-
1
-
-
0018360851
-
Creutzfeldt-Jakob Disease: Patterns of Worldwide Occurrence and the Significance of Familial and Sporadic Clustering
-
C.L. Masters, J.O. Harris, and D.C. Gajdusek, "Creutzfeldt-Jakob Disease: Patterns of Worldwide Occurrence and the Significance of Familial and Sporadic Clustering," Annals of Neurology, 5 (1978): 177-88.
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Annals of Neurology
, vol.5
, pp. 177-188
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-
Masters, C.L.1
Harris, J.O.2
Gajdusek, D.C.3
-
2
-
-
0346284799
-
-
See id. For example, Creutzfeldt-Jakob disease (CJD) is known to have a higher incidence among Libyan Jews and in Slovakia, Italy, and Chile
-
See id. For example, Creutzfeldt-Jakob disease (CJD) is known to have a higher incidence among Libyan Jews and in Slovakia, Italy, and Chile.
-
-
-
-
3
-
-
0015549846
-
The Clinical Characteristics of Transmissible Creutzfeldt-Jakob Disease
-
R. Roos, D.C. Gajdusek, and C.J. Gibbs, "The Clinical Characteristics of Transmissible Creutzfeldt-Jakob Disease," Brain, 96 (1973): at 7-11.
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Brain
, vol.96
, pp. 7-11
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-
Roos, R.1
Gajdusek, D.C.2
Gibbs, C.J.3
-
4
-
-
25944451127
-
-
Ottawa: Queen's Printer, Apr. 15
-
Health Canada, Canada Communicable Disease Report (Ottawa: Queen's Printer, vol. 22-8, Apr. 15, 1996): at 57-60.
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(1996)
Canada Communicable Disease Report
, vol.8-22
, pp. 57-60
-
-
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5
-
-
0026542737
-
From Slow Virus to Prion: A Review of Transmissible Spongiform Encephalopathies
-
P.L. Lantos, "From Slow Virus to Prion: A Review of Transmissible Spongiform Encephalopathies," Histopathology, 20 (1992): at 2.
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(1992)
Histopathology
, vol.20
, pp. 2
-
-
Lantos, P.L.1
-
6
-
-
0017871609
-
Subacute Spongiform Encephalopathy (Creutzfeldt-Jakob Disease): The Nature and Progression of Spongiform Change
-
C.L. Masters and E.P. Richardson Jr., "Subacute Spongiform Encephalopathy (Creutzfeldt-Jakob Disease): The Nature and Progression of Spongiform Change," Brain, 101 (1978): 333-44.
-
(1978)
Brain
, vol.101
, pp. 333-344
-
-
Masters, C.L.1
Richardson E.P., Jr.2
-
7
-
-
0027968896
-
The Dimensions of Creutzfeldt-Jakob Disease
-
The view that the infectious agent of CJD is viral is defended in L. Manuelidis, "The Dimensions of Creutzfeldt-Jakob Disease," Transfusion, 34 (1994): 915-28; and in E.E. Manuelidis and L. Manuelidis, "A Transmissible Creutzfeldt- Jakob Disease-Like Agent is Prevalent in the Human Population," Proceedings of the National Academy of Science, 90 (1993): 7724-28.
-
(1994)
Transfusion
, vol.34
, pp. 915-928
-
-
Manuelidis, L.1
-
8
-
-
0027295388
-
A Transmissible Creutzfeldt-Jakob Disease-Like Agent is Prevalent in the Human Population
-
The view that the infectious agent of CJD is viral is defended in L. Manuelidis, "The Dimensions of Creutzfeldt- Jakob Disease," Transfusion, 34 (1994): 915-28; and in E.E. Manuelidis and L. Manuelidis, "A Transmissible Creutzfeldt-Jakob Disease-Like Agent is Prevalent in the Human Population," Proceedings of the National Academy of Science, 90 (1993): 7724-28.
