Ewing sarcoma
Ewing sarcoma is the second most frequent bone tumour of childhood and adolescence that
can also arise in soft tissue. Ewing sarcoma is a highly aggressive cancer, with a survival of …
can also arise in soft tissue. Ewing sarcoma is a highly aggressive cancer, with a survival of …
Ewing sarcoma: current management and future approaches through collaboration
N Gaspar, DS Hawkins, U Dirksen, IJ Lewis… - Journal of Clinical …, 2015 - ascopubs.org
Ewing sarcoma (ES) is an aggressive sarcoma of bone and soft tissue occurring at any age
with a peak incidence in adolescents and young adults. The treatment of ES relies on a …
with a peak incidence in adolescents and young adults. The treatment of ES relies on a …
[CITAZIONE][C] DeVita, Hellman, and Rosenberg's cancer: principles & practice of oncology
VT DeVita - 2008 - books.google.com
Acclaimed by the worldwide medical community as" a staple reference text in the medical
oncologist's library"(JAMA), DeVita, Hellman, and Rosenberg's Cancer: Principles and …
oncologist's library"(JAMA), DeVita, Hellman, and Rosenberg's Cancer: Principles and …
[LIBRO][B] Pathology and genetics of head and neck tumours
L Barnes - 2005 - books.google.com
Pathology and Genetics of Head and Neck Tumoursis the latest volume in the new WHO
series, on histological and genetic ty** of human tumours. This authoritative, concise …
series, on histological and genetic ty** of human tumours. This authoritative, concise …
Ewing's sarcoma
NJ Balamuth, RB Womer - The lancet oncology, 2010 - thelancet.com
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 …
children and adolescents, has improved survival from about 10% in the period before …
PAX3-FKHR and PAX7-FKHR Gene Fusions Are Prognostic Indicators in Alveolar Rhabdomyosarcoma: A Report From the Children's Oncology Group
PHB Sorensen, JC Lynch, SJ Qualman… - Journal of Clinical …, 2002 - ascopubs.org
PURPOSE: Alveolar rhabdomyosarcoma (ARMS) is an aggressive soft tissue malignancy of
children and adolescents. Most ARMS patients express PAX3-FKHR or PAX7-FKHR gene …
children and adolescents. Most ARMS patients express PAX3-FKHR or PAX7-FKHR gene …
Common musculoskeletal tumors of childhood and adolescence
CAS Arndt, WM Crist - New England Journal of Medicine, 1999 - Mass Medical Soc
Common malignant tumors of the musculoskeletal system in children, adolescents, and
young adults (< 30 years old) include rhabdomyosarcoma, osteosarcoma, and Ewing's …
young adults (< 30 years old) include rhabdomyosarcoma, osteosarcoma, and Ewing's …
SYT–SSX Gene Fusion as a Determinant of Morphology and Prognosis in Synovial Sarcoma
A Kawai, J Woodruff, JH Healey… - … England Journal of …, 1998 - Mass Medical Soc
Background Synovial sarcomas account for up to 10 percent of soft-tissue sarcomas and
include two major histologic subtypes, biphasic and monophasic, defined respectively by the …
include two major histologic subtypes, biphasic and monophasic, defined respectively by the …
Impact of SYT-SSX Fusion Type on the Clinical Behavior of Synovial Sarcoma: A Multi-Institutional Retrospective Study of 243 Patients
Synovial sarcomas are aggressive spindle cell sarcomas containing in some cases areas of
epithelial differentiation. They consistently show a specific t (X; 18; p11; q11), which usually …
epithelial differentiation. They consistently show a specific t (X; 18; p11; q11), which usually …
Updates on cytogenetics and molecular genetics of bone and soft tissue tumors:: Ewing sarcoma and peripheral primitive neuroectodermal tumors
AA Sandberg, JA Bridge - Cancer genetics and cytogenetics, 2000 - Elsevier
Cytogenetics of Bone and Soft Tissue Tumors [1]. In view of the remarkable developments in
this field since 1994, both in the cytogenetic and particularly in the molecular genetic …
this field since 1994, both in the cytogenetic and particularly in the molecular genetic …