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Kidney Disease

Pathology - Research and Practice, 1980
The diagnostic highlights under electron microscopy in hereditary nephropathies and glomerulonephritides are reviewed: Alport's syndrome--lamellation, fragmentation and reticulation of glomerular basement membrane; benign essential (familial) hematuria--glomerular basement membrane thinning; nail patella syndrome--moth eaten holes and collagen like ...
M J, Mihatsch, H U, Zollinger
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Vasculitis and Kidney Disease

Pediatric Clinics of North America, 2022
Pediatric vasculitis is a complex group of disorders that commonly presents with multisystem involvement. Renal vasculitis can be isolated to the kidneys or can occur as part of a broader multiorgan vasculitis. Depending on severity, renal vasculitis may present as acute glomerulonephritis (AGN) often associated with hypertension and sometimes with a ...
Manpreet K, Grewal   +2 more
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Kidney Disease: Chronic Kidney Disease.

FP essentials, 2021
Chronic kidney disease (CKD) affects 37 million US adults. It is characterized by damage to the renal glomeruli, vascular supply, and/or tubulointerstitium through complex processes involving inflammation, fibrosis, and hyperfiltration. CKD typically is asymptomatic but may be detected incidentally via urinalysis showing proteinuria or blood test ...
Michael M, Braun, Maurice, Khayat
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Diseases of the Kidneys

Veterinary Clinics of North America: Equine Practice, 1986
Ultrasound examination offers important diagnostic and prognostic information in renal disease of the horse. Differentiation between acute nephrosis and chronic renal disease can usually be made because of the advanced degree of morphologic change usually prevalent in chronic conditions.
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HMGB1 in kidney diseases

Life Sciences, 2020
High mobility group box 1 (HMGB1) is a highly conserved nucleoprotein involving in numerous biological processes, and well known to trigger immune responses as the damage-associated molecular pattern (DAMP) in the extracellular environment. The role of HMGB1 is distinct due to its multiple functions in different subcellular location.
Zhi, Zhao   +3 more
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Chronic kidney disease and kidney stones

Current Opinion in Nephrology and Hypertension, 2020
Both chronic kidney disease (CKD) and kidney stones are major public health problems, which are closely interrelated. Recurrent kidney stones predispose to CKD although CKD seems to decrease risk of further kidney stone formation. Herein, we review new information of this interrelationship.Several epidemiological studies in the past have shown an ...
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Kidney Disease and Epilepsy

Journal of Stroke and Cerebrovascular Diseases, 2021
Chronic kidney disease and seizures often co-exist. When seizures are provoked in patients with kidney disease, their treatment poses a particular challenge. Seizures may be provoked in the context of uremia, and toxic substances associated with uremic encephalopathy. In that case, the mainstay of therapy is to treat the uremia before consideration for
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Chronic kidney disease

The Lancet, 2012
Chronic kidney disease is a general term for heterogeneous disorders affecting kidney structure and function. The 2002 guidelines for definition and classification of this disease represented an important shift towards its recognition as a worldwide public health problem that should be managed in its early stages by general internists.
Andrew S, Levey, Josef, Coresh
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Acupuncture and Kidney Disease

Advances in Chronic Kidney Disease, 2005
Acupuncture as a complex therapeutic system has been used to treat a variety of diseases and pathological conditions. Although the exact mechanism(s) of acupuncture remains unknown, some evidence suggests a mechanism initially involving signal transduction through connective tissue, with secondary involvement of other systems including the nervous ...
Gabriela E, Garcia   +2 more
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Multicystic Kidney Disease

Radiology, 1967
Multicystic kidney disease is commonly described as a congenital dysplasia which is usually unilateral and not productive of symptoms. The kidney is devoid of function, and there is no familial tendency (1). It often causes an abdominal mass and is most frequent in the neonatal period when nephroblastoma may be suspected (2).
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