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1 ;q11.2), which occurs in synovial sarcoma, a soft tissue tumor.
2 ibroblastic tumor (IMT) is a relatively rare soft tissue tumor.
3 ed patients with the aggressive form of this soft-tissue tumor.
4  in this highly aggressive group of bone and soft tissue tumors.
5 rcomas are a heterogeneous group of bone and soft tissue tumors.
6 t metastasis to bone, osteolytic tumors, and soft tissue tumors.
7 ce of GISTs and is rarely expressed in other soft tissue tumors.
8  that is being made in the classification of soft tissue tumors.
9  been found in a significant number of human soft tissue tumors.
10 examination of benign and malignant bond and soft tissue tumors.
11 s in 7 others; all below 2 years of age with soft tissue tumors.
12 esting new avenues for targeted treatment of soft tissue tumors.
13 c, colorectal, esophago-gastric, and sarcoma/soft-tissue tumors.
14 assess radiation dose to critical organs and soft-tissue tumors.
15  osteolytic bone disease and developed fewer soft-tissue tumors.
16 183 had primary bone tumors; 133 had primary soft-tissue tumors.
17 ypes, with the highest frequency observed in soft tissue tumors (20%), osteosarcomas (16%) and esopha
18                                Patients with soft tissue tumors accounted for 20% of the study popula
19 s therapeutics for the treatment of bone and soft tissue tumors along with other neoplasms driven by
20 te the expression of perilipins in 478 human soft tissue tumors and 60 respective normal tissues.
21 ree conditional models developed spontaneous soft tissue tumors and disseminated disease in the absen
22 -specific and applicable to the dosimetry of soft-tissue tumors and normal organs.
23 ronic acid protected Tax+ mice from bone and soft-tissue tumors and prolonged survival.
24 clear, an excess of non-Hodgkin's lymphomas, soft tissue tumors, and, in the case of adolescent girls
25     Because these tumors are rare and benign soft tissue tumors are common, many are initially though
26  readily distinguished from 27 other diverse soft tissue tumors based on their gene expression patter
27 xome and transcriptome sequencing of bone or soft tissue tumor biopsies from a cohort of 150 mCRPC af
28                                     Bone and soft tissue tumors (BSTT) are relatively poorly understo
29 -FDG PET scans also strongly correlated with soft-tissue tumor burden (P < 0.05).
30            Synovial sarcoma is an aggressive soft tissue tumor characterized by a chromosomal translo
31            Synovial sarcoma is an aggressive soft tissue tumor characterized by a specific chromosoma
32                                              Soft tissue tumors comprise a vast and heterogeneous gro
33                      Data from a prospective soft tissue tumor database was used to analyze clinical
34 anscription factor critical for the bone and soft tissue tumor Ewing sarcoma.
35 leading to ulnar nerve instability and focal soft tissue tumors (fibromas, lipomas, etc).
36 en utilized successfully to treat and ablate soft tissue tumors for over 15 years.
37 s some important recent work in two selected soft tissue tumors-gastrointestinal stromal tumor and in
38 ins as markers for differential diagnosis of soft tissue tumors has only been studied in a few cases.
39 omyosarcoma (RMS), the most common malignant soft tissue tumor in children, has several histologic su
40 (RMS) is the most commonly occurring type of soft tissue tumor in children.
41 oma (SS) is the second most common malignant soft tissue tumor in children.
42  Endothelial cell tumors are the most common soft tissue tumors in infants, yet little is known about
43  Endothelial cell tumors are the most common soft tissue tumors in infants.
44 was performed to evaluate a presumed forearm soft-tissue tumor in a 26-year-old man.
45 c rhabdomyosarcoma (ERMS) is the most common soft-tissue tumor in children.
46 r multiphasic bone scans may localize common soft-tissue tumors in neurofibromatosis.
47 radical ablative therapy in the treatment of soft-tissue tumors in the liver, kidney, prostate, and p
48 rkers exist, and the cell of origin for many soft tissue tumors is unknown.
49 and, theoretically, separates the gland from soft-tissue tumors lateral to the gland.
50 Lu-PSMA-617 than for [(177)Lu]Lu-PSMA-I&T in soft tissue tumor lesions (4.19 vs. 2.94 Gy/GBq; P = 0.2
51  synthetic DOG1 peptides was assessed on two soft tissue tumor microarrays.
52 onal IMD placement and retrieval in a rabbit soft tissue tumor model was technically feasible and saf
53 wing sarcoma (EWS) is an aggressive bone and soft tissue tumor of children and young adults in which
54 ation in Ewing Sarcoma, a malignant bone and soft tissue tumor of children and young adults.
55         Here, we report that SP cells from a soft tissue tumor of enigmatic origin termed undifferent
56      Ossifying fibromyxoid tumor (OFMT) is a soft tissue tumor of unknown lineage.
57          We systematically assessed bone and soft tissue tumors on 45 whole-body computed tomography
58 gland and primary orbital and ocular adnexal soft tissue tumors; reappraisal of diagnostic, prognosti
59 bility, CT characteristics, and frequency of soft tissue tumors represent new knowledge and offer a n
60 oxels of bone, lung, adipose tissue, muscle, soft tissue, tumor, steel, and aluminum meet the same cr
61 of MDM2 amplification than p53 mutation were soft tissue tumors, testicular germ cell cancers and neu
62                       Lipoblastomas are rare soft tissue tumors that occur primarily in young childre
63                  Ewing sarcoma is a bone and soft-tissue tumor that depends on the activity of the EW
64 y, at which time the common peripheral nerve soft-tissue tumors that occur in this syndrome (neurofib
65        Ewing sarcoma is a pediatric bone and soft tissue tumor treated with chemotherapy, radiation,
66                              The majority of soft tissue tumors were first delineated on the basis of
67       Patients with malignant skin tumors or soft tissue tumors were recruited if they had limited tr
68 omyosarcoma (RMS) is an aggressive childhood soft tissue tumor, which exists in oncoprotein PAX-FOXO1
69                    Leiomyosarcoma (LMS) is a soft tissue tumor with a significant degree of morpholog
70 wing sarcoma (EWS) is an aggressive bone and soft tissue tumor with high susceptibility to metastasiz
71 myosarcoma (ARMS) is an aggressive pediatric soft tissue tumor with striated muscle differentiation.
72          The tissue microarrays included 587 soft tissue tumors, with 149 GISTs, including 127 GIST c
73 e rare, locally aggressive, highly recurrent soft-tissue tumors without approved treatments.