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         Lipoid Nephrosis:     more detail

21. Arch Intern Med -- Abstract: Lipoid Nephrosis Appearing As Acute Oliguric Renal
This case suggests that lipoid nephrosis can appear as acute oliguric renalfailure without historical or physical evidence of preexisting nephrotic
http://archinte.ama-assn.org/cgi/content/abstract/140/3/403
Select Journal or Resource JAMA Archives of Dermatology Facial Plastic Surgery Family Medicine (1992-2000) General Psychiatry Internal Medicine Neurology Ophthalmology Surgery Student JAMA (1998-2004) JAMA CareerNet For The Media Meetings Peer Review Congress
Vol. 140 No. 3, March 1, 1980 Featured Link E-mail Alerts ARTICLE Article Options Send to a Friend Similar articles in this journal Literature Track Add to File Drawer Download to Citation Manager PubMed citation Articles in PubMed by Hulter HN Bonner EL Articles that cite this article Contact me when this article is cited
Lipoid nephrosis appearing as acute oliguric renal failure
H. N. Hulter and E. L. Bonner Jr
Acute oliguric renal failure previously was reported to develop in patients with preexisting idiopathic nephrotic syndrome in association with clinical evidence of vascular volume depletion. We describe an 81-year-old man without recent proteinuria or evidence of preexisting nephrotic syndrome in whom acute oliguric renal failure developed. Renal biopsy disclosed minimal change disease. Nephrotic range proteinuria without severe hypoalbuminemia

22. Lipoid Nephrosis; Clinical And Biochemical Studies Of 40 Children, With 10 Necro
lipoid nephrosis; Clinical and biochemical studies of 40 children, with 10 necropsies.WM Block, RL Jackson, G Stearns and MP Butsch
http://pediatrics.aappublications.org/cgi/content/abstract/1/6/733
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This Article P Rs: Submit a response Alert me when this article is cited Alert me when P ... Alert me if a correction is posted Services E-mail this article to a friend Similar articles in this journal Alert me to new issues of the journal Add to My File Cabinet ... Download to citation manager PubMed Articles by Block, W. M. Articles by Butsch, M. P. Pediatrics, Jun 1948, 733-753, Vol 1, No. 6
Lipoid nephrosis; Clinical and biochemical studies of 40 children, with 10 necropsies
WM Block, RL Jackson, G Stearns and MP Butsch
Department of Pediatrics, College of Medicine, State University of Iowa. Our purpose is to present experiences gained from the study of children with nephrosis observed in the Children's Hospital of the State University of Iowa during the past 15 years. The diagnosis of nephrosis was made only when the following criteria were met: presence of edema, proteinuria, good renal concentration ability, high blood fats and low blood protein with marked decrease in the albumin fraction; absence of retinopathy, persistent

23. Lipoid Nephrosis
lipoid nephrosis. Nephrotic syndrome. Electron micrograph. Previous Next 1 2 3 4 5 Return to Systemic Pathology Page.
http://biomed.brown.edu/Courses/BI279/Lec09/Lec09-D.htm
Lipoid Nephrosis
Nephrotic syndrome.
Electron micrograph.
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24. Intraglomerular Fibrin, Platelet Aggregation, And Subendothelial Deposits In Lip
platelet aggregates, and subendothelial deposits in lipoid nephrosis.Fibrin formation was found in 10 cases of active lipoid nephrosis.
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=322467

25. MUCOLYTIC ENZYME SYSTEMS. XI. HYALURONIDASE INHIBITOR AND SERUM MUCOPROTEINS IN
HYALURONIDASE INHIBITOR AND SERUM MUCOPROTEINS IN PATIENTS WITH lipoid nephrosisAND ACUTE GLOMERULONEPHRITIS 1. Vincent C. Kelley,2 Robert A. Good,3 David
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=436198

26. Lipoid Nephrosis » Medical Diagnosis
lipoid nephrosis. Medical Diagnosis » L » lipoid nephrosis 581.3 lipoidnephrosis (see images) Want to discuss this term?
http://www.medfamily.org/diagnosis/L/diagnosis-terms-Lipoid_nephrosis.phtml
Medical Diagnosis

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Lipoid nephrosis
Lipoid nephrosis
OVERVIEW:
Nephrosis characterized by edema, albuminuria, changes in lipids and proteins in the blood, accumulation of globules of cholesterol esters in the tubular epithelium of the kidney.
CAUSES:
TREATMENT
MISCELLANEOUS
SYNONYMS:
ICD-9-CM:
581.3 lipoid nephrosis
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Want to discuss this term? Visit our forum or our chat room SEE ALSO (Enter the keywords below into our search box or click on the link): Bulimia nervosa
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Hypokalemia

