All Stories

  1. Correlation of High-Grade Osteosarcoma Response to Chemotherapy with Enhanced Tissue Immunological Response: Analysis of CD95R, IFN-γ, Catalase, Hsp70, and VEGF
  2. Demographics and additional haematologic cancers of patients with histiocytic/dendritic cell neoplasms
  3. Transmembrane protein 14A protects glomerular filtration barrier integrity
  4. Immunological factors linked to geographical variation in vaccine responses
  5. Brown Tumour in Chronic Kidney Disease: Revisiting an Old Disease with a New Perspective
  6. Brown Tumour in Chronic Kidney Disease: Revisiting an Old Disease with a New Perspective
  7. Histone Deacetylase Inhibitors as a Therapeutic Strategy to Eliminate Neoplastic “Stromal” Cells from Giant Cell Tumors of Bone
  8. Outcomes from a mechanistic biomarker multi-arm and randomised study of liposomal MTP-PE (Mifamurtide) in metastatic and/or recurrent osteosarcoma (EuroSarc-Memos trial)
  9. Clinicopathologic and molecular features of denosumab-treated giant cell tumour of bone (GCTB): Analysis of 21 cases
  10. Mutations in the heparan sulfate backbone elongating enzymes EXT1 and EXT2 have no major effect on endothelial glycocalyx and the glomerular filtration barrier
  11. Cell Biology of Giant Cell Tumour of Bone: Crosstalk between m/wt Nucleosome H3.3, Telomeres and Osteoclastogenesis
  12. NTRK fusions are extremely rare in bone tumours
  13. The adapter protein Myd88 plays an important role in limiting mycobacterial growth in a zebrafish model for tuberculosis
  14. Co-existence of lung carcinoma metastasis and enchondroma in the femur of a patient with Ollier disease
  15. Surgical Outcome and Oncological Survival of Osteofibrous Dysplasia-Like and Classic Adamantinomas
  16. Mutation-driven epigenetic alterations as a defining hallmark of central cartilaginous tumours, giant cell tumour of bone and chondroblastoma
  17. Nikolay Ivanovich Pirogov (1810–1881): Anatomical research to develop surgery
  18. Glomerular permeability is not affected by heparan sulfate glycosaminoglycan deficiency in zebrafish embryos
  19. Quality of Life of Patients With Osteosarcoma in the European American Osteosarcoma Study-1 (EURAMOS-1): Development and Implementation of a Questionnaire Substudy
  20. Method to measure the mismatch between target and achieved received dose intensity of chemotherapy in cancer trials: a retrospective analysis of the MRC BO06 trial in osteosarcoma
  21. Adjuvant Zoledronic Acid in High-Risk Giant Cell Tumor of Bone: A Multicenter Randomized Phase II Trial
  22. Non‐ossifying fibroma: A RAS‐MAPK driven benign bone neoplasm
  23. A novel method to address the association between received dose intensity and survival outcome: benefits of approaching treatment intensification at a more individualised level in a trial of the European Osteosarcoma Intergroup
  24. Survival and prognosis with osteosarcoma: outcomes in more than 2000 patients in the EURAMOS-1 (European and American Osteosarcoma Study) cohort
  25. New indicators and indexes for benchmarking university–industry–government innovation in medical and life science clusters: results from the European FP7 Regions of Knowledge HealthTIES project
  26. Women in healthcare in Imperial Russia: The contribution of the surgeon Nikolay I Pirogov
  27. Conjunctival Leiomyosarcoma, a Rare Neoplasm Always Originating at the Limbus? Report of a New Case and Review of 11 Published Cases
  28. M-CSF and IL-34 expression as indicators for growth in sporadic vestibular schwannoma
  29. Increased dynamin expression precedes proteinuria in glomerular disease
  30. Introducing fluorescence guided surgery into orthopedic oncology: A systematic review of candidate protein targets for Ewing sarcoma
  31. Bioorthogonally Applicable Fluorescence Deactivation Strategy for Receptor Kinetics Study and Theranostic Pretargeting Approaches
  32. The incidence, mutational status, risk classification and referral pattern of gastro-intestinal stromal tumours in the Netherlands: a nationwide pathology registry (PALGA) study
  33. BCRP expression in schwannoma, plexiform neurofibroma and MPNST
  34. Hematopoietic Tumors Primarily Presenting in Bone
  35. Fluorescent CXCR4 targeting peptide as alternative for antibody staining in Ewing sarcoma
  36. Ten-Year Progression-Free and Overall Survival in Patients With Unresectable or Metastatic GI Stromal Tumors: Long-Term Analysis of the European Organisation for Research and Treatment of Cancer, Italian Sarcoma Group, and Australasian Gastrointestinal...
