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  • ¿µ¹®
    ÇѱÛ
  • amyloid nephrosis
    ¾Æ¹Ð·ÎÀ̵åÄáÆÏÁõ, ¾Æ¹Ð·ÎÀ̵å½ÅÀåÁõ
  • cryptogenic nephrosis
    ÀẹÄáÆÏÁõ, Àẹ½ÅÀåÁõ
  • hemoglobinuric nephrosis
    Çì¸ð±Û·Îºó´¢ÄáÆÏÁõ, Ç÷»ö¼Ò´¢½ÅÀåÁõ
  • myeloma nephrosis
    °ñ¼öÁ¾ÄáÆÏÁõ, °ñ¼öÁ¾½ÅÀåÁõ
  • nephrosis
    ÄáÆÏÁõ, ½ÅÀåÁõ
  • lipid
    ÁöÁú
  • lipid granule
    Áö¹æ°ú¸³
  • lipid infiltration
    ÁöÁúħÀ±
  • lipid layer
    ÁöÁúÃþ
  • lipid pneumonia
    ÁöÁúÆó·Å
  • lipid proteinosis
    ÁöÁú´Ü¹éÁõ
  • lipid solubility
    ÁöÁú¿ëÇØµµ
  • lipid storage disease
    ÁöÁúÃàÀûº´
  • lipid-soluble
    Áö¿ë¼º-
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  • ¿µ¹®
    ÇѱÛ
  • lipid
    ÁöÁú
  • nephrosis
    ÄáÆÏÁõ, ½ÅÀåÁõ
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  • ¿µ¹®
    ÇѱÛ
  • amyloid nephrosis
    ¾Æ¹Ð·ÎÀ̵åÄáÆÏÁõ
  • cryptogenic nephrosis
    ÀẹÄáÆÏÁõ
  • hemoglobinuric nephrosis
    Ç÷»ö¼Ò´¢ÄáÆÏÁõ
  • myeloma nephrosis
    °ñ¼öÁ¾ÄáÆÏÁõ
  • nephrosis
    ÄáÆÏÁõ, ½ÅÀåÁõ
  • toxic nephrosis
    µ¶¼ºÄáÆÏÁõ
  • lipid storage disease
    ÁöÁúÃàÀûº´
  • lipid granule
    Áö¹æ°ú¸³
  • lipid hypothesis
    ÁöÁú°¡¼³
  • lipid infiltration
    ÁöÁúħÀ±
  • lipid
    ÁöÁú
  • lipid-soluble
    Áö¿ë¼º-
  • lipid layer
    ÁöÁúÃþ
  • lipid pneumonia
    ÁöÁúÆó·Å
  • lipid proteinosis
    ÁöÁú´Ü¹éÁõ
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  • ¿µ¹®
    ÇѱÛ
  • amyloid nephrosis
    ¾Æ¹Ð·ÎÀ̵å½ÅÁõ(¡­ãìñø).
  • hemoglobinuric nephrosis
    Ç÷»ö¼Ò´¢¼º ½ÅÁõ.
  • hemoglobinuric nephrosis
    Ç÷»ö¼Ò´¢¼º ½ÅÁõ
  • Dorfman-Chanarin syndrome = neutral lipid storage disease
    Áß¼ºÁö¹æÃàÀûÁõ
  • Lipid Research Clinic
    ÁöÁú¿¬±¸Áø·á¼Ò
  • Lipid bilayer
    Áö¹æÀÌÁßÃþ(ò·Û¸ì£ñìöµ)
  • free radical formation,lipid peroxidation
    ÀÚÀ¯ ·¡µðÄ® Çü¼º, ÁöÁú °ú»êÈ­(ò·òõ Φ߫ûù)
  • granule, lipid
    Áö¹æ°ú¸³
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  • ¿µ¹®
    ÇѱÛ
  • amyloid nephrosis
    ¾Æ¹Ð·ÎÀ̵å½ÅÁõ(¡­ãìñø).
  • cryptogenic nephrosis
    Àẹ¼º ½ÅÁõ(¡­ãìñø).