Renal failure, acute (ARF)

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27. Karger Publishers
Cytokine mRNA Profile in lipoid nephrosis Evidence for Increased IL8 mRNAStability Paul F. Laflam, Soichi Haraguchi, Eduardo H. Garin
http://content.karger.com/ProdukteDB/produkte.asp?Doi=65022

28. Minimal Change Disease(lipoid Nephrosis)
Minimal change disease(lipoid nephrosis) Minimal change disease(lipoid nephrosis).Histologically normalappearing glomeruli are seen in a renal biopsy
http://ajoupath.ajou.ac.kr/slides/kd6.htm

29. A Study Of The Renal Handling Of Water In Lipoid Nephrosis -- Gur Et Al. 10 (3):
Children with lipoid nephrosis were studies during clinical relapse and aftercomplete remission. As expected, the calculated serum oncotic pressure was
http://www.pedresearch.org/cgi/content/abstract/10/3/197
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This Article correspondence: Submit a response Alert me when this article is cited Alert me when correspondence are posted Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager PubMed PubMed Citation Articles by Gur, A. Articles by Hayslett, J. P.
ARTICLES
A study of the renal handling of water in lipoid nephrosis
A Gur, PY Adefuin, NJ Siegel and JP Hayslett
Children with lipoid nephrosis were studies during clinical relapse and after complete remission. As expected, the calculated serum oncotic pressure was reduced severely from the remission value of 28.6 +/- 0.9 mm Hg to 15.4 +/- 1.1 (P less than 0.005) during relapse. Although no apparent change in plasma volume was noted using the volume of distribution of labeled human albumin, calculated plasma volume was reduced 13 +/- 8% during relapse when estimated from changes in hematocrit. After a water

30. Abnormal RNA Processing And Altered Expression Of Serin-Rich Proteins In Minimal
diagnosis, clinical course and treatment of lipoid nephrosis. Shalhoub RJ1974 Pathogenesis of lipoid nephrosis a disorder of Tcell function.
http://www.pedresearch.org/cgi/content/full/57/1/133
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Published online before print November 5, 2004
This Article Abstract Full Text (PDF) All Versions of this Article:
01.PDR.0000148013.53429.5Bv1

most recent correspondence: Submit a response Alert me when this article is cited Alert me when correspondence are posted Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager PubMed PubMed Citation Articles by GRIMBERT, P. Articles by SAHALI, D. Pediatric Research
International Pediatric Research Foundation, Inc.

DOI: 10.1203/01.PDR.0000148013.53429.5B
Abnormal RNA Processing and Altered Expression of Serin-Rich Proteins in Minimal-Change Nephrotic Syndrome
PHILIPPE GRIMBERT VINCENT AUDARD ASTA VALANCIUTE PHILIPPE LANG and DJILLALI SAHALI
ABSTRACT TOP
ABSTRACT INTRODUCTION METHODS RESULTS DISCUSSION NOTES REFERENCES Mechanisms underlying the pathophysiology of minimal-change nephrotic syndrome (MCNS), the most frequent glomerular disease

31. EMedicine - Nephrotic Syndrome : Article By Luther Travis, MD
Synonyms and related keywords NS, nephrosis, lipoid nephrosis, Briefly, thename was modified to lipoid nephrosis after the routine finding of lipid
http://www.emedicine.com/PED/topic1564.htm
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Nephrotic Syndrome
Last Updated: April 14, 2005 Rate this Article Email to a Colleague Synonyms and related keywords: NS, nephrosis, lipoid nephrosis, primary nephrotic syndrome, primary NS, PNS, idiopathic nephrotic syndrome, idiopathic NS, INS, secondary nephrotic syndrome, secondary NS, minimal change nephrotic syndrome, MCNS, minimal lesion nephrotic syndrome, MLNS, nil disease, steroid-sensitive nephrotic syndrome, SSNS, steroid-resistant nephrotic syndrome, SRNS, steroid-dependent nephrotic syndrome, SDNS, mesangial proliferative glomerulonephritis, MPN, immunoglobulin M nephropathy, focal segmental glomerulosclerosis, FSGS, membranoproliferative or mesangiocapillary glomerulonephritis, MPGN, hypocomplementemic glomerulonephritis, membranous glomerulonephritis, MGN, congenital nephrotic syndrome AUTHOR INFORMATION Section 1 of 10 Author Information Introduction Clinical Differentials ... Bibliography
Author: Luther Travis, MD

