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1. Conclusions and recommendations

2. Legal problems of pharming

3. The ethical evaluation of pharming

4. The role of patents in the development of pharming

5. Public views and attitudes to pharming

6. Risk assessment of plant pharming and animal pharming

7. The welfare of pharming animals

8. The technology of pharming

9. Introduction

10. Risk Evaluation and Communication

12. Hypothesis Testing and the Choice of the Dose-Response Model

13. Mathematical Models of Carcinogenesis

14. Glossary

15. Effects of Ionising Radiation in the Low-Dose Range — Radiobiological Basis

16. Epidemiological Perspectives on Low-Dose Exposure to Human Carcinogens

17. Toxicology of Chemical Carcinogens

18. Ethical Aspects of Risk

19. Abbreviations

20. Introduction

21. Zusammenfassung

23. Summary

24. Low Doses in Health-Related Environmental Law

25. The Importance of Economic Factors in Setting Combined Environmental Standards

26. Legal Problems of Assessing and Regulating Exposure to Combined Effects of Substances and Radiation

27. Scientific and Medical Foundations

28. Appraisal and Recommendations

29. Perception of Technical Risks

30. Methodological Foundations of Defining Environmental Standards

31. Introduction

32. Methodische Grundlagen der Festlegung von Umweltstandards

33. Beurteilung und Empfehlungen

34. Die Bedeutung des ökonomischen Faktors bei der Bestimmung kombinierter Umweltstandards

35. Naturwissenschaftlich-medizinische Grundlagen

36. Wahrnehmung technischer Risiken

37. Einleitung

38. Rechtliche Probleme der Ermittlung und Regulierung von Kombinationswirkungen von Stoffen und Strahlen

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