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1 the common features of thrombocytopenia and microangiopathic hemolytic anemia.
2 unction deteriorates, even in the absence of microangiopathic hemolytic anemia.
3 pathophysiological pathways that can lead to microangiopathic hemolytic anemia and a procoagulant sta
4 with the clinical features of hypertension, microangiopathic hemolytic anemia, and acute renal failu
5 drome (HUS), a disorder of thrombocytopenia, microangiopathic hemolytic anemia, and acute renal failu
6 ndrome characterized by acute renal failure, microangiopathic hemolytic anemia, and thrombocytopenia
8 ated with hemolytic uremic syndrome (HUS), a microangiopathic hemolytic anemia characterized by throm
9 TP) is characterized by thrombocytopenia and microangiopathic hemolytic anemia (MAHA) without an obvi
10 disorder characterized by thrombocytopenia, microangiopathic hemolytic anemia, mental status changes
11 ay also be associated with thrombocytopenia, microangiopathic hemolytic anemia, neurologic symptoms,
12 cell injury of various origins, resulting in microangiopathic hemolytic anemia, platelet consumption,
13 thrombotic microangiopathy characterized by microangiopathic hemolytic anemia, severe thrombocytopen
14 odes of small-vessel thrombosis resulting in microangiopathic hemolytic anemia, thrombocytopenia and
17 emolytic uremic syndrome (HUS) is a triad of microangiopathic hemolytic anemia, thrombocytopenia, and
18 tic microangiopathy that is characterized by microangiopathic hemolytic anemia, thrombocytopenia, and
19 me (aHUS), a rare condition characterized by microangiopathic hemolytic anemia, thrombocytopenia, and
20 ment at the cell surface level that leads to microangiopathic hemolytic anemia, thrombocytopenia, and
21 ura (TTP) is the common name for adults with microangiopathic hemolytic anemia, thrombocytopenia, wit
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