A Probabilistic Framework for the Reference Dose (Probabilistic RfD)
暂无分享,去创建一个
Michael Dourson | Paul S. Price | Russell E. Keenan | P. Price | M. Dourson | R. Keenan | H. Carlson-Lynch | Jeffrey C. Swartout | J. Swartout | Heather Carlson-Lynch
[1] D. Barnes,et al. Reference dose (RfD): description and use in health risk assessments. , 1988, Regulatory toxicology and pharmacology : RTP.
[2] E J Calabrese,et al. Lack of total independence of uncertainty factors (UFs): implications for the size of the total uncertainty factor. , 1993, Regulatory toxicology and pharmacology : RTP.
[3] E J Calabrese,et al. Improved method for selection of the NOAEL. , 1994, Regulatory toxicology and pharmacology : RTP.
[4] Max Henrion,et al. Uncertainty: A Guide to Dealing with Uncertainty in Quantitative Risk and Policy Analysis , 1990 .
[5] R J Kavlock,et al. Benchmark Dose Workshop: criteria for use of a benchmark dose to estimate a reference dose. , 1995, Regulatory toxicology and pharmacology : RTP.
[6] W Leisenring,et al. Statistical properties of the NOAEL. , 1992, Regulatory toxicology and pharmacology : RTP.
[7] R C Hertzberg,et al. A Statistical Model for Species Extrapolation Using Categorical Response Data , 1985, Toxicology and industrial health.
[8] R L Sielken,et al. Assessment of safety/risk of chemicals: inception and evolution of the ADI and dose-response modeling procedures. , 1991, Toxicology letters.
[9] I W Davidson,et al. Biological basis for extrapolation across mammalian species. , 1986, Regulatory toxicology and pharmacology : RTP.
[10] D W Gaylor,et al. Incidence of developmental defects at the no observed adverse effect level (NOAEL). , 1992, Regulatory toxicology and pharmacology : RTP.
[11] M J Small,et al. Deriving allowable daily intakes for systemic toxicants lacking chronic toxicity data. , 1987, Regulatory toxicology and pharmacology : RTP.
[12] C. P. Carpenter,et al. Relationship between single-peroral, one-week, and ninety-day rat feeding studies. , 1969, Toxicology and applied pharmacology.
[13] J. Hoekstra,et al. Alternatives for the no‐observed‐effect level , 1993 .
[14] Bruce D. Naumann,et al. Scientific basis for uncertainty factors used to establish occupational exposure limits for pharmaceutical active ingredients , 1995 .
[15] R. O. Gilbert. Statistical Methods for Environmental Pollution Monitoring , 1987 .
[16] D W Gaylor,et al. Issues in qualitative and quantitative risk analysis for developmental toxicology. , 1988, Risk analysis : an official publication of the Society for Risk Analysis.
[17] E J Calabrese,et al. Uncertainty factors and interindividual variation. , 1985, Regulatory toxicology and pharmacology : RTP.
[18] M L Dourson,et al. Regulatory history and experimental support of uncertainty (safety) factors. , 1983, Regulatory toxicology and pharmacology : RTP.
[19] C C Travis,et al. On the use of 0.75 as an interspecies scaling factor. , 1992, Risk analysis : an official publication of the Society for Risk Analysis.
[20] K S Crump,et al. A new method for determining allowable daily intakes. , 1984, Fundamental and applied toxicology : official journal of the Society of Toxicology.
[21] J. Aitchison,et al. The Lognormal Distribution. , 1958 .
[22] C C Travis,et al. Interspecific scaling of toxicity data. , 1988, Risk analysis : an official publication of the Society for Risk Analysis.
[23] D Hattis,et al. Human interindividual variability--a major source of uncertainty in assessing risks for noncancer health effects. , 1994, Risk analysis : an official publication of the Society for Risk Analysis.
[24] A. Fletcher,et al. Drug Safety Tests and Subsequent Clinical Experience , 1978, Journal of the Royal Society of Medicine.
[25] L. Goodman,et al. The Pharmacological Basis of Therapeutics , 1941 .
[26] John L. Adgate,et al. Subchronic to chronic exposure extrapolation: Toxicologic evidence for a reduced uncertainty factor , 1995 .
[27] W Slob,et al. Conversion factors estimating indicative chronic no-observed-adverse-effect levels from short-term toxicity data. , 1996, Regulatory toxicology and pharmacology : RTP.
[28] D W Gaylor,et al. The use of safety factors for controlling risk. , 1983, Journal of toxicology and environmental health.
[29] M L Dourson,et al. On Reference Dose (RFD) and Its Underlying Toxicity Data Base , 1992, Toxicology and industrial health.
[30] C. S. Weil,et al. Safety Evaluation of Chemicals, Relationship between Short-and Long-Term Feeding Studies in Designing an Effective Toxicity Test , 1963 .
[31] M L Dourson,et al. An Approach for Modeling Noncancer Dose Responses with an Emphasis on Uncertainty , 1997, Risk analysis : an official publication of the Society for Risk Analysis.
[32] A. Renwick. Data-derived safety factors for the evaluation of food additives and environmental contaminants. , 1993, Food additives and contaminants.
[33] D G Hoel. Statistical approaches to toxicological data. , 1979, Environmental health perspectives.
[34] Statistical uncertainty in the no-observed-adverse-effect level , 1989 .
[35] D Hattis,et al. Human variability in susceptibility to toxic chemicals--a preliminary analysis of pharmacokinetic data from normal volunteers. , 1987, Risk analysis : an official publication of the Society for Risk Analysis.