Incidence of Soft Tissue Sarcomas in Adults --;Clinical Management of Soft Tissue Sarcomas --;Soft Tissue Sarcomas in the Kiel Pediatric Tumor Registry --;Molecular Biological Aspects of Soft Tissue Tumors --;Characteristic Chromosome Abnormalities and Karyotype Profiles in Soft Tissue Tumors --;DNA Ploidy in Soft Tissue Tumors: An Evaluation of the Prognostic Implications in the Different Tumor Types --;Heterogeneity in Malignant Soft Tissue Tumors --;Grading of Soft Tissue Sarcomas: Proposal for a Reproducible, Albeit Limited Scheme --;Fibrous Tumors and Tumor-like Lesions of Childhood: Diagnosis, Differential Diagnosis, and Prognosis --;Malignant Fibrous Histiocytoma: 'A Fibrohistiocytic' or Primitive, Fibroblastic Sarcoma --;Recent Advances in Tumors of Adipose Tissue --;Classification of Rhabdomyosarcoma --;Spindle Cell Rhabdomyosarcoma: Histologic Variant of Embryonal Rhabdomyosarcoma with Association to Favorable Prognosis --;Alveolar Rhabdomyosarcoma: A Prognostically Unfavorable Rhabdomyosarcoma Type and Its Necessary Distinction from Embryonal Rhabdomyosarcoma --;Malignant Peripheral Neuroectodermal Tumor --;Leiomyosarcoma --;Malignant Peripheral Nerve Sheath Tumors --;Rare Soft Tissue Sarcomas.
یادداشتهای مربوط به خلاصه یا چکیده
متن يادداشت
Soft tissue tumors are a very heterogeneous group of tumors in terms of histogenesis, morphology, cytogenetics, molecular biology, clinical manifestation, and prognosis.
موضوع (اسم عام یاعبارت اسمی عام)
موضوع مستند نشده
Medicine.
موضوع مستند نشده
Oncology.
موضوع مستند نشده
Pathology.
رده بندی کنگره
شماره رده
RB1
نشانه اثر
.
E358
1995
نام شخص به منزله سر شناسه - (مسئولیت معنوی درجه اول )