about
Long-term health experience of jet engine manufacturing workers: V. Issues with the analysis of non-malignant central nervous system neoplasmsRegistering multiple primary tumors in central cancer registriesCohort follow-up: the 21st century proceduresThe effects of opt-out legislation on data collection and surveillance of birth defects by the New Hampshire Birth Conditions Program, New Hampshire, United States, 2007-2009Using NAPIIA to improve the accuracy of Asian race codes in registry data.Maximizing the cancer registry role and data utilization.Development and implementation of a distributed integrated data-management system for pediatric hematology/oncology service: a modular approach for a clinical outcome and research information system.Persistent socioeconomic inequalities in cancer survival in the United States: 1973-2007 surveillance, epidemiology and end results (SEER) data for breast cancer and non-Hodgkin's lymphoma.Avoiding sparse data bias: an example from gynecologic oncology.Workload and time management in central cancer registries: baseline data and implication for registry staffing.SEER and NAACCR data completeness methods: how do they impact data quality in Central Cancer Registries?The challenges of abstracting reliable information on patient race and ethnicity: initial observations from the Data Improvement Project on Patient Ethnicity and Race (DIPPER).Reality check: data are not always plentiful.Feasibility of using central registry data to assess timeliness of breast cancer care in Delaware.Construction of a comorbidity index for prostate cancer patients linking state cancer registry with inpatient and outpatient data.Registry data quality improvement by identifying discrepancies between assigned codes and text descriptions of birth defects.Conflicting race/ethnicity reports: lessons for improvement in data quality.Edits: an electronic tool for cancer registry data quality.The utility of the National Death Index as a supplemental data source in ascertaining 5-year mortality among Texas heterotaxy cases.Using an existing birth defects surveillance program to enhance surveillance data on stillbirths.Linking the Ohio Cancer Incidence Surveillance System with Medicare, Medicaid, and Clinical Data from Home Health Care and Long Term Care Assessment Instruments: Paving the Way for New Research Endeavors in Geriatric OncologyEnhancing central cancer registry treatment data using physician medical claims: a Florida pilot project.The value of billing data from oncology practice to supplement treatment information for cancer surveillance.Relative survival analysis using the Centers for Disease Control and Prevention's National Program of Cancer Registries Surveillance System Data, 2000-2007.Recent improvement in completeness of incidence data on acute myeloid leukemia in US cancer registries.Enhancing cancer registry data for comparative effectiveness research (CER) project: overview and methodology.Medicaid and cancer disparities: the need for comprehensive research data sets.An assessment of the reliability of race, Hispanic ethnicity, birthplace, and tobacco history data in the Massachusetts cancer registry, 2005-2009.Availability of TNM Staging Data Elements in the Medical Record and Training Needs Assessment: Results from the 2014 SEER Training Needs Assessment for TNM Study.Renal Cancer Patients with Unknown Ethnicity in Cancer Registry Data: Comparisons to Patients with Known Ethnicity.Registrars in Action: How Cancer Registry Data Are Used to Improve Public Health.Use of Population-Based Cancer Registry Data to Determine the Effect of Timely Treatment on the Survival of Colorectal Cancer Patients.Analysis of the National Cancer Data Base to Describe Treatment Trends in Stage IV Oral Cavity and Pharyngeal Cancers in the United States, 1998-2012.Improving the Completeness of Ascertainment in Florida's Birth Defects Surveillance Program: The Impact of Adding Infant Death and Emergency Department Data.Linking the National Health Interview Survey with the Florida Cancer Data System: A Pilot Study.Using Data on Tumor Grade in Cancer Registries to Enhance Surveillance of Oropharyngeal Cancers in Relation to the Human Papillomavirus Epidemic.Primary Payer at DX: Issues with Collection and Assessment of Data Quality.Identifying Class of Case to Improve Data Quality.Two Suspected Worksite or Occupational Cancer Clusters Investigated Using the Cancer Data Registry and Multiple Primary Standardized Incidence Ratios in SEER *Stat-Idaho, 2013-2014.A New Use for Your Cancer Registry Data.
P1433
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P1433
description
tijdschrift
@nl
name
Journal of registry management
@en
Journal of registry management
@it
Journal of registry management
@nl
type
label
Journal of registry management
@en
Journal of registry management
@it
Journal of registry management
@nl
prefLabel
Journal of registry management
@en
Journal of registry management
@it
Journal of registry management
@nl
P1055
P1156
19500157819
P1476
Journal of registry management
@en