  37. Predictive and prognostic factors associated with soft tissue sarcoma response to chemotherapy: a subgroup analysis of the European Organisation for Research and Treatment of Cancer 62012 study
  38. ECCO Essential Requirements for Quality Cancer Care: Soft Tissue Sarcoma in Adults and Bone Sarcoma. A critical review
  39. High prevalence of autoimmune disease in the rare inflammatory bone disorder sternocostoclavicular hyperostosis: survey of a Dutch cohort
  40. MRI appearances of atypical cartilaginous tumour/grade I chondrosarcoma after treatment by curettage, phenolisation and allografting
  41. Comparison of MAPIE versus MAP in patients with a poor response to preoperative chemotherapy for newly diagnosed high-grade osteosarcoma (EURAMOS-1): an open-label, international, randomised controlled trial
  42. Expression of CCL21 in Ewing sarcoma shows an inverse correlation with metastases and is a candidate target for immunotherapy
  43. Loss of H3K27 tri-methylation is a diagnostic marker for malignant peripheral nerve sheath tumors and an indicator for an inferior survival
  44. CXCR4 signaling is controlled by immobilization at the plasma membrane
  45. Nikolay Ivanovich Pirogov (1810–1881): A pioneering Russian surgeon and medical scientist
  46. Automation of Technology for Cancer Research
  47. Ewing sarcoma: The clinical relevance of the insulin-like growth factor 1 and the poly-ADP-ribose-polymerase pathway
  48. A translocation t(6;14) in two cases of leiomyosarcoma: Molecular cytogenetic and array-based comparative genomic hybridization characterization
  49. CXCL14, CXCR7 expression and CXCR4 splice variant ratio associate with survival and metastases in Ewing sarcoma patients
  50. Prognosis of Primary and Recurrent Chondrosarcoma of the Rib
  51. Inactivation of SDH and FH cause loss of 5hmC and increased H3K9me3 in paraganglioma/pheochromocytoma and smooth muscle tumors
  52. Novel splice variants of CXCR4 identified by transcriptome sequencing
  53. Pharmacological inhibition of Bcl-xL sensitizes osteosarcoma to doxorubicin
  54. Tumor Biology of Vestibular Schwannoma
  55. Sequencing Overview of Ewing Sarcoma: A Journey across Genomic, Epigenomic and Transcriptomic Landscapes
  56. Methotrexate, Doxorubicin, and Cisplatin (MAP) Plus Maintenance Pegylated Interferon Alfa-2b Versus MAP Alone in Patients With Resectable High-Grade Osteosarcoma and Good Histologic Response to Preoperative MAP: First Results of the EURAMOS-1 Good Resp...
  57. Chemotherapy in osteosarcoma
  58. Periosteal chondrosarcoma: a histopathological and molecular analysis of a rare chondrosarcoma subtype
  59. Neoadjuvant denosumab for extensive giant cell tumor in os ischium —a case report
  60. Doxorubicin-based adjuvant chemotherapy in soft tissue sarcoma: pooled analysis of two STBSG-EORTC phase III clinical trials
  61. EURAMOS-1, an international randomised study for osteosarcoma: results from pre-randomisation treatment
  62. Nikolay Ivanovich Pirogov: a surgeon's contribution to military and civilian anaesthesia
  63. De novodiscovery of phenotypic intratumour heterogeneity using imaging mass spectrometry
  64. In Reply
  65. Gene expression profiling of giant cell tumor of bone reveals downregulation of extracellular matrix components decorin and lumican associated with lung metastasis
  66. Quantification of the Heterogeneity of Prognostic Cellular Biomarkers in Ewing Sarcoma Using Automated Image and Random Survival Forest Analysis
  67. Ewing sarcoma inhibition by disruption of EWSR1-FLI1 transcriptional activity and reactivation of p53
  68. A phase 2 trial of R1507, a monoclonal antibody to the insulin-like growth factor-1 receptor (IGF-1R), in patients with recurrent or refractory rhabdomyosarcoma, osteosarcoma, synovial sarcoma, and other soft tissue sarcomas: Results of a Sarcoma Alliance
  69. Molecular genetics of chondroid tumours
  70. The Clinical Approach Toward Giant Cell Tumor of Bone
  71. Doxorubicin alone versus intensified doxorubicin plus ifosfamide for first-line treatment of advanced or metastatic soft-tissue sarcoma: a randomised controlled phase 3 trial
  72. GRM1 is upregulated through gene fusion and promoter swapping in chondromyxoid fibroma
  73. Possible effects of EXT2 on mesenchymal differentiation - lessons from the zebrafish
  74. Primary intraosseous manifestation of Rosai-Dorfman disease: 2 cases and review of literature
  75. Kinome and mRNA expression profiling of high-grade osteosarcoma cell lines implies Akt signaling as possible target for therapy
  76. Transactivating mutation of theMYOD1gene is a frequent event in adult spindle cell rhabdomyosarcoma
  77. Brostallicin versus doxorubicin as first-line chemotherapy in patients with advanced or metastatic soft tissue sarcoma: An European Organisation for Research and Treatment of Cancer Soft Tissue and Bone Sarcoma Group randomised phase II and pharmacogen...
