Results 161 to 170 of about 5,205 (214)
Dietary Oxalate Nephropathy Due to Pureed Feeds. [PDF]
Kidney MedPanchal RA +3 more
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The Dawn of Precision Medicine in Pediatric Nephrology: Lumasiran and the Era of siRNA Therapies for Primary Hyperoxaluria Type 1. [PDF]
J Pers MedDotis J, Fourikou M.
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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 SciLiu D, Guan Z, Du Y.
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Chronic leg ulcers in a patient with Hyperoxaluria type 1: a rare and challenging diagnosis. [PDF]
Oxf Med Case ReportsKabbou S, Eljouari O, Gallouj S.
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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
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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
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Primary Hyperoxaluria in Infancy
Australasian Radiology, 1986ABSTRACTPrimary 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
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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 +4 more
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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 +4 more
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THE RETINOPATHY OF PRIMARY HYPEROXALURIA
Retina, 1985The 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 +3 more
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Radiologic findings in primary hyperoxaluria
Skeletal Radiology, 1982Six out of seven patients with primary hyperoxaluria showed various degrees of oxalosis. The radiographic manifestations differ between patients younger than 15 years and those older than 45 years. The mild manifestations in children, only urolithiasis, can be explained by the, as yet, unimpaired renal function. The renal function in the older patients,
MARTIJN, A, THIJN, CJP
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