Sheri Spunt
0000-0002-1669-2676
180 papers found
Refreshing results…
Surgery alone is sufficient therapy for children and adolescents with low-risk synovial sarcoma: A joint analysis from the European paediatric soft tissue sarcoma Study Group and the Children's Oncology Group
Pleomorphic myxoid liposarcoma in an adolescent with Li–Fraumeni syndrome
Potential pitfalls of mass spectrometry to uncover mutations in childhood soft tissue sarcoma: A report from the Children’s Oncology Group
Pulmonary Function after Treatment for Childhood Cancer. A Report from the St. Jude Lifetime Cohort Study (SJLIFE)
Limited Margin Radiation Therapy for Children and Young Adults With Ewing Sarcoma Achieves High Rates of Local Tumor Control
Opportunities for Improvement in Pathology Reporting of Childhood Nonrhabdomyosarcoma Soft Tissue Sarcomas
Measurement of glomerular filtration rate by dynamic contrast‐enhanced magnetic resonance imaging using a subject‐specific two‐compartment model
MRI and CT of Low-Grade Fibromyxoid Sarcoma in Children: A Report From Children's Oncology Group Study ARST0332
Hemipelvectomie interne bilatérale pour ostéosarcome chez un patient pédiatrique antérieurement traité pour rhabdomyosarcome
Bilateral internal hemipelvectomy for osteosarcoma in a pediatric patient previously treated for rhabdomyosarcoma
Sarcoma
Subsequent Malignant Neoplasms in Pediatric Patients Initially Diagnosed With Neuroblastoma:
Phase I Clinical Trial of Ifosfamide, Oxaliplatin, and Etoposide (IOE) in Pediatric Patients With Refractory Solid Tumors:
Delayed primary excision with subsequent modification of radiotherapy dose for intermediate-risk rhabdomyosarcoma: A report from the Children's Oncology Group Soft Tissue Sarcoma Committee
Imaging Features of Alveolar Soft-Part Sarcoma: A Report From Children's Oncology Group Study ARST0332
Cumulative alkylating agent exposure and semen parameters in adult survivors of childhood cancer: a report from the St Jude Lifetime Cohort Study
Growth Plate Abnormalities in Pediatric Cancer Patients Undergoing Phase 1 Anti-Angiogenic Therapy: A Report From the Children's Oncology Group Phase I Consortium
Clinical features and outcomes of young patients with head and neck non-rhabdomyosarcoma soft tissue sarcomas
Targeting Oxidative Stress in Embryonal Rhabdomyosarcoma
Histologic and Clinical Characteristics Can Guide Staging Evaluations for Children and Adolescents With Rhabdomyosarcoma: A Report From the Children's Oncology Group Soft Tissue Sarcoma Committee
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