scholarly article | Q13442814 |
P50 | author | Jeffrey A. Kline | Q90429391 |
Alice M. Mitchell | Q93818746 | ||
P2860 | cites work | Potential impact of the HIPAA privacy rule on data collection in a registry of patients with acute coronary syndrome | Q30990472 |
Bias from requiring explicit consent from all participants in observational research: prospective, population based study | Q34089780 | ||
Institutional variability in a minimal risk, population-based study: recognizing policy barriers to health services research | Q34337572 | ||
Research without consent: current status, 2003. | Q35547732 | ||
Passive consent for clinical research in the age of HIPAA. | Q35688279 | ||
Conducting research using the emergency exception from informed consent: the Public Access Defibrillation (PAD) Trial experience. | Q35744549 | ||
Health Insurance Portability Accountability Act (HIPAA) regulations: effect on medical record research | Q35786532 | ||
Risk in emergency research using a waiver of/exception from consent: implications of a structured approach for institutional review board review | Q36258620 | ||
Electronic medical record review as a surrogate to telephone follow-up to establish outcome for diagnostic research studies in the emergency department | Q36258624 | ||
Research conditions that qualify for emergency exception from informed consent. | Q36303581 | ||
A qualitative study of institutional review board members' experience reviewing research proposals using emergency exception from informed consent | Q36807069 | ||
Waiver of informed consent: a survey of emergency medicine patients | Q39459723 | ||
Contribution of indirect computed tomography venography to computed tomography angiography of the chest for the diagnosis of thromboembolic disease in two United States emergency departments | Q39655389 | ||
Public perception of emergency research: a questionnaire | Q40368755 | ||
Distrust, race, and research | Q46863840 | ||
Factors that influence African-Americans' willingness to participate in medical research studies | Q46941182 | ||
Impracticability of informed consent in the Registry of the Canadian Stroke Network. | Q51941819 | ||
The Role of Community Consultation in the Ethical Conduct of Research Without Consent | Q57988501 | ||
P433 | issue | 3 | |
P921 | main subject | bias | Q742736 |
informed consent | Q764527 | ||
P304 | page(s) | 225-230 | |
P577 | publication date | 2008-03-01 | |
P1433 | published in | Academic Emergency Medicine | Q15755260 |
P1476 | title | Systematic bias introduced by the informed consent process in a diagnostic research study | |
P478 | volume | 15 |
Q34671655 | Antenatal consent in the SUPPORT trial: challenges, costs, and representative enrollment |
Q35830720 | Coordination and management of multicenter clinical studies in trauma: Experience from the PRospective Observational Multicenter Major Trauma Transfusion (PROMMTT) Study |
Q46327419 | Immediate complications of intravenous contrast for computed tomography imaging in the outpatient setting are rare |
Q33571334 | Incidence of contrast-induced nephropathy after contrast-enhanced computed tomography in the outpatient setting |
Q34758206 | Prospective multicenter evaluation of the pulmonary embolism rule-out criteria |
Q37721123 | Prospective study of the incidence of contrast-induced nephropathy among patients evaluated for pulmonary embolism by contrast-enhanced computed tomography |
Q43939070 | The effect of informed consent on results of a standard upper extremity intake questionnaire. |
Q58656949 | The ethics of uninsured participants accessing healthcare in biomedical research: A literature review |
Q33666469 | The use of delayed telephone informed consent for observational emergency medicine research is ethical and effective |
Q37096905 | Waiver of consent in noninterventional, observational emergency research: the PROMMTT experience |
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