Higher strength lanthanum carbonate provides serum phosphorus control with a low tablet burden and is preferred by patients and physicians: a multicenter study. (25/179)

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Long-term efficacy and safety profile of lanthanum carbonate: results for up to 6 years of treatment. (26/179)

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Molecular genetic and biochemical analyses of FGF23 mutations in familial tumoral calcinosis. (27/179)

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Peritoneal phosphate clearance is influenced by peritoneal dialysis modality, independent of peritoneal transport characteristics. (28/179)

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Efficacy and safety of sevelamer hydrochloride and calcium acetate in patients on peritoneal dialysis. (29/179)

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Tumoral calcinosis with vitamin D deficiency. (30/179)

A 50-year-old woman presented with recurrent calcified mass in the left gluteal region. The clinical, radiological, and biochemical profile confirmed the diagnosis of tumoral calcinosis. She also had associated vitamin D deficiency. The patient underwent surgical removal of the mass to relieve the sciatic nerve compression and was managed with acetazolamide, calcium carbonate, and aluminium hydroxide gel with which she showed significant improvement. The management implications and effect of vitamin D deficiency on phosphate metabolism in the setting of tumoral calcinosis is discussed.  (+info)

GALNT3, a gene associated with hyperphosphatemic familial tumoral calcinosis, is transcriptionally regulated by extracellular phosphate and modulates matrix metalloproteinase activity. (31/179)

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A case of familial tumoral calcinosis/hyperostosis-hyperphosphatemia syndrome due to a compound heterozygous mutation in GALNT3 demonstrating new phenotypic features. (32/179)

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