Am Med Assoc
, vol.282
, Issue.19
, pp. 1819-1825
-
-
Bruner, J.P.1
Tulipan, N.2
Paschall, R.L.3
-
136
-
-
0033579169
-
Improvement in hindbrain herniation demonstrated by serial fetal magnetic resonance imaging following fetal surgery for myelomeningocele
-
Sutton LN, Adzick NS, Bilaniuk LT, Johnson MP, Crombleholme TM, Flake AW. Improvement in hindbrain herniation demonstrated by serial fetal magnetic resonance imaging following fetal surgery for myelomeningocele. J Am Med Assoc 1999; 282(19):1826-1831.
-
(1999)
J Am Med Assoc
, vol.282
, Issue.19
, pp. 1826-1831
-
-
Sutton, L.N.1
Adzick, N.S.2
Bilaniuk, L.T.3
Johnson, M.P.4
Crombleholme, T.M.5
Flake, A.W.6
-
137
-
-
0037991398
-
Fetal surgery: for selected patients. The experiences of the Fetal Treatment Center in San Francisco
-
van Heurn LW, Harrison MR. Fetal surgery: for selected patients. The experiences of the Fetal Treatment Center in San Francisco. Ned Tijdschr Geneeskd 2003; 147(19):900-904.
-
(2003)
Ned Tijdschr Geneeskd
, vol.147
, Issue.19
, pp. 900-904
-
-
van Heurn, L.W.1
Harrison, M.R.2
-
138
-
-
0013652936
-
Operative fetoscopy
-
Rodeck CH, Whittle MJ, eds, London: Churchill Livingstone
-
Quintero RA, Carreño C. Operative fetoscopy. In: Rodeck CH, Whittle MJ, eds. Fetal Medicine: Basic Science and Clinical Practice. London: Churchill Livingstone, 1999:755-769.
-
(1999)
Fetal Medicine: Basic Science and Clinical Practice
, pp. 755-769
-
-
Quintero, R.A.1
Carreño, C.2
-
139
-
-
0035141962
-
Haematopoietic stem cell transplantation and gene therapy in the fetus: ready for clinical use?
-
Surbek DV, Holzgreve W, Nicolaides KH. Haematopoietic stem cell transplantation and gene therapy in the fetus: ready for clinical use? Hum Reprod Update 2001; 7(1):85-91.
-
(2001)
Hum Reprod Update
, vol.7
, Issue.1
, pp. 85-91
-
-
Surbek, D.V.1
Holzgreve, W.2
Nicolaides, K.H.3
-
140
-
-
0042128845
-
Stem cell and genetic therapies for the fetus
-
Flake AW. Stem cell and genetic therapies for the fetus. Semin Pediatr Surg 2003; 12(3):202-208.
-
(2003)
Semin Pediatr Surg
, vol.12
, Issue.3
, pp. 202-208
-
-
Flake, A.W.1
-
141
-
-
3042543750
-
Reappraisal of in utero stem cell transplantation based on long-term results
-
Touraine JL, Raudrant D, Golfier F, et al. Reappraisal of in utero stem cell transplantation based on long-term results. Fetal Diagn Ther 2004; 19(4):305-312.
-
(2004)
Fetal Diagn Ther
, vol.19
, Issue.4
, pp. 305-312
-
-
Touraine, J.L.1
Raudrant, D.2
Golfier, F.3
-
142
-
-
10744232558
-
The hopes and fears of in utero gene therapy for genetic disease-a review
-
Coutelle C, Themis M, Waddington S, et al. The hopes and fears of in utero gene therapy for genetic disease-a review. Placenta 2003; 24(Suppl B):S114-S121.
-
(2003)
Placenta
, vol.24
, pp. S114-S121
-
-
Coutelle, C.1
Themis, M.2
Waddington, S.3
-
143
-
-
0032821708
-
Prospects for in utero human gene therapy
-
Zanjani ED, Anderson WF. Prospects for in utero human gene therapy. Science 1999; 285(5436):2084-2088.
-
(1999)
Science
, vol.285
, Issue.5436
, pp. 2084-2088
-
-
Zanjani, E.D.1
Anderson, W.F.2
-
144
-
-
0029784268
-
Human fetal gene therapy: moral and ethical questions
-
Fletcher JC, Richter G. Human fetal gene therapy: moral and ethical questions. Hum Gene Ther 1996; 7(13):1605-1614.
-
(1996)
Hum Gene Ther
, vol.7
, Issue.13
, pp. 1605-1614
-
-
Fletcher, J.C.1
Richter, G.2
-
145
-
-
0029900007
-
The fetus as a patient: an essential ethical concept for maternal-fetal medicine
-
Chervenak FA, McCullough LB. The fetus as a patient: an essential ethical concept for maternal-fetal medicine. J Matern Fetal Med 1996; 5(3):115-119.
