| CID | 1) Carpal Instability Dissociative; 해리성 주근관절 불안정성 2) Cytomegalic Inclusio... |
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| AIE | acute inclusion-body encephalitis; acute infectious encephalitis; acute infective endocarditis |
| BII | beat inclusion index; Billroth II [operation]; butanol-insoluble iodine |
| CIBHA | congenital inclusion-body hemolytic anemia |
| CID | cellular immunodeficiency; charge injection device; chick infective dose; combined immunodeficiency ... |
| GPIC | Guinea pig inclusion conjunctivitis |
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| IBH | Inclusion Body Hepatitis |
| IB | Inclusion bodies |
| IBM | Inclusion body myositis |
| LBHI | Lewy body-like hyaline inclusion |
| inclusion | 1. The act of including, or the state of being included; limitation; restriction; as, the lines of inclusion of his policy. 2. <chemical> A foreign substance, either liquid or solid, usually of minute size, inclosed in the mass of a mineral. Origin: L. Inclusio: cf. F. Inclusion. See Include. Source: Websters Dictionary (01 Mar 1998) |
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| inclusion blennorrhoea | A neonatal conjunctivitis caused by Chlamydia trachomatis. (05 Mar 2000) |
| inclusion bodies | <cell biology> Nuclear or cytoplasmic structures with characteristic staining properties, usually found at the site of virus multiplication. Semi crystalline arrays of virions, capsids or other viral components. (13 Nov 1997) |
| inclusion bodies, viral | An area showing altered staining behaviour in the nucleus or cytoplasm of a virus-infected cell. Some inclusion bodies represent "virus factories" in which viral nucleic acid or protein is being synthesised; others are merely artifacts of fixation and staining. One example, negri bodies, are found in the cytoplasm or processes of nerve cells in animals that have died from rabies. (12 Dec 1998) |
| inclusion body disease | <disease> An illness in newborns caused by viral infection, symptoms includefever, cellular enlargement, microscopically-visible clumps of viralparticles or proteins in the cytoplasm and nuclei of affected cells, enlargementof the spleen and liver. Long-term effects of the disease may includemental retardation. (09 Oct 1997) |
| inclusion body encephalitis | <neurology> Chronic progressive illness seen in children a few years after measles infection and involving demyelination of the cerebral cortex. Virus apparently persists in brain cells: usually considered a slow virus disease. (18 Nov 1997) |
| inclusion body myositis | <radiology> Common form of inflamatory myopathy, most common in the elderly, equal sex incidence, sporadic idiopathic disease (very rarely familial), misdiagnosed as steroid-resistant polymyositis symptoms, presents as a painless slowly progressive proximal myopathy, may cause dysphagia, mild to moderate muscle wasting diagnosis, serum creatine kinase levels usually normal or only slightly elevated, EMG may show non-specific myopathic features, diagnosis on muscle biopsy, inclusion bodies seen in rimmed vacuoles in skeletal muscle fibres treatment, steroids and immunosuppression generally ineffective, rare patients reported who have made a response to treatment pathogenesis, unknown, ubiquitin, prion protein, tau protein found in inclusions, abnormal mitchondria seen in some case (12 Dec 1998) |
| inclusion body rhinitis | A respiratory disease of pigs caused by the cytomegalovirus porcine herpesvirus 2 and characterised by rhinitis and conjunctivitis in young pigs. (05 Mar 2000) |
| inclusion cell | i cell |
| inclusion cell disease | <biochemistry> Mucolipidosis of early onset and with severe symptoms like those in Hurler's syndrome but with normal urinary mucopolysaccharides, vacuolated lymphocytes, and inclusion bodies in cultured fibroblasts (I-cells). The lysosomes lack hydrolases but high concentrations of lysosomal enzymes are found in the extracellular fluids such as serum, spinal fluid, and urine. It is associated with a deficiency of N-acetylglucosaminyl-1-phosphotransferase. The gene defect responsible probably prevents the addition of the lysosome recognition marker mannose 6 phosphate) to these enzymes so that they are not directed into the lysosomes but are released. Inheritance: autosomal recessive. Synonym: I-cell disease, inclusion cell disease. (12 Jul 2000) |
| inclusion compound | The mechanical trapping of small molecules within spaces between other molecules; e.g., the inclusion of iodine molecules by starch molecules to form the well-known red-to-black "addition compound" (05 Mar 2000) |
| inclusion conjunctivitis | A follicular conjunctivitis caused by Chlamydia trachomatis. (05 Mar 2000) |
| inclusion conjunctivitis viruses | Former name for Chlamydia trachomatis. (05 Mar 2000) |
| inclusion cyst | Intradermal or subcutaneous saclike structure, the wall of which is stratified epithelium containing keratohyalin granules. (12 Dec 1998) |
| inclusion dermoid | A collection of cancerous cells which form cysts that contain one or more of the three primary embryonic germ layers: skin, hair or teeth. (27 Sep 1997) |
