Results 1 to 10 of about 34,123 (218)

Radiographic Imaging in Autosomal Dominant Polycystic Kidney Disease: A Claims Analysis

open access: yesInternational Journal of Nephrology and Renovascular Disease, 2021
Myrlene Sanon Aigbogun,1 Robert A Stellhorn,1 Christina S Pao,1 Stephen L Seliger2 1Otsuka Pharmaceutical Development & Commercialization, Inc, Princeton, NJ, USA; 2University of Maryland School of Medicine, Baltimore, MD, USACorrespondence: Stephen ...
Sanon Aigbogun M   +3 more
doaj  

Polycystic Kidney Disease in Cats

open access: yesVeterinary Quarterly, 1998
(1998). Polycystic Kidney Disease in Cats. Veterinary Quarterly: Vol. 20, Voorjaarsdagen Congress 1998, pp. S112-S113.
J T, Bosje, T S, van den Ingh
openaire   +2 more sources

Engineered Kidney Tubules for Modeling Patient-Specific Diseases and Drug Discovery

open access: yesEBioMedicine, 2018
The lack of engineering systems able to faithfully reproduce complex kidney structures in vitro has made it difficult to efficiently model kidney diseases and development.
Valentina Benedetti   +9 more
doaj   +1 more source

Polycystic liver disease with huge infected cyst displacing the pancreas, inferior vena cava and right kidney

open access: yesSaudi Journal of Medicine and Medical Sciences, 2016
Multiple liver cysts can be an isolated disease (isolated polycystic liver disease [PLD]) or they can be part of multi-organ involvement in other diseases, such as adult autosomal dominant polycystic disease (APD), which is the most frequently inherited ...
Adil H Al-Harthi   +2 more
doaj   +1 more source

Molecular and cellular pathogenesis of autosomal recessive polycystic kidney disease

open access: yesBrazilian Journal of Medical and Biological Research, 2006
Autosomal recessive polycystic kidney disease (ARPKD) is an inherited disease characterized by a malformation complex which includes cystically dilated tubules in the kidneys and ductal plate malformation in the liver.
L.F. Menezes, L.F. Onuchic
doaj  

Polycystic Diseases in Visceral Organs

open access: yesObstetrics and Gynecology International, 2011
Primary cilia are nonmotile, microtubule-based, antenna-like organelles projecting from the apical surface of most mammalian cells. Elegant studies have established the importance of ciliary structure and function in signal transduction and the sensory ...
Shakila Abdul-Majeed, Surya M. Nauli
doaj   +1 more source

CRISPR-Cas9 system in autosomal dominant polycystic kidney disease: a comprehensive review [PDF]

open access: yesChildhood Kidney Diseases
Genetic kidney diseases are caused by mutations in specific genes that significantly affect kidney development and function. Although the underlying pathogenic genes of many kidney diseases have been identified, an understanding of their mechanisms and ...
Seungyeon Kang   +4 more
doaj   +1 more source

Rare Combination of Phenotypes of Karyomegalic Interstitial Nephritis and Autosomal Recessive Polycystic Kidney Disease in an Omani Child

open access: yesOman Medical Journal
Autosomal recessive polycystic kidney disease is one of the most prevalent inherited cystic kidney diseases in infants and children, common in highly consanguineous societies such as Oman. Karyomegalic interstitial nephritis is a rare cause of hereditary
Intisar Al Alawi   +6 more
doaj   +1 more source

Autophagy in Chronic Kidney Diseases

open access: yesCells, 2019
Autophagy is a cellular recycling process involving self-degradation and reconstruction of damaged organelles and proteins. Current evidence suggests that autophagy is critical in kidney physiology and homeostasis.
Tien-An Lin   +2 more
doaj   +1 more source

Complications of polycystic kidney disease

open access: yesKidney International, 1997
A 33-year-old white man first presented to the Royal Infirmary Stirling, Scotland, 24 years ago with a history of recent-onset hematuria. Intravenous urography at that time showed a filling defect in the right kidney; a subsequent aortogram demonstrated a single simple cyst in the right kidney.
openaire   +2 more sources

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