• Vetter, J. (2004). Poison hemlock (Conium maculatum L.). Food and Chemical Toxicology, 42(9), 1373–1382.
• López, T., Cid, M., & Bianchini, M. (1999). Biochemistry of hemlock (Conium maculatum L.) alkaloids and their acute and chronic toxicity in livestock. A review. Toxicon, 37(6), 841–886
• Gardner, D., Ralphs, M., Turner, D., & Welsh, S. (2002). Taxonomic implications of diterpene alkaloids in three toxic tall larkspur species (Delphinium spp.). Biochemical Systematics and Ecology, 30(2), 77–90.
• Stern, E. S. (1954). Chapter 37 The Aconitum and Delphinium Alkaloids. The Alkaloids: Chemistry and Physiology, 275–333.
• Ronlán, A., & Wickberg, B. (1970). The structure of mezerein, a major toxic principle of daphne mezereum L. Tetrahedron Letters, 11(49), 4261–4264.
• Nelson, Lewis S.; Weil, Andrew; Goldfrank, L. R.; Shih, Richard D.; Balick, Michael J. Handbook of Poisonous and Injurious Plants. New York: Springer. P. 144.
• Lewis, R. J. Sax’s Dangerous Properties of Industrial Materials. 12 ed. Wiley, 2012. Vol. 1–5. P. 2861.
• Langford, S. D., & Boor, P. J. (1996). Oleander toxicity: an examination of human and animal toxic exposures. Toxicology, 109(1), 1–13.
• Cao, Y.-L., Zhang, M.-H., Lu, Y.-F., Li, C.-Y., Tang, J.-S., & Jiang, M.-M. (2018). Cardenolides from the leaves of Nerium oleander. Fitoterapia, 127, 293–300.
• Azzalini, E., Bernini, M., Vezzoli, S., Antonietti, A., & Verzeletti, A. (2019). A fatal case of self-poisoning through the ingestion of oleander leaves. Journal of Forensic and Legal Medicine, 65, 133–136.
• Gross, Michael; Baer, Harold; Fales, Henry M. (1975). «Urushiols of poisonous anacardiaceae». Phytochemistry. 14 (10): 2263.
• Aaron C., Gladman, M. (2006). Toxicodendron Dermatitis: Poison Ivy, Oak, and Sumac. Wilderness and Environmental Medicine, 17, 120–128.
• Salmaan Kanji, Pharm D., Robert D. MacLean (2012). Cardiac Glycoside Toxicity: More Than 200 Years and Counting. Critical Care Clinics, 28, 527–535.
• Wang, Y., Gao, W., Li, X., Wei, J., Jing, S., & Xiao, P. (2013). Chemotaxonomic study of the genus Paris based on steroidal saponins. Biochemical Systematics and Ecology, 48, 163–173.
• Mulkareddy, V., Sokach, C., Bucklew, E., Bukari, A., Sidlak, A., Harrold, I. M., Reis, S. (2020). Colchicine Toxicity. JACC: Case Reports, 2(4), 678–680.
• Finkelstein Y., Aks S. E., Hutson J. R., Juurlink D. N., Nguyen P., Dubnov-Raz G., Pollak U., Koren G., Bentur Y. (June 2010). “Colchicine poisoning: the dark side of an ancient drug”. Clinical Toxicology, 48 (5): 407–414.
• Francis, V., & Milne, N. (2013). Colchicine toxicity causing death. Pathology, 45, S68.
• Bolarinwa, Islamiyat F., Orfila, Caroline, Morgan, Michael R. A. (2014). «Amygdalin content of seeds, kernels and food products commercially-available in the UK». Food Chemistry, 152: 133–139.
• He, X.-Y., Wu, L.-J., Wang, W.-X., Xie, P.-J., Chen, Y.-H., & Wang, F. (2020). Amygdalin – A pharmacological and toxicological review. Vol. 254, Journal of Ethnopharmacology, 112–717.
• Cressey, P., & Reeve, J. (2019). Metabolism of cyanogenic glycosides: A review. Food and Chemical Toxicology, 125, 225–232.