All Stories

  1. Histiocytosis development and clinical variation through the lens of genomics
  2. Publisher Correction: Academia Europaea’s guidelines for the visualization of clinical outcomes
  3. Academia Europaea’s guidelines for the visualization of clinical outcomes
  4. Vaccination Against Extracellular Vimentin Plus Doxorubicin for Canine Hemangiosarcoma
  5. The impact of Leiden-educated Niels Stensen (Nicolas Steno) on the advancement of medical knowledge and practices
  6. Tanzanian gut microbiota profiles linked to high but rapidly waning yellow fever antibody titers
  7. Identification of novel small molecule inhibitors of ETS transcription factors
  8. Embryonic reprogramming of the tumor vasculature reveals targets for cancer therapy
  9. New evidence for fibrocartilaginous dysplasia representing a variant of fibrous dysplasia
  10. Recurrent ETV3::NCOA2 fusions and MAPK pathway mutations in indeterminate dendritic cell histiocytosis
  11. Histopathologic Challenges in the Diagnostic Stage
  12. Recurrent CLTC::SYK fusions and CSF1R mutations in juvenile xanthogranuloma of soft tissue
  13. Lifestyle score is associated with cellular immune profiles in healthy Tanzanian adults
  14. Immune response, Osteosarcoma and chemotherapy response
  15. Demographics and additional haematologic cancers of patients with histiocytic/dendritic cell neoplasms
  16. Transmembrane protein 14A protects glomerular filtration barrier integrity
  17. Immunological factors linked to geographical variation in vaccine responses
  18. Brown Tumour in Chronic Kidney Disease: Revisiting an Old Disease with a New Perspective
  19. Brown Tumour in Chronic Kidney Disease: Revisiting an Old Disease with a New Perspective
  20. The first, private and unknown small anatomical Ruijsch collection of Peter the Great
  21. Histone Deacetylase Inhibitors as a Therapeutic Strategy to Eliminate Neoplastic “Stromal” Cells from Giant Cell Tumors of Bone
  22. Outcomes from a mechanistic biomarker multi-arm and randomised study of liposomal MTP-PE (Mifamurtide) in metastatic and/or recurrent osteosarcoma (EuroSarc-Memos trial)
  23. Clinicopathologic and molecular features of denosumab-treated giant cell tumour of bone (GCTB): Analysis of 21 cases
  24. Mutations in the heparan sulfate backbone elongating enzymes EXT1 and EXT2 have no major effect on endothelial glycocalyx and the glomerular filtration barrier
  25. ALK-positive histiocytosis: a new clinicopathologic spectrum highlighting neurologic involvement and responses to ALK inhibition
  26. Case Report: Asymptomatic COVID-19 patient with a subtle hypercoagulable state and fluctuating D-dimer level
  27. Cell Biology of Giant Cell Tumour of Bone: Crosstalk between m/wt Nucleosome H3.3, Telomeres and Osteoclastogenesis
  28. NTRK fusions are extremely rare in bone tumours
  29. Frequent mutated B2M, EZH2, IRF8, and TNFRSF14 in primary bone diffuse large B-cell lymphoma reflect a GCB phenotype
  30. Medical instruments in Imperial Russia: from a blacksmith to a factory for medical instruments, headed by a leading surgeon N.L. Bidloo
  31. Non-Hodgkin lymphoma of bone of the femur and humerus: a case report and review of the literature
  32. The adapter protein Myd88 plays an important role in limiting mycobacterial growth in a zebrafish model for tuberculosis
  33. Dutch cultural heritage of Fredrik Ruijsch and Herman Boerhaave in the Military Medical Academy named after S. M. Kirov
  34. Co-existence of lung carcinoma metastasis and enchondroma in the femur of a patient with Ollier disease
  35. Nikolay Ivanovich Pirogov as an innovator in anatomy, surgery, and anaesthesiology. Part II
  36. Spectrum of histiocytic neoplasms associated with diverse haematological malignancies bearing the same oncogenic mutation
  37. Surgical Outcome and Oncological Survival of Osteofibrous Dysplasia-Like and Classic Adamantinomas
  38. Highlights of the professional activities of Nikolay Ivanovich Pirogov before and after his professoriate in Saint Petersburg (1841–1860). Part I
  39. Nikolay Ivanovich Pirogov: Forerunner, co-founder and Inspector-General of the Red Cross
  40. The Dutchman Herman Boerhaave and the Russian Nikolay Ivanovich Pirogov are brilliant medical scientists, whose remembrance will be eternal
  41. Mutation-driven epigenetic alterations as a defining hallmark of central cartilaginous tumours, giant cell tumour of bone and chondroblastoma
  42. The development of Russian Medicine in the Petrine era and the role of Dutch doctors in this process
  43. Nikolay Ivanovich Pirogov (1810–1881): Anatomical research to develop surgery
