| ¿µ¹® | atrophy | ÇÑ±Û | À§Ãà(Áõ) |
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| ET | educational therapy; effective temperature; ejection time; embryo transfer; endothelin; endotoxin; e... |
|---|---|
| ICL | idiopathic CD4 T-cell lymphocytopenia; iris-clip lens; isocitrate lyase |
| IRIS | integrated risk information system; interleukin regulation of immune system; International Research ... |
| VID | visible iris diameter |
| PMA | index of prevalence and severity of gingivitis, where P = papillary gingiva, M = marginal gingiva, a... |
| PRA | Progressive retinal atrophy |
|---|---|
| PMA | progressive muscular atrophy |
| IPE | Iris pigment epithelium |
| ICB | iris ciliary body |
| IPE | iris pigment epithelial |
| essential progressive atrophy of iris | Progressive atrophy of the iris without inflammatory signs, characterised by patchy loss of all layers of the iris with hole formation, migration of the pupil, degeneration of the corneal endothelium, peripheral anterior synechiae, and secondary glaucoma; usually unilateral, predominantly affecting women in their middle years. (05 Mar 2000) |
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| progressive choroidal atrophy | An x chromosome-linked abnormality characterised by atrophy of the choroid and degeneration of the retinal pigment epithelium causing night blindness. (12 Dec 1998) |
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| progressive circumscribed cerebral atrophy | Circumscribed atrophy of the cerebral cortex. Synonym: lobar sclerosis, progressive circumscribed cerebral atrophy. (05 Mar 2000) |
| progressive infantile spinal muscular atrophy | Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised. Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy. (05 Mar 2000) |
| progressive muscular atrophy | A serious neurologic disease that results from the progressive degeneration of the motor neurons. (27 Sep 1997) |
| progressive spinal muscular atrophy | One of the subgroups of motor neuron disease; a progressive degenerative disorder of the motor neurons of the spinal cord, manifested as progressive, often symmetrical, weakness and wasting, typically beginning in the distal portions of the limbs, particularly in the upper extremities, and spreading proximally; fasciculation potentials are often present, but evidence of corticospinal tract disease (e.g., increased deep tendon reflexes, Babinski sign) is not. (05 Mar 2000) |
| infantile progressive spinal muscular atrophy | Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised. Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy. (05 Mar 2000) |
| benign essential tremor | A benign tremor inherited as a dominant character; it may be a rapid oscillation resembling that seen in thyrotoxicosis, a coarse tremor during rest and inhibited by a voluntary effort, or one which appears only upon movement. Synonym: benign essential tremor, familial tremor. (05 Mar 2000) |
| drugs, essential | Drugs considered essential to meet the health needs of a population as well as to control drug costs. (world health organization action programme on essential drugs, 1994, p3) (12 Dec 1998) |
| osteolysis, essential | Syndromes of bone destruction where the cause is not obvious such as neoplasia, infection, or trauma. The destruction follows various patterns: massive (gorham disease), multicentric (hajdu-cheney syndrome, winchester syndrome), or carpal/tarsal. (12 Dec 1998) |
| Eagle's minimum essential medium | A tissue culture medium similar to Eagle's basal medium but with different amounts and a few exclusions (e.g., antibiotics and phenol red). (05 Mar 2000) |
| essential | 1. Belonging to the essence, or that which makes an object, or class of objects, what it is. "Majestic as the voice sometimes became, there was forever in it an essential character of plaintiveness." (Hawthorne) 2. Hence, really existing; existent. "Is it true, that thou art but a a name, And no essential thing?" (Webster (1623)) 3. Important in the highest degree; indispensable to the attainment of an object; indispensably necessary. "Judgment's more essential to a general Than courage." (Denham) "How to live? that is the essential question for us." (H. Spencer) 4. Containing the essence or characteristic portion of a substance, as of a plant; highly rectified; pure; hence, unmixed; as, an essential oil. "Mine own essential horror." 5. Necessary; indispensable; said of those tones which constitute a chord, in distinction from ornamental or passing tones. 6. <medicine> Idiopathic; independent of other diseases. <biology> Essential character, a class of volatile oils, extracted from plants, fruits, or flowers, having each its characteristic odour, and hot burning taste. They are used in essences, perfumery, etc, and include many varieties of compounds; as lemon oil is a terpene, oil of bitter almonds an aldehyde, oil of wintergreen an ethereal salt, etc.; called also volatile oils in distinction from the fixed or nonvolatile. Origin: Cf. F. Essentiel. See Essence. Source: Websters Dictionary (01 Mar 1998) |
| essential albuminuria | A collective term for types that are not the result of pathologic changes in the kidneys. Synonym: essential albuminuria. (05 Mar 2000) |
| essential amino acid | <biochemistry> Those amino acids that cannot be synthesised by an organism and must therefore be present in the diet. The term is often applied anthropocentrically to those amino acids required by humans (Ileu, Leu, Lys, Met, Phe, Thr, Try, & Val), though rats need two more (Arg & His). (18 Nov 1997) |
| essential amino acids | Alpha-amino acids nutritionally required by an organism and which must be supplied in its diet (i.e., cannot be synthesised by the organism) either as free amino acid or in proteins. (05 Mar 2000) |
| essential anaemia | An obsolete term for pernicious anaemia; also used formerly for any type of anaemia of unknown mechanism. (05 Mar 2000) |
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