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Autosomal Recessive Polycystic Kidney Disease
1990Autosomal recessive polycystic kidney disease (ARPKD) is a specific disease of the kidneys and liver, characterized by renal collecting tubule ectasia and invariably accompanied by biliary dysgenesis and portal fibrosis. In the past the disease has been called “infantile” polycystic kidney disease because of the predominant presentation in infancy.
Bernard S. Kaplan, Paige Kaplan
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Autosomal recessive polycystic kidney disease
2015Autosomal recessive polycystic kidney disease (ARPKD) is an important cause of childhood renal- and liver-related morbidity and mortality with variable disease expression. Many patients manifest peri- or neonatally with a mortality rate of 30–50%, whereas others survive to adulthood with only minor clinical features.
Carsten Bergmann, Klaus Zerres
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Autosomal Recessive Polycystic Kidney Diseases
2021Max C. Liebau, Lisa M. Guay-Woodford
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Autosomal Recessive Polycystic Kidney Disease
2004Abstract Autosomal recessive polycystic kidney disease (ARPKD) is an often devastating form of polycystic kidney disease. The typical onset occurs in neonates and infants and is characterized by cystic dilatation of the renal collecting ducts and dysgenesis of the biliary ductal plate.
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Onconephrology: The intersections between the kidney and cancer
Ca-A Cancer Journal for Clinicians, 2021, Kenar D Jhaveri, Mark A Perazella
exaly
American Cancer Society's report on the status of cancer disparities in the United States, 2021
Ca-A Cancer Journal for Clinicians, 2022Farhad Islami +2 more
exaly
Autosomal Dominant Polycystic Kidney Disease/Autosomal Recessive Polycystic Kidney Disease
2012Abdelaziz Y. Elzouki, Laurel Steinmetz
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Cancer statistics for adolescents and young adults, 2020
Ca-A Cancer Journal for Clinicians, 2020Kimberly D Miller +2 more
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