-
(1993)
Proceedings of the National Academy of Science
, vol.90
, pp. 7724-7728
-
-
Manuelidis, E.E.1
Manuelidis, L.2
-
9
-
-
0027724075
-
Overview of the Transmissible Spongiform Encephalopathies: Prion Protein Disorders
-
S.J. DeArmond, "Overview of the Transmissible Spongiform Encephalopathies: Prion Protein Disorders," British Medical Bulletin, 49 (1993): 725-37.
-
(1993)
British Medical Bulletin
, vol.49
, pp. 725-737
-
-
DeArmond, S.J.1
-
10
-
-
0020321767
-
Novel Proteinaceous Infectious Particles Cause Scrapie
-
The term prion was first introduced in S.B. Prusiner, "Novel Proteinaceous Infectious Particles Cause Scrapie," Science, 216 (1982): 136-44.
-
(1982)
Science
, vol.216
, pp. 136-144
-
-
Prusiner, S.B.1
-
11
-
-
0017226461
-
Familial Neurological Disease Associated with Spongiform Encephalopathy
-
N.P. Rosenthal et al., "Familial Neurological Disease Associated with Spongiform Encephalopathy," Archives of Neurology, 33 (1976): at 258; and S.B. Prusiner and K.K. Hsiao, "Human Prion Diseases," Annals of Neurology, 35 (1994): at 389-91.
-
(1976)
Archives of Neurology
, vol.33
, pp. 258
-
-
Rosenthal, N.P.1
-
12
-
-
0028270007
-
Human Prion Diseases
-
N.P. Rosenthal et al., "Familial Neurological Disease Associated with Spongiform Encephalopathy," Archives of Neurology, 33 (1976): at 258; and S.B. Prusiner and K.K. Hsiao, "Human Prion Diseases," Annals of Neurology, 35 (1994): at 389-91.
-
(1994)
Annals of Neurology
, vol.35
, pp. 389-391
-
-
Prusiner, S.B.1
Hsiao, K.K.2
-
13
-
-
0027716662
-
Epidemiology of Creutzfeldt-Jakob Disease
-
For a helpful summary, see R.G. Will, "Epidemiology of Creutzfeldt-Jakob Disease," British Medical Bulletin, 49 (1993): at 962-65.
-
(1993)
British Medical Bulletin
, vol.49
, pp. 962-965
-
-
Will, R.G.1
-
14
-
-
0026667331
-
'Friendly Fire' in Medicine: Hormones, Homografts, and Creutzfeldt-Jakob Disease
-
P. Brown, M.A. Preece, and R.G. Will, "'Friendly Fire' in Medicine: Hormones, Homografts, and Creutzfeldt-Jakob Disease," Lancet, 340 (1992): 24-27.
-
(1992)
Lancet
, vol.340
, pp. 24-27
-
-
Brown, P.1
Preece, M.A.2
Will, R.G.3
-
15
-
-
0017387067
-
Experimental Creutzfeldt-Jakob Disease Transmitted Via the Eye with Infected Cornea
-
E.E. Manuelidis et al., "Experimental Creutzfeldt-Jakob Disease Transmitted Via the Eye with Infected Cornea," N. Engl. J. Med., 296 (1977): 1334-36.
-
(1977)
N. Engl. J. Med.
, vol.296
, pp. 1334-1336
-
-
Manuelidis, E.E.1
-
16
-
-
0023804449
-
Creutzfeldt-Jakob Disease Probably Acquired from a Cadaveric Dura Mater Graft
-
V. Thadani et al., "Creutzfeldt-Jakob Disease Probably Acquired from a Cadaveric Dura Mater Graft," Journal of Neurosurgery, 69 (1988): 766-69.
-
(1988)
Journal of Neurosurgery
, vol.69
, pp. 766-769
-
-
Thadani, V.1
-
17
-
-
0017367439
-
Danger of Accidental Person-to-Person Transmission of Creutzfeldt-Jakob Disease by Surgery
-
C. Bernouilli et al., "Danger of Accidental Person-to-Person Transmission of Creutzfeldt-Jakob Disease by Surgery," Lancet, (1977): 478-79.
