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1  insulin resistance, multiple sclerosis, and idiopathic thrombocytopenic purpura.
2  a panel to develop a practice guideline for idiopathic thrombocytopenic purpura.
3 ctiveness of any treatment for patients with idiopathic thrombocytopenic purpura and persistent sever
4 telet production (Essential Thrombocythemia, Idiopathic Thrombocytopenic Purpura) and decreased upon
5 ause there are no specific tests that define idiopathic thrombocytopenic purpura, and management deci
6 on in various platelet disorders, especially idiopathic thrombocytopenic purpura, before consideratio
7 that the patient suffers from a rare form of idiopathic thrombocytopenic purpura caused by a GPVI-spe
8  if they were more than 16 years of age, had idiopathic thrombocytopenic purpura for more than 3 mont
9 aemorrhagic (IRR 1.47, 95%CI: 1.04-2.08) and idiopathic thrombocytopenic purpura (IRR 2.80, 95%CI: 1.
10                                              Idiopathic thrombocytopenic purpura is a common acquired
11              Treatment of chronic refractory idiopathic thrombocytopenic purpura is a dilemma because
12                     Because the incidence of idiopathic thrombocytopenic purpura is greatest in young
13 on was found between ChAdOx1 vaccination and idiopathic thrombocytopenic purpura (ITP) (0-27 d after
14           The incidence rate ratio (IRR) for idiopathic thrombocytopenic purpura (ITP) 14-20 days pos
15 a standard treatment for adult patients with idiopathic thrombocytopenic purpura (ITP) for more than
16 astic bone marrow patient and a patient with Idiopathic Thrombocytopenic Purpura (ITP) for the same p
17                  The pathogenesis of chronic idiopathic thrombocytopenic purpura (ITP) involves antib
18                                              Idiopathic thrombocytopenic purpura (ITP) is a common he
19                                     Although idiopathic thrombocytopenic purpura (ITP) is the most co
20                                              Idiopathic thrombocytopenic purpura (ITP) is the most co
21                             Indications were idiopathic thrombocytopenic purpura (ITP), hereditary sp
22 s from 63 sites in 23 countries with chronic idiopathic thrombocytopenic purpura (ITP), platelet coun
23 th platelet destructive disorders, including idiopathic thrombocytopenic purpura (ITP), posttransfusi
24 ic disorders, the authors concluded that, in idiopathic thrombocytopenic purpura (ITP), production of
25 a associated with myelodysplastic syndromes, idiopathic thrombocytopenic purpura, thrombocytopenia du
26               However, patients with chronic idiopathic thrombocytopenic purpura who harbor predomina