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1 time the clinical and pathologic features of hairy cell leukemia.
2 1 in both leukemia and lymphoma, and BRAF in hairy cell leukemia.
3 ll known and revolutionized the treatment of hairy cell leukemia.
4  signaling important for the pathogenesis of hairy cell leukemia.
5 ted kinase (ERK) in the hairy cells (HCs) of hairy cell leukemia.
6 mphomas with villous lymphocytes (SLVLs) and hairy cell leukemia.
7       Only 2 of 40 deaths were attributed to hairy cell leukemia.
8 denosine analog, is clinically effective for hairy cell leukemia.
9 y profile when administered to patients with hairy cell leukemia.
10  BRAF V600E is the genetic lesion underlying hairy-cell leukemia.
11 tive in patients with relapsed or refractory hairy-cell leukemia.
12 ia (29), T-cell prolymphocytic leukemia (3), hairy cell leukemia (1), adult T-cell leukemia/lymphoma
13 relapse-free survival times in patients with hairy cell leukemia, a disease that historically had bee
14 cally, this paper describes the frequency of hairy cell leukemia among all adult leukemias and charac
15 ons is helpful in the diagnosis of classical hairy cell leukemia and a number of histiocytic neoplasm
16  marker of disease activity in patients with hairy cell leukemia and adult T-cell leukemia/lymphoma.
17     Immunotoxin therapy is very effective in hairy cell leukemia and also has activity in other hemol
18 cladribine) is effective in the treatment of hairy cell leukemia and chronic lymphocytic leukemia.
19 lymphoid neoplasm subtypes, most notably for hairy cell leukemia and follicular lymphoma, black predo
20 ate of complete remissions in drug-resistant hairy cell leukemia and has a lower response rate in ped
21       RITs have shown efficacy in refractory hairy cell leukemia and in some children with acute lymp
22  with reports of only a few cases of variant hairy cell leukemia and neurological disease associated
23 ladribine is best known for the treatment of hairy cell leukemia and other lymphoid cancers, it also
24 e been used to treat many diseases including hairy-cell leukemia and hepatitis B and C and have also
25 CldAdo), which is the drug of choice against hairy-cell leukemia and other neoplasms, from 2'-deoxygu
26                     The hairy cells (HCs) of hairy-cell leukemia are intrinsically activated mature c
27                           The description of hairy cell leukemia as a specific clinical entity was pu
28 issions in most patients with drug-resistant hairy cell leukemia but had less activity in leukemias w
29        HA22 is very active in drug-resistant hairy cell leukemia but is less active in children with
30  V600E-expressing human primary melanoma and hairy cell leukemia cells.
31 B-Raf kinase (BRAF mutations) are present in hairy-cell leukemia, cutaneous melanoma, thyroid carcino
32                                          The Hairy Cell Leukemia Foundation convened an international
33 n bone marrow core biopsies of patients with hairy cell leukemia (HCL) after treatment with 2-chlorod
34 s, 28 low grade B-cell lymphomas, 4 cases of hairy cell leukemia (HCL) and 3 plasmacytomas.
