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         Glomerular Diseases:     more books (33)
  1. Renal Disease: Classification and Atlas of Glomerular Diseases by Jacob Churg, 1982-12
  2. Color atlas of kidney biopsy: Pathology of glomerular diseases by Wolfgang Rotter, 1985
  3. Pathology of Glomerular Disease (Contemporary Issues in Surgical Pathology) (Vol 1)
  4. The Official Patient's Sourcebook on Glomerular Disease: A Revised and Updated Directory for the Internet Age by Icon Health Publications, 2002-07
  5. Renal biopsy in glomerular diseases: Clinical, histological, immunohistological and electron-microscopic studies by Edit Beregi, 1978-01-01
  6. Nephrology... Obstruction, Stones and Tumours ... Glomerular Disease by A. W. & Moffat, D. B. & Sanders, E. Asscher, 1984
  7. Atlas of Glomerular Disease: Morphological and Clinical Correlation by Priscilla Kincaid-Smith, John P. Dowling, et all 1985-01
  8. Renal Glomerular Disease (Topics in Renal Disease) by P. Sharpstone, J.A. Trafford, 1981-05-31
  9. Slide Atlas of Nephrology. Obstuction, Stones and Tumours. Glomerular Disease. by A. William. [and] David B. Moffat. Eric Sanders. Asscher, 1984
  10. The Epidemic Challenge of Chronic Kidney Disease in Older Patients by MBChB, MSc, MRCP(UK), MD Ahmed H. Abdelhafi Z, MBChB, MRCP(UK) Evelyn Tan, et all 2010-05-17
  11. Glomerular Filtration Rate Is Used to Redefine Kidney Disease.: An article from: Internal Medicine News by Mitchel L. Zoler, 2001-07-15
  12. Pathophysiology of Renal Disease by Burton David Rose, 1987-03-01
  13. The Official Patient's Sourcebook on Glomerular Disease A Revised and Updated Directory for the Internet Age by Icon Health Publications, 1980
  14. Renal Glomerular Diseases: Atlas of Electron Microscopy with Histopathological Bases and Immunofluorescence Findings by Jonas Valaitis, 2002-08-14

81. CCHS Clinical Digital Library
Chapter 28 Primary Glomerular Disease Access document glomerular diseases that Cause Nephrotic Syndrome Access document
http://cchs-dl.slis.ua.edu/clinical/nephrology/glomerulonephritis/rapidly.htm
Clinical Resources by Topic: Nephrology
Rapidly Progressive Glomerulonephritis Clinical Resources
Emergency Pediatrics Geriatrics Atlases ... Miscellaneous Resources See also:

82. UNTSHC Clinic Digital Library
Chapter 148 Glomerular and Tubulointerstitial Disease Access document Chapter 13 glomerular diseases Table of contents
http://unthsc-dl.slis.ua.edu/clinical/nephrology/glomerulonephritis/chronic.htm
Clinical Resources by Topic: Nephrology
Chronic Glomerulonephritis Clinical Resources
Pediatrics Geriatrics Atlases Pathology ... Miscellaneous Resources See also:

83. ICD-10: Block N00-N08
N08*, glomerular disorders in diseases classified elsewhere N08.0*, glomerular disorders in infectious and parasitic diseases classified elsewhere
http://www3.who.int/icd/vol1htm2003/gn00.htm
Chapter XIV
Diseases of the genitourinary system
Glomerular diseases
Use additional code, if desired, to identify external cause (Chapter XX) or presence of renal failure (N17-N19). Excludes: hypertensive renal disease
The following fourth-character subdivisions classify morphological changes and are for use with categories N00-N07. Subdivisions .0-.8 should not normally be used unless these have been specifically identified (e.g. by renal biopsy or autopsy). The three-character categories relate to clinical syndromes. Minor glomerular abnormality Minimal change lesion
Focal and segmental glomerular lesions Focal and segmental:
Focal glomerulonephritis
Diffuse membranous glomerulonephritis Diffuse mesangial proliferative glomerulonephritis Diffuse endocapillary proliferative glomerulonephritis Diffuse mesangiocapillary glomerulonephritis Membranoproliferative glomerulonephritis, types 1 and 3, or NOS
Dense deposit disease Membranoproliferative glomerulonephritis, type 2
Diffuse crescentic glomerulonephritis Extracapillary glomerulonephritis
Other Proliferative glomerulonephritis NOS
Unspecified Acute nephritic syndrome [See before N00 for subdivisions Includes: acute: Excludes: acute infectious tubulo-interstitial nephritis nephritic syndrome NOS Rapidly progressive nephritic syndrome [See before N00 for subdivisions Includes: rapidly progressive: Excludes: nephritic syndrome NOS Recurrent and persistent haematuria [See before N00 for subdivisions Includes: haematuria: Excludes: haematuria NOS Chronic nephritic syndrome

