All Stories

  1. Transmembrane protein 14A protects glomerular filtration barrier integrity
  2. Immunological factors linked to geographical variation in vaccine responses
  3. Brown Tumour in Chronic Kidney Disease: Revisiting an Old Disease with a New Perspective
  4. Brown Tumour in Chronic Kidney Disease: Revisiting an Old Disease with a New Perspective
  5. Histone Deacetylase Inhibitors as a Therapeutic Strategy to Eliminate Neoplastic “Stromal” Cells from Giant Cell Tumors of Bone
  6. Clinicopathologic and molecular features of denosumab-treated giant cell tumour of bone (GCTB): Analysis of 21 cases
  7. Cell Biology of Giant Cell Tumour of Bone: Crosstalk between m/wt Nucleosome H3.3, Telomeres and Osteoclastogenesis
  8. NTRK fusions are extremely rare in bone tumours
  9. The adapter protein Myd88 plays an important role in limiting mycobacterial growth in a zebrafish model for tuberculosis
  10. Co-existence of lung carcinoma metastasis and enchondroma in the femur of a patient with Ollier disease
  11. Surgical Outcome and Oncological Survival of Osteofibrous Dysplasia-Like and Classic Adamantinomas
  12. Mutation-driven epigenetic alterations as a defining hallmark of central cartilaginous tumours, giant cell tumour of bone and chondroblastoma
  13. Nikolay Ivanovich Pirogov (1810–1881): Anatomical research to develop surgery
  14. Glomerular permeability is not affected by heparan sulfate glycosaminoglycan deficiency in zebrafish embryos
  15. Quality of Life of Patients With Osteosarcoma in the European American Osteosarcoma Study-1 (EURAMOS-1): Development and Implementation of a Questionnaire Substudy
  16. 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
  17. Adjuvant Zoledronic Acid in High-Risk Giant Cell Tumor of Bone: A Multicenter Randomized Phase II Trial
  18. Non‐ossifying fibroma: A RAS‐MAPK driven benign bone neoplasm
  19. 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
  20. Survival and prognosis with osteosarcoma: outcomes in more than 2000 patients in the EURAMOS-1 (European and American Osteosarcoma Study) cohort
  21. 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
  22. Women in healthcare in Imperial Russia: The contribution of the surgeon Nikolay I Pirogov
  23. Conjunctival Leiomyosarcoma, a Rare Neoplasm Always Originating at the Limbus? Report of a New Case and Review of 11 Published Cases
  24. M-CSF and IL-34 expression as indicators for growth in sporadic vestibular schwannoma
  25. Increased dynamin expression precedes proteinuria in glomerular disease
  26. Introducing fluorescence guided surgery into orthopedic oncology: A systematic review of candidate protein targets for Ewing sarcoma
  27. Bioorthogonally Applicable Fluorescence Deactivation Strategy for Receptor Kinetics Study and Theranostic Pretargeting Approaches
  28. The incidence, mutational status, risk classification and referral pattern of gastro-intestinal stromal tumours in the Netherlands: a nationwide pathology registry (PALGA) study
  29. BCRP expression in schwannoma, plexiform neurofibroma and MPNST
  30. Hematopoietic Tumors Primarily Presenting in Bone
  31. Fluorescent CXCR4 targeting peptide as alternative for antibody staining in Ewing sarcoma
  32. 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...
