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Authors:
Casarett, D
Karlawish, J
Sankar, P
Hirschman, KB
Asch, DA
Citation: D. Casarett et al., Obtaining informed consent for clinical pain research: patients' concerns and information needs, PAIN, 92(1-2), 2001, pp. 71-79
Authors:
Karlawish, JHT
Casarett, D
Klocinski, J
Sankar, P
Citation: Jht. Karlawish et al., How do AD patients and their caregivers decide whether to enroll in a clinical trial?, NEUROLOGY, 56(6), 2001, pp. 789-792
Authors:
Karlawish, JHT
Casarett, D
Klocinski, J
Clark, CM
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Citation: D. Casarett et Jl. Abrahm, Patients with cancer referred to hospice versus a bridge program: Patient characteristics, needs for care, and survival, J CL ONCOL, 19(7), 2000, pp. 2057-2063
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Citation: D. Casarett et al., Determining when quality improvement initiatives should be considered research - Proposed criteria and potential implications, J AM MED A, 283(17), 2000, pp. 2275-2280
Citation: D. Casarett et C. Helms, Systems errors versus physicians' errors: Finding the balance in medical education, ACAD MED, 74(1), 1999, pp. 19-22
Citation: D. Casarett, Commentary: Looking beyond vulnerability: The ethics and science of research involving dying patients, J PAIN SYMP, 18(2), 1999, pp. 144-145
Citation: D. Casarett et M. Siegler, Unilateral do-not-attempt-resuscitation orders and ethics consultation: A case series, CRIT CARE M, 27(6), 1999, pp. 1116-1120