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1 red with tryptase in estimating the need for bone marrow biopsy.
2 emic mastocytosis) and thus candidates for a bone marrow biopsy.
3  cell aggregates, and atypical mast cells on bone marrow biopsy.
4 fficient accuracy to replace routine staging bone marrow biopsy.
5 sponse to up to 31 drugs within 5 days after bone marrow biopsy.
6 , urine and serum immunoelectrophoresis, and bone marrow biopsy.
7  the diagnosis usually depends on results of bone marrow biopsy.
8 ng pure red cell aplasia (PRCA) confirmed by bone marrow biopsy.
9 pared with hematologic response criteria and bone marrow biopsies.
10 ot spot density compared with normal control bone marrow biopsies.
11 nical relevance of expression in 55 archival bone marrow biopsies.
12 e myeloid leukemia (AML) routinely undergo a bone marrow biopsy 7-10 days after induction chemotherap
13                                  Analysis of bone marrow biopsies after CTL019 revealed 8 patients wi
14      Response was assessed by weekly CBC and bone marrow biopsy after cycle 2 and after each subseque
15                                              Bone marrow biopsy analysis showed 5% plasma cells, whic
16 nohistochemically by factor VIII staining of bone marrow biopsies and quantified by assessment of mic
17 umbers of blood vessels were measured in 145 bone marrow biopsies and the levels of vascular endothel
18                                The patient's bone marrow biopsy and aspirate displayed unique patholo
19 enia and negligible gene marking, diagnostic bone marrow biopsy and aspirate were performed at day 88
20                                            A bone marrow biopsy and aspiration revealed a mildly hype
21 tiple myeloma was diagnosed and confirmed by bone marrow biopsy and aspiration.
22                           Congo red stain on bone marrow biopsy and fat pad aspirate was negative for
23 cible ischemia in Tc-99m SPECT who underwent bone marrow biopsy and were allocated to cells (n=16) or
24 cible ischemia in Tc-99m SPECT who underwent bone marrow biopsy and were allocated to cells (n=16) or
25 work-up consisted of a complete blood count, bone marrow biopsy, and immunohistochemical and histoche
26 agnosis, in the selection of those needing a bone marrow biopsy, and in the documentation of disease
27 ria to identify those patients who require a bone marrow biopsy, and whether the pathogenesis of IA i
28 s or suspicious lymphocytic infiltrates in a bone marrow biopsy as the sole suggestion of residual di
29 )At-radioimmunotherapy, after lymph node and bone marrow biopsies at 2-4 and/or 19 h after injection.
30     The diagnosis of 661 PMF patients with a bone marrow biopsy at presentation was revised according
31 one-metastatic CRPC who underwent transiliac bone marrow biopsy between October 2007 and March 2010.
32  B-cell lymphoma (DLBCL), the sensitivity of bone marrow biopsy (BMB) for the detection of bone marro
33                                     Skin and bone marrow biopsies can thus be used to generate de nov
34        A percutaneous biopsy of the mass and bone marrow biopsy confirmed the diagnosis of primary ad
35    Serum paraproteins and/or light chains or bone marrow biopsy defined response.
36 araspinal mass was discovered, and tumor and bone marrow biopsies disclosed rhabdomyosarcoma.
37 agrelide therapy should undergo surveillance bone marrow biopsy every 2 to 3 years and that those who
38                                              Bone marrow biopsy exhibited mostly mixed patterns of sm
39 r urticaria pigmentosa or the characteristic bone marrow biopsy finding of multifocal mast-cell aggre
40 iogenesis in plasmacytoma biopsy samples and bone marrow biopsies from 25 patients.
41                                 We evaluated bone marrow biopsies from 40 children with newly diagnos
42 iption factor (MITF), is highly expressed in bone marrow biopsies from 9 of 10 patients with systemic
43                                Evaluation of bone marrow biopsies from myeloma patients revealed a st
44                        Moreover, analysis of bone marrow biopsies from myeloma patients reveals a pos
45                                           In bone marrow biopsies from patients with DBA or del(5q) m
46 simultaneous analysis of WM patient sera and bone marrow biopsies identified a set of dysregulated cy
47 nohistochemical paraffin section staining of bone marrow biopsies in the staging of B-cell malignant
48                                     Although bone marrow biopsies in these patients showed increased
49 t optimal test indicating the necessity of a bone marrow biopsy in ISM-suspected patients.
50  commonly used test to estimate the need for bone marrow biopsy in patients suspected to have indolen
51  tumor DNA (ctDNA) is directly comparable to bone marrow biopsy in representing the genomic heterogen
52 o detected by immunohistochemistry in normal bone marrow biopsies, indicating an in vivo function.
53 oring response to therapy; also, the role of bone marrow biopsy is being revisited.
54                                            A bone marrow biopsy is no longer indicated for the routin
55                                              Bone marrow biopsies largely replaced by PCa were analyz
56                                              Bone marrow biopsy may reveal hemophagocytosis and marro
57 aranase activity in the plasma isolated from bone marrow biopsies of 100 patients reveals 86 positive
58 e to quantify IDO-1 expression on diagnostic bone marrow biopsies of AML patients in order to facilit
59  this cutoff correctly classifies diagnostic bone marrow biopsies of MPN,U patients specified upon fo
60                       In this investigation, bone marrow biopsies of the anterior iliac crest were ex
61                   Responses were assessed by bone marrow biopsy on day 15 of the first course and by
62 drome features with the exception that their bone marrow biopsy pathology revealed abundant neutrophi
63                                              Bone marrow biopsy performed in two of these five patien
64 g/gm Cr corresponded with the high degree of bone marrow biopsies positive for atypical mast cells, t
65 re staged using clinical assessment, CT, and bone marrow biopsy (RATHL stage).
66                                              Bone marrow biopsy revealed hypercellular marrow.
67                                              Bone marrow biopsy revealed no evidence of infectious or
68                       MAC loads in bilateral bone marrow biopsy samples from 7 subjects were highly c
69                                       Serial bone marrow biopsies showed normalization of trilineage
70                              Comparison with bone marrow biopsies showed that FDG-PET was not reliabl
71                                              Bone marrow biopsy showed 60% infiltration with lambda l
72                      Immunohistochemistry of bone marrow biopsy showed an increased number of plasma
73             After histologic analysis of the bone marrow biopsy specimen, diagnosis of Waldenstrom ma
74                               In this study, bone marrow biopsy specimens from 36 patients with T-cel
75   The TMA was constructed using pretreatment bone marrow biopsy specimens from 64 adult patients with
76 orulae were detected on peripheral smear and bone marrow biopsy specimens, and PCR amplified Ehrlichi
77 rum lgs, and immunohistochemical staining of bone marrow biopsy specimens.
78                                  Analysis of bone marrow-biopsy specimens obtained from two patients
79              Immunohistochemical analysis of bone marrow-biopsy specimens showed that only myeloma ce
80                      These data suggest that bone marrow biopsy using antigen-targeted magnetic nanop
81                                              Bone marrow biopsy was done on day -7 to estimate radiat
82 s was nondiagnostic, and lumbar puncture and bone marrow biopsies were negative.
83                      One hundred eighty-four bone marrow biopsies were obtained, and 48 had prostate
84                       Between 1989 and 1994, bone marrow biopsies were performed on 393 breast cancer
85    PDGFR-expressing tumor declined on serial bone marrow biopsies with combination therapy alone.

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