  44. Glomerular permeability is not affected by heparan sulfate glycosaminoglycan deficiency in zebrafish embryos
  45. Quality of Life of Patients With Osteosarcoma in the European American Osteosarcoma Study-1 (EURAMOS-1): Development and Implementation of a Questionnaire Substudy
  46. 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
  47. Adjuvant Zoledronic Acid in High-Risk Giant Cell Tumor of Bone: A Multicenter Randomized Phase II Trial
  48. Non‐ossifying fibroma: A RAS‐MAPK driven benign bone neoplasm
  49. 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
  50. Survival and prognosis with osteosarcoma: outcomes in more than 2000 patients in the EURAMOS-1 (European and American Osteosarcoma Study) cohort
  51. 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
  52. Women in healthcare in Imperial Russia: The contribution of the surgeon Nikolay I Pirogov
  53. Conjunctival Leiomyosarcoma, a Rare Neoplasm Always Originating at the Limbus? Report of a New Case and Review of 11 Published Cases
  54. Pleomorphic Sarcomas
  55. Markov moment for the agglomerative method of clustering in Euclidean space
  56. M-CSF and IL-34 expression as indicators for growth in sporadic vestibular schwannoma
  57. Increased dynamin expression precedes proteinuria in glomerular disease
  58. Introducing fluorescence guided surgery into orthopedic oncology: A systematic review of candidate protein targets for Ewing sarcoma
  59. Molecular genetics of Ewing sarcoma, model systems and finding novel (immuno-) therapeutic targets
  60. Bioorthogonally Applicable Fluorescence Deactivation Strategy for Receptor Kinetics Study and Theranostic Pretargeting Approaches
  61. The incidence, mutational status, risk classification and referral pattern of gastro-intestinal stromal tumours in the Netherlands: a nationwide pathology registry (PALGA) study
  62. Cancer of Bones and Joints
  63. BCRP expression in schwannoma, plexiform neurofibroma and MPNST
  64. Hematopoietic Tumors Primarily Presenting in Bone
  65. Fluorescent CXCR4 targeting peptide as alternative for antibody staining in Ewing sarcoma
  66. 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...
  67. 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
  68. ECCO Essential Requirements for Quality Cancer Care: Soft Tissue Sarcoma in Adults and Bone Sarcoma. A critical review
  69. High prevalence of autoimmune disease in the rare inflammatory bone disorder sternocostoclavicular hyperostosis: survey of a Dutch cohort
  70. MRI appearances of atypical cartilaginous tumour/grade I chondrosarcoma after treatment by curettage, phenolisation and allografting
  71. 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
  72. Erratum: Loss of H3K27 tri-methylation is a diagnostic marker for malignant peripheral nerve sheath tumors and an indicator for an inferior survival
  73. Expression of CCL21 in Ewing sarcoma shows an inverse correlation with metastases and is a candidate target for immunotherapy
  74. Loss of H3K27 tri-methylation is a diagnostic marker for malignant peripheral nerve sheath tumors and an indicator for an inferior survival
  75. CXCR4 signaling is controlled by immobilization at the plasma membrane
  76. Nikolay Ivanovich Pirogov (1810–1881): A pioneering Russian surgeon and medical scientist
  77. Molecular Genetics of Multiple Osteochondromas
  78. Automation of Technology for Cancer Research
  79. Ewing sarcoma: The clinical relevance of the insulin-like growth factor 1 and the poly-ADP-ribose-polymerase pathway
  80. MEK inhibition induces apoptosis in osteosarcoma cells with constitutive ERK1/2 phosphorylation
  81. A translocation t(6;14) in two cases of leiomyosarcoma: Molecular cytogenetic and array-based comparative genomic hybridization characterization
  82. CXCL14, CXCR7 expression and CXCR4 splice variant ratio associate with survival and metastases in Ewing sarcoma patients
  83. Prognosis of Primary and Recurrent Chondrosarcoma of the Rib
  84. Inactivation of SDH and FH cause loss of 5hmC and increased H3K9me3 in paraganglioma/pheochromocytoma and smooth muscle tumors
  85. Novel splice variants of CXCR4 identified by transcriptome sequencing
  86. Pharmacological inhibition of Bcl-xL sensitizes osteosarcoma to doxorubicin
  87. Tumor Biology of Vestibular Schwannoma
  88. Abstract 3780: Aven-mediated checkpoint kinase control regulates proliferation and resistance to chemotherapy in osteosarcoma cells
  89. Sequencing Overview of Ewing Sarcoma: A Journey across Genomic, Epigenomic and Transcriptomic Landscapes
  90. 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...
