| ECG | Electro-Cardio-Graphy(-Gram); 심전도 = EKG 1. Conducting System Structu... |
|---|---|
| IS | ileal segment; immediate sensitivity; immune serum; immunosuppression; impingement syndrome; incenti... |
| SM | Master of Science; sadomasochism; self-monitoring; silicon microphysiometer; simple mastectomy; skim... |
| DS | dead air space; dead space; deep sedative; deep sleep; defined substrate; dehydroepiandrosterone sul... |
| ICS | ileocecal sphincter; immotile cilia syndrome; impulse-conducting system; integrated case study; inte... |
| CMT | Charcot Marie Tooth |
|---|---|
| CMT | Charcot--Marie--Tooth disease |
| CMT1 | Charcot--Marie--Tooth disease type 1 |
| CMT1A | Charcot-Marie Tooth disease type 1A |
| CMTD | Charcot-Marie-Tooth Disease |
| quadrilateral space | Musculotendinous formation providing passageway for the axillary nerve, posterior humeral circumflex artery and accompanying veins as they run from the axilla to the superior posterior arm; as the neurovascular structures enter the formation anteriorly, it is bounded superiorly by the shoulder joint, medially by the lateral border of subscapularis, laterally by the surgical neck of the humerus, and inferiorly by the tendon of latissimus dorsi; as the vessels exit the formation posteriorly, it is bounded superiorly by the teres minor, medially by the long head of the triceps, laterally by the lateral head of the triceps and inferiorly by the teres major muscle or tendon; as they emerge, most of the neurovascular structures run on the deep surface of the deltoid muscle, which they supply. Synonym: quadrilateral space. (05 Mar 2000) |
|---|---|
| quadrilateral | 1. <geometry> A plane figure having four sides, and consequently four angles; a quadrangular figure; any figure formed by four lines. 2. An area defended by four fortresses supporting each other; as, the Venetian quadrilateral, comprising Mantua, Peschiera, Verona, and Legnano. <geometry> Complete quadrilateral, the figure made up of the six straight lines that can be drawn through four points, A, B, C, I, the lines being supposed to be produced indefinitely. Source: Websters Dictionary (01 Mar 1998) |
| Ampere, Andre-Marie | <person, radiobiology> French physicist responsible for much of what is known about the fundamentals of electromagnetism. (13 Nov 1997) |
| Andre-Marie Ampere | <person, radiobiology> French physicist responsible for much of what is known about the fundamentals of electromagnetism. (13 Nov 1997) |
| Bamberger-Marie disease | hypertrophic pulmonary osteoarthropathy |
| Bamberger-Marie syndrome | hypertrophic pulmonary osteoarthropathy |
| Blainville, Henri Marie Ducrotay de | <person> French zoologist and anthropologist, 1777-1850. See: Blainville ears. (05 Mar 2000) |
| Brissaud-Marie syndrome | <syndrome> Unilateral spasm of the tongue and lips, of hysterical nature. (05 Mar 2000) |
| Gelle, Marie-Ernst | <person> French otologist, 1834-1923. See: Gelle test. (05 Mar 2000) |
| Marie, Pierre | <person> French neurologist, 1853-1940. See: Marie's ataxia, Charcot-Marie-Tooth disease, Bamberger-Marie disease, Bamberger-Marie syndrome, Marie-Strumpell disease, Strumpell-Marie disease, Brissaud-Marie syndrome, Foix-Cavany-Marie syndrome. (05 Mar 2000) |
| Marie-Robinson syndrome | <syndrome> Insomnia and mild melancholia associated with alimentary levulosuria. (05 Mar 2000) |
| Marie's ataxia | An obsolete term for a variety of non-Friedreich hereditary ataxias. (05 Mar 2000) |
| Marie's disease | A hypertrophic osteopathy of dogs in which osseous changes of the limbs are associated with intrathoracic lesions such as pulmonary neoplasms; also occurs in horses, cattle, and sheep. (05 Mar 2000) |
| Marie-Strumpell disease | <rheumatology> A polyarthritis involving the spine, which is characterised by progressive, painful stiffening of the joints and ligaments. It almost exclusively affects young men. Interestingly the disease seems to be associated with HLA B27, those with this histocompatability antigen are 300 times more likely to get the disease, 90% of sufferers have HLA B27 (18 Nov 1997) |
| charcot-marie disease | A hereditary motor and sensory neuropathy transmitted as an autosomal dominant trait and characterised by progressive distal wasting and loss of reflexes in the muscles of the legs (occasionally of the arms). Onset is usually in the second to fourth decades. (12 Dec 1998) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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