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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
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
19 enia and negligible gene marking, diagnostic bone marrow biopsy and aspirate were performed at day 88
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
37 agrelide therapy should undergo surveillance bone marrow biopsy every 2 to 3 years and that those who
39 r urticaria pigmentosa or the characteristic bone marrow biopsy finding of multifocal mast-cell aggre
42 iption factor (MITF), is highly expressed in bone marrow biopsies from 9 of 10 patients with systemic
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
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.
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
62 drome features with the exception that their bone marrow biopsy pathology revealed abundant neutrophi
64 g/gm Cr corresponded with the high degree of bone marrow biopsies positive for atypical mast cells, t
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
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