Results 71 to 80 of about 2,344 (196)
Bony content of oxalate in patients with primary hyperoxaluria or oxalosis-unrelated renal failure
, 1995 Bony content of oxalate in patients with primary hyperoxaluria or oxalosis-unrelated renal failure. Oxalate retention occurs in end-stage renal failure. Regular dialysis treatment does not prevent progressive accumulation of oxalate in cases of ESRF due ...
Cadario, Anna +7 more
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Annals of Internal Medicine: Clinical CasesA 27-year-old man presented with influenza-like symptoms and rapidly progressing respiratory failure requiring mechanical ventilation and venovenous extracorporeal membrane oxygenation on the day of admission.
Salmina J. Guivala +8 more
doaj +1 more source
International Journal of Nephrology, 2011 Primary hyperoxalurias (PH) are inborn errors in the metabolism of glyoxylate and oxalate. PH type 1, the most common form, is an autosomal recessive disorder caused by a deficiency of the liver-specific enzyme alanine, glyoxylate aminotransferase (AGT ...
Jérôme Harambat +4 more
doaj +1 more source
, 2018 Primary hyperoxaluria type 1 (PH1) is a rare life-threatening genetic disease related to glyoxylate metabolism and characterized by accumulation of calcium oxalate crystals.
Moya-Garzón, María Dolores +8 more
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Aspergillus Niger Infection Associated with Systemic Oxalosis: An Autopsy Diagnosis Without Culture
, 2014 This case report presents a 60-year-old male with a past medical history that included diabetes mellitus type II, chronic alcoholism, Hepatitis C infection, and presumptive pneumonia who died following a cholecystectomy.
Albert Jenkins +2 more
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Isolated Nasopharyngeal Aspergillosis Caused by A flavus and Associated with Oxalosis
, 2004 We report a case of isolated nasopharyngeal aspergillosis in a 52-year-old woman with Hashimoto's thyroiditis. We found the nasopharyngeal lesion incidentally while evaluating bilateral cervical lymphadenopathy, which we had discovered during a ...
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, 2015 Hyperoxaluria type I (HPI) is a metabolic disorder secondary to liver alanine glyoxylate aminotransferase deficiency. Renal failure occurs due to the excessive production and precipitation of oxalate in the kidney. Combined liver-renal transplantation is
Sinangil A. +5 more
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Fatal outcome of infantile oxalosis: case reports from three families and a review of literature
The Turkish Journal of Pediatrics, 1998 Infantile oxalosis is a rare, autosomal recessive disorder. We present three unrelated cases of infantile oxalosis and their families, emphasizing its place as a cause of acute renal failure in infancy, and showing the clinical heterogeneity of ...
A Oner +4 more
doaj
, 1997 Tracer experiments in rats mimicking type II primary hyperoxaluria, with an expanded intracellular pool of hydroxypyruvate, showed that the excess formation of oxalate did not originate from its immediate precursor glyoxylate.
M. Lathika, Kunnathattu +6 more
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Bone involvement in primary oxalosis. Study of 20 cases
, 1991 International audienceThe authors report 20 cases of primary oxalosis with bone involvement, late revealed in adults in 19 cases. They have studied the clinical, radiological and histological manifestations of this bone oxalosis.
Lafage-Proust, Marie-Hélène +9 more
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