| CPK-BB | creatine phosphokinase, brain-type |
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| CR1 | complement receptor type 1 |
| CRPS | complex regional pain syndrome [type I and II] |
| CSB | contaminated small bowel; craniosynostosis, Boston type |
| DAT | delayed-action tablet; dementia Alzheimer's type; dental aptitude test; diacetylthiamine; diet as to... |
| Ellis type II | <nephrology> A type of nephritis that is characterised by low serum albumin, large amount of protein in the urine and swelling (oedema). Swelling, weight gain, high blood pressure and anorexia are key features. Nephrotic syndrome can be seen with a number of illness that cause damage to the kidney glomerulus. Examples include diabetes, hereditary disorders, lupus, multiple myeloma, amyloidosis, glomerulonephritis, minimal change disease and membranous glomerulonephritis. (27 Sep 1997) |
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| erotomanic type of paranoid disorder | The false belief that one is loved by another such as a movie star or a casual acquaintance. (05 Mar 2000) |
| tuberculin-type hypersensitivity | A local or generalised response that begins 24 to 48 hours after exposure to an antigen. See: cell-mediated reaction. Synonym: contact hypersensitivity, delayed hypersensitivity, late reaction, tuberculin-type hypersensitivity. (05 Mar 2000) |
| jealous type of paranoid disorder | The false belief that one's spouse or lover is unfaithful and leading to repeated confrontation, or the taking of extraordinary steps to intervene in the imagined infidelity. (05 Mar 2000) |
| Farr type assay | <investigation> Method of radioimmunoassay in which free antigen remains soluble and antibody antigen complexes are precipitated. (18 Nov 1997) |
| undifferentiated type fever | A term applied to illnesses resulting from infection by any one of the arboviruses pathogenic for man, in which the only constant manifestation is fever; rash, lymphadenopathy, or arthralgia (alone or in combination) may occur in some individuals but not in others; some arboviruses may induce infections in which undifferentiated type fever is the only manifestation, whereas other arboviruses may induce in some persons only undifferentiated fever, and in other persons similar fever followed by secondary manifestations, e.g., a haemorrhagic fever or encephalitis. (05 Mar 2000) |
| "e"-type cholinesterase | <enzyme, neurology, physiology> An enzyme that breaks down unused acetylcholine in the synaptic cleft (the space between neurons), this enzyme is necessary to restore the synaptic cleft so it is ready to transmit the next nerve impulse. (06 May 1997) |
| Langhans'-type giant cells | Multinucleated giant cell's seen in tuberculosis and other granulomas; the nuclei are arranged in an arciform manner at the periphery of the cell's. Synonym: Langhans'-type giant cells. Synonym: cytotrophoblastic cells. (05 Mar 2000) |
| Laron type dwarfism | Dwarfism associated with an absent or very low levels of somatomedin C (insulin-like growth factor I) or abnormalities in receptor activity. (05 Mar 2000) |
| F-type ATPase | <enzyme> One of three major classes of ion transport ATPase, characterised by a multi subunit structure and a lack of a phosphorylated intermediate. See: ATP synthase, P-type ATPase, V-type ATPase. (18 Nov 1997) |
| type |
The description of the data and the operations that can be performed on or by the data. See data type.
출처: davinci01.man.ac.uk/ibmcxx/glossary/t.htm
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| type II error |
The error made when a false null hypothesis is not rejected.
출처: www.measurementexperts.org/instrument/term_pocket_...
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| type II error |
In a hypothesis test, a Type II error occurs when the null hypothesis is not rejected when it is, in fact, false. For example, in a clinical trial of a new drug, the null hypothesis might be that the new drug is no better, on average, than the current drug. A Type II error would occur if it were concluded that the two drugs produced the same effect when, in fact, they produced different ones. Contrast with Type I error.
출처: www.etr.org/recapp/research/researchglossary.htm
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| type 1 d. mellitus |
one of the two major types of diabetes mellitus, characterized by abrupt onset of symptoms, insulinopenia, and dependence on exogenous insulin to sustain life; peak age of onset is 12 years, although onset can be at any age. It is due to lack of insulin production by the beta cells of the pancreas, which may result from viral infection, autoimmune reactions, and probably genetic factors; islet cell antibodies are usually detectable at diagnosis. When it is inadequately controlled, lack of insulin causes hyperglycemia, protein wasting, and production of ketone bodies owing to increased fat metabolism, and the hyperglycemia leads to overflow glycosuria, osmotic diuresis, hyperosmolarity, dehydration, and diabetic ketoacidosis. It is accompanied by angiopathy of blood vessels, particularly the small ones (microangiopathy), which affects the retinas, kidneys, and basement membrane of arterioles throughout the body. Other symptoms include polyuria, polydipsia, polyphagia, weight loss, paresthesias, blurred vision, and irritability; if untreated, diabetic ketoacidosis progresses to nausea and vomiting, stupor, and potentially fatal hyperosmolar coma. Called also insulin-dependent d. mellitus, juvenile or juvenile-onset d. mellitus, and Type I d. mellitus.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| type 1 renal tubular a. |
distal renal tubular a.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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