Results 161 to 170 of about 6,717 (218)

Real-world burden of primary hyperoxaluria with chronic kidney disease in the United States: a retrospective administrative claims analysis. [PDF]

BMC Nephrol
Goldfarb DS, Modersitzki F, Skaar JR, Li O, Salem S, Chen JV.   +5 more
europepmc   +1 more source

Re: Pierre Letourneau, Lara Cabezas, Aurélie De Mul, et al. Optimizing Screening Performance for the Risk of Hyperoxaluria and Urolithiasis Using the Urinary Oxalate/Creatinine Ratio: A Retrospective Analysis. Eur Urol Open Sci 2025;75:20-8. [PDF]

Eur Urol Open Sci
Liu D, Guan Z, Du Y.
europepmc   +1 more source

First retrospective study on pediatric nephrocalcinosis in Syria: clinical symptoms and causes. [PDF]

Front Pediatr
Ghanem H, Hassan M, Swideah S, Wannous H.   +3 more
europepmc   +1 more source

Lumasiran at birth changes the trajectory of primary hyperoxaluria type 1: same disease, different outcomes in two affected siblings. [PDF]

J Nephrol
Peruzzi L, Leporati M, Pediatric Oxal Turin Working Group.   +2 more
europepmc   +1 more source

Pathophysiology and Management of Hyperoxaluria and Oxalate Nephropathy: A Review

American Journal of Kidney Diseases, 2022
Hyperoxaluria results from either inherited disorders of glyoxylate metabolism leading to hepatic oxalate overproduction (primary hyperoxaluria), or increased intestinal oxalate absorption (secondary hyperoxaluria).
Nathalie Demoulin, Valentine Gillion, Johann Morelle   +2 more
exaly   +2 more sources

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The Primary Hyperoxalurias

Seminars in Nephrology, 2008
The primary hyperoxalurias (PHs) are rare autosomal-recessive inborn errors of metabolism. In the most severe form (type 1), recurrent kidney stones and progressive nephrocalcinosis lead to the loss of kidney function, accompanied by systemic oxalosis, and often requires dialysis and/or transplantation.
Amy E, Bobrowski, Craig B, Langman
openaire   +2 more sources

Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type I

FEBS Letters, 1986
Activities of alanine:glyoxylate aminotransferase in the livers of two patients with primary hyperoxaluria type I were substantially lower than those found in five control human livers.
P R Jennings, Christopher J Danpure
exaly   +2 more sources

Primary Hyperoxaluria

New England Journal of Medicine, 2017
Hiperoksalüri nefrolithiazis ve nefrokalsinozis ile karakterize, idrardaki kalsiyum oksalat/n süpersatürasyonu sonucu oluşur. Kalsiyum oksalat depozit/eri böbrek hasarı, böbrek yetmezliği ve diğer organlarda hasar/anmaya neden olabilir.
Dapeng, Jiang, Hongquan, Geng
openaire   +3 more sources

Oral Manifestations of Hyperoxaluria

Journal of Craniofacial Surgery, 2011
Primary hyperoxaluria is a rare, inherited autosomal recessive disease caused by defects in the metabolism of glyoxylate. Oral manifestations of hyperoxaluria are rare. However, bone and tooth resorption may be the result of chronic inflammation and the presence of osteoclastic cells surrounding the oxalate crystal deposit. A deposit of calcium oxalate
Eliete Neves da Silva, Guerra, Leonora, Vianna, Maria Nazareth, Sobreira, Flavio Nader Gross, de Araújo, Nilce Santos, de Melo   +4 more
openaire   +2 more sources