2007
DOI: 10.1201/b16160
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A Guide to Poisonous House and Garden Plants

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Cited by 30 publications
(41 citation statements)
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“…A popular South African lily, Clivia miniata (clivia) (Fig. 6), contains phenanthridine alkaloids (lycorine, clivonine, clivatine, miniatine, hippeastrine) in the leaves, stems and bulbs and is widely used as a garden or house plant, but rarely causes poisoning 36 . Irises (Iris spp.)…”
Section: Gastrointestinal Tractmentioning
confidence: 99%
“…A popular South African lily, Clivia miniata (clivia) (Fig. 6), contains phenanthridine alkaloids (lycorine, clivonine, clivatine, miniatine, hippeastrine) in the leaves, stems and bulbs and is widely used as a garden or house plant, but rarely causes poisoning 36 . Irises (Iris spp.)…”
Section: Gastrointestinal Tractmentioning
confidence: 99%
“…and Pieris spp. (PLUMLEE et al, 1992;KNIGHT, 2006;) and Nerium oleander (PEDROSO et al, 2009), should be included in the differential diagnosis. In the present study on R. simsii in goats, there were no signifi cant gross and microscopic alterations, similar to what was observed for cattle experimentally poisoned with R. indicum (TOKARNIA et al, 1996).…”
Section: Descrevementioning
confidence: 99%
“…S. halepense (Johnson grass), a naturalized and invasive plant present in Romania's spontaneous flora (Sîrbu, 2012), under certain soil and climate conditions, ie frost or drought, contain a cyanogen nitrile glycoside (durrhin) whose toxicity level is low, after Knight (2007). Durrhin, by hydrolysis at an alkaline pH or by crushing the plant, decomposes into glucose, oxybenzoic acid and hydrogen cyanide which inactivate cell ferments and produce respiratory center paralysis (Popescu et al, 1981) and cardiac arrest (D'Mello, 2002).…”
Section: Poisoning With Plants Containing Cyanogenic Glycosidesmentioning
confidence: 99%
“…Pteridium aquilinum (Bracken fern). All parts of the plant are toxic (Knight, 2007), having several principles: ptaquiloside -unstable glycoside (German, 2017) that, under alkaline conditions is transformed into conjugated dieneone which is readily added to various nucleophilic compounds, the exerted action being positively carcinogenic (http://ethnobotanical.info,); at least two carcinogenic potential principles: quercetin şi kaempferol (http://ethnobotanical.info,); prunasin which are glycoside; thiaminase, an enzyme that reduces the thiamine reserve of the body, present in the leaves and root (Stegelmeier, http://www.msdvetmanual.com; http://www. pfaf.org,).…”
Section: Poisoning With Plants Containing Other Toxic Principlesmentioning
confidence: 99%
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