84. What Kidneys Do And How They Fail - DaVita
glomerular disease has many causes, including other diseases such as diabetes, Toxic drugs and infection also can result in glomerular disease.
http://www.davita.com/articles/ckd/index.shtml?id=367

85. Introduction: Glomerular Disease - WrongDiagnosis.com
Introduction to glomerular Disease as a medical condition including symptoms, diagnosis, misdiagnosis, treatment, prevention, and prognosis.
http://www.wrongdiagnosis.com/g/glomerular_disease/intro.htm
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Current chapter:
Glomerular Disease
Next sections Basic Summary for Glomerular Disease Types of Glomerular Disease Causes of Glomerular Disease Symptoms of Glomerular Disease ... Diagnostic Tests for Glomerular Disease Next chapters: Lupus nephritis End-stage renal disease Kidney failure Acute kidney failure ... Feedback
Introduction: Glomerular Disease
Glomerular Disease: Condition affecting the glomerules in the kidney. Glomerular Disease: Many diseases affect kidney function by attacking the tiny units within the kidney where blood is cleaned. Glomerular diseases include many conditions with a variety of genetic and environmental causes, but they fall into two major categories:
  • Glomerulonephritis (gloh-MAIR-yoo-loh-neh-FRY-tis) describes the inflammation of the membrane tissue in the kidney that serves as a filter, separating wastes and extra fluid from the blood.
  • Glomerulosclerosis (gloh-MAIR-yoo-loh-skleh-ROH-sis) describes the scarring or hardening of the tiny blood vessels within the kidney.

86. UpToDate Differential Diagnosis Of Glomerular Disease
INTRODUCTION — The presence of some form of glomerular disease, CLINICAL PATTERNS OF glomerular DISEASE — Although there are many causes of glomerular
http://patients.uptodate.com/topic.asp?file=glomrdis/11292

87. Glomerular Disease - New Treatments, January 22, 2005
New treatments for glomerular disease, minimal change disease, focal glomerulosclerosis, January 22, 2005.
http://www.medical-library.org/journals2a/glomerular_disease.htm
Click here to view next page of this article
Glomerular Diseases
Major Renal Manifestations of Glomerular Disease
Abnormal urinalysis Only red cell casts, heavy proteinuria, and lipiduria are diagnostic
Approach to Patient with Hematuria
Historical clues suggesting a particular underlying disease: Unilateral flank pain with kidney stones Postinfectious glomerulonephritis or IgA nephropathy if post-URI Sickle cell trait or disease Family or personal history of renal failure or polycystic kidney disease Glomerular versus extraglomerular bleeding
Glomerular vs Extraglomerular Bleeding
Primary characteristics of glomerular hematuria: Majority of red cells have dysmorphic appearance - Red cell casts· Heavy proteinuria (primarily M)or light chain deposition disease (primarily M) · Lack of blood clots with renal bleeding, due perhaps to urokinase and TPA in tubular cells · Brown, "Coca-cola"-colored urine may be seen; unusual with extrarenal bleeding
Diagnosis of Isolated Glomerular Hematuria
IgA nephropathy May have recurrent episodes of gross hematuria Generally negative family history of renal disease Hereditary nephritis May have gross hematuria Family history of renal failure common Thin basement membrane disease
    Gross hematuria infrequent Autosomal dominant

88. ISN-India.com-Indian Society Of Nephrology-Publications-Glomerular Diseases
In addition to expression in glomerular podocytes, the reporter gene was expressed in the brain and pancreas of (+/) and (-/-) mice.
http://www.isn-india.com/glomdis.php
XXXVI ANNUAL CONFERENCE (ISNCON – 2005) COCHIN 1 ST TO 3 RD DECEMBER 2005 Glomerular Diseases
About the ISN
Newsroom Membership Member`s Directory ... ISNCON-2004
Scientific Editor
Vivekanand Jha, M.D., D.M. Associate Professor of Nephrology, Postgraduate Institute of Medical Education and Research Chandigarh 160012, INDIA Tel: +91(172) 721 368 Fax: +91(172) 744 401, 745 078 E-mail Address(es): vjha@iname.com
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89. AllRefer Health - Lupus Nephritis (Lupus Glomerular Disease, Nephritis - Lupus)
Lupus Nephritis (Lupus glomerular Disease, Nephritis Lupus) information center covers causes, prevention, symptoms, diagnosis, treatment, incidence,
http://health.allrefer.com/health/lupus-nephritis-info.html

