The pathogenesis of polycystic kidney disease.
Histology and histopathology, 1995 Polycystic kidney disease (PKD) is a genetic or acquired disorder characterized by progressive distention of multiple tubular segments and manifested by fluid accumulation, growth of non-neoplastic epithelial cells and remodeling of the extracellular matrix resulting ultimately in some degree of renal functional impairment, with the potential for ...
Carone, F.A., Bacallao, R., Kanwar, Y.S.
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A Classification-Based Adaptive Segmentation Pipeline: Feasibility Study Using Polycystic Liver Disease and Metastases from Colorectal Cancer CT Images [PDF]
Automated segmentation tools often encounter accuracy and adaptability issues when applied to images of different pathology. The purpose of this study is to explore the feasibility of building a workflow to efficiently route images to specifically trained segmentation models.
arxiv +1 more source
Clinical aspects of polycystic disease of the kidneys. [PDF]
, 1977 H. David Mitcheson +2 more
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Adult type of polycystic disease of kidneys and liver presenting in childhood [PDF]
, 1974 B. G. Ockenden
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Renal Parenchymal Area and Kidney Collagen Content [PDF]
arXiv, 2016 The extent of renal scarring in chronic kidney disease (CKD) can only be ascertained by highly invasive, painful and sometimes risky tissue biopsy. Interestingly, CKD-related abnormalities in kidney size can often be visualized using ultrasound. Nevertheless, not only does the ellipsoid formula used today underestimate true renal size but also the ...
arxiv
Non-ciliary Roles of IFT Proteins in Cell Division and Polycystic Kidney Diseases. [PDF]
Front Cell Dev Biol, 2020 Vitre B, Guesdon A, Delaval B.
europepmc +1 more source
Assessment of glycemic susceptibility across multiple urological and reproductive disorders
Diabetology & Metabolic SyndromeObjective To test the glycemic susceptibility in three urological cancers and eight urological/reproductive diseases using the Mendelian randomization (MR) method.
Xiongfeng Zeng +3 more
doaj +1 more source
Familial orofaciodigital syndrome type I presenting as adult polycystic kidney disease. [PDF]
, 1987 Dian Donnai, L Kerzin-Storrar, R Harris
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Engineered Kidney Tubules for Modeling Patient-Specific Diseases and Drug Discovery
EBioMedicine, 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
Congenital Hepatic Fibrosis and Polycystic Kidney Disease; Role of Porta-Caval Shunting and Transplantation in Three Patients [PDF]
, 1981 R J McGonigle +5 more
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