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Have you recently been diagnosed with reduced kidney function? View information on resources for those with chronic kidney disease (CKD) or at risk of developing CKD.
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Executive Director's Message A monthly column by AAKP's Executive Director & CEO, Kris Robinson.
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Synopses
Polycystic Kidney Disease: An Unrecognized Emerging Infectious Disease?
Marcia A. Miller-Hjelle,* J. Thomas Hjelle,* Monica Jones,* William R. Mayberry,† Mary Ann Dombrink-Kurtzman,‡ Stephen W. Peterson,‡ Deborah M. Nowak,* and Frank S. Darras*
*University of Illinois College of Medicine at Peoria, Peoria, Illinois, USA; †East Tennessee State University, Johnson City, Tennessee, USA; and ‡U.S. Department of Agriculture, Agricultural Research Service, Peoria, Illinois, USA
...
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Hereditary Nephritis (HN)
Version of August 31, 1999
WHAT IS HN?
HN is a problem of growing concern in the United States and throughout the world, according to the Hereditary Nephritis Foundation and to researchers at the University of Utah. HN is a group of inherited kidney diseases. The different varieties of HN have different patterns of inheritance, and different rates of progression. The kidney disease, manifested by microscopic traces of blood cells and proteins in urine, is present ...
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Inherited Renal Diseases
Ari Kostadaras, M.D.
The following session will highlight the main features of four unrelated diseases: 1) Alport Syndrome; 2) Autosomal Dominant Polycystic Kidney Disease; 3) Medullary Sponge Kidney; and 4) Medullary Cystic Disease. Medullary sponge kidney is the disorder in this group which is not usually inherited but the name may be confused with Medullary cystic disease.
Alport Syndrome
Alport syndrome (AS) is defined as progressive he ...
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Ed Friedlander, M.D., Pathologist
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Cyberfriends: The help you're looking for is probably here.
Welcome to Ed's Pathology Notes, placed here originally for the convenience of medical students at my school. You need to check the accuracy of any information, from any source, against other credible sources. I cannot diagnose or treat over the web, I cannot comment on the health care you have already received, and these notes cannot substitute for your o ...
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Welcome to the Canadian Pediatric Kidney Disease Research Centre Website
Centre canadien de recherche sur les maladies rénales infantiles
Nephrology Service --- Service de nephrologie
Children's Hospital of Eastern Ontario
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Urinary Tract Infections Common in Women, but Treatable
Urine is normally sterile. When bacteria or other microorganisms - usually from the digestive system - cling to the opening of the urethra, they can enter the urinary tract and begin to ...
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Why not add the latest features to your Internet Information Server?
Microsoft® Internet Information Server (IIS) makes it easier to do business with internal or external customers down the hall or around the world. To learn more about how Internet Information Server will help you in your business, browse the IIS online documentation.
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Very Special Athletes
Go for the Gold
2006 U.S. Transplant Games
They haven't hit the court or track yet and already this group of athletes has performed death-defying feats. They all carry an inner trophy -- a new organ that qualifies them for the dream team in the game of life. Their ultimate trial will kick off at various venues in Louisville, the host site for the 2006 U.S. Transplant Games.
Early Detection
Kidney E ...
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Register Today!
The mission of the National Kidney Foundation of Upstate New York is to prevent kidney and urinary tract diseases, improve the health and well-being of individuals and families affected by these diseases, and increase the availability of all organs for transplantation.
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Polycystic Kidney Disease
(PKD)
What is Polycystic Kidney Disease?
What is autosomal dominant PKD?
What are the symptoms of autosomal dominant PKD?
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Pathology of Renal Cystic Disease
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Recessive Polycystic Kidney Disease (RPKD)
This condition is inherited in an autosomal recessive pattern, giving a 25% recurrence risk for parents having subsequent children. The kidneys are affected bilaterally, so that in utero, there is typically oligohydramnios because of poor renal function and failure to form significant amounts of fetal urine. ...
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