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  • ¿µ¹®
    ÇѱÛ
  • lumbar spinal stenosis
    Ç㸮ôÃß°üÇùÂø(Áõ), ¿äÃßôÃß°üÇùÂø(Áõ)
  • posterior spinal sclerosis
    µÚô¼ö°æÈ­Áõ, ô¼öÈÄ»è°æÈ­Áõ
  • progressive spastic spinal paralysis
    ÁøÇà°­Á÷ô¼ö¸¶ºñ
  • progressive spinal amyotrophy
    ÁøÇàô¼ö±Ù(À°)À§Ãà(Áõ)
  • spasmodic spinal paralysis
    ¿¬Ãàô¼ö¸¶ºñ
  • spastic spinal paralysis
    °­Á÷ô¼ö¸¶ºñ
  • spinal
    1. °¡½Ã- 2. ôÃß- 3. ôÁÖ- 4. ô¼ö-
  • spinal accessory nerve
    ô¼ö´õºÎ½Å°æ, ô¼öºÎ½Å°æ
  • spinal accessory-facial nerve crossover
    ô¼ö´õºÎ¾ó±¼½Å°æ±³Â÷(¼ú), ô¼öºÎ¾È¸é½Å°æ±³Â÷(¼ú)
  • spinal anesthesia
    ô¼ö¸¶Ãë, ôÃ߸¶Ãë
  • spinal angiogram
    ô¼öÇ÷°üÁ¶¿µ»ó
  • spinal animal
    ô¼öµ¿¹°
  • spinal arachnoid
    ô¼ö°Å¹Ì¸·, ô¼öÁöÁÖ¸·
  • spinal artery
    ô¼öµ¿¸Æ
  • spinal automatism
    ô¼öÀÚµ¿Áõ
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  • ¿µ¹®
    ÇѱÛ
  • spinal shock
    ô¼ö¼îÅ©
  • spinal sign
    ô¼ö¡ÈÄ
  • spinal stenosis
    ôÁÖ°üÇùÂøÁõ
  • spinal tap
    (¢¡lumbar puncture) Ç㸮õÀÚ, ¿äÃßõÀÚ, ¿äÃß¶Õ±â
  • spinal cord softening
    ô¼ö¿¬È­(Áõ)
  • abortive type
    ºÎÀüÇü
  • anovulatory type
    ¹«¹è¶õÇü
  • asthenic type
    ¹«·ÂüÇü
  • athletic type
    °ÇÀåÇü
  • precision type attachment
    Á¤¹ÐÇüºÎÂø
  • type specific antigen
    ÇüƯÀÌÇ׿ø
  • blood type
    Ç÷¾×Çü
  • bubble type vaporizer
    ±âÆ÷Çü±âÈ­±â
  • cellular type
    ¼¼Æ÷Çü
  • culture type
    Ç¥ÁرÕÁÖ, ±âÁØÁÖ
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  • ¿µ¹®
    ÇѱÛ
  • herpes simplex virus type 1
    Á¦1Çü ´Ü¼øÆ÷Áø¹ÙÀÌ·¯½º
  • herpes simplex virus type 2
    Á¦2Çü ´Ü¼øÆ÷Áø¹ÙÀÌ·¯½º
  • htlv,type i
    type 1Çü
  • human T cell leukemia virus type I
    Á¦1Çü »ç¶÷ T¼¼Æ÷¹éÇ÷º´¹ÙÀÌ·¯½º
  • human T cell leukemia virus type I
    Á¦1Çü »ç¶÷ T ¼¼Æ÷ ¹éÇ÷º´ ¹ÙÀÌ·¯½º
  • human T cell leukemia virus type II
    Á¦2Çü »ç¶÷ T¼¼Æ÷¹éÇ÷º´¹ÙÀÌ·¯½º
  • human T cell leukemia virus type II
    Á¦2Çü »ç¶÷ T ¼¼Æ÷ ¹éÇ÷º´ ¹ÙÀÌ·¯½º
  • hyperlipoproteinemia type III
    °íÁö´Ü¹éÇ÷Áõ III
  • hyperlipoproteinemia type IV
    °í´Ü¹éÇ÷Áõ IV Çü
  • hyperlipoprotenemia type II
    °íÁö´Ü¹éÇ÷Áõ II Çü
  • hyperproteinemia type III
    ´Ü¹é°úÀ×Ç÷(Áõ) III Çü
  • hypersensitivity reactions,delayed-type
    Áö¿¬Çü(òÀæÅû¡)
  • hypersensitivity reactions,type i(anaphylactic)
    IÇü
  • hypersensitivity reactions,type ii(antibody-dependent cell-mediate cyt
    IIÇü
  • hypersensitivity reactions,type iii(imune complex-mediated)
    IIIÇü
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  • pigmentary atrophy
    »ö¼Ò¼º À§Ãà(ßäáÈàõ ê×õê)
  • postinflammatory optic atrophy
    ¿°ÁõÈĽýŰæÀ§Ãà
  • postneuritic optic atrophy
    ¿°ÁõÈĽýŰæÀ§Ãà
  • pressure atrophy
    ¾Ð¹ÚÀ§Ãà(äâÚÞê×õê).
