18 hasil untuk "Maria Frezza"
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Artikel Jurnal
Loisir e sport: identità e dinamiche sociali
Recensione del volume: Loisir e sport: identità e dinamiche sociali. Bortoletto, N. (2024). Tracce per una sociologia dello sport in Italia: 1948-1962, FrancoAngeli
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Attaccante fino alla fine: identità sportiva, celebrità, malattia e autobiografia nell’esperienza di Stefano Borgonovo
This study analyses, from a sociological perspective, the transformation of the identity of Stefano Borgonovo, a former professional footballer, following his diagnosis with amyotrophic lateral sclerosis (ALS). Through a phenomenological-interpretative analysis of his posthumous autobiography…
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Espiritualidade na formação acadêmica em psicologia no Rio Grande do Sul
Embora estudos científicos recentes comprovem correlação positiva entre espiritualidade e saúde, outros apontam a espiritualidade do psicólogo como menor que a da população em geral. Visando analisar a espiritualidade de acadêmicos de psicologia, foram investigados 1.064 estudantes (672 calouros e…
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Artikel Jurnal
Systemic treatment in advanced soft tissue sarcoma: what is standard, what is new
Abstract For metastatic soft tissue sarcoma (STS) patients not eligible for surgery, systemic treatments, including standard chemotherapy and newer biological compounds, still play the most relevant role in the management of the disease. An anthracycline and alkylating agent combination has formed…
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Artikel Jurnal
Rechallenge of denosumab in jaw osteonecrosis of patients with unresectable giant cell tumour of bone: a case series analysis and literature review
Objectives Giant cell tumour of bone (GCTB) is a rare tumour, generally managed with surgery. Treatment of the very rare unresectable advanced/metastatic GCTB is challenging and denosumab is the only current available medical option, an anti-RANKL monoclonal antibody inhibiting osteolysis. An…
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Artikel Jurnal
Rechallenge of denosumab in advanced giant cell tumor of the bone after atypical femur fracture: A case report and review of literature
Giant cell tumor of the bone (GCTB) is a locally aggressive neoplasm where surgery is often curative. However, it can rarely give rise to distant metastases. Currently, the only available active therapeutic option for unresectable GCTB is denosumab, an anti-RANKL monoclonal antibody that dampens…
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Artikel Jurnal
Long‐term survivors with desmoplastic small round cell tumor (DSRCT): Results from a retrospective single‐institution case series analysis
Abstract Objective To report on a retrospective study of primary DSRCT aiming at characterizing long‐term survivors (LTS). Methods All consecutive patients treated at our institution for a primary DSRCT between 2000 and 2021 were retrospectively identified. Patients received multiagent chemotherapy…
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Artikel Jurnal
CINSARC in high‐risk soft tissue sarcoma patients treated with neoadjuvant chemotherapy: Results from the ISG‐STS 1001 study
Abstract Background The Complexity INdex in SARComas (CINSARC) is a transcriptional signature derived from the expression of 67 genes involved in mitosis control and chromosome integrity. This study aims to assess CINSARC value of in an independent series of high‐risk patients with localized soft…
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Management of patients with rare adult solid cancers: objectives and evaluation of European reference networks (ERN) EURACAN
Summary: About 500,000 patients with rare adult solid cancers (RASC) are diagnosed yearly in Europe. Delays and unequal quality of management impact negatively their survival. Since 2017, European reference networks (ERN) aim to improve the quality of care of patients with rare disease. The…
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The management of desmoid tumours: A joint global consensus-based guideline approach for adult and paediatric patients
Desmoid tumor (DT; other synonymously used terms: Desmoid-type fibromatosis, aggressive fibromatosis) is a rare and locally aggressive monoclonal, fibroblastic proliferation characterised by a variable and often unpredictable clinical course. Previously surgery was the standard primary treatment…
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Ultra‐rare sarcomas: A consensus paper from the Connective Tissue Oncology Society community of experts on the incidence threshold and the list of entities
BACKGROUND: Among sarcomas, which are rare cancers, many types are exceedingly rare; however, a definition of ultra-rare cancers has not been established. The problem of ultra-rare sarcomas is particularly relevant because they represent unique diseases, and their rarity poses major challenges for…
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The observational EURACAN prospective clinical registry dedicated to epithelioid hemangioendothelioma: The protocol of an international and collaborative effort on an ultra-rare entity
Introduction: Epithelioid hemangioendothelioma (EHE) is an ultra-rare sarcoma, marked by distinctive molecular and pathological features and with a variable clinical behavior. Its natural history is still partially understood, reliable prognostic and predictive factors are lacking and many…