-
Lancet
, vol.1977
, pp. 478-479
-
-
Bernouilli, C.1
-
18
-
-
0025963199
-
Creutzfeldt-Jakob Disease in Pituitary Growth Hormone Recipients in the United States
-
J.E. Fradkin et al., "Creutzfeldt-Jakob Disease in Pituitary Growth Hormone Recipients in the United States," JAMA, 265 (1991): 880-84.
-
(1991)
JAMA
, vol.265
, pp. 880-884
-
-
Fradkin, J.E.1
-
19
-
-
0348175479
-
-
See Manuelidis, supra note 7
-
See Manuelidis, supra note 7.
-
-
-
-
20
-
-
0346284783
-
Current Status of Creutzfeldt-Jakob Disease and Blood Product Safety
-
B.L. Evatt, "Current Status of Creutzfeldt-Jakob Disease and Blood Product Safety," Haemophilia World, 2, no. 2 (1995): 3-4. But see A. Créange et al., "Creutzfeldt-Jakob Disease After Liver Transplantation," Annals of Neurology, 38 (1995): 269-72. Reports of earlier studies suggesting the possibility of transmission by blood transfusion include E.E. Manuelidis, E.J. Gorgacz, and L. Manuelidis, "Viremia in Experimental Creutzfeldt-Jakob Disease," Science, 200 (1978): 1063-65.
-
(1995)
Haemophilia World
, vol.2
, Issue.2
, pp. 3-4
-
-
Evatt, B.L.1
-
21
-
-
0029125679
-
Creutzfeldt-Jakob Disease after Liver Transplantation
-
B.L. Evatt, "Current Status of Creutzfeldt-Jakob Disease and Blood Product Safety," Haemophilia World, 2, no. 2 (1995): 3-4. But see A. Créange et al., "Creutzfeldt-Jakob Disease After Liver Transplantation," Annals of Neurology, 38 (1995): 269-72. Reports of earlier studies suggesting the possibility of transmission by blood transfusion include E.E. Manuelidis, E.J. Gorgacz, and L. Manuelidis, "Viremia in Experimental Creutzfeldt-Jakob Disease," Science, 200 (1978): 1063-65.
-
(1995)
Annals of Neurology
, vol.38
, pp. 269-272
-
-
Créange, A.1
-
22
-
-
0018099217
-
Viremia in Experimental Creutzfeldt-Jakob Disease
-
B.L. Evatt, "Current Status of Creutzfeldt-Jakob Disease and Blood Product Safety," Haemophilia World, 2, no. 2 (1995): 3-4. But see A. Créange et al., "Creutzfeldt-Jakob Disease After Liver Transplantation," Annals of Neurology, 38 (1995): 269-72. Reports of earlier studies suggesting the possibility of transmission by blood transfusion include E.E. Manuelidis, E.J. Gorgacz, and L. Manuelidis, "Viremia in Experimental Creutzfeldt-Jakob Disease," Science, 200 (1978): 1063-65.
-
(1978)
Science
, vol.200
, pp. 1063-1065
-
-
Manuelidis, E.E.1
Gorgacz, E.J.2
Manuelidis, L.3
-
23
-
-
0027409810
-
Creutzfeldt-Jakob Disease and Blood Transfusion
-
See T.G.F. Esmonde et al., "Creutzfeldt-Jakob Disease and Blood Transfusion," Lancet, 341 (1993): 205-07; and a similar study by N. Heye, S. Hensen, and N. Muller, "Creutzfeldt-Jakob Disease and Blood Transfusion," Lancet, 343 (1994): 298-99.
