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1 f SYK, and it is believed to be the cause of peripheral T cell lymphoma.
2 transplant lymphoproliferative disorder, and peripheral T cell lymphoma.
3 (ALCL) is the most common type of pediatric peripheral T-cell lymphoma.
4 ted T-cell lymphoma (EATL) is a rare type of peripheral T-cell lymphoma.
5 stigation for the treatment of patients with peripheral T-cell lymphoma.
6 with large-cell transformation), and two had peripheral T-cell lymphoma.
7 ed adult T-cell leukaemia-lymphoma and other peripheral T-cell lymphomas.
8 e T-cell leukemia (T-ALL) and in a subset of peripheral T-cell lymphomas.
9 of lymphomas, which included a large set of peripheral T-cell lymphomas.
10 a, adult T-cell leukemia/lymphoma, and other peripheral T-cell lymphomas.
11 n TEL-FGFR3 associated with t(4;12)(p16;p13) peripheral T-cell lymphomas.
12 anaplastic large-cell lymphomas, 2/12 nodal peripheral T-cell lymphomas, 1/3 CD8+ cutaneous T-cell l
13 ated HD (100%) and EBV+ Malaysian and Danish peripheral T-cell lymphomas (100%, 61% respectively), bu
14 as (15.3%), classic Hodgkin lymphomas (13%), peripheral T-cell lymphomas (6.3%) of which angioimmunob
15 ;q22) translocation was found in a subset of peripheral T cell lymphomas and was shown to result in a
16 le the diagnosis of unusual entities such as peripheral T-cell lymphomas and Hodgkin disease in patie
17 CD134 may be helpful in subclassification of peripheral T-cell lymphomas and that the patterns of TNF
18 s that can easily be mistaken for intestinal peripheral T-cell lymphoma, and lead to aggressive thera
21 is study was to compare in a large series of peripheral T cell lymphoma, as a model of diffuse diseas
22 FGFR3 TDII-induced pre-B cell lymphoma, or a peripheral T-cell lymphoma associated TEL-FGFR3 fusion-i
23 ve been approved for relapsed and refractory peripheral T-cell lymphomas based on their activity, alt
24 status (PS) >/= 2; the Prognostic Index for Peripheral T-Cell Lymphoma, comprising: age >/= 60 years
28 th fulminant hepatic failure from an unusual peripheral T cell lymphoma involving the liver and splee
30 xate in Patients with Relapsed or Refractory Peripheral T-Cell Lymphoma) is the largest prospective s
31 astic large cell lymphoma (BIA-ALCL), a rare peripheral T-cell lymphoma, is increasing in incidence.
32 ogies included DLBCL (n = 21), MCL (n = 13), peripheral T-cell lymphoma (n = 8), transformed follicul
33 ymphomas, n = 10; mycosis fungoides, n = 13; peripheral T-cell lymphoma, n = 5; other T-cell lymphoma
34 nts (112 anaplastic large-cell lymphoma, 102 peripheral T-cell lymphoma not otherwise specified, 27 a
35 le to successfully separate ALK(-) ALCL from peripheral T-cell lymphoma not otherwise specified, with
36 s, 9 angioimmunoblastic T-cell lymphomas, 11 peripheral T-cell lymphomas not otherwise specified (PTC
37 mphoma (AITL) and in 22 of 58 (38%) cases of peripheral T-cell lymphoma, not otherwise specified (PTC
42 ted by T-cell responses were associated with peripheral T-cell lymphoma (OR = 2.14, 95% CI: 1.35, 3.3
45 Anaplastic large cell lymphoma (ALCL) is a peripheral T-cell lymphoma presenting mostly in children
49 n addition, a significant subset of cases of peripheral T cell lymphoma (PTCL), 39 of 81 cases (48%),
50 lymphocytic leukemia (CLL) and CD8-positive peripheral T cell lymphomas (PTCL) in EmuSRalpha-tTA;Tet
52 ion of Lin28b in vivo leads to an aggressive peripheral T-cell lymphoma (PTCL) characterized by wides
82 cells (TFH) represent a large proportion of peripheral T-cell lymphomas (PTCLs) with poorly understo
83 dotin was reported for CD30(+) nonanaplastic peripheral T-cell lymphomas (PTCLs) with promising effic
86 e differential diagnosis among the commonest peripheral T-cell lymphomas (PTCLs; ie, PTCL not otherwi
87 anned subset analysis included patients with peripheral T-cell lymphomas (PTCLs; n = 35), specificall
88 t T-cell leukaemia-lymphoma, four with other peripheral T-cell lymphomas) receiving lenalidomide, dos
90 absence of a mass lesion or lymphadenopathy, peripheral T cell lymphoma should be included in the dif
92 ive adult T-cell leukaemia-lymphoma or other peripheral T-cell lymphoma subtypes, and at least one pr
95 a had a partial response, and 1 patient with peripheral T-cell lymphoma, unspecified, had a complete
98 ho had relapsed cutaneous T-cell lymphoma or peripheral T-cell lymphoma with prominent cutaneous dise
99 ll lymphoma (AITL) is the second most common peripheral T-cell lymphoma with unusual clinical and pat
101 motherapy because of an initial diagnosis of peripheral T-cell lymphoma, with little or no response,
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