  91. Mesenchymal stromal cells of osteosarcoma patients do not show evidence of neoplastic changes during long-term culture
  92. Chemotherapy in osteosarcoma
  93. Periosteal chondrosarcoma: a histopathological and molecular analysis of a rare chondrosarcoma subtype
  94. Neoadjuvant denosumab for extensive giant cell tumor in os ischium —a case report
  95. Epidemiology of primary bone tumors and economical aspects of bone metastases
  96. Doxorubicin-based adjuvant chemotherapy in soft tissue sarcoma: pooled analysis of two STBSG-EORTC phase III clinical trials
  97. EURAMOS-1, an international randomised study for osteosarcoma: results from pre-randomisation treatment
  98. Nikolay Ivanovich Pirogov: a surgeon's contribution to military and civilian anaesthesia
  99. De novodiscovery of phenotypic intratumour heterogeneity using imaging mass spectrometry
  100. In Reply
  101. Gene expression profiling of giant cell tumor of bone reveals downregulation of extracellular matrix components decorin and lumican associated with lung metastasis
  102. Quantification of the Heterogeneity of Prognostic Cellular Biomarkers in Ewing Sarcoma Using Automated Image and Random Survival Forest Analysis
  103. 2013 AHA/ACC Guideline on Lifestyle Management to Reduce Cardiovascular Risk
  104. Ewing sarcoma inhibition by disruption of EWSR1-FLI1 transcriptional activity and reactivation of p53
  105. 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
  106. Molecular genetics of chondroid tumours
  107. The Clinical Approach Toward Giant Cell Tumor of Bone
  108. Doxorubicin alone versus intensified doxorubicin plus ifosfamide for first-line treatment of advanced or metastatic soft-tissue sarcoma: a randomised controlled phase 3 trial
  109. GRM1 is upregulated through gene fusion and promoter swapping in chondromyxoid fibroma
  110. Possible effects of EXT2 on mesenchymal differentiation - lessons from the zebrafish
  111. Primary intraosseous manifestation of Rosai-Dorfman disease: 2 cases and review of literature
  112. Kinome and mRNA expression profiling of high-grade osteosarcoma cell lines implies Akt signaling as possible target for therapy
  113. Transactivating mutation of theMYOD1gene is a frequent event in adult spindle cell rhabdomyosarcoma
  114. 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...