-
(1993)
Lancet
, vol.341
, pp. 205-207
-
-
Esmonde, T.G.F.1
-
24
-
-
0028128111
-
Creutzfeldt-Jakob Disease and Blood Transfusion
-
See T.G.F. Esmonde et al., "Creutzfeldt-Jakob Disease and Blood Transfusion," Lancet, 341 (1993): 205-07; and a similar study by N. Heye, S. Hensen, and N. Muller, "Creutzfeldt-Jakob Disease and Blood Transfusion," Lancet, 343 (1994): 298-99.
-
(1994)
Lancet
, vol.343
, pp. 298-299
-
-
Heye, N.1
Hensen, S.2
Muller, N.3
-
26
-
-
0347545857
-
-
June 23
-
Roger Dodd, American Red Cross, Remarks at Special Meeting of Food and Drug Administration Special Advisory Panel on Creutzfeldt-Jakob Disease and Blood Products (June 22, 1995). See Council of Community Blood Centers, CCBC Newsletter, June 23, 1995, at 9-10.
-
(1995)
CCBC Newsletter
, pp. 9-10
-
-
-
27
-
-
0347545845
-
BPAC Recommends Component Retrieval for Previous Donations from CJD-Infected Donors
-
This was reported at a meeting on December 15-16, 1994. See "BPAC Recommends Component Retrieval for Previous Donations from CJD-Infected Donors," AABB Blood Bank Week, 11, no. 45 (1994).
-
(1994)
AABB Blood Bank Week
, vol.11
, Issue.45
-
-
-
28
-
-
0347545843
-
-
note
-
It was passed by a vote of six to five, with two abstentions, at a special meeting held on June 22, 1995. For a report of the proceedings, see Council of Community Blood Centers, supra note 20.
-
-
-
-
29
-
-
0346284793
-
-
note
-
Memorandum from the European Agency for the Evaluation of Medicinal Products (Feb. 13, 1995) (on file with author); and Position Paper of the European Association of the Plasma Products Industry (July 18, 1995) (on file with author).
-
-
-
-
30
-
-
0346284798
-
-
note
-
Information Letter from Health Canada (Oct. 20, 1993) (on file with author).
-
-
-
-
31
-
-
0346914903
-
-
note
-
Letter from Dr. Bert Aye, National Director of Blood Services, to all Blood Bank directors and chief executive officers (July 17, 1995) (on file with author); and Memorandum from Dr. Bert Aye, National Director of Blood Services, to all Blood Bank directors and chief executive officers (July 24, 1995) (on file with author).
-
-
-
-
32
-
-
0348175478
-
-
note
-
For example, the Hospital for Sick Children in Toronto and the Calgary Regional Health Authority both undertook notification campaigns. However, Vancouver General Hospital, Alberta Capital Health Authority, and Winnipeg's Health Sciences Centre have each decided not to notify specific recipients.
-
-
-
-
34
-
-
0346914904
-
-
note
-
In addition, in the event that life or health insurance companies include questions about exposure to CJD in application questionnaires, those notified may find life or health insurance either unavailable or more expensive.
-
-
-
-
35
-
-
25944458764
-
Blood Recipients Joining Forces
-
May 1
-
R. Walker, "Blood Recipients Joining Forces," Herald (Calgary), May 1, 1996, at B1.
-
(1996)
Herald (Calgary)
-
-
Walker, R.1
-
36
-
-
25944440460
-
Hospital Warns Parents of Blood Risk
-
May 4
-
W. Immen, "Hospital Warns Parents of Blood Risk," Globe and Mail (Toronto), May 4, 1996, at A1.
-
(1996)
Globe and Mail (Toronto)
-
-
Immen, W.1
-
37
-
-
0346914902
-
-
note
-
I acknowledge that the analogy is not as persuasive as hoped. Aside from young children, those tested for Huntington disease already know that they are at some risk of developing the disease. The test simply makes the prognosis more or less certain. Notifying of possible CJD exposure introduces this risk to persons theretofore totally unaware of it.