  78. Zebrafish as a Model for Human Osteosarcoma
  79. The density of CD8+ T-cell infiltration and expression of BCL2 predicts outcome of primary diffuse large B-cell lymphoma of bone
  80. Recurrent Chromosome 22 Deletions in Osteoblastoma Affect Inhibitors of the Wnt/Beta-Catenin Signaling Pathway
  81. Frequent truncating mutations of STAG2 in bladder cancer
  82. Results of a phase II pilot study of moderate dose radiotherapy for inoperable desmoid-type fibromatosis—an EORTC STBSG and ROG study (EORTC 62991–22998)
  83. CD99-positive undifferentiated round cell sarcoma diagnosed on fine needle aspiration cytology, later found to harbour aCIC-DUX4translocation: a recently described entity
  84. IR/IGF1R signaling as potential target for treatment of high-grade osteosarcoma
  85. FXR regulates CETP
  86. Screening for Potential Targets for Therapy in Mesenchymal, Clear Cell, and Dedifferentiated Chondrosarcoma Reveals Bcl-2 Family Members and TGFβ as Potential Targets
  87. Imaging Mass Spectrometry-based Molecular Histology Differentiates Microscopically Identical and Heterogeneous Tumors
  88. Genome-wide analyses on high-grade osteosarcoma: Making sense of a genomically most unstable tumor
  89. Tumor-Associated Macrophages Are Related to Volumetric Growth of Vestibular Schwannomas
  90. Nuclear factor-κB activation in primary lymphoma of bone
  91. MicroRNAs at the human 14q32 locus have prognostic significance in osteosarcoma
  92. Inactivation of Patched1 in Mice Leads to Development of Gastrointestinal Stromal-Like Tumors That Express Pdgfrα but Not Kit
  93. Mutations affecting BRAF, EGFR, PIK3CA, and KRAS are not associated with sporadic vestibular schwannomas
  94. Osteosarcoma of the hands and feet: a distinct clinico-pathological subgroup
  95. The activities of Smad and Gli mediated signalling pathways in high-grade conventional osteosarcoma
  96. Integrative Analysis Reveals Relationships of Genetic and Epigenetic Alterations in Osteosarcoma
  97. ‘The chicken or the egg?’ dilemma strikes back for the controlling mechanism in chordoma#
  98. Adjuvant chemotherapy with doxorubicin, ifosfamide, and lenograstim for resected soft-tissue sarcoma (EORTC 62931): a multicentre randomised controlled trial
  99. High frequency of MYC gene amplification is a common feature of radiation‐induced sarcomas. Further results from EORTC STBSG TL 01/01
  100. Malignant fibrous histiocytoma and fibrosarcoma of bone: a re-assessment in the light of currently employed morphological, immunohistochemical and molecular approaches
  101. Interobserver reliability in the histopathological diagnosis of cartilaginous tumors in patients with multiple osteochondromas
  102. Three new chondrosarcoma cell lines: one grade III conventional central chondrosarcoma and two dedifferentiated chondrosarcomas of bone
  103. Alternate Splicing of the p53 Inhibitor HDMX Offers a Superior Prognostic Biomarker than p53 Mutation in Human Cancer
  104. Imaging mass spectrometry statistical analysis
  105. A multidisciplinary approach to giant cell tumors of tendon sheath and synovium—A critical appraisal of literature and treatment proposal
  106. Expression of ERG, an Ets family transcription factor, identifies ERG-rearranged Ewing sarcoma
  107. Low-Grade Chondrosarcoma of Long Bones Treated with Intralesional Curettage Followed by Application of Phenol, Ethanol, and Bone-Grafting
  108. The management of diffuse-type giant cell tumour (pigmented villonodular synovitis) and giant cell tumour of tendon sheath (nodular tenosynovitis)
  109. Intratumoral hemorrhage, vessel density, and the inflammatory reaction contribute to volume increase of sporadic vestibular schwannomas
  110. Molecular pathology and its diagnostic use in bone tumors
  111. Smooth muscle actin expression in primary bone tumours
  112. Identification of osteosarcoma driver genes by integrative analysis of copy number and gene expression data
  113. An osteosarcoma zebrafish model implicates Mmp‐19 and Ets‐1 as well as reduced host immune response in angiogenesis and migration
  114. Intact interferon signaling in peripheral blood leukocytes of high-grade osteosarcoma patients
  115. Presence of chemotherapy-induced toxicity predicts improved survival in patients with localised extremity osteosarcoma treated with doxorubicin and cisplatin: A report from the European Osteosarcoma Intergroup
  116. The clinical impact of molecular techniques on diagnostic pathology of soft tissue and bone tumours
  117. Anti-EGFR Antibody Cetuximab Enhances the Cytolytic Activity of Natural Killer Cells toward Osteosarcoma
  118. HSPG-Deficient Zebrafish Uncovers Dental Aspect of Multiple Osteochondromas
  119. The First European Interdisciplinary Ewing Sarcoma Research Summit
  120. Analysis of stromal cells in osteofibrous dysplasia and adamantinoma of long bones
  121. Automated microinjection of cell-polymer suspensions in 3D ECM scaffolds for high-throughput quantitative cancer invasion screens
