Búsqueda | Biblioteca Virtual en Salud

1.

Attitudes of clinicians following large-scale pharmacogenomics implementation.

Peterson, J F; Field, J R; Shi, Y; Schildcrout, J S; Denny, J C; McGregor, T L; Van Driest, S L; Pulley, J M; Lubin, I M; Laposata, M; Roden, D M; Clayton, E W.

Pharmacogenomics J ; 16(4): 393-8, 2016 08.

Artículo en Inglés | MEDLINE | ID: mdl-26261062

2.

Parents' responses to vaccine information pamphlets.

Clayton, E W; Hickson, G B; Miller, C S.

Pediatrics ; 93(3): 369-72, 1994 Mar.

Artículo en Inglés | MEDLINE | ID: mdl-8115193

3.

Should promethazine in liquid form be available without prescription?

Hickson, G B; Altemeier, W A; Clayton, E W.

Pediatrics ; 86(2): 221-5, 1990 Aug.

Artículo en Inglés | MEDLINE | ID: mdl-2196521

4.

Removing the shadow of the law from the debate about genetic testing of children.

Clayton, E W.

Am J Med Genet ; 57(4): 630-4, 1995 Jul 17.

Artículo en Inglés | MEDLINE | ID: mdl-7573143

5.

Whose DNA is it anyway? Relationships between families and researchers.

Hannig, V L; Clayton, E W; Edwards, K M.

Am J Med Genet ; 47(2): 257-60, 1993 Aug 15.

Artículo en Inglés | MEDLINE | ID: mdl-8213916

6.

Satisfaction with obstetric care: relation to neonatal intensive care.

Hickson, G B; Clayton, E W; Miller, C S; Pichert, J W; Entman, S S.

Obstet Gynecol ; 91(2): 288-92, 1998 Feb.

Artículo en Inglés | MEDLINE | ID: mdl-9469291

7.

Legal and ethical commentary: the dangers of reading duty too broadly.

Clayton, E W.

J Law Med Ethics ; 25(1): 19-21, 2, 1997.

Artículo en Inglés | MEDLINE | ID: mdl-11066470

8.

From Rogers to Rivers: the rights of the mentally ill to refuse medication.

Clayton, E W.

Am J Law Med ; 13(1): 7-52, 1987.

Artículo en Inglés | MEDLINE | ID: mdl-3332562

9.

Risks of compulsory genetic databases-Response.

Hazel, J W; Clayton, E W; Malin, B A; Slobogin, C.

Science ; 363(6430): 940, 2019 03 01.

Artículo en Inglés | MEDLINE | ID: mdl-30819956

10.

Is it time for a universal genetic forensic database?

Hazel, J W; Clayton, E W; Malin, B A; Slobogin, C.

Science ; 362(6417): 898-900, 2018 11 23.

Artículo en Inglés | MEDLINE | ID: mdl-30467160

11.

Operational implementation of prospective genotyping for personalized medicine: the design of the Vanderbilt PREDICT project.

Pulley, J M; Denny, J C; Peterson, J F; Bernard, G R; Vnencak-Jones, C L; Ramirez, A H; Delaney, J T; Bowton, E; Brothers, K; Johnson, K; Crawford, D C; Schildcrout, J; Masys, D R; Dilks, H H; Wilke, R A; Clayton, E W; Shultz, E; Laposata, M; McPherson, J; Jirjis, J N; Roden, D M.

Clin Pharmacol Ther ; 92(1): 87-95, 2012 Jul.

Artículo en Inglés | MEDLINE | ID: mdl-22588608

12.

False positive newborn screening results are not always benign.

Morrison, D R; Clayton, E W.

Public Health Genomics ; 14(3): 173-7, 2011.

Artículo en Inglés | MEDLINE | ID: mdl-21178328

13.

Issues in state newborn screening programs.

Clayton, E W.

Pediatrics ; 90(4): 641-6, 1992 Oct.

Artículo en Inglés | MEDLINE | ID: mdl-1344065

14.

What should be the role of public health in newborn screening and prenatal diagnosis?

Clayton, E W.

Am J Prev Med ; 16(2): 111-5, 1999 Feb.

Artículo en Inglés | MEDLINE | ID: mdl-10343887

15.

Why the use of anonymous samples for research matters.

Clayton, E W.

J Law Med Ethics ; 23(4): 375-7, 1995.

Artículo en Inglés | MEDLINE | ID: mdl-8715059

16.

Are you and your waiting room's televised "expert" saying the same thing?

Hickson, G B; Clayton, E W.

Clin Pediatr (Phila) ; 32(3): 172-4, 1993 Mar.

Artículo en Inglés | MEDLINE | ID: mdl-8453837

17.

The dispersion of genetic technologies and the law.

Clayton, E W.

Hastings Cent Rep ; 25(3): S13-5, 1995.

Artículo en Inglés | MEDLINE | ID: mdl-7649733

18.

Baby Aaron and the elders.

Clayton, E W; Kodish, E.

Hastings Cent Rep ; 29(5): 20; discussion 20-1, 1999.

Artículo en Inglés | MEDLINE | ID: mdl-10587806

19.

Potential liability in cases of child abuse and neglect.

Clayton, E W.

Pediatr Ann ; 26(3): 173-7, 1997 Mar.

Artículo en Inglés | MEDLINE | ID: mdl-9084053

20.

What should the law say about disclosure of genetic information to relatives?

Clayton, E W.

J Health Care Law Policy ; 1(2): 373-90, 1998.

Artículo en Inglés | MEDLINE | ID: mdl-16281334

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Attitudes of clinicians following large-scale pharmacogenomics implementation.

Parents' responses to vaccine information pamphlets.

Should promethazine in liquid form be available without prescription?

Removing the shadow of the law from the debate about genetic testing of children.

Whose DNA is it anyway? Relationships between families and researchers.

Satisfaction with obstetric care: relation to neonatal intensive care.

Legal and ethical commentary: the dangers of reading duty too broadly.

From Rogers to Rivers: the rights of the mentally ill to refuse medication.

Risks of compulsory genetic databases-Response.

Is it time for a universal genetic forensic database?

Operational implementation of prospective genotyping for personalized medicine: the design of the Vanderbilt PREDICT project.

False positive newborn screening results are not always benign.

Issues in state newborn screening programs.

What should be the role of public health in newborn screening and prenatal diagnosis?

Why the use of anonymous samples for research matters.

Are you and your waiting room's televised "expert" saying the same thing?

The dispersion of genetic technologies and the law.

Baby Aaron and the elders.

Potential liability in cases of child abuse and neglect.

What should the law say about disclosure of genetic information to relatives?