  • hemoglobinuric nephrosis
    Ç÷»ö¼Ò´¢¼º ½ÅÁõ.
  • hemoglobinuric nephrosis
    Ç÷»ö¼Ò´¢¼º ½ÅÁõ
  • lipoid nephrosis
    ¸®Æ÷À̵å½ÅÁõ(¡­ãìñø), À¯ÁöÁú½ÅÁõ.
  • lipoid nephrosis
    À¯ÁöÁú ½ÅÁõ, ¹Ì¼Òº´º¯ ½ÅÁõÈıº(Ú°á³Ü»Ü¨ ãìñøý¦ÏØ)
  • lower nephron nephrosis
    ÇϺγ×ÇÁ·Ð½ÅÁõ(ù»Ý»¡­ãìñø).
  • myeloma nephrosis
    °ñ¼öÁ¾¼º ½ÅÁõ(¡­àõ ãìñø)
  • nephrosis
    ½ÅÁõ
  • nephrosis
    ½ÅÁõ(ãìñø).
  • nephrosis
    ½ÅÁõ(¡­ñø)
  • syphilitic nephrosis
    ¸Åµ¶¼º ½ÅÁõ(¡­ãìñø).
  • toxic nephrosis
    Áßµ¶¼º½ÅÁõ(¡­ãìñø)
  • blood lipid
    Ç÷¾×ÁöÁú(úìäûò·òõ).
  • fecal lipid
    ºÐº¯Áö¹æ
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  • ¿µ¹®
    ÇѱÛ
  • Lipid drop
    Áö¹æ¹æ¿ï
    [¿¾ ¿ë¾î] Áö¹æ¼ÒÀû
  • Lipid droplet
    Áö¹æ¹æ¿ï
    [¿¾ ¿ë¾î] Áö¹æ¼ÒÀû
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    ÇѱÛ
  • bare lipid membrane
    ¾Ë¸ö ÁöÁú¸·(ò·òõد)
  • bilayer lipid membrane
    ¾çÃþ ÁöÁú¸·(å»öµ ò·òõد)
  • bimolecular lamellar lipid membrane
    À̺ÐÀÚ(ì£ÝÂí­) ÆÇ»óÁöÁú¸·(÷ùßÒò·òõد)
  • bimolecular lipid membrane
    À̺ÐÀÚ ÁöÁú¸·(ì£ÝÂí­ò·òõد)
  • black lipid membrane
    Èæ ÁöÁú¸·(ýÙò·òõد)
  • C55 lipid carrier
    "C55 ÁöÁú¿î¹Ýü(ò·òõê¡Úæô÷),(ÔÒ) bactoprenol"
  • complex lipid
    º¹ÇÕÁöÁú(ÜÜùêò·òõ)
  • compound lipid
    "È­ÇÕÁöÁú(ûùùêò·òõ), (ÔÒ) complex lipid"
  • derived lipid
    À¯µµÁöÁú(ë¯Óôò·òõ)
  • diol lipid
    ´ÙÀÌ¿ÃÁöÁú(ò·òõ)
  • high-lipid lipoprotein
    °íÁöÁú ÁöÁú´Ü¹éÁú(ÍÔò·òõò¢òõÓ±ÛÜòõ)
  • lipid
    ÁöÁú(ò·òõ)
  • lipid bilayer
    ÁöÁú¾çÃþ(ò·òõÕ×öµ)
  • lipid-globular protein mosaic model
    "ÁöÁú-±¸»ó´Ü¹éÁú(ò·òõϹßÒÓ±ÛÜòõ) , ¸ðÀÚÀÌÅ©¸ðµ¨"
  • lipid imbibition theory
    ÁöÁúÈí¼öÀÌ·Ð(ò·òõýåâ¥ìµÖå)
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    ÇѱÛ
  • nephrosis
    ½ÅÁõ
  • lipid bound proton
    Áö¹æ°áÇվ缺ÀÚ
  • lipid-laden