  33. 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
  34. ECCO Essential Requirements for Quality Cancer Care: Soft Tissue Sarcoma in Adults and Bone Sarcoma. A critical review
  35. High prevalence of autoimmune disease in the rare inflammatory bone disorder sternocostoclavicular hyperostosis: survey of a Dutch cohort
  36. MRI appearances of atypical cartilaginous tumour/grade I chondrosarcoma after treatment by curettage, phenolisation and allografting
  37. 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
  38. Expression of CCL21 in Ewing sarcoma shows an inverse correlation with metastases and is a candidate target for immunotherapy
  39. Loss of H3K27 tri-methylation is a diagnostic marker for malignant peripheral nerve sheath tumors and an indicator for an inferior survival
  40. CXCR4 signaling is controlled by immobilization at the plasma membrane
  41. Nikolay Ivanovich Pirogov (1810–1881): A pioneering Russian surgeon and medical scientist
  42. Automation of Technology for Cancer Research
  43. Ewing sarcoma: The clinical relevance of the insulin-like growth factor 1 and the poly-ADP-ribose-polymerase pathway
  44. A translocation t(6;14) in two cases of leiomyosarcoma: Molecular cytogenetic and array-based comparative genomic hybridization characterization
  45. CXCL14, CXCR7 expression and CXCR4 splice variant ratio associate with survival and metastases in Ewing sarcoma patients
  46. Inactivation of SDH and FH cause loss of 5hmC and increased H3K9me3 in paraganglioma/pheochromocytoma and smooth muscle tumors
  47. Sequencing Overview of Ewing Sarcoma: A Journey across Genomic, Epigenomic and Transcriptomic Landscapes
  48. 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...
  49. Chemotherapy in osteosarcoma
  50. Periosteal chondrosarcoma: a histopathological and molecular analysis of a rare chondrosarcoma subtype
  51. Neoadjuvant denosumab for extensive giant cell tumor in os ischium —a case report
  52. Doxorubicin-based adjuvant chemotherapy in soft tissue sarcoma: pooled analysis of two STBSG-EORTC phase III clinical trials
  53. EURAMOS-1, an international randomised study for osteosarcoma: results from pre-randomisation treatment
  54. Nikolay Ivanovich Pirogov: a surgeon's contribution to military and civilian anaesthesia
  55. De novodiscovery of phenotypic intratumour heterogeneity using imaging mass spectrometry
  56. Gene expression profiling of giant cell tumor of bone reveals downregulation of extracellular matrix components decorin and lumican associated with lung metastasis
  57. Quantification of the Heterogeneity of Prognostic Cellular Biomarkers in Ewing Sarcoma Using Automated Image and Random Survival Forest Analysis
  58. Ewing sarcoma inhibition by disruption of EWSR1-FLI1 transcriptional activity and reactivation of p53
  59. 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
  60. Molecular genetics of chondroid tumours
  61. The Clinical Approach Toward Giant Cell Tumor of Bone
  62. Primary intraosseous manifestation of Rosai-Dorfman disease: 2 cases and review of literature
  63. Transactivating mutation of theMYOD1gene is a frequent event in adult spindle cell rhabdomyosarcoma
  64. 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...
  65. Frequent truncating mutations of STAG2 in bladder cancer
  66. 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)
  67. CD99-positive undifferentiated round cell sarcoma diagnosed on fine needle aspiration cytology, later found to harbour aCIC-DUX4translocation: a recently described entity
  68. IR/IGF1R signaling as potential target for treatment of high-grade osteosarcoma
  69. FXR regulates CETP
  70. Imaging Mass Spectrometry-based Molecular Histology Differentiates Microscopically Identical and Heterogeneous Tumors
  71. Genome-wide analyses on high-grade osteosarcoma: Making sense of a genomically most unstable tumor
  72. Tumor-Associated Macrophages Are Related to Volumetric Growth of Vestibular Schwannomas
  73. Inactivation of Patched1 in Mice Leads to Development of Gastrointestinal Stromal-Like Tumors That Express Pdgfrα but Not Kit
  74. Mutations affecting BRAF, EGFR, PIK3CA, and KRAS are not associated with sporadic vestibular schwannomas
  75. Osteosarcoma of the hands and feet: a distinct clinico-pathological subgroup