-
-
-
-
38
-
-
0029095678
-
Emotional and Functional Impact of DNA Testing on Patients with Symptoms of Huntington's Disease
-
J. Jankovic, J. Beach, and T. Ashizawa, "Emotional and Functional Impact of DNA Testing on Patients with Symptoms of Huntington's Disease," Journal of Medical Genetics, 32 (1995): 516-18. The authors found no significant differences in psychological scores, depression, functional capacity, symptom interference, independence, or other measures of mood and behavior two weeks and three months following testing. However, see M. Bloch et al., "Diagnosis of Huntington Disease," American Journal of Medical Genetics, 47 (1993): 368-74; and A. Tibben et al., "DNA Testing for Huntington's Disease in the Netherlands," American Journal of Medical Genetics, 44 (1992): 94-99. Both studies found profound effects when patients were advised of their Huntington disease status.
-
(1995)
Journal of Medical Genetics
, vol.32
, pp. 516-518
-
-
Jankovic, J.1
Beach, J.2
Ashizawa, T.3
-
39
-
-
0027265353
-
Diagnosis of Huntington Disease
-
J. Jankovic, J. Beach, and T. Ashizawa, "Emotional and Functional Impact of DNA Testing on Patients with Symptoms of Huntington's Disease," Journal of Medical Genetics, 32 (1995): 516-18. The authors found no significant differences in psychological scores, depression, functional capacity, symptom interference, independence, or other measures of mood and behavior two weeks and three months following testing. However, see M. Bloch et al., "Diagnosis of Huntington Disease," American Journal of Medical Genetics, 47 (1993): 368-74; and A. Tibben et al., "DNA Testing for Huntington's Disease in the Netherlands," American Journal of Medical Genetics, 44 (1992): 94-99. Both studies found profound effects when patients were advised of their Huntington disease status.
-
(1993)
American Journal of Medical Genetics
, vol.47
, pp. 368-374
-
-
Bloch, M.1
-
40
-
-
0026657732
-
DNA Testing for Huntington's Disease in the Netherlands
-
J. Jankovic, J. Beach, and T. Ashizawa, "Emotional and Functional Impact of DNA Testing on Patients with Symptoms of Huntington's Disease," Journal of Medical Genetics, 32 (1995): 516-18. The authors found no significant differences in psychological scores, depression, functional capacity, symptom interference, independence, or other measures of mood and behavior two weeks and three months following testing. However, see M. Bloch et al., "Diagnosis of Huntington Disease," American Journal of Medical Genetics, 47 (1993): 368-74; and A. Tibben et al., "DNA Testing for Huntington's Disease in the Netherlands," American Journal of Medical Genetics, 44 (1992): 94-99. Both studies found profound effects when patients were advised of their Huntington disease status.
-
(1992)
American Journal of Medical Genetics
, vol.44
, pp. 94-99
-
-
Tibben, A.1
-
41
-
-
0027134654
-
Risk Factors for Suicide in Huntington's Disease
-
H. Lipe, A. Schultze, and T.D. Bird, "Risk Factors for Suicide in Huntington's Disease," American Journal of Medical Genetics, 48 (1993): 231-33; and L.A. Farrer, "Suicide and Attempted Suicide in Huntington Disease," American Journal of Medical Genetics, 24 (1986): 305-11.
-
(1993)
American Journal of Medical Genetics
, vol.48
, pp. 231-233
-
-
Lipe, H.1
Schultze, A.2
Bird, T.D.3
-
42
-
-
0022548975
-
Suicide and Attempted Suicide in Huntington Disease
-
H. Lipe, A. Schultze, and T.D. Bird, "Risk Factors for Suicide in Huntington's Disease," American Journal of Medical Genetics, 48 (1993): 231-33; and L.A. Farrer, "Suicide and Attempted Suicide in Huntington Disease," American Journal of Medical Genetics, 24 (1986): 305-11.