    Áö¹æÀûÀç
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
LN Lesch-Nyhan [syndrome]; lipoid nephrosis; Lisch nodule; low necrosis; lupus nephritis; lymph node
Neph nephron; nephritis; nephrosis
ALLHAT Antihypertensive and Lipid Lowering Treatment to Prevent Heart Attack Trial
ANRL antihypertensive neutral renomedullary lipid
BLM bilayer lipid membrane; bimolecular liquid membrane; bleomycin; buccolinguomasticatory
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
PAN Puromycin Aminonucleoside nephrosis
LN lipoid nephrosis
MLA 4'-Monophosphoryl lipid A
ALBP Adipocyte lipid binding protein
ABLC Amphotericin B Lipid Complex
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • lipid bilayer
    Áö¹æÁú Ãþ
    ¼¼Æ÷¸·Àº ÁöÁú ÀÌÁß ÃþÀ̶ó Çϸç, ÀÌ Áö¹æÁú ÃþÀº ÁÖ·Î ÀÎ ÁöÁú¿¡ ÀÇÇØ ±¸¼ºµÇ¾î ÀÖ´Ù. ÀÎ ÁöÁúÀº Ä£¼ö¼º°ú ¼Ò¼ö¼º ºÎÀ§·Î ±¸¼ºµÇ¾î ¼¼Æ÷¸·ÀÇ ¹°Áú À̵¿¿¡ ¿µÇâÀ» ³¢Ä£´Ù. ¶Ç Áö¹æÁú ÃþÀÇ ÄÝ·¹½ºÅ×·ÑÀº ÀÌ ÃþÀÇ ¾ÈÁ¤È­¸¦ µ½´Â´Ù.
  • lipid metabolism
    ÁöÁú ´ë»ç
    °£¿¡¼­ ÈçÈ÷ ÀϾ¸ç Áö¹æ»êÀÇ º£Å¸-»êÈ­ ¹× ¾Æ¼¼Æ® ¾Æ¼¼Å×ÀÌÆ® Çü¼º, ´ç ÁöÁú »ý¼º, ÄÝ·¹½ºÅ×·Ñ ¹× ÀÎ ÁöÁú Çü¼º, ´ç°ú ´Ü¹éÁú·ÎºÎÅÍ Áö¹æÀÇ Àüȯ µîÀÌ °¡Àå ´ëÇ¥ÀûÀÌ´Ù.
  • lipid proteinosis
    ÁöÁú ´Ü¹éÁõ
  • lipid storage
    Áö¹æ ÀúÀå
    Áö¹æ ¼¼Æ÷°¡ ´ã´çÇÏ´Â ±â´ÉÀ¸·Î ü³»¿¡ Èí¼öµÈ Áö¹æÀº ų·Î¹ÌÅ©·ÐÀÇ ÇüÅ·Πü¼øÈ¯À» ÇÏ°Ô µÇ¸ç, Áö¹æ Á¶Á÷ÀÇ ¸ð¼¼Ç÷°ü¿¡ À̸£¸é ³»ÇÇ ¼¼Æ÷ÀÇ ´çÁöÁú ¸®ÆÄ¾ÆÁ¦ÀÇ ÀÛ¿ëÀ¸·Î À¯¸® Áö¹æ»ê°ú ´Ü´ç·ù·Î ºÐÇØµÇ¾î Áö¹æ ¼¼Æ÷¿¡ ÀÇÇØ ´Ü¼ø È®»êÀ¸·Î ¼·ÃëµÈ´Ù. ÀÌ Áö¹æ»êÀº Áö¹æ ÇÕ¼º È¿¼Ò¿¡ ÀÇÇÏ¿© Áß¼º Áö¹æÀ¸·Î ÇÕ¼ºµÇ¸ç Áö¹æ ºÐÇØ È¿¼Ò¸¦ ¾ïÁ¦ÇÏ¿© Áö¹æÀ» ÃàÀû½ÃŲ´Ù.
  • lipid-filled histocyte
    ÁöÁú·Î ä¿öÁø Á¶Á÷±¸
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
acute lobar nephrosis A severe but localised bacterial infection of the renal parenchyma that may produce a mass effect simulating a renal abscess.
