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期刊名:Clinical sarcoma research

缩写:CLIN SARCOMA RES

ISSN:2045-3329

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IF/分区:0.0/

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共收录本刊相关文章索引197
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Abhishek Mahajan,Bharat Rekhi,Siddhartha Laskar et al. Abhishek Mahajan et al.
Background: Primary pulmonary artery sarcomas are rare malignant vascular tumors and carry a very poor prognosis. Due to overlapping clinical and radiological features, the differentiation between pulmonary artery thrombo...
Jason Roszik,Wei-Lien Wang,John A Livingston et al. Jason Roszik et al.
Background: PRAME (preferentially expressed antigen in melanoma), a member of the cancer-testis antigen family, has been shown to have increased expression in solid tumors, including sarcoma, and PRAME-specific therapies ...
Enrico Pinotti,Marta Sandini,Simone Famularo et al. Enrico Pinotti et al.
Background: Leiomyosarcoma of the head and neck is a rare cancer with high local aggressiveness. Radical surgery and adjuvant treatment offer the best chance for cure, nonetheless 5-years recurrence rate remains high. Des...
Sarah Bétrian,Christophe Bergeron,Jean-Yves Blay et al. Sarah Bétrian et al.
Background: Desmoplastic small round cell tumor (DSRCT) is a very rare mesenchymal tumor that mainly affects teenagers and young adults with a mean age at diagnosis around 20-25 years. Although initial management still ne...
Christian Koelsche,Daniel Schrimpf,Lars Tharun et al. Christian Koelsche et al.
Background: Histone 3.3 (H3.3) hotspot mutations in bone tumors occur in the vast majority of giant cell tumors of bone (GCTBs; 96%), chondroblastomas (95%) and in a few cases of osteosarcomas. However, clinical presentat...
Arjen H G Cleven,Johnny Suijker,Georgios Agrogiannis et al. Arjen H G Cleven et al.
Background: Mutations in isocitrate dehydrogenase (IDH)1 or -2 are found in ~50% of conventional central chondrosarcomas and in up to 87% of their assumed benign precursors enchondromas. The mutant enzyme acquires the act...
Anna Paioli,Michele Rocca,Luca Cevolani et al. Anna Paioli et al.
[This corrects the article DOI: 10.1186/s13569-017-0067-5.].
Ian Judson,Ramesh Bulusu,Beatrice Seddon et al. Ian Judson et al.
Background: Soft tissue sarcomas (STS) are rare tumours arising in mesenchymal tissues. Gastrointestinal stromal tumour (GIST) is the commonest STS and arises within the wall of the gastrointestinal (GI) tract. While most...
K Behi,M Ayadi,E Mezni et al. K Behi et al.
Background: Cardiac tumors are a very rare entity. Leiomyosarcoma represents less than 1% of cases. Case presentation: a 51-year-old wo...
Emanuela Marchesi,Celeste Cagnazzo,Irene Quattrini et al. Emanuela Marchesi et al.
Background: The Italian Sarcoma Group (ISG) is a nonprofit group of professionals established in 1997 aimed to improve the quality of care and promote the independent research in sarcomas. The increased regulatory require...