-
(1986)
American Journal of Medical Genetics
, vol.24
, pp. 305-311
-
-
Farrer, L.A.1
-
43
-
-
0026514328
-
Predictive Testing for Huntington Disease in Canada
-
M. Bloch et al., "Predictive Testing for Huntington Disease in Canada," American Journal of Medical Genetics, 42 (1992): 499-507.
-
(1992)
American Journal of Medical Genetics
, vol.42
, pp. 499-507
-
-
Bloch, M.1
-
44
-
-
0028022712
-
Psychological Costs and Benefits of Predictive Testing for Huntington's Disease
-
A. Codori and J. Brandt, "Psychological Costs and Benefits of Predictive Testing for Huntington's Disease," American Journal of Medical Genetics, 54 (1994): 174-84.
-
(1994)
American Journal of Medical Genetics
, vol.54
, pp. 174-184
-
-
Codori, A.1
Brandt, J.2
-
45
-
-
0348175462
-
-
See, for example, Stanback v. Parke, Davis & Co., 657 F.2d 642 (4th Cir. 1981); Doe v. Miles Laboratories, 927 F.2d 187 (4th Cir 1991); and Tarasoff v. Regents of the University of California, 551 P.2d 334 (Cal. Sup. Ct. 1976)
-
See, for example, Stanback v. Parke, Davis & Co., 657 F.2d 642 (4th Cir. 1981); Doe v. Miles Laboratories, 927 F.2d 187 (4th Cir 1991); and Tarasoff v. Regents of the University of California, 551 P.2d 334 (Cal. Sup. Ct. 1976).
-
-
-
-
46
-
-
0346284781
-
-
For example, Christopher v. Cutter Laboratories, 53 F.3d 1184 (11th Cir. 1995) (alleging that the defendant supplier of blood products failed to warn prior to the transfusion that might have transmitted HIV to the hemophiliac patient)
-
For example, Christopher v. Cutter Laboratories, 53 F.3d 1184 (11th Cir. 1995) (alleging that the defendant supplier of blood products failed to warn prior to the transfusion that might have transmitted HIV to the hemophiliac patient).
-
-
-
-
47
-
-
0348175475
-
-
927 F.2d 187
-
927 F.2d 187.
-
-
-
-
48
-
-
0346284710
-
In re Sealed Case
-
D.C. Cir.
-
In re Sealed Case, 67 F.3d 965 (D.C. Cir. 1995).
-
(1995)
F.3d
, vol.67
, pp. 965
-
-
-
49
-
-
0348175459
-
-
See id.; and Pittman Estate v. Bain [1994] 112 D.L.R.4th 257, 403-12 (Ont. High Ct.)
-
See id.; and Pittman Estate v. Bain [1994] 112 D.L.R.4th 257, 403-12 (Ont. High Ct.).
-
-
-
-
50
-
-
0347545858
-
-
927 F.2d at 193; and 112 D.L.R.4th at 310
-
927 F.2d at 193; and 112 D.L.R.4th at 310.
-
-
-
-
51
-
-
0346284775
-
-
Arato v. Avedon, 858 P.2d 598, 605 (Cal. 1993) (noting duty to disclose "dire prognosis")
-
Arato v. Avedon, 858 P.2d 598, 605 (Cal. 1993) (noting duty to disclose "dire prognosis").
-
-
-
-
52
-
-
0347545853
-
-
112 D.L.R.4th at 372
-
112 D.L.R.4th at 372.
-
-
-
-
53
-
-
0347545850
-
-
Daly v. United States, 946 F.2d 1467 (9th Cir. 1991)
-
Daly v. United States, 946 F.2d 1467 (9th Cir. 1991).
-
-
-
-
54
-
-
0348175468
-
-
Union Carbide & Carbon Corp. v. Stapleton, 237 F.2d 229 (6th Cir. 1956)
-
Union Carbide & Carbon Corp. v. Stapleton, 237 F.2d 229 (6th Cir. 1956).
