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  • amyloidosis primary
    ¿ø¹ß¼º(ê«Û¡àõ) ¾Æ¹Ð·ÎÀ̵åÁõ.
  • amyloidosis ulcer
    À¯ÀüºÐÁõ(ëºîþÝÏñø) ±Ë¾ç(Ï÷åË)
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  • amyloidosis primary
    ¿ø¹ß¼º(ê«Û¡àõ) ¾Æ¹Ð·ÎÀ̵åÁõ.
  • amyloidosis ulcer
    À¯ÀüºÐÁõ(ëºîþÝÏñø) ±Ë¾ç(Ï÷åË)
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AP   1) Alkaline Phosphatase
    = ALP
  2) Amyloid Plasm...
FAC Familial Amyloid Cardiomyopathy
FAP Familial Amyloid Polyneuropathy
IAPP Insulinoma Amyloid Poly-Peptide
SAA   1) Severe Aplastic Anemia
  2) Serum Amyloid A protein
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APLP amyloid precursor-like protein
APP Amyloid Protein Precursor
A beta Amyloid beta
A beta Amyloid beta peptide
APP Amyloid beta precursor protein
CancerWEB ¿µ¿µ ÀÇÇлçÀü ¸ÂÃã °Ë»ö °á°ú : 9 ÆäÀÌÁö: 2
amyloid protein saa A serum protein believed to be a circulating precursor to amyloid protein aa. It is present in low concentrations in normal sera, but found in much higher concentrations in sera of older persons and in patients with amyloidosis or with diseases known to predispose to amyloidosis. Very high levels of this protein have been reported during acute inflammatory episodes. Antisera to amyloid protein aa cross-react with protein saa.
(12 Dec 1998)
amyloid tumour A localised form of amyloidosis in which amyloid occurs as masses or nodules beneath the skin or mucous membranes, e.g., in the larynx.
Synonym: amyloid tumour, focal amyloidosis.
(05 Mar 2000)
amyloidal Resembling or containing amyl; starchlike.
<medicine> Amyloid degeneration, a diseased condition of various organs of the body, produced by the deposit of an albuminous substance, giving a blue colour with iodine and sulphuric acid.
Synonym: waxy or lardaceous degeneration.
Origin: L. Amylum starch.
Source: Websters Dictionary
(01 Mar 1998)
amyloidogenic glycoprotein <protein> An integral membrane glycoprotein of the brain and related to the Drosophila vnd gene product. A precursor of _ amyloid, that accumulates in Alzheimer's disease and Down's syndrome.
See: amyloid precursor protein.
(18 Nov 1997)
amyloidosis Deposition of amyloid. A common complication of several diseases (leprosy, tuberculosis), often associated with perturbation of the immune system, although there may be immunosuppression or enhancement.
(18 Nov 1997)
amyloidosis cutis Localised cutaneous amyloidosis with pruritic brownish-red papules, most commonly on the lower legs, due to amyloid infiltration of the papillary dermis.
Synonym: amyloidosis cutis, lichen amyloidosis.
Origin: G. Leichen, lichen, a lichen-like eruption + eidos, resemblance
(05 Mar 2000)
amyloidosis of multiple myeloma Foci of amyloidosis in mesenchymal tissues of some persons with multiple myeloma; no direct relation between amyloid and Bence Jones protein is conclusively known.
(05 Mar 2000)
amyloidosis: bone manifestations <radiology> Joint pain without radiographic findings, osteoporosis, especially in axial skeleton, lytic lesions that destroy cortex and invade soft tissue, wrist, scaphoid and lunate lesions that may extend into the carpal tunnel, inducing the classic complaints of carpal tunnel syndrome amyloid arthropathy Differential diagnosis: pigmented villonodular synovitis, synovial chondromatosis, rheumatoid arthritis, TB
(12 Dec 1998)
amyloidosis: gastrointestinal manifestations <radiology> Oesophagus, loss of peristalsis, megaesophagus, stomach, small and rigid (simulate linitis plastica), effaced rugal pattern, diminished/absent peristalsis, may be localised to antrum, amyloidoma: well defined submucosal mass, small bowel, diffuse form (more common), diffuse, uniform thickening of valvulae conniventes, broadened flat undulated mucosal folds (mucosal atrophy), jejunalization of ileum, impaired motility, small bowel dilatation, localised form: multiple small deposits; associated with pseudoobstruction, colon, psudopolyps
(12 Dec 1998)
MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 3 ÆäÀÌÁö: 2
  • Amyloid Precursor Protein Secretases - »õâ Endopeptidases that are specific for AMYLOID PROTEIN PRECURSOR. Three secretase subtypes referred to as alpha, beta, and gamma have been identified based upon the region of amyloid protein precursor they cleave.
    Synonyms : APP Secretase, Amyloid Precursor Protein Secretase, Secretase, Secretases, alpha-Secretase, beta-Secretase, gamma-Secretase, Secretase, APP, alpha Secretase, beta Secretase, gamma Secretase
  • Amyloidosis - »õâ A group of sporadic, familial and/or inherited, degenerative, and infectious disease processes, linked by the common theme of abnormal protein folding and deposition of AMYLOID. As the amyloid deposits enlarge they displace normal tissue structures, causing disruption of function. Various signs and symptoms depend on the location and size of the deposits.
    Synonyms : Amyloidoses
  • Amyloidosis, Familial - »õâ Diseases in which there is a familial pattern of AMYLOIDOSIS.
    Synonyms : Amyloidoses, Familial, Amyloidoses, Hereditary, Familial Amyloidoses, Familial Amyloidosis, Hereditary Amyloidoses, Hereditary Amyloidosis
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amyloidosis A group of diseases in which protein is deposited in specific organs (localized amyloidosis) or throughout the body (systemic amyloidosis). Amyloidosis may be either primary (with no known cause) or secondary (caused by another disease, including some types of cancer). Generally, primary amyloidosis affects the nerves, skin, tongue, joints, heart, and liver; secondary amyloidosis often affects the spleen, kidneys, liver, and adrenal glands.
Ãâó: www.stjude.org/glossary
amyloidosis A rare condition in which certain blood cells produce an abnormal protein that deposits in the tissues. If the deposits are in the heart, heart failure can result.
Ãâó: www.bdid.com/termsa.htm
amyloid Of spore walls, spore ornamentation, hyphal walls, ascus tips, etc.: Staining blue or grayish to blackish-violet in Melzer's reagent, presumably because of the presence of starch or a starch-like compound. (17)
Ãâó: ppathw3.cals.cornell.edu/glossary/Defs_A.htm
amyloidosis a disease characterized by extracellular deposition in connective tissue of a carbohydrate-protein material, amyloid
Ãâó: www.southalabama.edu/alliedhealth/cls/Ravine/gloss...
amyloid the extracellular protein substance deposited in amyloidosis. It is a waxy, amorphous, eosinophilic, hyalinelike material that exhibits red-green birefringence under polarized light when stained with Congo red. Amyloid deposits are composed of straight, non-branching fibrils with a diameter of 7.5 to 10 nm and indefinite length. ...
Ãâó: www.uwo.ca/pathol/glossary.html
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