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Alternate Names : Lupus Glomerular Disease, Nephritis - Lupus Definition Lupus nephritis is a kidney disorder that is a complication of systemic lupus erythematosus , characterized by damage to the glomerulus and progressive loss of kidney function.
Male Urinary System Lupus nephritis is one complication of systemic lupus erythematosus SLE ). It is related to the autoimmune process of lupus, where the immune system produces antibodies antinuclear antibody and others) against body components. Complexes of these antibodies and

90. AllRefer Health - Lupus Nephritis Diagnosis & Tests (Lupus Glomerular Disease, N
Lupus Nephritis (Lupus glomerular Disease, Nephritis Lupus) information center covers Diagnosis Tests.
http://health.allrefer.com/health/lupus-nephritis-diagnosis-tests.html

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Alternate Names : Lupus Glomerular Disease, Nephritis - Lupus Examination indicates decreased kidney functioning with edema and may indicate renal failure Blood pressure may be high. Abnormal sounds may be heard on auscultation of the heart and lungs, indicating fluid overload. Lupus nephritis is usually discovered during investigation of the causes of reduced kidney function. Fewer than one-half have other symptoms of systemic lupus erythematosus at the time of diagnosis of lupus nephritis.

91. Clinical And Pathological Characteristics Of Patients With Glomerular Diseases A
OBJECTIVE To examine the prevalence of glomerular disease in Hong Kong. PATIENTS All patients who presented with suspected glomerular disease from
http://www.hkmj.org.hk/hkmj/abstracts/v5n3/240.htm
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Clinical and pathological characteristics of patients with glomerular diseases at a university teaching hospital: 5-year prospective review
KW Chan, TM Chan, IKP Cheng
Department of Pathology, The University of Hong Kong, Queen Mary Hospital, Pokfulam, Hong Kong OBJECTIVE: To examine the prevalence of glomerular disease in Hong Kong.
DESIGN: Prospective review.
SETTING: University teaching hospital, Hong Kong.
PATIENTS: All patients who presented with suspected glomerular disease from 1993 through 1997.
MAIN OUTCOME MEASURES: Histopathological diagnosis from biopsy examination and clinical features of presentation.
RESULTS: A total of 1629 consecutive percutaneous renal biopsies of native kidneys showed glomerular disease in 1413 cases. The most common clinical indication for renal biopsy was persistent proteinuria (n=735; 52.0%), while the most frequently found glomerular lesion was immunoglobulin A nephropathy (n=338; 23.9%). Minimal-change nephrotic syndrome (n=125; 8.8%) and immunoglobulin M nephropathy (n=11; 0.8%), were the most common glomerular diseases that presented with nephrotic syndrome. The male to female ratio for lupus nephritis was 1:14 (n=290), whereas for minimal-change nephrotic syndrome, the ratio was 1.8:1 (n=125). Immunoglobulin A nephropathy and membranous glomerulonephritis (n=117) affected approximately equal numbers of male and female patients. Familial fibrillary glomerulonephritis, a disease hitherto unknown in Hong Kong, was diagnosed in two siblings.

92. Glomercular Disease Collaborative Network
The glomerular Disease Collaborative Network (GDCN) was established as a collaborative effort between private practice community nephrology offices and the
http://medicine.med.unc.edu/centers/gdcn.htm
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The PubMed The Glomerular Disease Collaborative Network (GDCN) was established as a collaborative effort between private practice community nephrology offices and the University of North Carolina at Chapel Hill School of Medicine to seek the best possible treatment alternatives for patients with various glomerular diseases. The co-founders and co-directors of the Network are Dr. Ronald J. Falk
, Chief of the Division of Nephrology and Professor of Medicine, and Dr. J. Charles Jennette , Director of the Nephropathology Laboratory and Professor of Medicine in the Division of Pathology, both at the University of North Carolina at Chapel Hill. While the Network was started in 1985 as a group of only 15 nephrologists in North Carolina, it has since grown to include over 400 nephrologists throughout North Carolina, Virginia, South Carolina, Georgia, Florida, Washington and Minnesota. The Network has also vastly expanded the development and management of its clinical trials as well as sixteen large patient registries which follow the course of several different kidney diseases. In addition, a yearly meeting is held for the Network as a whole, functioning not only as a source for continuing education, but also as a consultation center for the participating physicians.

