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Surgical management of sacral chordoma.[The effect of resistance-related proteins on the prognosis and survival of patients with osteosarcoma: an immunohistochemical analysis].Incidence, predictive factors, and prognosis of chondrosarcoma in patients with Ollier disease and Maffucci syndrome: an international multicenter study of 161 patientsThe clinical effect of a positive surgical margin and adjuvant postoperative radiotherapy in the treatment of resectable desmoid tumors.Childhood osteosarcoma: multimodal therapy in a single-institution Turkish series.Osteosarcoma After Hematopoietic Stem Cell Transplantation in Children and Adolescents: Case Report and Review of the Literature.Clinical management of a challenging malignancy, osteoblastoma-like osteosarcoma: a report of four cases and a review of the literature.Lung Metastasis Mimicking Fingertip Infection.Giant Extraarticular Pigmented Villonodular Tenosynovitis; TWIST-MRA Findings.Polygonal triple (Kotz) osteotomy (over 10 years experience).[Evaluation of prognostic factors affecting recurrences and disease-free survival in extra-abdominal desmoid tumors].Ewing's sarcoma of the axial system in patients older than 15 years: dismal prognosis despite intensive multiagent chemotherapy and aggressive local treatment.Biological reconstruction of the femur using double free vascularized fibular autografts in a vertical array because of a large defect following wide resection of an osteosarcoma: a case report with 7 years of follow-up.Methylenetetrahydrofolate reductase C677T gene polymorphism in osteosarcoma and chondrosarcoma patients.A phase II study of cisplatin, ifosfamide and epirubicin combination chemotherapy in adults with nonmetastatic and extremity osteosarcomas.[Isolated bone tuberculosis of the talus. Case report]Management of primary malignant bone and soft tissue tumors of foot and ankle: Is it worth salvaging?Neoadjuvant radiotherapy for myxoid liposarcomas: Oncologic outcomes and histopathologic correlations.Survival and prognostic factors in adult patients with recurrent or refractory ewing sarcoma family tumours: a 13-years retrospective study in Turkey.Surgical treatment of malignant tumors of the foot and ankle.Malignant transformation of aggressive osteoblastoma to ostesarcoma.CT and MR characteristics of hibernoma: six cases.Midfoot reconstruction with free vascularized fibular graft after wide resection: a case report.Comparison of Tc-99m MIBI and Tl-201 uptake in musculoskeletal lesionsMalignant peripheral nerve sheath tumors associated with neurofibromatosis type 1Articulated distraction of the hip joint in the treatment of benign aggressive tumors located around the hip joint[Surgical treatment of Langerhans cell histiocytosis with bone and soft tissue involvement in pediatric patients][Posterior interosseous nerve palsy due to lipoma][Sarcomas of the hand][Ossifying subperiosteal hematoma associated with neurofibromatosis type 1: a report of two cases][Survival analysis and the effects of prognostic factors in patients treated for osteosarcoma][Familial tumoral calcinosis in three patients in the same family]Paraoxonase 1 192 and 55 polymorphisms in osteosarcomaCorrection of forearm deformities in children with multiple osteochondroma, by corrective radial osteotomy and ulnar lengthening by distraction osteogenesisNeuropathic arthropathy of the shoulder associated with syringomyelia: a report of six casesForequarter amputation as a life-saving procedure[Applications of external fixation for management of complications associated with musculoskeletal tumors and related surgery]Primary epiphyseal Ewing sarcoma: a case reportAvulsion fractures involving the straight and reflected heads of the rectus femorisMMP-3 gene polymorphisms and Osteosarcoma
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P50
description
researcher ORCID ID = 0000-0001-5033-7531
@en
wetenschapper
@nl
name
Harzem Ozger
@ast
Harzem Ozger
@en
Harzem Ozger
@es
Harzem Ozger
@nl
type
label
Harzem Ozger
@ast
Harzem Ozger
@en
Harzem Ozger
@es
Harzem Ozger
@nl
prefLabel
Harzem Ozger
@ast
Harzem Ozger
@en
Harzem Ozger
@es
Harzem Ozger
@nl
P106
P31
P496
0000-0001-5033-7531