  122. Osteosarcoma Models: From Cell Lines to Zebrafish
  123. Peripheral chondrosarcoma progression is associated with increased type X collagen and vascularisation
  124. Epiphyseal growth plate and secondary peripheral chondrosarcoma: the neighbours matter
  125. Chemotherapeutic adjuvant treatment for osteosarcoma: Where do we stand?
  126. Identification of a novel, recurrent HEY1‐NCOA2 fusion in mesenchymal chondrosarcoma based on a genome‐wide screen of exon‐level expression data
  127. Survival from high-grade localised extremity osteosarcoma: combined results and prognostic factors from three European Osteosarcoma Intergroup randomised controlled trials
  128. Multiple Statistical Analysis Techniques Corroborate Intratumor Heterogeneity in Imaging Mass Spectrometry Datasets of Myxofibrosarcoma
  129. mRNA expression profiles of primary high-grade central osteosarcoma are preserved in cell lines and xenografts
  130. 1q gain and CDT2 overexpression underlie an aggressive and highly proliferative form of Ewing sarcoma
  131. Secondary peripheral chondrosarcoma evolving from osteochondroma as a result of outgrowth of cells with functional EXT
  132. Functional characterization of osteosarcoma cell lines provides representative models to study the human disease
  133. A ΔRaf1–ER‐inducible oncogenic zebrafish liver cell model identifies hepatocellular carcinoma signatures
  134. Breakpoint characterization of large deletions in EXT1 or EXT2 in 10 Multiple Osteochondromas families
  135. A short-term in vivo model for giant cell tumor of bone
  136. IDH1 and IDH2 mutations are frequent events in central chondrosarcoma and central and periosteal chondromas but not in other mesenchymal tumours
  137. IGF1R Signaling in Ewing Sarcoma Is Shaped by Clathrin-/Caveolin-Dependent Endocytosis
  138. Maffucci syndrome: A genome‐wide analysis using high resolution single nucleotide polymorphism and expression arrays on four cases
  139. The immunophenotype of osteoclasts and macrophage polykaryons
  140. Growth plate regulation and osteochondroma formation: insights from tracing proteoglycans in zebrafish models and human cartilage
  141. Podoplanin expression in adamantinoma of long bones and osteofibrous dysplasia
  142. Tumor-Infiltrating Macrophages Are Associated with Metastasis Suppression in High-Grade Osteosarcoma: A Rationale for Treatment with Macrophage Activating Agents
  143. Survival after recurrent osteosarcoma: Data from 3 European Osteosarcoma Intergroup (EOI) randomized controlled trials
  144. Concise Review: Mesenchymal Tumors: When Stem Cells Go Mad
  145. Chemotherapy-resistant osteosarcoma is highly susceptible to IL-15-activated allogeneic and autologous NK cells
  146. Genome-wide analysis of Ollier disease: Is it all in the genes?
  147. Cartilage ultrastructure in proteoglycan‐deficient zebrafish mutants brings to light new candidate genes for human skeletal disorders
  148. Opening the archives for state of the art tumour genetic research: sample processing for array-CGH using decalcified, formalin-fixed, paraffin-embedded tissue-derived DNA samples
  149. Distinct histological features characterize primary angiosarcoma of bone
  150. First-line chemotherapy for malignant peripheral nerve sheath tumor (MPNST) versus other histological soft tissue sarcoma subtypes and as a prognostic factor for MPNST: an EORTC Soft Tissue and Bone Sarcoma Group study
  151. Late sarcoma development after curettage and bone grafting of benign bone tumors
  152. Pro-inflammatory chemokine-chemokine receptor interactions within the Ewing sarcoma microenvironment determine CD8+ T-lymphocyte infiltration and affect tumour progression
  153. The role of epidermal growth factor receptor in chordoma pathogenesis: a potential therapeutic target
  154. Tiling resolution array-CGH shows that somatic mosaic deletion of the EXT gene is causative in EXT gene mutation negative multiple osteochondromas patients
  155. Role of the transcription factor T (brachyury) in the pathogenesis of sporadic chordoma: a genetic and functional‐based study
  156. Cancer biology and genomics: translating discoveries, transforming pathology
  157. A nation‐wide study comparing sporadic and familial adenomatous polyposis‐related desmoid‐type fibromatoses
  158. Array-based comparative genomic hybridisation analysis reveals recurrent chromosomal alterations in primary diffuse large B cell lymphoma of bone
  159. No Haploinsufficiency but Loss of Heterozygosity for EXT in Multiple Osteochondromas
  160. Kinome profiling of myxoid liposarcoma reveals NF-kappaB-pathway kinase activity and Casein Kinase II inhibition as a potential treatment option
  161. Critical role of endoglin in tumor cell plasticity of Ewing sarcoma and melanoma
  162. Coactivated Platelet-Derived Growth Factor Receptor α and Epidermal Growth Factor Receptor Are Potential Therapeutic Targets in Intimal Sarcoma
  163. Imaging mass spectrometry of myxoid sarcomas identifies proteins and lipids specific to tumour type and grade, and reveals biochemical intratumour heterogeneity
  164. Heterogeneous and Complex Rearrangements of Chromosome Arm 6q in Chondromyxoid Fibroma
  165. Bisphosphonate treatment of aggressive primary, recurrent and metastatic Giant Cell Tumour of Bone
  166. Small deletions but not methylation underlie CDKN2A/p16 loss of expression in conventional osteosarcoma