  115. Zebrafish as a Model for Human Osteosarcoma
  116. The Molecular Mechanisms of Gradient Sensing by CXCR4
  117. The density of CD8+ T-cell infiltration and expression of BCL2 predicts outcome of primary diffuse large B-cell lymphoma of bone
  118. Recurrent Chromosome 22 Deletions in Osteoblastoma Affect Inhibitors of the Wnt/Beta-Catenin Signaling Pathway
  119. Frequent truncating mutations of STAG2 in bladder cancer
  120. 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)
  121. Mesenchymal stem cell transformation and sarcoma genesis
  122. CD99-positive undifferentiated round cell sarcoma diagnosed on fine needle aspiration cytology, later found to harbour aCIC-DUX4translocation: a recently described entity
  123. IR/IGF1R signaling as potential target for treatment of high-grade osteosarcoma
  124. FXR regulates CETP
  125. Screening for Potential Targets for Therapy in Mesenchymal, Clear Cell, and Dedifferentiated Chondrosarcoma Reveals Bcl-2 Family Members and TGFβ as Potential Targets
  126. Imaging Mass Spectrometry-based Molecular Histology Differentiates Microscopically Identical and Heterogeneous Tumors
  127. Genome-wide analyses on high-grade osteosarcoma: Making sense of a genomically most unstable tumor
  128. Tumor-Associated Macrophages Are Related to Volumetric Growth of Vestibular Schwannomas
  129. Nuclear factor-κB activation in primary lymphoma of bone
  130. MicroRNAs at the human 14q32 locus have prognostic significance in osteosarcoma
  131. Inactivation of Patched1 in Mice Leads to Development of Gastrointestinal Stromal-Like Tumors That Express Pdgfrα but Not Kit
  132. Pleomorphic Sarcomas
  133. Understanding the Molecular Mechanism of Gradient Sensing
  134. NFATC2 (nuclear factor of activated T-cells, cytoplasmic, calcineurin-dependent 2)
  135. Mutations affecting BRAF, EGFR, PIK3CA, and KRAS are not associated with sporadic vestibular schwannomas
  136. Osteosarcoma of the hands and feet: a distinct clinico-pathological subgroup
  137. The activities of Smad and Gli mediated signalling pathways in high-grade conventional osteosarcoma
  138. Integrative Analysis Reveals Relationships of Genetic and Epigenetic Alterations in Osteosarcoma
  139. ‘The chicken or the egg?’ dilemma strikes back for the controlling mechanism in chordoma#
  140. Adjuvant chemotherapy with doxorubicin, ifosfamide, and lenograstim for resected soft-tissue sarcoma (EORTC 62931): a multicentre randomised controlled trial
  141. Gastrointestinal stromal tumors: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up
  142. Bone sarcomas: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up
  143. High frequency of MYC gene amplification is a common feature of radiation‐induced sarcomas. Further results from EORTC STBSG TL 01/01
  144. Malignant fibrous histiocytoma and fibrosarcoma of bone: a re-assessment in the light of currently employed morphological, immunohistochemical and molecular approaches
  145. Interobserver reliability in the histopathological diagnosis of cartilaginous tumors in patients with multiple osteochondromas
  146. Three new chondrosarcoma cell lines: one grade III conventional central chondrosarcoma and two dedifferentiated chondrosarcomas of bone
  147. Alternate Splicing of the p53 Inhibitor HDMX Offers a Superior Prognostic Biomarker than p53 Mutation in Human Cancer
  148. Imaging mass spectrometry statistical analysis
  149. A multidisciplinary approach to giant cell tumors of tendon sheath and synovium—A critical appraisal of literature and treatment proposal
  150. Expression of ERG, an Ets family transcription factor, identifies ERG-rearranged Ewing sarcoma
  151. Low-Grade Chondrosarcoma of Long Bones Treated with Intralesional Curettage Followed by Application of Phenol, Ethanol, and Bone-Grafting
  152. The management of diffuse-type giant cell tumour (pigmented villonodular synovitis) and giant cell tumour of tendon sheath (nodular tenosynovitis)
  153. Intratumoral hemorrhage, vessel density, and the inflammatory reaction contribute to volume increase of sporadic vestibular schwannomas
  154. Molecular pathology and its diagnostic use in bone tumors
  155. Smooth muscle actin expression in primary bone tumours
  156. Abstract 5128: Identification of osteosarcoma driver genes by integrative analysis of copy number and gene expression data
  157. Identification of osteosarcoma driver genes by integrative analysis of copy number and gene expression data
  158. Phenol levels during intralesional curettage and local adjuvant treatment of benign and low-grade malignant bone tumours
  159. An osteosarcoma zebrafish model implicates Mmp‐19 and Ets‐1 as well as reduced host immune response in angiogenesis and migration
