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Aconitum napellus, monkshood, [2] aconite, Venus' chariot or wolfsbane, is a species of highly toxic flowering plants in the genus Aconitum of the family ...
Monkshood, Aconitum napellus. Monkshood and other members of the genus Aconitum contain substantial amounts of the highly toxic aconitine and related alkaloids, especially in their roots and tubers. [3] As little as 2 mg of aconitine or 1 g of plant may cause death from respiratory paralysis or heart failure. [3]
A Aconitum abietetorum W.T.Wang & L.Q.Li Aconitum × acuminatum Rchb. Aconitum acutiusculum H.R.Fletcher & Lauener Aconitum × acutum Rchb. Aconitum ajanense Steinb.
The term "non-dialysis-dependent chronic kidney disease" (NDD-CKD) is a designation used to encompass the status of those persons with an established CKD who do not yet require the life-supporting treatments for kidney failure known as kidney replacement therapy (RRT, including maintenance dialysis or kidney transplantation).
Chronic kidney disease–mineral and bone disorder (CKD–MBD) is one of the many complications associated with chronic kidney disease. It represents a systemic disorder of mineral and bone metabolism due to CKD manifested by either one or a combination of the following: [ 1 ] [ 2 ]
Aconitum lycoctonum (wolf's-bane [2] or northern wolf's-bane) [3] is a species of flowering plant in the genus Aconitum, of the family Ranunculaceae, native to much of Europe and northern Asia. [ 4 ] [ 5 ] It is found in lowlands to the subalpine zone, mainly in forests and shaded habitats. [ 6 ]
Risk factors for kidney disease include diabetes, high blood pressure, family history, older age, ethnic group and smoking. For most patients, a GFR over 60 (mL/min)/(1.73 m 2) is adequate. But significant decline of the GFR from a previous test result can be an early indicator of kidney disease requiring medical intervention.
Cystic kidney disease includes various conditions related to the formation of cysts in one or both kidneys. The most common subset is polycystic kidney disease (PKD), which is a genetic anomaly with two subsets, autosomal recessive polycystic kidney disease (ARPKD) and autosomal dominant polycystic kidney disease (ADPKD).