35  V600E mutation was reported in all cases of hairy cell leukemia (HCL) but not in other peripheral B-
36  BRAFV600E mutation was recently detected in hairy cell leukemia (HCL) by whole exome sequencing.
37 tic leukemia (CLL) cases, 100% (32 of 32) of hairy cell leukemia (HCL) cases, 15% (5 of 34) of mantle
38                                              Hairy cell leukemia (HCL) derives from a mature B cell a
39       The discovery of effective therapy for hairy cell leukemia (HCL) has increased the relevance of
40                                              Hairy cell leukemia (HCL) is a chronic B-cell leukemia n
41                                              Hairy cell leukemia (HCL) is a chronic lymphoproliferati
42                                              Hairy cell leukemia (HCL) is a chronic mature B-cell neo
43                                              Hairy cell leukemia (HCL) is a distinct clinicopathologi
44                                              Hairy cell leukemia (HCL) is a distinct clinicopathologi
45                                              Hairy cell leukemia (HCL) is a rare, indolent B-cell dis
46                                              Hairy cell leukemia (HCL) is an indolent B-cell neoplasm
47                                              Hairy cell leukemia (HCL) is an uncommon, indolent, chro
48                                              Hairy cell leukemia (HCL) is characterized by underexpre
49                      Cladribine treatment of hairy cell leukemia (HCL) is complicated by neutropenic
50                                              Hairy cell leukemia (HCL) is marked by near 100% mutatio
51                                          One hairy cell leukemia (HCL) patient achieved a complete re
52                                              Hairy cell leukemia (HCL) shows unique clinicopathologic
53 iral oncogene homolog B1 (BRAF) mutations in hairy cell leukemia (HCL) subsets, demonstrating that BR
54                                   To compare hairy cell leukemia (HCL) with chronic lymphocytic leuke
55 produce high response rates in patients with hairy cell leukemia (HCL), a significant number of patie
56 ), 7 of 7 follicular lymphoma (FL), 13 of 17 hairy cell leukemia (HCL), and 2 of 3 mantle cell lympho
57 ch as chronic lymphocytic leukemia (CLL) and hairy cell leukemia (HCL), are associated with myelosupp
58  target on B-cell malignancies, particularly hairy cell leukemia (HCL), but its soluble extracellular
59 sions (CRs) in the majority of patients with hairy cell leukemia (HCL), neither the actual relapse ra
60       These included Hodgkin's disease (HD), hairy cell leukemia (HCL), non-Hodgkin's lymphoma (NHL),
61 e (BRAF V600E) is the key driver mutation in hairy cell leukemia (HCL), suggesting opportunities for
62                                  However, in hairy cell leukemia (HCL), these processes are particula
63  defining the BRAF-V600E driving mutation in hairy cell leukemia (HCL),provide extensive laboratory s
64 ious CDKN1B mutation in 16% of patients with hairy cell leukemia (HCL).
65  recently described as a molecular marker of hairy cell leukemia (HCL).
66 duces protracted remissions in patients with hairy cell leukemia (HCL).
67 nd also occurs in the hematopoietic neoplasm hairy cell leukemia (HCL).
68  accepted as the agent of choice in treating hairy cell leukemia (HCL).
69 tibody, rituximab, in relapsed or refractory hairy cell leukemia (HCL).
70 ates when used as first-line monotherapy for hairy cell leukemia (HCL); however, patients continue to
71  low-grade follicular lymphoma (FL; n = 44), hairy cell leukemia (HCL; n = 15), and reactive lymphoid
72 ity against chronic lymphocytic leukemia and hairy cell leukemia, in general, monoclonal antibodies h
73 ibine followed by rituximab in patients with hairy cell leukemia including the vari-ant form (HCLv).
74                                              Hairy cell leukemia is a chronic B-cell disorder that fo
75                                              Hairy cell leukemia is an indolent, chronic B-cell lymph
76                                              Hairy cell leukemia is an uncommon hematologic malignanc
77                                     Although hairy cell leukemia is uniquely sensitive to interferon-
78 , an immunotoxin with impressive activity in hairy cell leukemia, is in phase II trials in CLL as wel
79 N-alpha2b were approved for the treatment of hairy cell leukemia just 11 years ago.
80 al blood samples obtained from patients with hairy cell leukemia, marginal zone lymphoma, and chronic
81 lymphoma, CLL, acute lymphoblastic leukemia, hairy cell leukemia, non-Hodgkin lymphoma (including rit
82 splenomegaly, constitutional symptoms due to hairy cell leukemia, or recurrent serious infections.
83        Enormous progress in the treatment of hairy cell leukemia over the last five decades has emerg
84                                 Treatment of hairy cell leukemia should be considered for symptomatic
85         Immunophenotypic features in classic hairy cell leukemia show that the leukemic cells express
86 entostatin is a highly effective regimen for hairy cell leukemia that produces durable complete respo
87  BRAF inhibitor vemurafenib in patients with hairy-cell leukemia that had relapsed after treatment wi
88                                              Hairy-cell leukemia that is resistant to treatment with
89  induce complete remissions in patients with hairy-cell leukemia that is resistant to treatment with
90 utcome of young patients with a diagnosis of hairy cell leukemia treated with cladribine.
91                                              Hairy cell leukemia variant (HCLv) presents with high di
92 isms driving variant and IGHV4-34-expressing hairy-cell leukemias, we performed whole-exome sequencin
93                 A total of 358 patients with hairy cell leukemia were treated with cladribine at 0.08
94 d many complete remissions in drug-resistant hairy-cell leukemia when several cycles of the agent can
95 d many complete remissions in drug-resistant Hairy cell leukemia, where many treatment cycles can be
96 notoxin treatment and report that samples of hairy cell leukemia with high levels of Bim protein resp
97 ts profound impact on the natural history of hairy cell leukemia, with responses approaching 100% and

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