  • primary optic atrophy
    ¿ø¹ß½Ã½Å°æÀ§Ãà(ê«Û¡ãÊãêÌèê×õê).
  • primary optic atrophy
    ¿ø¹ß(¼º) ½Ã½Å°æÀ§Ãà(ê«Û¡(àõ) ãÊãêÌèê×õê)
  • progressive unilateral facial atrophy
    ÁøÇ༺ Æí¾È¸éÀ§Ãà(òäú¼àõø¸äÔØüê×õê ).
  • progressive unilateral facial atrophy
    ÁøÇ༺ Æí¾È¸éÀ§Ãà(òäú¼àõ ø¸äÔØüê×õê )
  • red atrophy
    Àû»öÀ§Ãà(îåßäê×õê)
  • renal atrophy
    ½ÅÀ§Ãà
  • renal atrophy
    ½ÅÀ§Ãà(ãìê×õê).
  • renal atrophy
    ½ÅÀ§Ãà(ãìê×õê)
  • reticular atrophy
    ¸Á»óÀ§Ãà(ØÑßÒê×õê)
  • secondary macula atrophy
    ÀÌÂ÷¹Ý¹®Çü À§Ãà(¡­ÚèÚ£û¡ê×õê)
  • secondary optic atrophy
    ¼Ó¹ß½Ã½Å°æÀ§Ãà(áÙÛ¡àõãÊãêÌèê×õê).
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LCCA late cortical cerebellar atrophy; leukoclastic angiitis
LOA leave of absence; Leber optic atrophy; left occipitoanterior [fetal position]
MSA major serologic antigen; male-specific antigen; mannitol salt agar; Medical Services Administration;...
OA obstructive apnea; occipital artery; occipito-anterior; occiput anterior; octanoic acid; ocular albi...
OAK Kjer optic atrophy
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 8
mdg Muscular dysgenesis
MMD Myotonic muscular dystrophy
MyD Myotonic muscular dystrophy
OPMD Oculopharyngeal muscular dystrophy
SCARMD Severe childhood autosomal recessive muscular dystrophy
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    ¼³¸í
  • bilateral type
    ¾çÃøÇü
  • blood type
    Ç÷¾×Çü
  • body type
    üÇü
    ¸öÀÇ »ý±è»ý±è.
  • brush type vessel arrangement
    ¼Ö ¸ð¾çÀÇ Ç÷°ü ¹è¿­
  • C-type virus particle
    CÇü ¹ÙÀÌ·¯½º ÀÔÀÚ
  • cylindroid type
    ¿øÁÖÇü
    ¿©·¯ °¡Áö ±âÀΰú Çü»óÀ» °¡Áø ¿äÁßÀÇ ¿øÁÖ.
  • defiant type
    ¹ÝÇ×Àû Çൿ À¯Çü
  • delayed-type hyperseneitivity
    Áö¿¬Çü °ú¹ÎÁõ
    °¨ÀÛµÈ T ¸²ÇÁ±¸¿¡ ÀÇÇÏ¿© Àü´ÞµÇ´Â °ú¹ÎÁõ. Ç×ü¿¡ ÀÇÇÏ¿© ¹ß»ýÇÏ´Â °ú¹ÎÁõÀÌ ¾Æ´Ï°í º¸Åë ¸²ÇÁ±¸¿Í macro
  • Diego blood type
    µð¿¡°í½Ä Ç÷¾×Çü
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  • distal step type
    ¿ø½É °è´ÜÇü
  • Dombrock blood type
    µ¼ºê·Ï½Ä Ç÷¾×Çü
    Ç÷¾×ÇüÀÇ Çϳª. »ç¶÷ÀÇ Ç÷±¸ °¡¿îµ¥ Ç×Do Ç×ü¿Í ÀÀÁý ¹ÝÀÀÀ» ÀÏÀ¸Å°´Â Do
  • dorsolumbal type
    Èä¿äºÎ Çü, ¹èÃø ¿äºÎ Çü
  • dysplastic type
    ¹ßÀ° ºÎÀü ü°Ý
  • epidermoid type cell
    À¯Ç¥ÇÇ ¼¼Æ÷
  • ferm-type design
    ¾çÄ¡·ù ÇüÅÂÀÇ µðÀÚÀÎ
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 8
progressive circumscribed cerebral atrophy Circumscribed atrophy of the cerebral cortex.