93. Berger Disease - Medstudents - Neprhology
A review of Berger Disease giving most importance to etiology,treatment to be the most common form of primary glomerular disease throughout the world.
http://www.medstudents.com.br/nefro/nefro2.htm
Nephrology
Bernardo Boaventura Liberato
Medstudents' Homepage
Berger Disease
Also known as primary IgA nephropathy, glomerulonephritis with IgA and IgG deposits and IgA mesangial nephropathy, Berger disease has a wide pattern of distribution and is believed to be the most common form of primary glomerular disease throughout the world. Although highly prevalent, geographic variations occur, which could be due to genetic as well as enviromental influences. Extensive mesangial IgA deposits (the characteristic pathologic feature of Berger disease), may also occur in a variety of multisystem, neoplastic and infectious diseases; when this occurs the term Secondary IgA Nephropathy should be applied. Examples of the most common causes are: Multisystem disease
  • Schönlein-Henoch purpura
  • Celiac Disease
  • Dermatitis Herpetiformis
  • Crohn Disease
    Neoplasia
  • Carcinoma of lungs, larynx, pharynx and pancreas
    Infection
  • Leprosy
  • Toxoplasmosis
  • HIV infection
    Others
  • Chronic liver disease
  • Portosystemic shunts
    In spite of the extremely varied clinical presentation, the most common feature leading to the diagnosis, by renal biopsy, is recurring episodes of macroscopic hematuria (which is generally the initial complaint). More than 80% of patients are between the ages of 16 to 35 years at the time of diagnosis. However, the disorder may be found at any age, although being uncommon before the age of 10 and after the age of 50. Thus, it should be considered a disease of children and young adults. There is a predilection for males (2:1), which disappears when affecting black persons (this disease is uncommon in blacks).
  • 94. Pathology PIMP
    glomerular Disease. 1. Remember 3 types of cells in glomerulus Final common outcome of many forms of longstanding glomerular disease.
    http://www.utmed.com/medpimp/path/pathrenal.html
    PATHOLOGY PIMP:
    Glomerular Disease
    1. Remember 3 types of cells in glomerulus: 2. Immune complex glomerulonephritis results from deposition within the glomerulus of formed in 3. If complexes are formed in an excess of Ab then depositions will be . If complexes are formed in excess of Ag then deposits will be 4. Ag-Ab complexes can be located in these locations 5. Smaller complexes are generally deposited in location and usually contain IgG. Larger complexes are usually deposited in locations and usually contain 5. In contrast to immune complex glomerulonephritis, antiglomerular basement membrane disease (antiGBM) results when Ab are formed against the not from circulation. 6. There is evidence that same Ab in anti-GBM disease cross-reacts with 7. Nephrotic syndrome includes:
  • 8. Nephritic syndrome includes:
  • 9. Minimal change disease:

    • Major cause of
    • Disease primarily of
    • Glomeruli appear by light microscopy.
    • By EM there is
    • Prognosis is
    • Treat with
    10. Idiopathic focal segmental glomerulosclerosis (FSGS):

    • Causes
    • Afflicts mostly
    • IF is
    • Prognosis is
    11. Membranous glomerulopathy:
  • 95. Glomerulonephritis - VeterinaryPartner.com - A VIN Company!
    When glomerular disease exists, holes are punched out in this filtration system allowing Albumin can be lost (urinated away) in glomerular disease,
    http://www.veterinarypartner.com/Content.plx?P=A&A=1352&S=1&SourceID=42

