Results 191 to 200 of about 37,353 (245)
Curatively Resected Mesenteric Lymph Node Recurrence of Ewing Sarcoma. [PDF]
Surg Case RepTachikawa A +10 more
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The Efficacy of High-Dose Chemotherapy Followed by Autologous Stem Cell Transplantation in Ewing Sarcoma Patients. [PDF]
J Clin MedKuzu ÖF +9 more
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Ortopediia travmatologiia i protezirovanie, 2002 B N, TSYPKIN, A A, ZAPOROZHETS
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cIAP1 inhibitor of apoptosis is a tumor suppressor in Ewing sarcoma
Cidre-Aranaz F +12 more
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The Lancet Oncology, 2010
Progress in the treatment of Ewing's sarcoma, the second most common bone tumour in children and adolescents, has improved survival from about 10% in the period before chemotherapy was introduced to about 75% today for patients with localised tumours. However, patients with metastases still fare badly, and the therapy carries short-term and long-term ...
Naomi J, Balamuth, Richard B, Womer
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Progress in the treatment of Ewing's sarcoma, the second most common bone tumour in children and adolescents, has improved survival from about 10% in the period before chemotherapy was introduced to about 75% today for patients with localised tumours. However, patients with metastases still fare badly, and the therapy carries short-term and long-term ...
Naomi J, Balamuth, Richard B, Womer
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Radiologic Clinics of North America, 1993
Ewing's sarcoma is a highly malignant tumor of uncertain origin. A strong relationship is suggested between Ewing's sarcoma and tumors of neural origin. The radiologic manifestation of Ewing's sarcoma are protean and lesions may be lytic, mixed lytic-sclerotic, or rarely, predominantly sclerotic.
K D, Eggli, T, Quiogue, R P, Moser
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Ewing's sarcoma is a highly malignant tumor of uncertain origin. A strong relationship is suggested between Ewing's sarcoma and tumors of neural origin. The radiologic manifestation of Ewing's sarcoma are protean and lesions may be lytic, mixed lytic-sclerotic, or rarely, predominantly sclerotic.
K D, Eggli, T, Quiogue, R P, Moser
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Current Treatment Options in Oncology, 2000
Patients with Ewing's sarcoma should be transferred to a comprehensive cancer center for evaluation and management when the diagnosis is suspected. Proper biopsy technique is essential to preserve all therapeutic options, including limb preservation surgery.
P A, Meyers, A S, Levy
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Patients with Ewing's sarcoma should be transferred to a comprehensive cancer center for evaluation and management when the diagnosis is suspected. Proper biopsy technique is essential to preserve all therapeutic options, including limb preservation surgery.
P A, Meyers, A S, Levy
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Seminars in Diagnostic Pathology, 2014
Classification of small round cell tumors of bone is often challenging due to overlapping clinicopathologic features. The purpose of this article is to review the clinical, radiological, histologic, and molecular features of Ewing sarcoma and to provide a discussion of the differential diagnosis of small round cell tumors of bone.
Eun-Young K, Choi +4 more
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Classification of small round cell tumors of bone is often challenging due to overlapping clinicopathologic features. The purpose of this article is to review the clinical, radiological, histologic, and molecular features of Ewing sarcoma and to provide a discussion of the differential diagnosis of small round cell tumors of bone.
Eun-Young K, Choi +4 more
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Oral Surgery, Oral Medicine, Oral Pathology, 1971
Abstract Ewing's sarcoma, a rare neoplasm that usually occurs in persons under 25 years of age, is considered the most lethal of all bone tumors. Treatment usually consists of radiation therapy. Although the value of prophylactic chemotherapy has not been established, encouraging results have been achieved with the use of Cytoxan at periodic ...
W, Carl +3 more
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Abstract Ewing's sarcoma, a rare neoplasm that usually occurs in persons under 25 years of age, is considered the most lethal of all bone tumors. Treatment usually consists of radiation therapy. Although the value of prophylactic chemotherapy has not been established, encouraging results have been achieved with the use of Cytoxan at periodic ...
W, Carl +3 more
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Virchows Archiv A Pathological Anatomy and Histology, 1978
Clinicopathologic study of five cases of soft tissue tumors revealed distinct differences from skeletal Ewing's sarcoma in preferential localisation and mean age. The cases examined here are similar to cases described earlier as "extraskeletal Ewing's sarcomas".
P, Meister, J M, Gokel
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Clinicopathologic study of five cases of soft tissue tumors revealed distinct differences from skeletal Ewing's sarcoma in preferential localisation and mean age. The cases examined here are similar to cases described earlier as "extraskeletal Ewing's sarcomas".
P, Meister, J M, Gokel
openaire +2 more sources