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1. Controversy on health-based guidance values for bisphenol A—the need of criteria for studies that serve as a basis for risk assessment

2. Commentary of the SKLM to the EFSA opinion on risk assessment of N-nitrosamines in food

3. Correction: Commentary of the SKLM to the EFSA opinion on risk assessment of N-nitrosamines in food

6. Direct addition of flavors, including taste and flavor modifiers

7. List of contributors

8. Stellungnahme zu Acetaldehyd als Aromastoff: Aspekte der Risikobewertung

9. Evaluation of the genotoxic potential of acrylamide: Arguments for the derivation of a tolerable daily intake (TDI value)

11. Salivary nitrate/nitrite and acetaldehyde in humans: potential combination effects in the upper gastrointestinal tract and possible consequences for the in vivo formation of N-nitroso compounds—a hypothesis

13. In response to the Letter to the Editor from Xiao regarding our article, “FEMA GRAS assessment of natural flavor complexes: Asafetida oil, garlic oil and onion oil”

14. Contribution to the ongoing discussion on fluoride toxicity

15. Acetaldehyde as a Food Flavoring Substance: Aspects of Risk Assessment

18. Toxicity of fluoride: critical evaluation of evidence for human developmental neurotoxicity in epidemiological studies, animal experiments and in vitro analyses

24. FEMA GRAS assessment of natural flavor complexes: Allspice, anise, fennel-derived and related flavoring ingredients

25. FEMA GRAS assessment of natural flavor complexes: Lemongrass oil, chamomile oils, citronella oil and related flavoring ingredients

26. Letter to the Editors regarding “10% body weight (gain) change as criterion for the maximum tolerated dose: A critical analysis”

27. FEMA GRAS assessment of derivatives of basil, nutmeg, parsley, tarragon and related allylalkoxybenzene-containing natural flavor complexes

31. The role of endogenous versus exogenous sources in the exposome of putative genotoxins and consequences for risk assessment

41. Acrylamide and Glycidamide: Approach towards Risk Assessment Based on Biomarker Guided Dosimetry of Genotoxic/Mutagenic Effects in Human Blood

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