Results 121 to 130 of about 4,332 (175)

Investigation of the multifactorial regulatory mechanisms underlying compositional changes in recurrent urinary stones and development of a machine learning-based personalized predictive model. [PDF]

Sci Rep
Maimaiti M, Xianmuxiding W, Chen X, Atawula M, Yu G.   +4 more
europepmc   +1 more source

Normal urinary oxalate excretion in 4-hydroxy-2-oxo-glutarate aldolase 1 (HOGA1) deficient mice with AGT expression in peroxisomes and not in mitochondria. [PDF]

Biochim Biophys Acta Mol Basis Dis
Boffa I, Ferriero R, Cancelliere M, Nusco E, Gatticchi L, Palmer D, Ng P, Piccolo P, Cellini B, Wood K, Knight J, Brunetti-Pierri N.   +11 more
europepmc   +1 more source

Dietary Oxalate Nephropathy Due to Pureed Feeds. [PDF]

Kidney Med
Panchal RA, Rytting H, Chinnadurai AV, Greenbaum LA.   +3 more
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Extraintestinal Manifestations of Inflammatory Bowel Disease: A Focus on Kidney Complications. [PDF]

Int J Mol Sci
Wu H, Lin A, Chi J, Zhang J, Peng B, Ni D, Hao H, Liu Z.   +7 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

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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

Primary Hyperoxaluria in Infancy

Australasian Radiology, 1986
ABSTRACTPrimary Hyperoxaluria is a rare autosomal recessive disorder causing progressive renal failure and death before adulthood in most cases1. Acute renal failure due to Primary Hyperoxaluria with renal oxalosis is rare in infancy2‐ 3 and we report such a case emphasizing the importance of ultrasonographic examination in the diagnosis of this ...
H N, Srinivas, C, Ramkumar
openaire   +2 more sources

PRIMARY HYPEROXALURIA

Pediatrics, 1960
The clinical and pathologic findings in a case of primary hyperoxaluria and calcium oxalate nephrocalcinosis in a 7-year-old boy are described and discussed in relation to similar reported cases. The diagnosis was suspected because of nephrocalcinosis in the absence of an abnormality of calcium metabolism and proven by the demonstration of increased ...
Thomas H. Shepard, S. Allison Creighton, Edwin G. Krebs, Lou-sein W. Lee, Horace C. Thuline   +4 more
openaire   +2 more sources

THE RETINOPATHY OF PRIMARY HYPEROXALURIA

Retina, 1985
The ophthalmoscopic and fluorescein angiographic findings in a seven-year-old boy with primary hyperoxaluria presented. The retinal findings in this condition have been reported previously in only ten patients. The fluorescein pattern which is considered to be very suggestive was reported previously in only one patient.
E I, Traboulsi, F, el-Baba, A Y, Barakat, B M, Faris   +3 more
openaire   +2 more sources