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Autosomal dominant polycystic kidney disease: Disrupted pathways and potential therapeutic interventions

Journal of Cellular Physiology, 2019
Autosomal dominant polycystic kidney disease (ADPKD) is a monogenic inherited renal cystic disease that occurs in different races worldwide. It is characterized by the development of a multitude of renal cysts, which leads to massive enlargement of the ...
Talieh Malekshahabi   +3 more
semanticscholar   +1 more source

MRI in autosomal dominant polycystic kidney disease

Journal of Magnetic Resonance Imaging, 2019
Magnetic resonance imaging (MRI) is increasingly used in autosomal dominant polycystic kidney disease (ADPKD) for diagnosis, classification, assessment of disease progression and treatment response, and for identifying complications. Herein we review the
Weiguo Zhang, J. Blumenfeld, M. Prince
semanticscholar   +1 more source

Autosomal Dominant Polycystic Kidney Disease

2004
Abstract Autosomal dominant polycystic kidney disease (ADPKD) typically presents in the third or fourth decade with haematuria, loin (flank) pain or hypertension. It is characterized by the progressive development and enlargement of bilateral renal cysts and often leads to end-stage renal disease (ESRD) by late middle age.
Anand K Saggar-Malik, Stefan Somlo
openaire   +1 more source

Autosomal dominant polycystic kidney disease.

American Family Physician, 2014
A. Srivastava, Neel Patel
semanticscholar   +1 more source

[Autosomal-dominant polycystic kidney disease].

Deutsche medizinische Wochenschrift (1946), 1992
G, Fick, M, Weber
openaire   +3 more sources

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