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An update on primary hyperoxaluria
Nature Reviews Nephrology, 2012The autosomal recessive inherited primary hyperoxalurias types I, II and III are caused by defects in glyoxylate metabolism that lead to the endogenous overproduction of oxalate. Type III primary hyperoxaluria was first described in 2010 and further types are likely to exist. In all forms, urinary excretion of oxalate is strongly elevated (>1 mmol/1.73
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Hyperoxaluria and Bowel Disease
New England Journal of Medicine, 1972Recurrent calcium oxalate nephrolithiasis is a frequent and serious complication in patients with disease or resection of the distal ileum. Hofmann et al. first noted that renal calculi formation in these patients was associated with excessive urinary excretion of oxalate.1 , 2 They suggested that failure to absorb conjugated bile salts in the distal ...
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Pathophysiology and Management of Hyperoxaluria and Oxalate Nephropathy: A Review
American Journal of Kidney Diseases, 2022Nathalie Demoulin +2 more
exaly
[Primary hyperoxaluria and pregnancy].
Minerva urologica e nefrologica = The Italian journal of urology and nephrology, 2005A rare case of pregnancy in a patient with primary hyperoxaluria type 1 is reported offering a clinical contribution for the prognostic study of a natural event such as the pregnancy on these patients. It is underlined how epicriticity of the hepatorenal system is remarkably altered during the last weeks of pregnancy with a great increase of calciuria ...
CIMINO, SEBASTIANO +6 more
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New England Journal of Medicine, 1967
C C, Solomons, S I, Goodman, C M, Riley
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C C, Solomons, S I, Goodman, C M, Riley
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