  167. Hierarchical clustering of flow cytometry data for the study of conventional central chondrosarcoma
  168. DOG1 and CD117 are the antibodies of choice in the diagnosis of gastrointestinal stromal tumours
  169. Primary cilia organization reflects polarity in the growth plate and implies loss of polarity and mosaicism in osteochondroma
  170. Cartilage tumours and bone development: molecular pathology and possible therapeutic targets
  171. A Reappraisal of Hemangiopericytoma of Bone; Analysis of Cases Reclassified as Synovial Sarcoma and Solitary Fibrous Tumor of Bone
  172. Bone sarcomas: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up
  173. Impact of EWS-ETS Fusion Type on Disease Progression in Ewing's Sarcoma/Peripheral Primitive Neuroectodermal Tumor: Prospective Results From the Cooperative Euro-E.W.I.N.G. 99 Trial
  174. Correlation of hypoxic signalling to histological grade and outcome in cartilage tumours
  175. Langerhans cell histiocytosis: fascinating dynamics of the dendritic cell–macrophage lineage
  176. Soft tissue sarcomas: introduction to the Virchows Archiv review issue
  177. Anti-inflammatory M2 type macrophages characterize metastasized and tyrosine kinase inhibitor-treated gastrointestinal stromal tumors
  178. Epidemiology of Primary Bone Tumors and Economical Aspects of Bone Metastases
  179. Prognostic and predictive factors for outcome to first-line ifosfamide-containing chemotherapy for adult patients with advanced soft tissue sarcomas
  180. Erratum: Profiling of high-grade central osteosarcoma and its putative progenitor cells identifies tumourigenic pathways
  181. Improved diagnosis and treatment of soft tissue sarcoma patients after implementation of national guidelines: A population-based study
  182. Sdhd and Sdhd/H19 Knockout Mice Do Not Develop Paraganglioma or Pheochromocytoma
  183. A balanced t(5;17) (p15;q22-23) in chondroblastoma: frequency of the re-arrangement and analysis of the candidate genes
  184. Genome‐wide transcriptome analyses reveal p53 inactivation mediated loss of miR‐34a expression in malignant peripheral nerve sheath tumours
  185. Prognostic factors in pulmonary metastasized high‐grade osteosarcoma
  186. Profiling of high-grade central osteosarcoma and its putative progenitor cells identifies tumourigenic pathways
  187. Dedifferentiated peripheral chondrosarcomas: regulation of EXT-downstream molecules and differentiation-related genes
  188. The Journal of Pathology 2008 Jeremy Jass Prize for Research Excellence in Pathology
  189. Imatinib Mesylate in Patients with WHO B3 Thymomas and Thymic Carcinomas
  190. Molecular characterization of commonly used cell lines for bone tumor research: A trans‐European EuroBoNet effort
  191. Molecular pathology of sarcomas: concepts and clinical implications
  192. Inactive Wnt/β-catenin pathway in conventional high-grade osteosarcoma
  193. Central chondrosarcoma progression is associated with pRb pathway alterations: CDK4 down-regulation and p16 overexpression inhibit cell growth in vitro
  194. Benign Cartilaginous Tumors of Bone
  195. Primary lymphoma of bone: extranodal lymphoma with favourable survival independent of germinal centre, post-germinal centre or indeterminate phenotype
  196. Osteosarcoma originates from mesenchymal stem cells in consequence of aneuploidization and genomic loss of Cdkn2
  197. Running GAGs: myxoid matrix in tumor pathology revisited
  198. Absence of Progression As Assessed by Response Evaluation Criteria in Solid Tumors Predicts Survival in Advanced GI Stromal Tumors Treated With Imatinib Mesylate: The Intergroup EORTC-ISG-AGITG Phase III Trial
  199. Gastrointestinal Stromal Tumors I: Pathology, Pathobiology, Primary Therapy, and Surgical Issues
  200. Kinome Profiling of Chondrosarcoma Reveals Src-Pathway Activity and Dasatinib as Option for Treatment
  201. Cellular/intramuscular myxoma and grade I myxofibrosarcoma are characterized by distinct genetic alterations and specific composition of their extracellular matrix
  202. Lymphopenia as a Prognostic Factor for Overall Survival in Advanced Carcinomas, Sarcomas, and Lymphomas
  203. Cell Cycle/Apoptosis Molecule Expression Correlates with Imatinib Response in Patients with Advanced Gastrointestinal Stromal Tumors
  204. Reduced human leukocyte antigen expression in advanced-stage Ewing sarcoma: implications for immune recognition
  205. Sclerostin in Mineralized Matrices and van Buchem Disease
  206. Similar gene expression profiles of sporadic, PGL2-, and SDHD-linked paragangliomas suggest a common pathway to tumorigenesis
  207. Genomic Profiling of Chondrosarcoma: Chromosomal Patterns in Central and Peripheral Tumors
  208. Extra‐abdominal subcutaneous metastasis of a gastrointestinal stromal tumor: report of a case and a review of the literature
  209. The molecular and cellular basis of exostosis formation in hereditary multiple exostoses
  210. The NFATc2 Gene Is Involved in a Novel Cloned Translocation in a Ewing Sarcoma Variant That Couples Its Function in Immunology to Oncology
  211. Aberrant Heparan Sulfate Proteoglycan Localization, Despite Normal Exostosin, in Central Chondrosarcoma
  212. Superior performance of liquid-based versus conventional cytology in a population-based cervical cancer screening program
  213. Genomic instability in giant cell tumor of bone. A study of 52 cases using DNA ploidy, relocalization FISH, and array‐CGH analysis
