Яды: вокруг и внутри. Путеводитель по самым опасным веществам на планете - Сакина Зейналова Страница 36
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Белладонна
• Kwakye, G. F., Jiménez, J., Jiménez, J. A., & Aschner, M. (2018). Atropa belladonna neurotoxicity: Implications to neurological disorders. Food and Chemical Toxicology, 116, 346–353.
• Mazzanti, G., Tita, B., Bolle, P., Bonanomi, M., & Piccinelli, D. (1988). A comparative study of behavioural and autonomic effects of atropine and Atropa belladonna. Pharmacological Research Communications, 20, 49–53.
• Mateo, Montoya A., Mavrakanas, N., Schutz, J. S. (2009). “Acute anticholinergic syndrome from Atropa belladonna mistaken for blueberries”. Eur. J. Ophthalmol. 19 (1): 170–172.
• Prusakov, P. A. (2014). Belladonna Alkaloids. Encyclopedia of Toxicology, 399–401.
• Van der Meer, M. J.; Hundt, H. K.; Müller, F. O. (October 1986). “The metabolism of atropine in man”. The Journal of Pharmacy and Pharmacology, 38 (10): 781–784
Белена
• Мазнев Н. И. Энциклопедия лекарственных растений. 3-е изд., испр. и доп. М.: Мартин, 2004. С. 92–93. 496 с.
Стрихнос ядоносный
• Philippe, G., Angenot, L., Tits, M., & Frédérich, M. (2004). About the toxicity of some Strychnos species and their alkaloids. Toxicon, 44(4), 405–416.
• Burr, S. A., & Leung, Y. L. (2014). Curare (d-Tubocurarine). Encyclopedia of Toxicology, 1088–1089.
• Bennett, A. E., 1968. The history of the introduction of curare into medicine. Anesth. Analg. 47, 484–492.
• Rivera, H. L., & Barrueto, F. (2014). Strychnine. Encyclopedia of Toxicology, 407–408.
• Садритдипов Ф. С., Курмуков А. Г. Фармакология растительных алкалоидов и их применение в медицине. VTam., 1980.
Вёх
• Гусынин И. А. Токсикология ядовитых растений. М.: ОГИЗ-Сельхозгиз, 1974. С. 55–56.
• Химическая энциклопедия. Т. 5. М.: Советская энциклопедия, 1999. С. 531.
• Шишкин Б. К. Род 1001. Вех – Cicuta L. // Флора СССР: в 30 т. / Начато при рук. и под гл. ред. В. Л. Комарова. М.; Л.: Изд-во АН СССР, 1950. Т. 16 / Ред. тома Б. К. Шишкин. С. 376–378. 648 с.
Наперстянка
• Emswiler, M. P., & Wills, B. K. (2014). Digitalis Glycosides. Encyclopedia of Toxicology, 151–154.
Чемерица Лобеля
• Heretsch, P., & Giannis, A. (2015). The Veratrum and Solanum Alkaloids. The Alkaloids: Chemistry and Biology, 201–232.
Клещевина и абрус
• Wright, H. T., & Robertus, J. D. (1987). The intersubunit disulfide bridge of ricin is essential for cytotoxicity. Archives of Biochemistry and Biophysics, 256(1), 280–284.
• Муравьева Д. А. Тропические и субтропические лекарственные растения. М.: Медицина, 1983. 336 с.
• Bradberry, S. (2016). Ricin and abrin. Medicine, 44(2), 109–110.
• Alipour, M., Pucaj, K., Smith, M. G., & Suntres, Z. E. (2012). Toxicity of ricin toxin A chain in rats. Drug and Chemical Toxicology, 36(2), 224–230.
• Alipour, M., Pucaj, K., Smith, M.G., Suntres, Z.E., 2013. Toxicity of ricin toxin A chains in rats. Drug Chem. Toxicol. 36, 224–230.
Аконит
• Banasik, M., & Stedeford, T. (2014). Plants, Poisonous (Humans). Encyclopedia of Toxicology, 970–978.
• Beike J., Frommherz L., Wood M., Brinkmann B., Köhler H. (2004). “Determination of aconitine in body fluids by LC-MS-MS”. International Journal of Legal Medicine. 118 (5): 289–293.
• Chan T. Y. K. Aconite poisoning. Clin Toxicol 2009; 47: 279e85.
• Chen S. P. L., Ng S. W., Poon W. T., et al. Aconite poisoning over 5 years: a case series in Hong Kong and lessons towards herbal safety. Drug Saf. 2012; 35: 575e87.
Болиголов
• 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
Живокость
• 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.
Волчеягодник
• 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.
Олеандр
• 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.
Ядовитый плющ
• 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.
Ландыш майский
• Salmaan Kanji, Pharm D., Robert D. MacLean (2012). Cardiac Glycoside Toxicity: More Than 200 Years and Counting. Critical Care Clinics, 28, 527–535.
Вороний глаз
• 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.
Безвременник
• 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.
Жалоба
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