32. EMedicine - Nephrotic Syndrome : Article Excerpt By: Luther Travis, MD
Synonyms, Key Words, and Related Terms NS, nephrosis, lipoid nephrosis, Briefly, the name was modified to lipoid nephrosis after the routine finding of
http://www.emedicine.com/ped/byname/nephrotic-syndrome.htm
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Excerpt from Nephrotic Syndrome
Synonyms, Key Words, and Related Terms: NS, nephrosis, lipoid nephrosis, primary nephrotic syndrome, primary NS, PNS, idiopathic nephrotic syndrome, idiopathic NS, INS, secondary nephrotic syndrome, secondary NS, minimal change nephrotic syndrome, MCNS, minimal lesion nephrotic syndrome, MLNS, nil disease, steroid-sensitive nephrotic syndrome, SSNS, steroid-resistant nephrotic syndrome, SRNS, steroid-dependent nephrotic syndrome, SDNS, mesangial proliferative glomerulonephritis, MPN, immunoglobulin M nephropathy, focal segmental glomerulosclerosis, FSGS, membranoproliferative or mesangiocapillary glomerulonephritis, MPGN, hypocomplementemic glomerulonephritis, membranous glomerulonephritis, MGN, congenital nephrotic syndrome
Please click here to view the full topic text: Nephrotic Syndrome
Background: The term nephrosis, or nephrotic syndrome, had its origin in the early 20th century and was introduced primarily to distinguish it from nephritis, a label used to denote a clinical state associated with hematuria, proteinuria, and a cellular proliferation of the glomerulus. It describes a clinical condition of edema and proteinuria in which the renal histology (light microscopy) demonstrates fatty degeneration of the tubules associated with normal appearing glomeruli. Briefly, the name was modified to lipoid nephrosis after the routine finding of lipid droplets in the urine of affected patients. The subcategories of PNS are based on histologic descriptions, but clinical-pathological correlations have been made. Even though knowledge of specific causes of NS are too limited for more precise classification, the variants of PNS/INS will be considered as clinical disease states with well-defined histopathologic processes. The histologic type at onset makes it possible to generalize about such things as response to therapy and ultimate prognosis. When possible, the authors use the definitions, descriptions, and nomenclature developed by the International Study of Kidney Diseases in Children (ISKDC). Most attention will be devoted to minimal change nephrotic syndrome (MCNS) and focal segmental glomerulosclerosis (FSGS) with only modest attention to familial or congenital nephrosis, membranoproliferative glomerulonephritis (MPGN), and membranous glomerulonephritis (MGN).

33. Nephrosis, Lipoid
Nephrosis, Lipoid Medical.WebEnds.com. Nephrosis, Lipoid. Glomerulonephritis,Minimal Change; Nephropathy, Minimal Change; Nephrotic Syndrome,
http://medical.webends.com/kw/Nephrosis, Lipoid
Medical.WebEnds.com - Medical Terminology Dictionary
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Nephrosis, Lipoid
Glomerulonephritis, Minimal Change; Nephropathy, Minimal Change; Nephrotic Syndrome, Minimal Change; Glomerulonephritides, Minimal Change; Lipoid Nephroses; Lipoid Nephrosis; Minimal Change Glomerulonephritides; Nephroses, Lipoid Glomerular disease causing heavy proteinuria characterized by absence of obvious histologic glomerular changes on light microscopy . It is also called minimal change glomerular disease and minimal lesion glomerulonephritis
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34. HEALTHMEDNET ILLNESS AND DISEASE URL DIRECTORY
lipoid nephrosis http//directory.ansme.com/health/168.html. lipoid nephrosis (5)http//directory.google.co.nz/Top/Health/Conditions_and_Diseases
http://www.healthmednet.com/LIP-LUN.htm

35. Kidneys - Nephrotic Syndrome
Minimal change (lipoid nephrosis) this type is most common in children, Minimal Change disease (lipoid nephrosis) is the most common form of
http://www.betterhealth.vic.gov.au/bhcv2/bhcarticles.nsf/pages/Kidneys_nephrotic

36. Minimal Change Disease
Alternative Names. Minimal change nephrotic syndrome; Nil disease; lipoid nephrosis;Idiopathic nephrotic syndrome of childhood
http://www.ehendrick.org/healthy/000496.htm
Injury Disease Nutrition Poison ... Prevention
Minimal change disease
Definition
Minimal change disease is a kidney disorder. Each kidney is made of more than a million units called nephrons. Each nephron has a tuft of blood vessels called a glomerulus, which is surrounded by a Bowman's Capsule. Together, these structures filter blood and form urine. Minimal change disease is one cause of nephrotic syndrome . It is named "minimal change" because the nephrons appear totally normal under a light microscope. The condition is only seen using an electron microscope, which reveals changes in the Bowman's Capsule in the nephrons. Urine tests also show high protein levels.
Alternative Names
Minimal change nephrotic syndrome; Nil disease; Lipoid nephrosis; Idiopathic nephrotic syndrome of childhood
Causes
Minimal change disease is the most common cause of nephrotic syndrome in children. It is also frequently seen in adults. The cause is unknown, but the disease may be preceded by viral infection, allergic reactions, or recent immunizations. Minimal change disease does not reduce the amount of urine produced. It rarely progresses to

