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"benign myalgic encephalitis"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
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  • ¿µ¹®
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  • eastern equine encephalitis
    µ¿ºÎ¸¶³ú¿°(ÔÔݻةÒàæú).
  • eastern equine encephalitis
    µ¿ºÎ¸¶³ú¿°(ÔÔݻةÒàæú)
  • eastern equine encephalitis
    µ¿ºÎ¸¶³ú¿°(ÔÔݻةÒàæú)
  • encephalitis
    ³ú¿°
  • encephalitis
    ³ú¿°.(Òàæú)
  • encephalitis epidemica<³ª>
    À¯Ç༺ ³ú¿°(êüú¼àõÒàæú).
  • encephalitis haemorrhagica superior<³ª>
    Ç¥À缺 ÃâÇ÷¼º ³ú¿°.
  • encephalitis hyperplastica<³ª>
    Áõ½Ä¼º ³ú¿°(ñòãÖàõÒàæú).
  • encephalitis lethargica
    ±â¸é¼º ³ú¿°
  • encephalitis lethargica
    ±â¸é¼º ³ú¿°
  • encephalitis lethargica<³ª>
    ±â¸é¼º(ÐîØùàõ) ³ú¿°.
  • encephalitis neonatorum<³ª>
    ½Å»ý¾Æ³ú¿°.
  • encephalitis periaxialis diffusa<³ª>
    ¹Ì¸¸¼º Ãà»èÁÖÀ§(گؼàõõîßãñ²êÌ)³ú¿°.
  • encephalitis periaxialis scleroticans<³ª>
    °æÈ­¼º Ãà»èÁÖÀ§³ú¿°.
  • encephalitis siderans<³ª>
    Àü°Ý¼º(ï³Ìªàõ)³ú¿°.
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CETE Central European tick-borne encephalitis
CEV California encephalitis virus; Citrus exocortis viroid
EAE experimental allergic encephalomyelitis; experimental autoimmune encephalitis
EE embryo extract; end-to-end; end expiration; energy expenditure; Enterobacteriaceae enrichment [broth...
EEE eastern equine encephalitis; eastern equine encephalomyelitis; experimental enterococcal endocarditi...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 4
GABEB Generalised atrophic benign epidermolysis bullosa
BPH benign hyperplasia
BPH benign prostate hypertrophy
BPE benign prostatic enlargement
BPO benign prostatic obstruction
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 4
glossitis, benign migratory An inflammatory disease of the tongue of unknown aetiology, characterised by multiple annular areas of desquamation of the filiform papillae on the dorsal surface of the tongue, usually presenting pinkish-red central lesions outlined by thin, yellowish lines or bands that change patterns and shift from one area to another every few days.
(12 Dec 1998)
pemphigoid, benign mucous membrane A chronic blistering disease with predilection for mucous membranes and less frequently the skin, and with a tendency to scarring. It is sometimes called ocular pemphigoid because of conjunctival mucous membrane involvement.
(12 Dec 1998)
pemphigus, benign familial Rare hereditary disease characterised by recurrent eruptions of vesicles and bullae mainly on the neck, axillae, and groin. It exhibits autosomal dominant inheritance and is unrelated to pemphigus vulgaris though it closely resembles that disease.
(12 Dec 1998)
monoclonal gammopathies, benign Conditions characterised by the presence of a monoclonal serum (or urine) protein without clinical manifestations of plasma cell dyscrasia.
(12 Dec 1998)
hereditary benign intraepithelial dyskeratosis An autosomal dominant condition consisting of white spongy lesions of the buccal mucosa, floor of the mouth, ventral lateral tongue, gingiva and palate. Transient gelatinous plaques form over the cornea, which may produce temporary blindness, hereditary benign intraepithelial dyskeratosis.
Synonym: hereditary benign intraepithelial dyskeratosis.
(05 Mar 2000)
epidemic benign dry pleurisy An acute infectious disease usually occurring in epidemic form, characterised by paroxysms of pain, usually in the chest, and associated with strains of Enterovirus coxsackievirus type B.
Synonym: benign dry pleurisy, Bornholm disease, Daae's disease, devil's grip, diaphragmatic pleurisy, epidemic benign dry pleurisy, epidemic diaphragmatic pleurisy, epidemic myalgia, epidemic myositis, myositis epidemica acuta, epidemic transient diaphragmatic spasm, Sylvest's disease.
(05 Mar 2000)
unconjugated benign bilirubinaemia <gastroenterology> An inherited disorder that affects the way bilirubin in handled by the liver. Thought to be due to an inborn error of bilirubin metabolism.
Symptoms include mild jaundice, weakness, fatigue, nausea and abdominal pain.
Origin: Gr. Haima = blood
(27 Sep 1997)
late benign syphilis Late syphilis, manifested by serologic evidence of infection, but without any clinical manifestations.
(05 Mar 2000)
acute haemorrhagic encephalitis Encephalitis of apoplectoid character due to blood extravasation.
Synonym: encephalitis haemorrhagica.
(05 Mar 2000)
acute inclusion body encephalitis The most common acute encephalitis, caused by HSV-1; affects persons of any age; preferentially involves the inferomedial portions of the temporal lobe and the orbital portions of the frontal lobes; pathologically, severe haemorrhagic necrosis is present along with, in the acute stages, intranuclear eosinophilic inclusion bodies in the neurons and glial cells.
Synonym: acute inclusion body encephalitis, herpes encephalitis.
(05 Mar 2000)
acute necrotizing encephalitis An acute form of encephalitis, characterised by destruction of brain parenchyme.
(05 Mar 2000)
arthritis-encephalitis virus, caprine A species of lentivirus, subgenus ovine-caprine lentiviruses (lentiviruses, ovine-caprine), closely related to visna-maedi virus and causing acute encephalomyelitis, chronic arthritis, pneumonia, mastitis, and glomerulonephritis in goats. It is transmitted mainly in the colostrum and milk.
(12 Dec 1998)
Australian X encephalitis A severe encephalitis with a high mortality rate occurring in the Murray Valley of Australia; the disease is most severe in children and is characterised by headache, fever, malaise, drowsiness or convulsions, and rigidity of the neck; extensive brain damage may result; it is caused by the Murray Valley encephalitis virus (genus Flavivirus).
Synonym: Australian X disease, Australian X encephalitis.
(05 Mar 2000)
bacterial encephalitis Encephalitis of bacterial aetiology.
Synonym: encephalitis pyogenica, purulent encephalitis, suppurative encephalitis.
(05 Mar 2000)
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)
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