-
-
-
-
55
-
-
0346284788
-
-
M.M.H. v. United States, 966 F.2d 285 (7th Cir. 1992)
-
M.M.H. v. United States, 966 F.2d 285 (7th Cir. 1992).
-
-
-
-
56
-
-
0347545847
-
Miles
-
Miles, 927 F.2d at 194-95.
-
F.2d
, vol.927
, pp. 194-195
-
-
-
57
-
-
0347545852
-
-
Hoemke v. New York Blood Center, 912 F.2d 550 (2d Cir. 1990)
-
Hoemke v. New York Blood Center, 912 F.2d 550 (2d Cir. 1990).
-
-
-
-
58
-
-
0348175473
-
-
See id. at 554
-
See id. at 554.
-
-
-
-
59
-
-
0347545854
-
-
Spann v. Irwin Memorial Blood Centers, 40 Cal. Rptr. 2d 360 (Cal. Ct. App. 1995)
-
Spann v. Irwin Memorial Blood Centers, 40 Cal. Rptr. 2d 360 (Cal. Ct. App. 1995).
-
-
-
-
60
-
-
0004094981
-
-
St. Louis: Mosby, 3rd ed.
-
American College of Legal Medicine, Legal Medicine (St. Louis: Mosby, 3rd ed., 1995): at 283.
-
(1995)
Legal Medicine
, pp. 283
-
-
-
61
-
-
0347545851
-
-
Miceikis v. Field, 347 N.E.2d 320, 324 (Ill. App. Ct. 1976) ("excessive disclosure of remote risks would tend to do more harm than good to the patient"); see also, Pardy v. United States, 783 F.2d 710 (7th Cir. 1986); and McInerney v. McDonald [1992] 93 D.L.R.4th 415, 429-30 (Can.)
-
Miceikis v. Field, 347 N.E.2d 320, 324 (Ill. App. Ct. 1976) ("excessive disclosure of remote risks would tend to do more harm than good to the patient"); see also, Pardy v. United States, 783 F.2d 710 (7th Cir. 1986); and McInerney v. McDonald [1992] 93 D.L.R.4th 415, 429-30 (Can.).
-
-
-
-
62
-
-
0348175467
-
-
note
-
This is the manner of notification used, for example, by the Calgary Regional Health Authority and Toronto's Hospital for Sick Children.
-
-
-
-
63
-
-
0023184757
-
Psychiatric Implications of Presymptomatic Testing for Huntington's Disease
-
S. Kessler, "Psychiatric Implications of Presymptomatic Testing for Huntington's Disease," American Journal of Orthopsychiatry, 57 (1987): 212-19.
-
(1987)
American Journal of Orthopsychiatry
, vol.57
, pp. 212-219
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Kessler, S.1
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64
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0029007707
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Exploration of the Effects of Predictive Testing for Huntingdon Disease on Intimate Relationships
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K.A. Quaid and M.K. Wesson, "Exploration of the Effects of Predictive Testing for Huntingdon Disease on Intimate Relationships," American Journal of Medical Genetics, 57 (1995): 46-51.
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(1995)
American Journal of Medical Genetics
, vol.57
, pp. 46-51
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-
Quaid, K.A.1
Wesson, M.K.2
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65
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25944442479
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-
May 11
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This is the approach adopted by Winnipeg's Health Sciences Centre when it faced this dilemma. See Free Press (Winnipeg), May 11, 1996, at A2.
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(1996)
Free Press (Winnipeg)
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-
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66
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-
0346284790
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This is the method preferred by Health Canada. See Informanon Letter from Health Canada, Health Protection Branch (Oct. 20, 1995) (on file with author)
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This is the method preferred by Health Canada. See Informanon Letter from Health Canada, Health Protection Branch (Oct. 20, 1995) (on file with author).
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67
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-
0346284787
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Pittman Estate v. Bain suggests that it may not. See Pittman, 112 D.L.R.4th at 382-83
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Pittman Estate v. Bain suggests that it may not. See Pittman, 112 D.L.R.4th at 382-83.
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