  214. Telomere‐associated proteins: cross‐talk between telomere maintenance and telomere‐lengthening mechanisms
  215. Assessment of Interobserver Variability and Histologic Parameters to Improve Reliability in Classification and Grading of Central Cartilaginous Tumors
  216. CD33+ CD14− Phenotype Is Characteristic of Multinuclear Osteoclast‐Like Cells in Giant Cell Tumor of Bone
  217. No genomic aberrations in Langerhans cell histiocytosis as assessed by diverse molecular technologies
  218. Reduced leucocyte cholesteryl ester transfer protein expression in acute coronary syndromes
  219. The cytotoxic effect of phenol and ethanol on the chondrosarcoma-derived cell line OUMS-27: AN IN VITRO EXPERIMENT
  220. Paclitaxel in patients with advanced angiosarcomas of soft tissue: A retrospective study of the EORTC soft tissue and bone sarcoma group
  221. NK cells recognize and lyse Ewing sarcoma cells through NKG2D and DNAM-1 receptor dependent pathways
  222. Distribution and prognostic value of histopathologic data and immunohistochemical markers in gastrointestinal stromal tumours (GISTs): An analysis of the EORTC phase III trial of treatment of metastatic GISTs with imatinib mesylate
  223. A chondrogenic gene expression signature in mesenchymal stem cells is a classifier of conventional central chondrosarcoma
  224. Results of Diagnostic Review in Pediatric Bone Tumors and Tumorlike Lesions
  225. Critical illness VR rehabilitation device (X-VR-D): Evaluation of the potential use for early clinical rehabilitation
  226. The Clinical Approach Towards Chondrosarcoma
  227. A Phase II Study of Gefitinib for Patients with Advanced HER-1 Expressing Synovial Sarcoma Refractory to Doxorubicin-Containing Regimens
  228. The Clinical Approach Towards Chondrosarcoma
  229. Myxoid tumours of soft tissue: the so‐called myxoid extracellular matrix is heterogeneous in composition
  230. Telomere biology in giant cell tumour of bone
  231. Incidence of Biopsy-Proven Bone Tumors in Children
  232. Lymphatics and bone
  233. EWSR1-CREB1 and EWSR1-ATF1 Fusion Genes in Angiomatoid Fibrous Histiocytoma
  234. Frequent deletion of the CDKN2A locus in chordoma: analysis of chromosomal imbalances using array comparative genomic hybridisation
  235. CT‐guided, COBRA‐FISH‐assisted diagnosis of well‐differentiated liposarcoma (inflammatory subtype) of the retroperitoneum
  236. Increased HIF1α in SDH and FH deficient tumors does not cause microsatellite instability
  237. Phase III Trial of Two Investigational Schedules of Ifosfamide Compared With Standard-Dose Doxorubicin in Advanced or Metastatic Soft Tissue Sarcoma: A European Organisation for Research and Treatment of Cancer Soft Tissue and Bone Sarcoma Group Study
  238. Does parosteal liposarcoma differ from other atypical lipomatous tumors/well-differentiated liposarcomas? A molecular cytogenetic study using combined multicolor COBRA-FISH karyotyping and array-based comparative genomic hybridization
  239. The role of noncartilage‐specific molecules in differentiation of cartilaginous tumors
  240. MR imaging characteristics in primary lymphoma of bone with emphasis on non-aggressive appearance
  241. Functional imaging of multidrug resistance in an orthotopic model of osteosarcoma using 99mTc-sestamibi
  242. Differences in telomerase expression by the CD1a+ cells in Langerhans cell histiocytosis reflect the diverse clinical presentation of the disease
  243. The Role of EXT1 in Nonhereditary Osteochondroma: Identification of Homozygous Deletions
  244. Identification of markers to characterize and sort human articular chondrocytes with enhanced in vitro chondrogenic capacity
  245. Improvement in Histologic Response But Not Survival in Osteosarcoma Patients Treated With Intensified Chemotherapy: A Randomized Phase III Trial of the European Osteosarcoma Intergroup
  246. Decreased EXT expression and intracellular accumulation of heparan sulphate proteoglycan in osteochondromas and peripheral chondrosarcomas
  247. Detection and molecular cytogenetic characterization of a novel ring chromosome in a histological variant of Ewing sarcoma
  248. Expression of Cellular FLICE Inhibitory Protein, Caspase-8, and Protease Inhibitor-9 in Ewing Sarcoma and Implications for Susceptibility to Cytotoxic Pathways
  249. Basic fibroblast growth factor and fibroblastic growth factor receptor–1 may contribute to head and neck paraganglioma development by an autocrine or paracrine mechanism
  250. Brostallicin, an agent with potential activity in metastatic soft tissue sarcoma: A phase II study from the European Organisation for Research and Treatment of Cancer Soft Tissue and Bone Sarcoma Group
  251. Sarcoma Derived from Cultured Mesenchymal Stem Cells
  252. Multidrug resistance mediated by ABC transporters in osteosarcoma cell lines: mRNA analysis and functional radiotracer studies
  253. Pathology of primary malignant bone and cartilage tumours
  254. Chondroid lipoma: findings on radiography and MRI (2006:7b)
  255. Array‐comparative genomic hybridization of central chondrosarcoma
  256. Giant cell tumors of the tendon sheath may present radiologically as intrinsic osseous lesions
  257. Peripheral chondrosarcoma progression is accompanied by decreased Indian Hedgehog signalling
  258. Nora’s lesion, a distinct radiological entity?
  259. Molecular cytogenetic characterization of four previously established and two newly established Ewing sarcoma cell lines