| 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) |
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| conjunctivitis, inclusion | An infection of the eyes characterised by the presence in conjunctival epithelial cells of inclusion bodies indistinguishable from those of trachoma. It is acquired by infants during birth and by adults from swimming pools. The aetiological agent is chlamydia trachomatis whose natural habitat appears to be the genito-urinary tract. Inclusion conjunctivitis is a less severe disease than trachoma and usually clears up spontaneously. (12 Dec 1998) |
| Cowdry's type A inclusion bodies | Droplet-like masses of acidophilic material surrounded by clear halos within nuclei, with margination of chromatin on the nuclear membrane. (05 Mar 2000) |
| Cowdry's type B inclusion bodies | Droplet-like masses of acidophilic material surrounded by clear halos within nuclei, without other nuclear changes during early stages of development of the inclusion. (05 Mar 2000) |
| myositis, inclusion body | A progressive inflammatory myopathy primarily involving muscles of the pelvic region and legs, usually seen in older people. The muscles are infiltrated by mononuclear inflammatory cells, sarcoplasmic vacuoles, masses of filaments and filamentous microtubules, and sometimes eosinophilic bodies. (12 Dec 1998) |
| cytomegalic inclusion disease | <disease> An illness in newborns caused by viral infection, symptoms includefever, cellular enlargement, microscopically-visible clumps of viralparticles or proteins in the cytoplasm and nuclei of affected cells, enlargementof the spleen and liver. Long-term effects of the disease may includemental retardation. (09 Oct 1997) |
| cytoplasmic inclusion bodies | See: inclusion bodies. (05 Mar 2000) |
| psittacosis inclusion bodies | Intracytoplasmic chlamydial microcolonies observed in bronchial epithelial cells infected with Chlamydia psittaci. (05 Mar 2000) |
| subacute inclusion body encephalitis | <neurology> Chronic progressive illness seen in children a few years after measles infection and involving demyelination of the cerebral cortex. Virus apparently persists in brain cells: usually considered a slow virus disease. (18 Nov 1997) |
| nuclear inclusion bodies | See: inclusion bodies. (05 Mar 2000) |
| epidermoid inclusion cyst | <radiology> Well-circumscribed radiolucent lesion showing a thin cortical margin that may not be visible in its entirety, frequently in the terminal phalanx, history of penetrating trauma is often elicited Differential diagnosis: ABC, enchondroma (12 Dec 1998) |
| foetal inclusion | Unequal conjoined twins in which the incompletely developed parasite is wholly enclosed in the autosite. (05 Mar 2000) |
Synonyms : Bodies, Inclusion, Body, Inclusion, Cellular Inclusion, Cytoplasmic Inclusion, Inclusion Body, Inclusion, Cellular, Inclusion, Cytoplasmic, Inclusions, Cellular, Inclusions, Cytoplasmic
Synonyms : Negri Body, Bodies, Negri, Bodies, Viral Inclusion, Body, Negri, Body, Viral Inclusion, Inclusion Body, Viral, Viral Inclusion Body
| inclusion body encephalitis |
subacute sclerosing panencephalitis: a rare chronic progressive encephalitis caused by the measles virus and occurring primarily in children and young adults; death usually occurs within three years; characterized by primary measles infection before the age of two years
출처: wordnet.princeton.edu/perl/webwn
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| inclusion |
the state of being included the relation of comprising something; "he admired the inclusion of so many ideas in such a short work" inclusion body: any small intracellular body found within another (characteristic of certain diseases); "an inclusion in the cytoplasm of the cell" the act of including
출처: wordnet.princeton.edu/perl/webwn
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| inclusion body |
any small intracellular body found within another (characteristic of certain diseases); "an inclusion in the cytoplasm of the cell"
출처: wordnet.princeton.edu/perl/webwn
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| inclusion body myositis |
myositis characterized by weakness of limb muscles (especially the thighs and wrists and fingers); sometimes involves swallowing muscles; onset after 50 and slowly progressive; seen more often in men than in women
출처: wordnet.princeton.edu/perl/webwn
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| inclusion |
(in
출처: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
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| inclusion | the act of including |
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| inclusion | any small intracellular body found within another (characteristic of certain diseases) |
| inclusion | the relation of comprising something |
| inclusion | the state of being included |
| inclusion | any small intracellular body found within another (characteristic of certain diseases) |
| inclusion | a rare chronic progressive encephalitis caused by the measles virus and occurring primarily in children and young adults |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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