  76. The activities of Smad and Gli mediated signalling pathways in high-grade conventional osteosarcoma
  77. Integrative Analysis Reveals Relationships of Genetic and Epigenetic Alterations in Osteosarcoma
  78. Adjuvant chemotherapy with doxorubicin, ifosfamide, and lenograstim for resected soft-tissue sarcoma (EORTC 62931): a multicentre randomised controlled trial
  79. High frequency of MYC gene amplification is a common feature of radiation‐induced sarcomas. Further results from EORTC STBSG TL 01/01
  80. Three new chondrosarcoma cell lines: one grade III conventional central chondrosarcoma and two dedifferentiated chondrosarcomas of bone
  81. Imaging mass spectrometry statistical analysis
  82. A multidisciplinary approach to giant cell tumors of tendon sheath and synovium—A critical appraisal of literature and treatment proposal
  83. Expression of ERG, an Ets family transcription factor, identifies ERG-rearranged Ewing sarcoma
  84. Low-Grade Chondrosarcoma of Long Bones Treated with Intralesional Curettage Followed by Application of Phenol, Ethanol, and Bone-Grafting
  85. The management of diffuse-type giant cell tumour (pigmented villonodular synovitis) and giant cell tumour of tendon sheath (nodular tenosynovitis)
  86. Intratumoral hemorrhage, vessel density, and the inflammatory reaction contribute to volume increase of sporadic vestibular schwannomas
  87. An osteosarcoma zebrafish model implicates Mmp‐19 and Ets‐1 as well as reduced host immune response in angiogenesis and migration
  88. 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
  89. Anti-EGFR Antibody Cetuximab Enhances the Cytolytic Activity of Natural Killer Cells toward Osteosarcoma
  90. The First European Interdisciplinary Ewing Sarcoma Research Summit
  91. Osteosarcoma Models: From Cell Lines to Zebrafish
  92. Epiphyseal growth plate and secondary peripheral chondrosarcoma: the neighbours matter
  93. Identification of a novel, recurrent HEY1‐NCOA2 fusion in mesenchymal chondrosarcoma based on a genome‐wide screen of exon‐level expression data
  94. Survival from high-grade localised extremity osteosarcoma: combined results and prognostic factors from three European Osteosarcoma Intergroup randomised controlled trials
  95. 1q gain and CDT2 overexpression underlie an aggressive and highly proliferative form of Ewing sarcoma
  96. Secondary peripheral chondrosarcoma evolving from osteochondroma as a result of outgrowth of cells with functional EXT
  97. Functional characterization of osteosarcoma cell lines provides representative models to study the human disease
  98. Breakpoint characterization of large deletions in EXT1 or EXT2 in 10 Multiple Osteochondromas families
  99. A short-term in vivo model for giant cell tumor of bone
  100. IGF1R Signaling in Ewing Sarcoma Is Shaped by Clathrin-/Caveolin-Dependent Endocytosis
  101. Maffucci syndrome: A genome‐wide analysis using high resolution single nucleotide polymorphism and expression arrays on four cases
  102. The immunophenotype of osteoclasts and macrophage polykaryons
  103. Growth plate regulation and osteochondroma formation: insights from tracing proteoglycans in zebrafish models and human cartilage
  104. Podoplanin expression in adamantinoma of long bones and osteofibrous dysplasia
  105. Tumor-Infiltrating Macrophages Are Associated with Metastasis Suppression in High-Grade Osteosarcoma: A Rationale for Treatment with Macrophage Activating Agents
  106. Survival after recurrent osteosarcoma: Data from 3 European Osteosarcoma Intergroup (EOI) randomized controlled trials
  107. Chemotherapy-resistant osteosarcoma is highly susceptible to IL-15-activated allogeneic and autologous NK cells
  108. Cartilage ultrastructure in proteoglycan‐deficient zebrafish mutants brings to light new candidate genes for human skeletal disorders
  109. 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
  110. Distinct histological features characterize primary angiosarcoma of bone
  111. Late sarcoma development after curettage and bone grafting of benign bone tumors
  112. Pro-inflammatory chemokine-chemokine receptor interactions within the Ewing sarcoma microenvironment determine CD8+ T-lymphocyte infiltration and affect tumour progression
  113. The role of epidermal growth factor receptor in chordoma pathogenesis: a potential therapeutic target