(05 Mar 2000)
acute nephrosis Acute oliguric renal failure, especially that caused by certain poisons.
(05 Mar 2000)
amyloid nephrosis The nephrotic syndrome due to deposition of amyloid in the kidney.
See: renal amyloidosis.
(05 Mar 2000)
bile nephrosis <gastroenterology, nephrology> Acute renal failure occurring in a patient with liver failure. The exact causal relationship in unclear, but those with alcoholic cirrhosis and alcoholic hepatitis are at greatest risk.
Symptoms include decreased or absent urine production, jaundice, abdominal swelling, delirium, confusion, nausea and vomiting. Prognosis is very poor.
(27 Sep 1997)
vacuolar nephrosis Vacuolation of the epithelial cytoplasm of renal convoluted tubules in patients seriously depleted of potassium; vacuoles do not contain fat or glycogen, concentrating ability is impaired, polyuria and polydipsia are common, and pyelonephritis may develop.
Synonym: vacuolar nephrosis.
(05 Mar 2000)
cholaemic nephrosis An obsolete term for the occurrence of acute renal failure in jaundiced patients; the kidneys contain tubular casts of bile and may show tubular necrosis, but there is little evidence that jaundice or bile casts directly damage the kidneys.
(05 Mar 2000)
cholemic nephrosis <nephrology> Acute renal failure occurring in a patient with liver failure. The exact causal relationship in unclear, but those with alcoholic cirrhosis and alcoholic hepatitis are at greatest risk.
Symptoms include decreased or absent urine production, jaundice, abdominal swelling, delirium, confusion, nausea and vomiting. Prognosis is very poor.
(15 Jan 1998)
haemoglobinuric nephrosis Acute oliguric renal failure associated with haemoglobinuria, due to massive intravascular haemolysis, e.g., following an incompatible blood transfusion; the kidneys show the morphologic changes of hypoxic nephrosis.
(05 Mar 2000)
hypoxic nephrosis Acute oliguric renal failure following haemorrhage, burns, shock, or other causes of hypovolaemia and reduced renal blood flow; frequently associated with patchy tubular necrosis, tubulorrhexis, and distal tubular casts of haemoglobin.
(05 Mar 2000)
nephrosis 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)
nephrosis, lipoid Glomerular disease causing heavy proteinuria characterised by absence of obvious histologic glomerular changes on light microscopy. It is also called minimal change glomerular disease and minimal lesion glomerulonephritis.
(12 Dec 1998)
osmotic nephrosis Swelling of renal tubular epithelium associated with glomerular filtration of sugars and dextrose; the swelling is due to formation of cytoplasmic vesicles by pinocytosis, and is reversible, probably with no dysfunction, when produced by glucose or mannitol.
(05 Mar 2000)
toxic nephrosis Acute oliguric renal failure due to chemical poisons, septicaemia, or bacterial toxaemia; frequently associated with extensive necrosis of proximal convoluted tubules.
(05 Mar 2000)
familial nephrosis The nephrotic syndrome appearing in sibs in infancy, without nerve deafness.
(05 Mar 2000)
lipoid nephrosis <nephrology> A disorder of the kidneys which largely affects the glomerulus, the blood filtering structure. This disorder is one common cause of nephrotic syndrome in children affecting 2 to 3 children per 100,000 population under age 16 in the us. Minimal change disease is also seen rarely in adults.
The cause is unknown but may be related to an autoimmune illness. Risk factors include a history for a immune disorder, recent immunisation or a bee sting.
Diagnosis is made by renal biopsy. Treatment include systemic corticosteroids which are usually quite effective in curing this disease. Other medications include chlorambucil and cyclophosphamide. In most cases, a moderate protein diet (1 gram protein per Kg body weight per day) will be recommended. Salt (sodium) restriction can be helpful to reduce swelling and vitamin D is usually supplemented.
(27 Sep 1997)
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  • nephrosis
    (º´¸®)»óÇǼº ½ÅÀåÁõ
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