Results 11 to 20 of about 34,123 (218)
Polycystic kidney disease [PDF]
Nature Reviews Disease Primers, 2018 Cystic kidneys are common causes of end-stage renal disease, both in children and in adults. Autosomal dominant polycystic kidney disease (ADPKD) and autosomal recessive polycystic kidney disease (ARPKD) are cilia-related disorders and the two main forms of monogenic cystic kidney diseases.
Dorien Peters +2 more
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MicroRNAs and Polycystic Kidney Disease [PDF]
Kidney Medicine, 2020 Important advances have been made regarding the diagnosis and management of polycystic kidney diseases. Care of patients with polycystic kidney diseases has moved beyond supportive care for complications and chronic kidney disease to new potentially ...
Dantong Li, Liangzhong Sun
doaj +3 more sources
Polycystic liver and kidney diseases
Annals of Medicine, 2005 There have been remarkable advances in research on polycystic liver and kidney diseases recently, covering cloning of new genes, refining disease classifications, and advances in understanding more about the molecular pathology of these diseases. Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary disease affecting ...
Krister Höckerstedt +1 more
exaly +3 more sources
Molecular Diagnosis and Identification of Novel Pathogenic Variants in a Large Cohort of Italian Patients Affected by Polycystic Kidney Diseases [PDF]
Genes, 2023 Ersilia Nigro +2 more
exaly +2 more sources
Insights Into the Molecular Mechanisms of Polycystic Kidney Diseases [PDF]
Frontiers in Physiology, 2021 Anastasia Sudarikova +1 more
exaly +2 more sources
Radiological Imaging Diagnosis of Adult Renal Cystic Diseases and Management
The Iraqi Journal of Medical Sciences, 2020 Background: Renal cysts are a heterogonous group of cystic renal diseases that present in approximately 40% of the patients undergoing imaging. Objective: To describe the role of the radiological imaging methods for the diagnosis of adult renal ...
Saleh Akares, Ahmed Bahomil
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Polycystic Kidney Disease [PDF]
Annual Review of Medicine, 2009 A number of inherited disorders result in renal cyst development. The most common form, autosomal dominant polycystic kidney disease (ADPKD), is a disorder most often diagnosed in adults and caused by mutation in PKD1 or PKD2. The PKD1 protein, polycystin-1, is a large receptor-like protein, whereas polycystin-2 is a transient receptor potential ...
Peter C, Harris, Vicente E, Torres
+7 more sources
ADAMs family in kidney physiology and pathology
EBioMedicine, 2021 A disintegrin and metalloproteinases (ADAMs) family are proteolytic transmembrane proteases that modulate diverse cell functions and coordinate intercellular communication.
Huanhuan Zhu +4 more
doaj +1 more source
Polycystic Kidney Disease [PDF]
New England Journal of Medicine, 1989 The Polycystic Kidney Disease (PKD) is a genetic disease which is characterized by the gradual emergence of cystic lesions in the kidneys, which replace the renal parenchyma causing deterioration of its function to stage 5. The PKD is one of the causes of Chronic Kidney Disease on renal replacement therapy (RRT).
Lavie, C.J. +3 more
openaire +4 more sources
Acta Medica Lituanica, 2021 Kidney cysts are the most common kidney lesion, while congenital kidney cysts are mostly found in pediatric population. Neonatal kidney cysts can develop due to fetal malformations, rare genetic disorders or can be acquired which is very rare.
Dovilė Ruzgienė +4 more
doaj +1 more source