  114. Tiling resolution array-CGH shows that somatic mosaic deletion of the EXT gene is causative in EXT gene mutation negative multiple osteochondromas patients
  115. Role of the transcription factor T (brachyury) in the pathogenesis of sporadic chordoma: a genetic and functional‐based study
  116. Array-based comparative genomic hybridisation analysis reveals recurrent chromosomal alterations in primary diffuse large B cell lymphoma of bone
  117. No Haploinsufficiency but Loss of Heterozygosity for EXT in Multiple Osteochondromas
  118. Kinome profiling of myxoid liposarcoma reveals NF-kappaB-pathway kinase activity and Casein Kinase II inhibition as a potential treatment option
  119. Critical role of endoglin in tumor cell plasticity of Ewing sarcoma and melanoma
  120. Coactivated Platelet-Derived Growth Factor Receptor α and Epidermal Growth Factor Receptor Are Potential Therapeutic Targets in Intimal Sarcoma
  121. Heterogeneous and Complex Rearrangements of Chromosome Arm 6q in Chondromyxoid Fibroma
  122. Bisphosphonate treatment of aggressive primary, recurrent and metastatic Giant Cell Tumour of Bone
  123. Small deletions but not methylation underlie CDKN2A/p16 loss of expression in conventional osteosarcoma
  124. Hierarchical clustering of flow cytometry data for the study of conventional central chondrosarcoma
  125. DOG1 and CD117 are the antibodies of choice in the diagnosis of gastrointestinal stromal tumours
  126. Primary cilia organization reflects polarity in the growth plate and implies loss of polarity and mosaicism in osteochondroma
  127. Cartilage tumours and bone development: molecular pathology and possible therapeutic targets
  128. A Reappraisal of Hemangiopericytoma of Bone; Analysis of Cases Reclassified as Synovial Sarcoma and Solitary Fibrous Tumor of Bone
  129. Bone sarcomas: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up
  130. 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
  131. Correlation of hypoxic signalling to histological grade and outcome in cartilage tumours
  132. Langerhans cell histiocytosis: fascinating dynamics of the dendritic cell–macrophage lineage
  133. Soft tissue sarcomas: introduction to the Virchows Archiv review issue
  134. Anti-inflammatory M2 type macrophages characterize metastasized and tyrosine kinase inhibitor-treated gastrointestinal stromal tumors
  135. Prognostic and predictive factors for outcome to first-line ifosfamide-containing chemotherapy for adult patients with advanced soft tissue sarcomas
  136. Improved diagnosis and treatment of soft tissue sarcoma patients after implementation of national guidelines: A population-based study
  137. Sdhd and Sdhd/H19 Knockout Mice Do Not Develop Paraganglioma or Pheochromocytoma
  138. Genome‐wide transcriptome analyses reveal p53 inactivation mediated loss of miR‐34a expression in malignant peripheral nerve sheath tumours
  139. Prognostic factors in pulmonary metastasized high‐grade osteosarcoma
  140. Profiling of high-grade central osteosarcoma and its putative progenitor cells identifies tumourigenic pathways
  141. Dedifferentiated peripheral chondrosarcomas: regulation of EXT-downstream molecules and differentiation-related genes
  142. The Journal of Pathology 2008 Jeremy Jass Prize for Research Excellence in Pathology
  143. Imatinib Mesylate in Patients with WHO B3 Thymomas and Thymic Carcinomas
  144. Molecular characterization of commonly used cell lines for bone tumor research: A trans‐European EuroBoNet effort
  145. Molecular pathology of sarcomas: concepts and clinical implications
  146. Inactive Wnt/β-catenin pathway in conventional high-grade osteosarcoma
  147. Central chondrosarcoma progression is associated with pRb pathway alterations: CDK4 down-regulation and p16 overexpression inhibit cell growth in vitro
  148. Osteosarcoma originates from mesenchymal stem cells in consequence of aneuploidization and genomic loss of Cdkn2
  149. Running GAGs: myxoid matrix in tumor pathology revisited
  150. Kinome Profiling of Chondrosarcoma Reveals Src-Pathway Activity and Dasatinib as Option for Treatment
  151. Cellular/intramuscular myxoma and grade I myxofibrosarcoma are characterized by distinct genetic alterations and specific composition of their extracellular matrix
  152. Lymphopenia as a Prognostic Factor for Overall Survival in Advanced Carcinomas, Sarcomas, and Lymphomas
