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Current Strategies for the Treatment of Aneurysmal Bone Cysts

Orthopedic Reviews, 2015-12, Vol.7 (4), p.6182-6182

2015

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Disruption of the TP53 locus in osteosarcoma leads to TP53 promoter gene fusions and restoration of parts of the TP53 signalling pathway

The Journal of pathology, 2024-02, Vol.262 (2), p.147-160

2024

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Reconstruction of metastatic acetabular defects using a modified Harrington procedure: Good outcome after surgical treatment of 70 patients

Acta orthopaedica, 2015-11, Vol.86 (6), p.690-694

2015

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Drug sensitivity testing on patient-derived sarcoma cells predicts patient response to treatment and identifies c-Sarc inhibitors as active drugs for translocation sarcomas

British journal of cancer, 2019-02, Vol.120 (4), p.435-443

2019

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Sclerotherapy with polidocanol for treatment of aneurysmal bone cysts: Good results in 37 of 38 consecutive patients

Acta orthopaedica, 2013-10, Vol.84 (5), p.502-505

2013

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Genomic Profiling of Chondrosarcoma: Chromosomal Patterns in Central and Peripheral Tumors

Clinical cancer research, 2009-04, Vol.15 (8), p.2685-2694

2009

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Drug sensitivity testing on patient-derived sarcoma cells predicts patient response to treatment and identifies c-Sarc inhibitors as active drugs for translocation sarcomas

British journal of cancer, 2019-02, Vol.120 (4), p.435-443

2019

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Neoadjuvant Chemotherapy With High-Dose Ifosfamide, High-Dose Methotrexate, Cisplatin, and Doxorubicin for Patients With Localized Osteosarcoma of the Extremity: A Joint Study by the Italian and Scandinavian Sarcoma Groups

Journal of clinical oncology, 2005-12, Vol.23 (34), p.8845-8852

2005

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Insulin-Like Growth Factor Type 1 Receptor Expression Correlates to Good Prognosis in Highly Malignant Soft Tissue Sarcoma

Clinical cancer research, 2005-01, Vol.11 (1), p.206-216

2005

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Comprehensive genetic analysis identifies a pathognomonic NAB2/STAT6 fusion gene, nonrandom secondary genomic imbalances, and a characteristic gene expression profile in solitary fibrous tumor

Genes chromosomes & cancer, 2013-10, Vol.52 (10), p.873-886

2013

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Loss of NF2 defines a genetic subgroup of non‐FOS‐rearranged osteoblastoma

The journal of pathology. Clinical research, 2020-10, Vol.6 (4), p.231-237

2020

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The chimeric FUS/CREB3l2 gene is specific for low-grade fibromyxoid sarcoma

Genes chromosomes & cancer, 2004-07, Vol.40 (3), p.218-228

2004

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Different patterns of clonal evolution among different sarcoma subtypes followed for up to 25 years

Nature communications, 2018-09, Vol.9 (1), p.3662-8, Article 3662

2018

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Reconstruction with modular megaprostheses for sarcomas of the lower extremity

Orthopedics (Thorofare, N.J.), 2015-05, Vol.38 (5), p.e401

2015

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Genetic profiling of a chondroblastoma‐like osteosarcoma/malignant phosphaturic mesenchymal tumor of bone reveals a homozygous deletion of CDKN2A, intragenic deletion of DMD, and a targetable FN1‐FGFR1 gene fusion

Genes chromosomes & cancer, 2019-10, Vol.58 (10), p.731-736

2019

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Fusion, Disruption, and Expression of HMGA2 in Bone and Soft Tissue Chondromas

Modern pathology, 2003-11, Vol.16 (11), p.1132-1140

2003

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Improved Prognosis for Patients with Ewing Sarcoma in the Sacrum Compared with the Innominate Bones: The Scandinavian Sarcoma Group Experience

Journal of bone and joint surgery. American volume, 2016-02, Vol.98 (3), p.199-210

2016

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Recurrent PRDM10 gene fusions in undifferentiated pleomorphic sarcoma

Clinical cancer research, 2015-02, Vol.21 (4), p.864-869

2015

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Synovial sarcoma - a rare and highly malignant, tumor with an ambiguous clinical picture at times

Läkartidningen, 2020-01, Vol.117

2020

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Synovial sarcoma - a rare and highly malignant, tumor with an ambiguous clinical picture at times

