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1 g the high restriction of VJ region usage in POEMS syndrome.
2               We identified 99 patients with POEMS syndrome.
3 nopathy Monoclonal-protein and Skin Changes (POEMS) syndrome.
4     This review discusses several aspects of POEMS syndrome and includes the most recently published
5 ion of features that should strongly suggest POEMS syndrome as part of the differential diagnosis.
6               The clinical manifestations of POEMS syndrome can be debilitating; therefore, early dia
7                                          The POEMS syndrome (coined to refer to polyneuropathy, organ
8  in the University College London Hospital's POEMS syndrome database (n=100) and from the National Im
9                        Sixteen patients with POEMS syndrome have undergone PBSCT at Mayo.
10 isease entities showing higher serum VEGF in POEMS syndrome; however, it is unknown whether serum lev
11 help establish or eliminate the diagnosis of POEMS syndrome in uncertain cases.
12 the bone marrow (BM) of 83% of patients with POEMS syndrome, including some in whom BM tests routinel
13 de that the median survival of patients with POEMS syndrome is 165 months, independent of the number
14                                              POEMS syndrome is a paraneoplastic syndrome whose acrony
15                                              POEMS syndrome is a rare plasma cell dyscrasia presentin
16                                          The POEMS syndrome is associated with elevated vascular endo
17                                              POEMS syndrome is characterized by peripheral neuropathy
18   These findings imply that the pathology of POEMS syndrome is diffusely distributed (uniform demyeli
19                                    PBSCT for POEMS syndrome is effective therapy but may also be asso
20 hy, monoclonal gammopathy, and skin changes (POEMS) syndrome is a rare multisystem disease resulting
21                                              POEMS syndrome may be underdiagnosed because of its rari
22                                          The POEMS syndrome (polyradiculoneuropathy, organomegaly, mu
23                 Among selected patients with POEMS syndrome, radiation produces durable, meaningful r
24                              Misdiagnosis in POEMS syndrome results in diagnostic delay, disease prog
25                     Of the 146 patients with POEMS syndrome seen at the Mayo Clinic between January 1
26                                              POEMS syndrome should be considered in the differential
27                                   NCS/EMG of POEMS syndrome suggests both axonal loss and demyelinati
28 wth factor (VEGF) more accurately identifies POEMS syndrome than the current standard of care.
29                                              POEMS syndrome (the acronym reflects the common features
30 ed plasma levels of VEGF in 29 patients with POEMS syndrome with those of other disorders (n = 76).
31 urine and neuropathy should be evaluated for POEMS syndrome with use of imaging to assess whether scl
32 abundance PC clones in BM and assign them to POEMS syndrome, with all the consequences for therapeuti