  153. Reduced human leukocyte antigen expression in advanced-stage Ewing sarcoma: implications for immune recognition
  154. Genomic Profiling of Chondrosarcoma: Chromosomal Patterns in Central and Peripheral Tumors
  155. Extra‐abdominal subcutaneous metastasis of a gastrointestinal stromal tumor: report of a case and a review of the literature
  156. The molecular and cellular basis of exostosis formation in hereditary multiple exostoses
  157. The NFATc2 Gene Is Involved in a Novel Cloned Translocation in a Ewing Sarcoma Variant That Couples Its Function in Immunology to Oncology
  158. Aberrant Heparan Sulfate Proteoglycan Localization, Despite Normal Exostosin, in Central Chondrosarcoma
  159. Superior performance of liquid-based versus conventional cytology in a population-based cervical cancer screening program
  160. Genomic instability in giant cell tumor of bone. A study of 52 cases using DNA ploidy, relocalization FISH, and array‐CGH analysis
  161. Assessment of Interobserver Variability and Histologic Parameters to Improve Reliability in Classification and Grading of Central Cartilaginous Tumors
  162. CD33+ CD14− Phenotype Is Characteristic of Multinuclear Osteoclast‐Like Cells in Giant Cell Tumor of Bone
  163. Reduced leucocyte cholesteryl ester transfer protein expression in acute coronary syndromes
  164. The cytotoxic effect of phenol and ethanol on the chondrosarcoma-derived cell line OUMS-27: AN IN VITRO EXPERIMENT
  165. Paclitaxel in patients with advanced angiosarcomas of soft tissue: A retrospective study of the EORTC soft tissue and bone sarcoma group
  166. NK cells recognize and lyse Ewing sarcoma cells through NKG2D and DNAM-1 receptor dependent pathways
  167. 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
  168. Results of Diagnostic Review in Pediatric Bone Tumors and Tumorlike Lesions
  169. The Clinical Approach Towards Chondrosarcoma
  170. A Phase II Study of Gefitinib for Patients with Advanced HER-1 Expressing Synovial Sarcoma Refractory to Doxorubicin-Containing Regimens
  171. The Clinical Approach Towards Chondrosarcoma
  172. Myxoid tumours of soft tissue: the so‐called myxoid extracellular matrix is heterogeneous in composition
  173. Telomere biology in giant cell tumour of bone
  174. Incidence of Biopsy-Proven Bone Tumors in Children
  175. EWSR1-CREB1 and EWSR1-ATF1 Fusion Genes in Angiomatoid Fibrous Histiocytoma
  176. CT‐guided, COBRA‐FISH‐assisted diagnosis of well‐differentiated liposarcoma (inflammatory subtype) of the retroperitoneum
  177. Increased HIF1α in SDH and FH deficient tumors does not cause microsatellite instability
  178. 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
  179. 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
  180. The role of noncartilage‐specific molecules in differentiation of cartilaginous tumors
  181. MR imaging characteristics in primary lymphoma of bone with emphasis on non-aggressive appearance
  182. Functional imaging of multidrug resistance in an orthotopic model of osteosarcoma using 99mTc-sestamibi
  183. The Role of EXT1 in Nonhereditary Osteochondroma: Identification of Homozygous Deletions
  184. Identification of markers to characterize and sort human articular chondrocytes with enhanced in vitro chondrogenic capacity
  185. Improvement in Histologic Response But Not Survival in Osteosarcoma Patients Treated With Intensified Chemotherapy: A Randomized Phase III Trial of the European Osteosarcoma Intergroup
  186. Decreased EXT expression and intracellular accumulation of heparan sulphate proteoglycan in osteochondromas and peripheral chondrosarcomas
  187. Detection and molecular cytogenetic characterization of a novel ring chromosome in a histological variant of Ewing sarcoma
  188. Expression of Cellular FLICE Inhibitory Protein, Caspase-8, and Protease Inhibitor-9 in Ewing Sarcoma and Implications for Susceptibility to Cytotoxic Pathways
  189. Basic fibroblast growth factor and fibroblastic growth factor receptor–1 may contribute to head and neck paraganglioma development by an autocrine or paracrine mechanism
  190. 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
  191. Sarcoma Derived from Cultured Mesenchymal Stem Cells
  192. Multidrug resistance mediated by ABC transporters in osteosarcoma cell lines: mRNA analysis and functional radiotracer studies
