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Das atypische hämolytisch-urämische Syndrom (aHUS) als eine der drei Hauptformen der thrombotischen Mikroangiopathie ist gekennzeichnet durch genetische Veränderungen im Bereich der Komplementkaskade. Diese lassen sich bei 40–60 % aller Patienten mit aHUS nachweisen. Mittlerweile sind Mutationen in über 10 verschiedenen Genen identifiziert worden. Am häufigsten und klinisch relevantesten sind Mutationen,...
Set the date range to filter the displayed results. You can set a starting date, ending date or both. You can enter the dates manually or choose them from the calendar.