Synonym: lobar sclerosis, progressive circumscribed cerebral atrophy.
(05 Mar 2000)
progressive muscular dystrophy A form of progressive muscular atrophy in which the disease begins in the muscle and not in the spinal centres.
Synonym: Erb atrophy, idiopathic muscular atrophy.
(05 Mar 2000)
scapulohumeral atrophy Progressive spinal muscular atrophy beginning in the shoulder.
Synonym: scapulohumeral atrophy.
(05 Mar 2000)
scapulohumeral muscular dystrophy One of the less well-defined types of muscular dystrophy, probably heterogenous in nature. Onset usually in childhood or early adulthood and both sexes affected. Characterised by weakness and wasting, usually symmetrical, of the pelvic girdle muscles, the shoulder girdle muscles, or both, but not the facial muscles. Muscle pseudohypertrophy, heart involvement, and mental retardation are absent. Variable inheritance.
Synonym: Leyden-Mobius muscular dystrophy, pelvofemoral muscular dystrophy, scapulohumeral muscular dystrophy.
(05 Mar 2000)
pseudohypertrophic muscular dystrophy The most common childhood muscular dystrophy, with onset usually before age 6. Characterised by symmetrical weakness and wasting of first the pelvic and crural muscles and then the pectoral and proximal upper extremity muscles; pseudohypertrophy of some muscles, especially the calf; heart involvement; sometimes mild mental retardation; progressive course and early death, usually in adolescence. X-linked inheritance (affects males and transmitted by females).
Synonym: childhood muscular dystrophy, Duchenne's disease, pseudohypertrophic muscular dystrophy.
(05 Mar 2000)
pulp atrophy Diminution in size and/or cellular elements of the dental pulp due to interference with the blood supply.
(05 Mar 2000)
horizontal atrophy A progressive loss of alveolar and supporting bone surrounding the teeth, beginning at the most coronal level of the bone.
Synonym: horizontal resorption.
(05 Mar 2000)
senile atrophy Wasting of tissues and organs with advancing age from decreased catabolic or anabolic processes, at times due to endocrine changes, decreased use, or ischemia.
Synonym: geromarasmus.
(05 Mar 2000)
serous atrophy A degenerative change occurring in fat cells, the fat being absorbed and its place being taken by a serous fluid.
(05 Mar 2000)
Hunt's atrophy An obsolete term for atrophy of the small muscles of the hand without sensory disturbances; two types are recognised: thenar, from compression of the thenar branch of the median nerve; hypothenar, from compression of the deep palmar branch of the ulnar nerve.
(05 Mar 2000)
smooth muscular sphincter A sphincter of smooth musculature.
Synonym: smooth muscular sphincter.
Origin: G. Lissos, smooth, + sphincter
(05 Mar 2000)
neuritic atrophy Abnormalities of the skin, hair, nails, subcutaneous tissues and bone, caused by peripheral nerve lesions.
Synonym: neuritic atrophy, neurogenic atrophy, neurotrophic atrophy, trophic changes.
(05 Mar 2000)
neurogenic atrophy Abnormalities of the skin, hair, nails, subcutaneous tissues and bone, caused by peripheral nerve lesions.
Synonym: neuritic atrophy, neurogenic atrophy, neurotrophic atrophy, trophic changes.
(05 Mar 2000)
neurotrophic atrophy Abnormalities of the skin, hair, nails, subcutaneous tissues and bone, caused by peripheral nerve lesions.
Synonym: neuritic atrophy, neurogenic atrophy, neurotrophic atrophy, trophic changes.
(05 Mar 2000)
striate atrophy of skin Bands of thin wrinkled skin, initially red but becoming purple and white, which occur commonly on the abdomen, buttocks, and thighs at puberty and/or during and following pregnancy, and result from atrophy of the dermis and overextension of the skin; also associated with ascites and Cushing's syndrome.
Synonym: atrophoderma striatum, lineae albicantes, lineae atrophicae, linear atrophy, stretch marks, stria, striae atrophicae, striate atrophy of skin, traction atrophy, vergeture.
(05 Mar 2000)
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