-
(1996)
J Matern Fetal Med
, vol.5
, Issue.3
, pp. 115-119
-
-
Chervenak, F.A.1
McCullough, L.B.2
-
146
-
-
0036077287
-
A comprehensive ethical framework for fetal research and its application to fetal surgery for spina bifida
-
Chervenak FA, McCullough LB. A comprehensive ethical framework for fetal research and its application to fetal surgery for spina bifida. Am J Obstet Gynecol 2002; 187(1):10-14.
-
(2002)
Am J Obstet Gynecol
, vol.187
, Issue.1
, pp. 10-14
-
-
Chervenak, F.A.1
McCullough, L.B.2
-
147
-
-
4243548721
-
Ethical issues in maternal-fetal medicine
-
Rodeck CH, Whittle MJ, eds, London: Chrchill Livingstone
-
Bewley S. Ethical issues in maternal-fetal medicine. In: Rodeck CH, Whittle MJ, eds. Fetal Medicine: Basic Science and Clinical Practice. London: Chrchill Livingstone, 1999:265-279.
-
(1999)
Fetal Medicine: Basic Science and Clinical Practice
, pp. 265-279
-
-
Bewley, S.1
-
148
-
-
0034802429
-
Toward the ethical evaluation and use of maternal-fetal surgery
-
Lyerly AD, Gates EA, Cefalo RC, Sugarman J. Toward the ethical evaluation and use of maternal-fetal surgery. Obstet Gynecol 2001; 98(4):689-697.
-
(2001)
Obstet Gynecol
, vol.98
, Issue.4
, pp. 689-697
-
-
Lyerly, A.D.1
Gates, E.A.2
Cefalo, R.C.3
Sugarman, J.4
-
149
-
-
0034193478
-
Limitations of informed consent for in utero gene transfer research: implications for investigators and institutional review boards
-
Burger IM, Wilfond BS. Limitations of informed consent for in utero gene transfer research: implications for investigators and institutional review boards. Hum Gene Ther 2000; 11(7):1057-1063.
-
(2000)
Hum Gene Ther
, vol.11
, Issue.7
, pp. 1057-1063
-
-
Burger, I.M.1
Wilfond, B.S.2
-
150
-
-
0033968036
-
The ethical challenges of in utero gene therapy
-
Caplan AL, Wilson JM. The ethical challenges of in utero gene therapy. Nat Genet 2000; 24(2):107.
-
(2000)
Nat Genet
, vol.24
, Issue.2
, pp. 107
-
-
Caplan, A.L.1
Wilson, J.M.2
-
151
-
-
0033021870
-
In utero gene therapy: the case against
-
Billings PR. In utero gene therapy: the case against. Nat Med 1999; 5(3):255-256.
-
(1999)
Nat Med
, vol.5
, Issue.3
, pp. 255-256
-
-
Billings, P.R.1
-
152
-
-
0242407171
-
Fetal surgery for congenital diaphragmatic hernia
-
Wenstrom KD. Fetal surgery for congenital diaphragmatic hernia. N Engl J Med 2003; 349(20):1887-1888.
-
(2003)
N Engl J Med
, vol.349
, Issue.20
, pp. 1887-1888
-
-
Wenstrom, K.D.1
-
153
-
-
3042728865
-
Endoscopic laser surgery versus serial amnioreduction for severe twin-to-twin transfusion syndrome
-
Senat MV, Deprest J, Boulvain M, Paupe A, Winer N, Ville Y. Endoscopic laser surgery versus serial amnioreduction for severe twin-to-twin transfusion syndrome. N Engl J Med 2004; 351(2):136-144.
-
(2004)
N Engl J Med
, vol.351
, Issue.2
, pp. 136-144
-
-
Senat, M.V.1
Deprest, J.2
Boulvain, M.3
Paupe, A.4
Winer, N.5
Ville, Y.6
-
154
-
-
0242658928
-
A randomized trial of fetal endoscopic tracheal occlusion for severe fetal congenital diaphragmatic hernia
-
Harrison MR, Keller RL, Hawgood SB, et al. A randomized trial of fetal endoscopic tracheal occlusion for severe fetal congenital diaphragmatic hernia. N Engl J Med 2003; 349(20):1916-1924.
-
(2003)
N Engl J Med
, vol.349
, Issue.20
, pp. 1916-1924
-
-
Harrison, M.R.1
Keller, R.L.2
Hawgood, S.B.3
-
155
-
-
1142286325
-
Ethical questions raised by in utero therapeutics with stem cells and gene therapy
-
Sicard D. Ethical questions raised by in utero therapeutics with stem cells and gene therapy. Fetal Diagn Ther 2004; 19(2):124-126.
-
(2004)
Fetal Diagn Ther
, vol.19
, Issue.2
, pp. 124-126
-
-
Sicard, D.1
|