  260. Clinico-histologic parameters of osteosarcoma patients with late relapse
  261. Soft tissue pathology
  262. Brachyury and chordoma: the chondroid–chordoid dilemma resolved?
  263. Local recurrence of myxofibrosarcoma is associated with increase in tumour grade and cytogenetic aberrations, suggesting a multistep tumour progression model
  264. Tumor Cell Plasticity in Ewing Sarcoma, an Alternative Circulatory System Stimulated by Hypoxia
  265. Central high-grade osteosarcoma of bone: Diagnostic and genetic considerations
  266. Incidence of gastrointestinal stromal tumours is underestimated: Results of a nation-wide study
  267. Limited Rescue of Osteoclast‐Poor Osteopetrosis After Successful Engraftment by Cord Blood From an Unrelated Donor
  268. The histopathological differential diagnosis of mesenchymal tumours of the skin
  269. Estrogen Signaling Is Active in Cartilaginous Tumors: Implications for Antiestrogen Therapy as Treatment Option of Metastasized or Irresectable Chondrosarcoma
  270. TGF‐β1 drives partial myofibroblastic differentiation in chondromyxoid fibroma of bone
  271. Accuracy of radiography in grading and tissue-specific diagnosis—a study of 200 consecutive bone tumors of the hand
  272. Desmoplastic fibroma of bone: an immunohistochemical study including -catenin expression and mutational analysis for -catenin
  273. Initial and Late Resistance to Imatinib in Advanced Gastrointestinal Stromal Tumors Are Predicted by Different Prognostic Factors: A European Organisation for Research and Treatment of Cancer–Italian Sarcoma Group–Australasian Gastrointestinal Trials G...
  274. Emerging pathways in the development of chondrosarcoma of bone and implications for targeted treatment
  275. cDNA expression profiling of chondrosarcomas: Ollier disease resembles solitary tumours and alteration in genes coding for components of energy metabolism occurs with increasing grade
  276. Corrections to “Consensus meeting for the management of gastrointestinal stromal tumors Report of the GIST Consensus Conference of 20–21 March 2004, under the auspices of ESMO”
  277. Consensus meeting for the management of gastrointestinal stromal tumors
 Report of the GIST Consensus Conference of 20–21 March 2004, under the auspices of ESMO
  278. Presence of osteoclast-like multinucleated giant cells in the bone and nonostotic lesions of Langerhans cell histiocytosis
  279. The use of Bcl-2 and PTHLH immunohistochemistry in the diagnosis of peripheral chondrosarcoma in a clinicopathological setting
  280. Prenatal Detection of Orbital Rhabdomyosarcoma
  281. Absence of IHH and retention of PTHrP signalling in enchondromas and central chondrosarcomas
  282. Chondromyxoid fibroma resemblesin vitro chondrogenesis, but differs in expression of signalling molecules
  283. Bifurcation of the femur with tibial agenesis and additional anomalies
  284. Doxorubicin and cisplatin chemotherapy in high-grade spindle cell sarcomas of the bone, other than osteosarcoma or malignant fibrous histiocytoma: a European Osteosarcoma Intergroup Study
  285. Mutation screening of EXT1 and EXT2 by direct sequence analysis and MLPA in patients with multiple osteochondromas: splice site mutations and exonic deletions account for more than half of the mutations
  286. Aggressive angiomyxoma: a clinicopathological and immunohistochemical study of 11 cases with long-term follow-up
  287. Enchondromatosis (Ollier disease, Maffucci syndrome) is not caused by the PTHR1 mutation p.R150C
  288. Primary synovial sarcoma of the heart: a cytogenetic and molecular genetic analysis combining RT-PCR and COBRA-FISH of a case with a complex karyotype
  289. Soft-Tissue Tumors: Value of Static and Dynamic Gadopentetate Dimeglumine–enhanced MR Imaging in Prediction of Malignancy
  290. Magnetic resonance imaging of knee cartilage using a water selective balanced steady‐state free precession sequence
  291. Progression-free survival in gastrointestinal stromal tumours with high-dose imatinib: randomised trial
  292. Multicolor fluorescence in situ hybridization analysis of a synovial sarcoma of the larynx with a t(X;18)(p11.2;q11.2) and trisomies 2 and 8
  293. Changing concepts in the pathological basis of soft tissue and bone sarcoma treatment
  294. A phase II study of ET-743/trabectedin (`Yondelis') for patients with advanced gastrointestinal stromal tumours
  295. Solitary fibrous tumour: the emerging clinicopathologic spectrum of an entity and its differential diagnosis
  296. Expression Profiling of t(12;22) Positive Clear Cell Sarcoma of Soft Tissue Cell Lines Reveals Characteristic Up-Regulation of Potential New Marker Genes Including ERBB3
  297. Overexpression of the HER-2 oncogene does not play a role in high-grade osteosarcomas
  298. Somatic loss of maternal chromosome 11 causes parent-of-origin-dependent inheritance in SDHD-linked paraganglioma and phaeochromocytoma families
  299. Chondroma and chondrosarcoma of the larynx
  300. Molecular analysis of the INK4A/INK4A‐ARF gene locus in conventional (central) chondrosarcomas and enchondromas: indication of an important gene for tumour progression
  301. Langerhans cell histiocytosis: A pathologic combination of oncogenesis and immune dysregulation
  302. A distinct phenotype characterizes tumors from a putative genetic trait involving chondrosarcoma and breast cancer occurring in the same patient
  303. Dedifferentiated Adamantinoma With Revertant Mesenchymal Phenotype
  304. SDHD mutations in head and neck paragangliomas result in destabilization of complex II in the mitochondrial respiratory chain with loss of enzymatic activity and abnormal mitochondrial morphology
  305. Imatinib mesylate (STI-571 Glivec®, Gleevec™) is an active agent for gastrointestinal stromal tumours, but does not yield responses in other soft-tissue sarcomas that are unselected for a molecular target
