| BSE | behavior summarized evaluation; bilateral intranasal sphenoethmoiclectomy; bilateral symmetrical and... |
|---|---|
| SE | saline enema; sanitary engineering; side effect; smoke exposure; solid extract; sphenoethmoidal; spi... |
| SSE | saline solution enema; skin self-examination; soapsuds enema; steady state exercise; subacute spongi... |
| AE | above-elbow [amputation]; acrodermatitis enteropathica; activation energy; adult erythrocyte; advers... |
| HE | half-scan with extrapolation; hard exudate; hektoen enteric [agar]; hemagglutinating encephalomyelit... |
| BSE | Bovine Spongiform Encephalopathy |
|---|---|
| TSE | Transmissible Spongiform Encephalopathy |
| TSE | Transmissible Spongiform Encephalopathies |
| TSEs | Transmissible Spongiform Encephalopathies |
| EIEE | Early infantile epileptic encephalopathy |
| spongiform encephalopathy | An encephalopathy characterised by vacuolation within nerve and glial cells. (05 Mar 2000) |
|---|
| bovine spongiform encephalopathy | A new disease of cattle, first reported in 1986 in Great Britain, characterised clinically by apprehensive behaviour, hyperesthesia, and ataxia and histopathologically by spongiform changes in the gray-matter neuropil of the brain stem; it is thought to be caused by an agent, possibly a prion, similar to that observed as the cause of scrapie. Synonym: mad cow disease. (05 Mar 2000) |
|---|---|
| subacute spongiform encephalopathy | A form of spongiform encephalopathy that is associated with a "slow virus", which to date has not been adequately described, is transmissible, and has a rapidly progressive, fatal course; e.g., Creutzfeldt-Jakob disease, kuru, Gerstmann-Straussler syndrome, scrapie. (05 Mar 2000) |
| encephalopathy, bovine spongiform | Scrapie-like neurological disorder of cattle. The infection appears to be caused by the consumption of scrapie-infected ruminant-derived protein (prions). (12 Dec 1998) |
| bovine spongiform encephalitis | <pathology> A neuro-degenerative disease found in domestic cattle which is related to a number of other similar diseases found in other animal species, including humans. The most well-known of these other diseases are scrapie, found in sheep, and Creutzfeldt-Jakob Disease, found in humans. The family of diseases is caused by an abnormally-configured protein called a prion. The function of the protein in its normal configuration is not certain. The diseases are similar to Alzheimer's disease in humans, except the progressive loss of brain function is more rapid. (09 Oct 1997) |
| spongiform | 1. Soft, and full of cavities; of an open, loose, pliable texture; as, a spongy excrescence; spongy earth; spongy cake; spongy bones. 2. Wet; drenched; soaked and soft, like sponge; rainy. "Spongy April." 3. Having the quality of imbibing fluids, like a sponge. <chemistry> Spongy lead, sponge lead. See Sponge. Spongy platinum. See Platinum. Source: Websters Dictionary (01 Mar 1998) |
| spongiform encephalopathies | A group of diseases characterised by long incubation and fatal progressive course with characteristic spongiform degeneration of grey matter of the cortex. The two main human diseases are kuru and Creutzfeldt Jakob disease. Diseases such as scrapie, mink encephalopathy and bovine spongiform encephalopathy (BSE) are considered to be similar. Controversy still surround the causative agent, the two main theories being slow viruses or prions. See: Gerstmann Straussler Scheinker syndrome. (18 Nov 1997) |
| alcoholic encephalopathy | <neurology> Encephalopathy associated with thiamin deficiency. Usually associated with chronic alcohol abuse. Other features include loss of memory and confabulation. Origin: Gr. Pathos = disease (27 Sep 1997) |
| bilirubin encephalopathy | <paediatrics> Disorder due to jaundice in a newborn baby with high blood levels of the pigment bilirubin that is deposited in the brain resulting in damage. The level of bilirubin is monitored in newborns to determine whether treatment is needed to prevent kernicterus. With brain affected, it is also called bilirubin encephalopathy. (12 Dec 1998) |
| Binswanger's encephalopathy | One of the causes of multiinfarct dementia, in which there are many infarcts and lacunes in the white matter, with relative sparing of the cortex and basal ganglia. Synonym: Binswanger's encephalopathy, encephalitis subcorticalis chronica, subcortical arteriosclerotic encephalopathy. (05 Mar 2000) |
| palindromic encephalopathy | A relatively mild form which tends to recur. (05 Mar 2000) |
| pancreatic encephalopathy | A metabolic encephalopathy associated with extensive pancreatic necrosis. (05 Mar 2000) |
| recurrent encephalopathy | A progressive form of encephalopathy occurring in young members of the same family; characterised by headache, vertigo, truncal ataxia, drowsiness and stupor, speech impairments, choreic-athetoid movements, and sometimes convulsions. (05 Mar 2000) |
| metabolic encephalopathy | Encephalopathy characterised by memory loss, vertigo, and generalised weakness, due to metabolic brain disease including hypoxia, ischemia, hypoglycaemia, or secondary to other organ failure such as liver or kidney. (05 Mar 2000) |
| Wernicke-Korsakoff encephalopathy | See: Wernicke's syndrome, Korsakoff's syndrome. (05 Mar 2000) |
| Wernicke's encephalopathy | <neurology> Encephalopathy associated with thiamin deficiency. Usually associated with chronic alcohol abuse. Other features include loss of memory and confabulation. Origin: Gr. Pathos = disease (27 Sep 1997) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|