Daniela Santon

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The disease complex medullary cystic disease/familial juvenile hyperuricemic nephropathy (MCKD/FJHN) is characterized by alteration of urinary concentrating ability, frequent hyperuricemia, tubulo-interstitial fibrosis, cysts at the cortico-medullary junction and renal failure. MCKD/FJHN is caused by mutations of the gene encoding uromodulin, the most(More)
previous study indicated that the sequential hourly and daily changes in plasma ␤-globin DNA concentrations after trauma were different between mildly and severely injured patients and between patients with and without organ failure (19). The differences may also be useful for monitoring the progress of post-trauma complications (19). Further studies will(More)
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