| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/(SICI)1097-0142(19990815)86:4<647::AID-CNCR13>3.0.CO;2-G |
| P698 | PubMed publication ID | 10440692 |
| P2093 | author name string | Parker B | |
| Sugarman J | |||
| Schildkraut J | |||
| Regan K | |||
| Bluman LG | |||
| P2860 | cites work | Medical record confidentiality and data collection: current dilemmas | Q30619456 |
| The public health information infrastructure. A national review of the law on health information privacy | Q38480092 | ||
| Using a population-based cancer registry for recruitment in a pilot cancer control study | Q43570436 | ||
| Recruitment for controlled clinical trials: literature summary and annotated bibliography | Q49109414 | ||
| A comparison of methods of recruitment to a health promotion program for university seniors. | Q52903913 | ||
| Consent, confidentiality, and research. | Q53601269 | ||
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | medical ethics | Q237151 |
| research ethics | Q1132684 | ||
| P304 | page(s) | 647-651 | |
| P577 | publication date | 1999-08-01 | |
| P1433 | published in | Cancer | Q326041 |
| P1476 | title | Ethical ramifications of alternative means of recruiting research participants from cancer registries | |
| P478 | volume | 86 |
| Q33516495 | A cost-effectiveness analysis of subject recruitment strategies in the HIPAA era: results from a colorectal cancer screening adherence trial |
| Q34832109 | An automated communication system in a contact registry for persons with rare diseases: scalable tools for identifying and recruiting clinical research participants |
| Q36597644 | Are cancer registries a viable tool for cancer survivor outreach? A feasibility study. |
| Q34976096 | Building a registry of research volunteers among older urban African Americans: recruitment processes and outcomes from a community-based partnership |
| Q51898907 | Developing registries of volunteers: key principles to manage issues regarding personal information protection: Figure 1 |
| Q33430032 | Ethical issues in using data from quality management programs |
| Q40684782 | Making effective use of tumor registries for cancer survivorship research |
| Q37343172 | Maximizing Efficiency of Enrollment for School-Based Educational Research |
| Q36500221 | On using a cancer center cancer registry to identify newly affected women eligible for hereditary breast cancer syndrome testing: practical considerations |
| Q47113516 | Recruiting former melanoma patients via hospitals in comparison to office-based dermatologists in a register-based cohort study that required indirect contact |
| Q36771364 | Recruitment approaches for family studies: attitudes of index patients and their relatives. |
| Q33793645 | Recruitment of representative samples for low incidence cancer populations: do registries deliver? |
| Q90462680 | Recruitment of trial participants through electronic medical record patient portal messaging: A pilot study |
| Q53251599 | Research recruitment through US central cancer registries: balancing privacy and scientific issues. |
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