[1] WolthersD. A questionnaire on factors influencing children’s assent and dissent to non- therapeutic research[J].J Med Ethics,2006.
[2] Abramovitch R,Freedman J.L,Henry K,Van BrunschotM. Children’s capacity to agree to psychological research:Knowledge of risks and benefits and voluntariness[J].Ethics & Behavior,1995.
[3] Jean-Marie Bruzzese,Celia B.Fisher. Assessing and enhancing the research consent capacity of children and youth[J].Applied Developmental Science,2003.
[4] Broome ME,Richards DJ,Hall J.Children in research:The experience of ill children and adolescents[J].Journal of Family Nursing,2001.
[5] Kodish E,EderM,NollR B,Ruccione K,LangeB,AngiolilloA.Communication of randomization in childhood leukemia trials[J].Journal of the American Medical Association,2004.
[6] Department of Health and Human Services. Code of Federal Regulations. Title 45,Part 46,Protection of Human Subjects,45CFR46.405. Available at:http://www.hhs.gov/ohrp/humansubjects/gui dance/45cfr46.htm[Accessed:5 April2010].
[7] Wendler D,Varma S:Minimal Risk in Pediatric Research[J].The Journal of Pediatrics,2006.
[8] Miller VA,Drotar D,Burant C,Kodish E.Clinician-parent communication during informed consent for pediatric leukemia trials[J]. Journal of Pediatric Psychology,2005.
[9] 田海平. 中国生命伦理学的“问题域”还原[J].道德与文明,2013.
[10] H.T.恩格尔哈特.生命伦理学基础[M].范瑞平,译.北京:北京大学出版社,2006.
[11] 康德. 道德形而上学奠基[M]杨云飞,译;邓晓芒,校.北京:人民出版社,2013.
[12] 韩跃红,绪宗刚.尊严的价值内涵及伦理意义[J].伦理学研究,2011.
[13] 汤姆·比彻姆,詹姆士·邱卓思.生命医学伦理原则(第5版)[M].李伦,等译.北京:北京大学出版社,2014.
[14] WC Rossi,W Reynolds,RM Nelson.Child Assent and Parental Permission in Pediatric Research[J].Theoretical medicine and bioethics,2003.
[15] 陈化,李红文.论知情同意的家庭主义模式[J].道德与文明,2015(5).
[16] 那力,何志鹏,王彦志.WTO与公共健康[M].北京:清华大学出版社,2005.
[17] 约翰·穆勒.功利主义[M].徐大建,译.北京:商务印书馆,2014.
[18] 史军.公共健康实践的伦理原则探析科学技术与辩证法,2007(2). |