  306. Pathology of soft tissue sarcomas with emphasis on molecular diagnostic techniques
  307. Langerhans-cell histiocytosis: neoplasia or unbridled inflammation?
  308. Multiple primary malignancies in osteosarcoma patients. Incidence and predictive value of osteosarcoma subtype for cancer syndromes related with osteosarcoma
  309. G2M arrest, blocked apoptosis, and low growth fraction may explain indolent behavior of head and neck paragangliomas
  310. Aberrant Chemokine Receptor Expression and Chemokine Production by Langerhans Cells Underlies the Pathogenesis of Langerhans Cell Histiocytosis
  311. Langerhans-cell histiocytosis 'insight into DC biology'
  312. Dynamic contrast-enhanced MR imaging in monitoring response to isolated limb perfusion in high-grade soft tissue sarcoma: initial results
  313. Amplification of 17p11.2∼p12, including PMP22, TOP3A, and MAPK7, in high-grade osteosarcoma
  314. Clear cell sarcoma of the stomach
  315. Expression of Cell Cycle–Related Gene Products in Langerhans Cell Histiocytosis
  316. Does the histological subtype of high-grade central osteosarcoma influence the response to treatment with chemotherapy and does it affect overall survival? A study on 570 patients of two consecutive trials of the European Osteosarcoma Intergroup
  317. Gemcitabine in advanced adult soft-tissue sarcomas. A phase II study of the EORTC Soft Tissue and Bone Sarcoma Group
  318. Diffusion‐weighted MRI in the characterization of soft‐tissue tumors
  319. Scale‐invariant segmentation of dynamic contrast‐enhanced perfusion MR images with inherent scale selection
  320. Cartilage-forming tumours of bone and soft tissue and their differential diagnosis
  321. Chromosome 9 Alterations and Trisomy 22 in Central Chondrosarcoma: A Cytogenetic and DNA Flow Cytometric Analysis of Chondrosarcoma Subtypes
  322. Retain or sacrifice the posterior cruciate ligament in total knee arthroplasty? A histopathological study of the cruciate ligament in osteoarthritic and rheumatoid disease
  323. Synovial sarcoma: dynamic contrast-enhanced MR imaging features
  324. The histopathological differential diagnosis of gastrointestinal stromal tumours
  325. Adamantinoma-like Ewing's sarcoma and Ewing's-like adamantinoma. The t(11; 22), t(21; 22) status
  326. Malignant melanoma is genetically distinct from clear cell sarcoma of tendons and aponeurosis (malignant melanoma of soft parts)
  327. Infantile‐type digital fibromatosis tumour in an adult
  328. Malignant progression in multiple enchondromatosis (Ollier's disease): An autopsy-based molecular genetic study
  329. Detection of areas with viable remnant tumor in postchemotherapy patients with Ewing’s sarcoma by dynamic contrast-enhanced MRI using pharmacokinetic modeling
  330. MR imaging of clear cell sarcoma (malignant melanoma of the soft parts): a multicenter correlative MRI-pathology study of 21 cases and literature review
  331. An update of diagnostic strategies using molecular genetic and magnetic resonance imaging techniques for musculoskeletal tumors
  332. A phase II study of cisplatin, ifosfamide and doxorubicin in operable primary, axial skeletal and metastatic osteosarcoma
  333. Myxoid tumours of soft tissue
  334. EXT-Mutation Analysis and Loss of Heterozygosity in Sporadic and Hereditary Osteochondromas and Secondary Chondrosarcomas
  335. Ring Chromosome 4 as the Sole Cytogenetic Anomaly in a Chondroblastoma
  336. Maligne Knorpeltumoren
  337. Chondroblastic osteosarcoma: characterisation by gadolinium-enhanced MR imaging correlated with histopathology
  338. Preoperative evaluation and monitoring chemotherapy in patients with high-grade osteogenic and Ewing's sarcoma: review of current imaging modalities
  339. How is the mutational status for tumor suppressors p53 and p16INK4A in MFH of the bone?
  340. MR imaging based strategies in limb salvage surgery for osteosarcoma of the distal femur
  341. Cytogenetic analysis of adamantinoma of long bones: Further indications for a common histogenesis with osteofibrous dysplasia
  342. Skin Metastases of Osteogenic Sarcoma
  343. Distribution of extracellular matrix components in adamantinoma of long bones suggests fibrous-to-epithelial transformation
  344. Molecular Identification of a Partial Hydatidiform Mole
  345. Tumor-associated eosinophilic infiltrate of cervical cancer is indicative for a less effective immune response
  346. Can conventional radiographs be used to monitor the effect of neoadjuvant chemotherapy in patients with osteogenic sarcoma?
  347. Calcified meningioma of the skull base simulating chondrosarcoma
  348. Translocation Identification of an Ews-Pseudogene Using Detection by RT-PCR in Ewings-Sarcoma
  349. Can MRI predict the histopathological response in patients with osteosarcoma after the first cycle of chemotherapy?
  350. Classification of histopathologic changes following chemotherapy in Ewing's sarcoma of bone
  351. Monitoring the effect of chemotherapy in Ewing's sarcoma of bone with MR imaging
  352. Metastasis of Breast Carcinoma to a Primary Mucinous Cystadenocarcinoma of the Ovary
  353. Adamantinoma of the Long Bones: Keratin Subclass Immunoreactivity Pattern with Reference to Its Histogenesis
  354. Antigen size influences the type of glomerular pathology in chronic serum sickness
  355. Unusual Manifestations of Yersinia enterocolitica Infections Diagnosed Using Novel Methods