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24. [Primary hyperoxaluria type 1-a rare hereditary metabolic disorder as cause of livedo racemosa]. Linse KP; Enk A; Toberer F Dermatologie (Heidelb); 2024 Apr; 75(4):321-324. PubMed ID: 38167780 [TBL] [Abstract][Full Text] [Related]
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31. [Secondary oxalosis following small bowel resection with kidney insufficiency and oxalate vasculopathy]. Kiss D; Meier R; Gyr K; Wegmann W Schweiz Med Wochenschr; 1992 May; 122(22):854-7. PubMed ID: 1604291 [TBL] [Abstract][Full Text] [Related]
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