37. Medical Image Database, Radiology Teaching Files And Cases, MedPix™: Single
Minimal Change Disease (lipoid nephrosis) Factoid 2531 Created 2001-07-20090922-04 - Modified 2001-08-24 072230-04. ACR Codes 8.8
http://rad.usuhs.mil/medpix/radpix.html?mode=single&comebackto=mode=geo_browse&r

38. JN 2003; Vol.16 N°1: 148-153
One patient had focal glomerulosclerosis and lipoid nephrosis. lipoid nephrosisand focal glomerulosclerosis in a patient with polymyositis.
http://www.sin-italy.org/jnonline/vol16n1/148.html
Table of Contents Case report J NEPHROL 2003; 16: 148-153 Unexpected IgA nephropathy during the treatment of a young woman with idiopathic dermatomyositis: Case report and review of the literature Tzung-Hai Yen , Jeng-Yi Huang , Chen-Yin Chen Department of Nephrology, Department of Pediatrics, Chang Gung Memorial Hospital, Taipei, Taiwan - China
ABSTRACT: This article reports the unexpected discovery of IgA nephropathy in a 26-year-old Chinese woman 1.5 years after the onset of idiopathic dermatomyositis. The patient was taking immunosuppressive agents, prednisolone 25 mg and azathioprine 75 mg daily. Glomerulonephritis associated with idiopathic polymyositis/dermatomyositis is rare. A review of the medical literature indicates that the most common pattern seen in idiopathic polymyositis is mesangial proliferative glomerulonephritis. However, both membranous and mesangial proliferative glomerulonephritis are often seen in idiopathic dermatomyositis. It is still not clear, however, whether the humorally- mediated immune process in dermatomyositis and the cell-mediated immune process in polymyositis can explain the different patterns of occurrence of glomerular lesions in these two closely related disease entities.
Key words: Dermatomyositis, Polymyositis, Nephrotic syndrome, IgA nephropathy

39. REFERENCES
Pathogenesis of lipoid nephrosis a disorder of Tcell function. Lancet 1974;2 (7880) 556-60. 47.Candiano G, Musante L, Zennaro C, Bruschi M, Carraro M,
http://www.sin-italy.org/jnonline/forum/fsgs/references.htm
REFERENCES
1.Rich AR. A hitherto undescribed vulnerability of the juxtamedullary glomeruli in lipoid nephrosis. Bull John Hopkins Hosp 1957; 100: 173-86.
2.D’Agati VD. The many masks of focal segmental glomerulosclerosis. Kidney Int 1994; 46: 1223-41.
3.Cameron JS. The enigma of focal segmental glomerulosclerosis. Kidney Int 1996; 57 (suppl): S119-31.
4.Cortes L, Tejani A. The dilemma of focal segmental glomerulosclerosis. Kidney Int 1996; 49 (suppl): S57-61.
5.Korbet SM, Schwartz MM, Lewis EJ. Primary focal segmental glomerulosclerosis: Clinical course and response to therapy. Am J Kidney Dis 1994; 23: 773-83.
6.Haas M, Spargo BH, Coventry S. Increasing incidence of segmental glomerulosclerosis among adult nephropathies: 20 years of biopsy study. Am J Kidney Dis 1995; 26: 740-50.
7.Haas M, Meehan SM, Karrison TG, Spargo BH. Changing etiologies of unexplained adult nephrotic syndrome: A comparison of renal biopsy findings from 1976 to 1979 and 1995 to 1997. Am J Kidney Dis 1997; 30: 621-31.
8.Bonilla-Felix M, Parra C, Ferris M, Swinford RD, Brannan P, Portman RJ. Focal segmental glomerular sclerosis (FSGS) in children with idiopathic nephrotic syndrome (NS): Is the incidence increasing. J Am Soc Nephrol 1997; 8: 82A.

40. Penn State Faculty Research Expertise Database (FRED)
, Glomerular disease causing heavy proteinuria Lipoid Nephroses, lipoid nephrosis. Minimal Change Glomerulonephritides......Nephrosis, Lipoid.
http://fred.hmc.psu.edu/ds/retrieve/fred/meshdescriptor/D009402

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