  193. Pathology of primary malignant bone and cartilage tumours
  194. Chondroid lipoma: findings on radiography and MRI (2006:7b)
  195. Array‐comparative genomic hybridization of central chondrosarcoma
  196. Giant cell tumors of the tendon sheath may present radiologically as intrinsic osseous lesions
  197. Peripheral chondrosarcoma progression is accompanied by decreased Indian Hedgehog signalling
  198. Nora’s lesion, a distinct radiological entity?
  199. Molecular cytogenetic characterization of four previously established and two newly established Ewing sarcoma cell lines
  200. Clinico-histologic parameters of osteosarcoma patients with late relapse
  201. Soft tissue pathology
  202. Brachyury and chordoma: the chondroid–chordoid dilemma resolved?
  203. Local recurrence of myxofibrosarcoma is associated with increase in tumour grade and cytogenetic aberrations, suggesting a multistep tumour progression model
  204. Central high-grade osteosarcoma of bone: Diagnostic and genetic considerations
  205. Incidence of gastrointestinal stromal tumours is underestimated: Results of a nation-wide study
  206. Limited Rescue of Osteoclast‐Poor Osteopetrosis After Successful Engraftment by Cord Blood From an Unrelated Donor
  207. Estrogen Signaling Is Active in Cartilaginous Tumors: Implications for Antiestrogen Therapy as Treatment Option of Metastasized or Irresectable Chondrosarcoma
  208. TGF‐β1 drives partial myofibroblastic differentiation in chondromyxoid fibroma of bone
  209. Accuracy of radiography in grading and tissue-specific diagnosis—a study of 200 consecutive bone tumors of the hand
  210. Desmoplastic fibroma of bone: an immunohistochemical study including -catenin expression and mutational analysis for -catenin
  211. 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...
  212. Emerging pathways in the development of chondrosarcoma of bone and implications for targeted treatment
  213. cDNA expression profiling of chondrosarcomas: Ollier disease resembles solitary tumours and alteration in genes coding for components of energy metabolism occurs with increasing grade
  214. 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”
  215. 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
  216. Presence of osteoclast-like multinucleated giant cells in the bone and nonostotic lesions of Langerhans cell histiocytosis
  217. The use of Bcl-2 and PTHLH immunohistochemistry in the diagnosis of peripheral chondrosarcoma in a clinicopathological setting
  218. Chondromyxoid fibroma resemblesin vitro chondrogenesis, but differs in expression of signalling molecules
  219. 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
  220. 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
  221. Aggressive angiomyxoma: a clinicopathological and immunohistochemical study of 11 cases with long-term follow-up
  222. 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
  223. Soft-Tissue Tumors: Value of Static and Dynamic Gadopentetate Dimeglumine–enhanced MR Imaging in Prediction of Malignancy
  224. Magnetic resonance imaging of knee cartilage using a water selective balanced steady‐state free precession sequence
  225. 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
  226. A phase II study of ET-743/trabectedin (`Yondelis') for patients with advanced gastrointestinal stromal tumours
  227. Solitary fibrous tumour: the emerging clinicopathologic spectrum of an entity and its differential diagnosis
  228. 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
  229. Somatic loss of maternal chromosome 11 causes parent-of-origin-dependent inheritance in SDHD-linked paraganglioma and phaeochromocytoma families
