ライフサイエンスコーパス: unclassifiable

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1 Approximately 10% of the patients were unclassifiable.

2 ther patterns were subcortical myoclonus and unclassifiable.

3 2%), respectively, and 144 studies (5%) were unclassifiable.

4 1% (n=4), G6a: 1% (n=8), G6e: <1% (n=1), and unclassifiable: 1% (n=9).

5 to 6.1%, p < 0.0001), and 41.7% decrease in unclassifiable (13.9% to 8.1%, p < 0.0001) scans during

6 lomonocytic leukemia (CMML; 48%) and MDS/MPD-unclassifiable (38%).

7 lomonocytic leukemia, isolated 5q- syndrome, unclassifiable, and therapy-related MDS were excluded.

8 uring clinical subtyping, some patients were unclassifiable by the 2011 guidelines whereas others sim

9 The ten patients who were initially unclassifiable by the LPD analyses were subclassified by

10 ardial infarction and definite, possible, or unclassifiable coronary deaths in men and women aged 35-

11 related; 1076 non-AIDS-defining; 509 unknown/unclassifiable deaths).

12 chaemia, 92 critical limb ischaemia); and 62 unclassifiable deaths.

13 latter of which included both ABC DLBCL and unclassifiable DLBCL) on the basis of immunophenotype by

14 Interestingly, most of the unclassifiable-DLBCL by GEP showed a strong similarity t

15 tory central cell and the remaining two were unclassifiable excitatory cells.

16 ptom criteria were applied, 100 (21.6%) were unclassifiable including 21 (21.0%) with definite pulmon

17 th right temporal lobe presentations, and 11 unclassifiable including eight with motor neuron disease

18 pression (1 B-CLL, 1 blastoid mantle cell, 1 unclassifiable low grade B-cell lymphoma).

19 kin's lymphoma (3%), B-cell lymphoma (1.4%), unclassifiable lymphoma (2.8%), or a diagnosis other tha

20 tinctive enough to allow its separation from unclassifiable MDS/MPN (MDS/MPN-U).

21 19 lentigo maligna melanomas, 18 AMs, and 12 unclassifiable melanomas) using fluorescence in situ hyb

22 Combining the unclassifiable MI group with either STEMI or NSTEMI did

23 vents occurred (829 NSTEMIs, 249 STEMIs, 296 unclassifiable MIs).

24 urine MPN model with features of a pediatric unclassifiable mixed MDS/MPN and mimics many clinical ma

25 (ET); primary myelofibrosis (PMF); and MPN, unclassifiable (MPN,U).

26 vera, 547 with myelofibrosis, and 1720 with unclassifiable MPNs) and 4.3 (95% CI, 4.1-4.4) for the 7

27 myelofibrosis, and 1.5 (95% CI, 1.1-2.1) for unclassifiable MPNs.

28 themia, polycythemia vera, myelofibrosis, or unclassifiable MPNs.

29 ified 6217 PV, 2838 ET, 1172 MF, and 812 MPN unclassifiable (NOS) patients diagnosed in Sweden, 43 55

30 .9%) as "probable asthma," 1,193 (29.1%) as "unclassifiable obstructive airway disease, " 626 (15.3%)

31 .8%) as "probable asthma," 1,996 (31.1%) as "unclassifiable obstructive airway disease," 228 (3.5%) a

32 Longitudinal evaluations of initially unclassifiable patients showed that the semantic variant

33 n-subtype B viruses in both classifiable and unclassifiable PR genes, with 36I being the predominant

34 s were unclassifiable, whereas 2% (7 of 301) unclassifiable PR sequences were reported for a global c

35 , atypical chronic myeloid leukemia, MDS/MPN-Unclassifiable, ring sideroblasts associated with marked

36 Compared with classifiable PR sequences, unclassifiable sequences had significantly more dual and

37 nsonism associated with chromosome 17, three unclassifiable tauopathy, and one argyrophilic grain dis

38 ach), 22 were subtype A1 (10.2%), and 9 were unclassifiable (UC) (4.2%).

39 PTCL-unclassifiable was molecularly heterogeneous, but we wer

40 s from the remaining 25 (23%) specimens were unclassifiable, whereas 2% (7 of 301) unclassifiable PR

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