Results 171 to 180 of about 7,435 (215)

An update on primary hyperoxaluria

Nature Reviews Nephrology, 2012
The 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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Primary Hyperoxaluria

Journal of Urology, 1963
D, SWARTZ, S, ISRAELS
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Primary hyperoxaluria

Urology, 1995
P C, Peters, G M, Preminger
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PRIMARY HYPEROXALURIA

The Lancet, 1957
H E, ARCHER, A E, DORMER, E F, SCOWEN, R W, WATTS   +3 more
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Treatment of Hyperoxaluria

New England Journal of Medicine, 1967
C C, Solomons, S I, Goodman, C M, Riley
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Primary Hyperoxaluria

Annals of Internal Medicine, 1961
A W, MCLAURIN, W R, BEISEL, G J, MCCORMICK, R, SCALETTAR, R H, HERMAN   +4 more
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Primary Hyperoxaluria

New England Journal of Medicine, 2013
Iraj, Rezvani, Victor H, Auerbach
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Primary Hyperoxaluria

New England Journal of Medicine, 2017
Dapeng, Jiang, Hongquan, Geng
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Determinants of Kidney Failure in Primary Hyperoxaluria Type 1: Findings of the European Hyperoxaluria Consortium

Kidney International Reports, 2023
Michiel J S Oosterveld, Thomas J Neuhaus, Sally-Anne Hulton   +2 more
exaly  

PRIMARY HYPEROXALURIA

Nutrition Reviews, 2009
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