  230. Chondroma and chondrosarcoma of the larynx
  231. Dedifferentiated Adamantinoma With Revertant Mesenchymal Phenotype
  232. 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
  233. 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
  234. Pathology of soft tissue sarcomas with emphasis on molecular diagnostic techniques
  235. Langerhans-cell histiocytosis: neoplasia or unbridled inflammation?
  236. Multiple primary malignancies in osteosarcoma patients. Incidence and predictive value of osteosarcoma subtype for cancer syndromes related with osteosarcoma
  237. G2M arrest, blocked apoptosis, and low growth fraction may explain indolent behavior of head and neck paragangliomas
  238. Aberrant Chemokine Receptor Expression and Chemokine Production by Langerhans Cells Underlies the Pathogenesis of Langerhans Cell Histiocytosis
  239. Langerhans-cell histiocytosis 'insight into DC biology'
  240. Dynamic contrast-enhanced MR imaging in monitoring response to isolated limb perfusion in high-grade soft tissue sarcoma: initial results
  241. Amplification of 17p11.2∼p12, including PMP22, TOP3A, and MAPK7, in high-grade osteosarcoma
  242. Clear cell sarcoma of the stomach
  243. 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
  244. Gemcitabine in advanced adult soft-tissue sarcomas. A phase II study of the EORTC Soft Tissue and Bone Sarcoma Group
  245. Diffusion‐weighted MRI in the characterization of soft‐tissue tumors
  246. Chromosome 9 Alterations and Trisomy 22 in Central Chondrosarcoma: A Cytogenetic and DNA Flow Cytometric Analysis of Chondrosarcoma Subtypes
  247. Retain or sacrifice the posterior cruciate ligament in total knee arthroplasty? A histopathological study of the cruciate ligament in osteoarthritic and rheumatoid disease
  248. Synovial sarcoma: dynamic contrast-enhanced MR imaging features
  249. Adamantinoma-like Ewing's sarcoma and Ewing's-like adamantinoma. The t(11; 22), t(21; 22) status
  250. Infantile‐type digital fibromatosis tumour in an adult
  251. Malignant progression in multiple enchondromatosis (Ollier's disease): An autopsy-based molecular genetic study
  252. An update of diagnostic strategies using molecular genetic and magnetic resonance imaging techniques for musculoskeletal tumors
  253. EXT-Mutation Analysis and Loss of Heterozygosity in Sporadic and Hereditary Osteochondromas and Secondary Chondrosarcomas
  254. Ring Chromosome 4 as the Sole Cytogenetic Anomaly in a Chondroblastoma
  255. Maligne Knorpeltumoren
  256. Chondroblastic osteosarcoma: characterisation by gadolinium-enhanced MR imaging correlated with histopathology
  257. Preoperative evaluation and monitoring chemotherapy in patients with high-grade osteogenic and Ewing's sarcoma: review of current imaging modalities
  258. How is the mutational status for tumor suppressors p53 and p16INK4A in MFH of the bone?
  259. MR imaging based strategies in limb salvage surgery for osteosarcoma of the distal femur
  260. Cytogenetic analysis of adamantinoma of long bones: Further indications for a common histogenesis with osteofibrous dysplasia
  261. Skin Metastases of Osteogenic Sarcoma
  262. Distribution of extracellular matrix components in adamantinoma of long bones suggests fibrous-to-epithelial transformation
  263. Molecular Identification of a Partial Hydatidiform Mole
  264. Calcified meningioma of the skull base simulating chondrosarcoma
  265. Translocation Identification of an Ews-Pseudogene Using Detection by RT-PCR in Ewings-Sarcoma
  266. Can MRI predict the histopathological response in patients with osteosarcoma after the first cycle of chemotherapy?
  267. Monitoring the effect of chemotherapy in Ewing's sarcoma of bone with MR imaging
  268. Metastasis of Breast Carcinoma to a Primary Mucinous Cystadenocarcinoma of the Ovary
  269. Adamantinoma of the Long Bones: Keratin Subclass Immunoreactivity Pattern with Reference to Its Histogenesis
  270. Antigen size influences the type of glomerular pathology in chronic serum sickness
  271. Unusual Manifestations of Yersinia enterocolitica Infections Diagnosed Using Novel Methods