About: Marco Fiore

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher (ORCID 0000-0001-8220-424X)

Attributes	Values
rdf:type	Item
description	forskare (sv) ikertzailea (eu) 연구원 (ko) গবেষক (bn) 研究者 (ja) ഗവേഷകൻ (ml) araştırmacı (tr) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq) researcher (ORCID 0000-0001-8220-424X) (en)
exact match	wds:Q39185017-6E77AD7B-9B06-452D-8689-07F554B16863
exact match	https://scigraph.springernature.com/person.01346363063.49
rdfs:label	Marco Fiore (en) Marco Fiore (es) Marco Fiore (it) Marco Fiore (nl) Marco Fiore (sl) Marco Fiore (ast)
skos:prefLabel	Marco Fiore (en) Marco Fiore (es) Marco Fiore (it) Marco Fiore (nl) Marco Fiore (sl) Marco Fiore (ast)
name	Marco Fiore (en) Marco Fiore (es) Marco Fiore (it) Marco Fiore (nl) Marco Fiore (sl) Marco Fiore (ast)
Scopus author ID	wds:Q39185017-ACF710A4-7D44-4183-9C71-2EFE2054FD1C
Scopus author ID	7102171752
given name	wds:Q39185017-C152226B-6292-44C6-BEF1-45D12E40763E
given name	Marco
instance of	wds:Q39185017-5B2E3174-F0F3-4BFF-AEC4-114F40E0FAE9
instance of	Homo sapiens
occupation	wds:Q39185017-CC8F7827-B6A2-442B-8863-61772C654205
employer	wds:Q39185017-16269BA3-7856-4624-84A9-5E53EBBEEBA2
sex or gender	wds:Q39185017-C81B0EBD-71D3-459D-8721-5FEA02B9984F
VIAF ID	wds:Q39185017-53a4abc4-7976-4446-8676-fc05329a2397
GND ID	wds:Q39185017-c4fef2ed-fdfc-4ffc-83cd-0f848d2d80e6
family name	wds:Q39185017-A0403223-73CE-4E64-A132-5B63E93CB526
VIAF ID	http://viaf.org/viaf/3759162985507086300001
GND ID	https://d-nb.info/gnd/1239304021
occupation	researcher
employer	National Cancer Institute
sex or gender	male
VIAF ID	3759162985507086300001
GND ID	1239304021
family name	Fiore
ORCID iD	wds:Q39185017-F9C65C91-0346-4C87-9148-3610FB960431
Dimensions author ID	wds:Q39185017-ABAFF7C5-606D-4988-AD0D-BCD5B503FEBF
ORCID iD	https://orcid.org/0000-0001-8220-424X
ORCID iD	0000-0001-8220-424X
Dimensions author ID	01346363063.49
ResearcherID	wds:Q39185017-05D5A7E3-71F6-456D-8F3E-A25AA01650B0
Publons author ID	wds:Q39185017-27e7fd38-45c1-4268-a5c8-79bc62c4822a
ResearcherID	M-6587-2016
Publons author ID	395824
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q39185017
is author of	Retroperitoneal soft tissue sarcomas: patterns of recurrence in 167 patients treated at a single institution. Head and neck soft tissue sarcomas: prognostic factors and outcome in a series of patients treated at a single institution RHABDOMYOSARCOMA OF THE EXTREMITIES: A Focus on Tumors Arising in the Hand and Foot Quality of surgery and outcome in extra-abdominal aggressive fibromatosis: a series of patients surgically treated at a single institution. Prognostic Effect of Re-Excision in Adult Soft Tissue Sarcoma of the Extremity Surgery of residual disease following molecular-targeted therapy with imatinib mesylate in advanced/metastatic GIST. Aggressive fibromatosis in children and adolescents: the Italian experience Myxoid/round cell and pleomorphic liposarcomas: prognostic factors and survival in a series of patients treated at a single institution Validation and adaptation of a nomogram for predicting the survival of patients with extremity soft tissue sarcoma using a three-grade system Neoadjuvant imatinib in locally advanced gastrointestinal stromal tumors (GIST): the EORTC STBSG experience. Long-term follow-up of patients with GIST undergoing metastasectomy in the era of imatinib -- analysis of prognostic factors (EORTC-STBSG collaborative study). Status of Surgical Margins and Prognosis in Adult Soft Tissue Sarcomas of the Extremities: A Series of Patients Treated at a Single Institution Extremity Soft Tissue Sarcoma in a Series of Patients Treated at a Single Institution The prognostic impact of dedifferentiation in retroperitoneal liposarcoma: a series of surgically treated patients at a single institution Quality of surgery and neoadjuvant combined therapy in the ISG-GEIS trial on soft tissue sarcomas of limbs and trunk wall. Myxofibrosarcoma: Prognostic Factors and Survival in a Series of Patients Treated at a Single Institution Chordoma: natural history and results in 28 patients treated at a single institution. Development and external validation of two nomograms to predict overall survival and occurrence of distant metastases in adults after surgical resection of localised soft-tissue sarcomas of the extremities: a retrospective analysis Epithelioid sarcoma: prognostic factors and survival in a series of patients treated at a single institution Sporadic desmoid-type fibromatosis: a stepwise approach to a non-metastasising neoplasm--a position paper from the Italian and the French Sarcoma Group Malignant peripheral nerve sheath tumors The symptom interval in children and adolescents with soft tissue sarcomas Alveolar soft part sarcoma: clinical presentation, treatment, and outcome in a series of 33 patients at a single institution. Desmoid-type fibromatosis: a front-line conservative approach to select patients for surgical treatment. Preoperative imatinib mesylate for unresectable or locally advanced primary gastrointestinal stromal tumors (GIST). Is autophagy rather than apoptosis the regression driver in imatinib-treated gastrointestinal stromal tumors? c-Kit/PDGFRA gene status alterations possibly related to primary imatinib resistance in gastrointestinal stromal tumors. Peritoneal Sarcomatosis: Is There a Subset of Patients Who May Benefit from Cytoreductive Surgery and Hyperthermic Intraperitoneal Chemotherapy? Post-imatinib surgery in advanced/metastatic GIST: is it worthwhile in all patients? Extremity Soft Tissue Sarcoma: Adding to the Prognostic Meaning of Local Failure Aggressive Surgical Policies in a Retrospectively Reviewed Single-Institution Case Series of Retroperitoneal Soft Tissue Sarcoma Patients Technical considerations in surgery for retroperitoneal sarcomas: position paper from E-Surge, a master class in sarcoma surgery, and EORTC-STBSG. Frontline extended surgery is associated with improved survival in retroperitoneal low- to intermediate-grade soft tissue sarcomas.

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