Läkartidningen, 2020-01, Vol.117

2020

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Fusion of the FUS and BBF2H7 genes in low grade fibromyxoid sarcoma

Human molecular genetics, 2003-09, Vol.12 (18), p.2349-2358

2003

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Femoral Metastasis from Penile Carcinoma: Report of 2 Cases

Case reports in urology, 2015, Vol.2015 (2015), p.1-3

2015

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Recurrent chromosome 22 deletions in osteoblastoma affect inhibitors of the Wnt/beta-catenin signaling pathway

PloS one, 2013-11, Vol.8 (11), p.e80725

2013

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Molecular genetic characterization of the EWS/CHN and RBP56/CHN fusion genes in extraskeletal myxoid chondrosarcoma

Genes chromosomes & cancer, 2002-12, Vol.35 (4), p.340-352

2002

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Retained Heterodisomy Is Associated with High Gene Expression in Hyperhaploid Inflammatory Leiomyosarcoma

Neoplasia (New York, N.Y.), 2012-09, Vol.14 (9), p.807-IN5

2012

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Current Strategies for the Treatment of Aneurysmal Bone Cysts

Disruption of the TP53 locus in osteosarcoma leads to TP53 promoter gene fusions and restoration of parts of the TP53 signalling pathway

Reconstruction of metastatic acetabular defects using a modified Harrington procedure: Good outcome after surgical treatment of 70 patients

Drug sensitivity testing on patient-derived sarcoma cells predicts patient response to treatment and identifies c-Sarc inhibitors as active drugs for translocation sarcomas

Sclerotherapy with polidocanol for treatment of aneurysmal bone cysts: Good results in 37 of 38 consecutive patients

Genomic Profiling of Chondrosarcoma: Chromosomal Patterns in Central and Peripheral Tumors

Drug sensitivity testing on patient-derived sarcoma cells predicts patient response to treatment and identifies c-Sarc inhibitors as active drugs for translocation sarcomas

Neoadjuvant Chemotherapy With High-Dose Ifosfamide, High-Dose Methotrexate, Cisplatin, and Doxorubicin for Patients With Localized Osteosarcoma of the Extremity: A Joint Study by the Italian and Scandinavian Sarcoma Groups

Insulin-Like Growth Factor Type 1 Receptor Expression Correlates to Good Prognosis in Highly Malignant Soft Tissue Sarcoma

Comprehensive genetic analysis identifies a pathognomonic NAB2/STAT6 fusion gene, nonrandom secondary genomic imbalances, and a characteristic gene expression profile in solitary fibrous tumor

Loss of NF2 defines a genetic subgroup of non‐FOS‐rearranged osteoblastoma

The chimeric FUS/CREB3l2 gene is specific for low-grade fibromyxoid sarcoma

Different patterns of clonal evolution among different sarcoma subtypes followed for up to 25 years

Reconstruction with modular megaprostheses for sarcomas of the lower extremity

Genetic profiling of a chondroblastoma‐like osteosarcoma/malignant phosphaturic mesenchymal tumor of bone reveals a homozygous deletion of CDKN2A, intragenic deletion of DMD, and a targetable FN1‐FGFR1 gene fusion

Fusion, Disruption, and Expression of HMGA2 in Bone and Soft Tissue Chondromas

Improved Prognosis for Patients with Ewing Sarcoma in the Sacrum Compared with the Innominate Bones: The Scandinavian Sarcoma Group Experience

Recurrent PRDM10 gene fusions in undifferentiated pleomorphic sarcoma

Synovial sarcoma - a rare and highly malignant, tumor with an ambiguous clinical picture at times

Synovial sarcoma - a rare and highly malignant, tumor with an ambiguous clinical picture at times

Fusion of the FUS and BBF2H7 genes in low grade fibromyxoid sarcoma

Femoral Metastasis from Penile Carcinoma: Report of 2 Cases

Recurrent chromosome 22 deletions in osteoblastoma affect inhibitors of the Wnt/beta-catenin signaling pathway

Molecular genetic characterization of the EWS/CHN and RBP56/CHN fusion genes in extraskeletal myxoid chondrosarcoma

Retained Heterodisomy Is Associated with High Gene Expression in Hyperhaploid Inflammatory Leiomyosarcoma

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