    96. Acute Renal Failure: Urinalysis And Cytodiagnostic Microscopy May Help Diagnose
    glomerular disease was more likely in patients with acute renal disease who had renal biopsy, if there was. blood on the dipstick (LR+2.7)
    http://www.eboncall.org/CATs/1673.htm
    Acute renal failure: urinalysis and cytodiagnostic microscopy may help diagnose glomerular and interstitial renal disease.
    Clinical bottom line (level 2b)
  • Glomerular disease was more likely in patients with acute renal disease who had renal biopsy, if there was:
    • blood on the dipstick (LR+2.7) proteinuria 2 or more on dipstick (LR+1.9) dysmorphic red blood cells on microscopy (LR+4.7)
    It was less likely if there was/were:
    • no blood on dipstick (LR-0.16) no dysmorphic red blood cells on microscopy (LR-0.080)
    Interstitial disease was more likely if there were:
    • lymphocytes 10 or more per 10 high power fields (LR+3.0) granular casts 5 or more per 10 high power fields (LR+2.1)
    Interstitial disease was less likely if there were fewer lymphocytes than this (LR-0.28) .
  • Marcussen et al: American Journal of Kidney Disease 1992; 20 (6): 618-628
    Expires July 2003 The study Setting: university hospital, Canada
    77 patients (aged mean 40 years, 50%% male) 47 patients (53% male, mean age 43) with native kidney biopsies (mean creatinine 236 micromol/l; urea 11.2 mmol/l); 30 patients (47% male, mean age 37) with renal transplants (mean creatinine 338 micromol/l; urea 12.5 mmol/l)
    Independent blinded reference standard, applied in all patients from a consecutive inappropriate spectrum.

    97. Hepatitis C Virus-Associated Glomerular Disease In Patients With Human Immunodef
    Hepatitis C VirusAssociated glomerular Disease in Patients with Human Immunodeficiency Virus Coinfection. JEN-TSE CHENG* , HERMAN L. ANDERSON, JR.
    http://www.jasn.org/cgi/content/abstract/10/7/1566
    HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author:
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    This Article Full Text Full Text (PDF) Alert me when this article is cited ... Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Cited by other online articles PubMed PubMed Citation Articles by CHENG, J.-T. Articles by D'AGATI, V. D. J Am Soc Nephrol 10:1566-1574, 1999
    American Society of Nephrology
    REGULAR ARTICLES
    Hepatitis C Virus-Associated Glomerular Disease in Patients with Human Immunodeficiency Virus Coinfection
    JEN-TSE CHENG HERMAN L. ANDERSON, JR. GLEN S. MARKOWITZ GERALD B. APPEL VELVIE A. POGUE and VIVETTE D. D'AGATI Department of Medicine at Harlem Hospital Center, New York, New York.
    Department of Medicine at Columbia Presbyterian Medical Center, New York, New York.
    Department of Pathology, Columbia University College of Physicians and Surgeons, New York, New York.
    Correspondence to Dr. Jen-Tse Cheng, Department of Medicine, Harlem Hospital Center, 506 Lenox Avenue, Room 12-101 KP, New York, NY 10037. Phone: 212-939-1453; Fax: 212-939-1306; E-mail:

    98. The Official Patient's Sourcebook On Glomerular Disease - OSTG.com: The Open Sou
    The Official Patient s Sourcebook on glomerular Disease. (English) A Revised and Updated Directory for the Internet Age
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    99. Glomerular Disease Workshop
    both basic science and clinical investigators interested in glomerular disease, diagnosis and therapeutic intervention for human glomerular disease.
    http://www.niddk.nih.gov/fund/other/glomerular/

    The Gladys Hirschman Symposium

    A Tribute to a Career Advocating for Kidney Disease Research
    A workshop for both basic science and clinical investigators interested in glomerular disease, that will discuss recent observations and potential opportunities for improving diagnosis and therapeutic intervention for human glomerular disease.
    Educational Objectives
    Understand the recent scientific advances in the study of glomerular disease.
    Discuss how new technologies might expand the scope of glomerular disease research.
    Appreciate potential new avenues of therapy for some forms of glomerular disease, as well as strategies for clinical testing of new reagents.
    Target Audience
    The target audience is primarily physician-researchers involved in the treatment of patients with glomerular diseases. The National Institutes of Health/Foundation for the Advanced Education in the Sciences (NIH/FAES) is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians.
    US Department of Health and Human Services
    National Institutes of Health

    100. Idiopathic Primary Renal Hematuric/proteinuric Syndrome
    . This syndrome, also known as Berger s disease or IgA nephropathy,...... kidney glomeruli (filtering structures) that may lead to kidney failure.
    http://www.healthatoz.com/healthatoz/Atoz/ency/idiopathic_primary_renal_hematuri

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