  160. Intact interferon signaling in peripheral blood leukocytes of high-grade osteosarcoma patients
  161. 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
  162. The clinical use of biomarkers as prognostic factors in Ewing sarcoma
  163. The clinical impact of molecular techniques on diagnostic pathology of soft tissue and bone tumours
  164. Anti-EGFR Antibody Cetuximab Enhances the Cytolytic Activity of Natural Killer Cells toward Osteosarcoma
  165. HSPG-Deficient Zebrafish Uncovers Dental Aspect of Multiple Osteochondromas
  166. The CXCR4-CXCL12 axis in Ewing sarcoma: promotion of tumor growth rather than metastatic disease
  167. Histone deacetylase inhibitors enhance expression of NKG2D ligands in Ewing sarcoma and sensitize for natural killer cell-mediated cytolysis
  168. Comprehensive analysis of published phase I/II clinical trials between 1990-2010 in osteosarcoma and Ewing sarcoma confirms limited outcomes and need for translational investment
  169. The First European Interdisciplinary Ewing Sarcoma Research Summit
  170. Paratesticular desmoplastic small round cell tumor: an unusual tumor with an unusual fusion, cytogenetic and molecular genetic analysis combining RT-PCR and COBRA-FISH
  171. Analysis of stromal cells in osteofibrous dysplasia and adamantinoma of long bones
  172. Automated microinjection of cell-polymer suspensions in 3D ECM scaffolds for high-throughput quantitative cancer invasion screens
  173. Osteosarcoma Models: From Cell Lines to Zebrafish
  174. Molecular Mechanisms of Gradient Sensing in Ewing's Sarcoma Cells
  175. Incidence, Predictive Factors, and Prognosis of Chondrosarcoma in Patients with Ollier Disease and Maffucci Syndrome: An International Multicenter Study of 161 Patients
  176. Peripheral chondrosarcoma progression is associated with increased type X collagen and vascularisation
  177. Epiphyseal growth plate and secondary peripheral chondrosarcoma: the neighbours matter
  178. Chemotherapeutic adjuvant treatment for osteosarcoma: Where do we stand?
  179. Identification of a novel, recurrent HEY1‐NCOA2 fusion in mesenchymal chondrosarcoma based on a genome‐wide screen of exon‐level expression data
  180. Survival from high-grade localised extremity osteosarcoma: combined results and prognostic factors from three European Osteosarcoma Intergroup randomised controlled trials
  181. Reclassification and subtyping of so-called malignant fibrous histiocytoma of bone: comparison with cytogenetic features
  182. Multiple Statistical Analysis Techniques Corroborate Intratumor Heterogeneity in Imaging Mass Spectrometry Datasets of Myxofibrosarcoma
  183. mRNA expression profiles of primary high-grade central osteosarcoma are preserved in cell lines and xenografts
  184. Workshop Report on the European Bone Sarcoma Networking Meeting: Integration of Clinical Trials with Tumor Biology
  185. 1q gain and CDT2 overexpression underlie an aggressive and highly proliferative form of Ewing sarcoma
  186. Secondary peripheral chondrosarcoma evolving from osteochondroma as a result of outgrowth of cells with functional EXT
  187. Functional characterization of osteosarcoma cell lines provides representative models to study the human disease
  188. Expression of aromatase and estrogen receptor alpha in chondrosarcoma, but no beneficial effect of inhibiting estrogen signaling both in vitro and in vivo
  189. A ΔRaf1–ER‐inducible oncogenic zebrafish liver cell model identifies hepatocellular carcinoma signatures
  190. Breakpoint characterization of large deletions in EXT1 or EXT2 in 10 Multiple Osteochondromas families
  191. A short-term in vivo model for giant cell tumor of bone
  192. Exploratory analysis of prognostic factors for patients (pts) with advanced soft tissue sarcoma (ASTS) receiving combination chemotherapy: A joined study of the EORTC Soft Tissue and Bone Sarcoma Group and the French Sarcoma Group.
  193. IDH1 and IDH2 mutations are frequent events in central chondrosarcoma and central and periosteal chondromas but not in other mesenchymal tumours
  194. IGF1R Signaling in Ewing Sarcoma Is Shaped by Clathrin-/Caveolin-Dependent Endocytosis
  195. Maffucci syndrome: A genome‐wide analysis using high resolution single nucleotide polymorphism and expression arrays on four cases
  196. The immunophenotype of osteoclasts and macrophage polykaryons
  197. Growth plate regulation and osteochondroma formation: insights from tracing proteoglycans in zebrafish models and human cartilage
  198. Podoplanin expression in adamantinoma of long bones and osteofibrous dysplasia
  199. Tumor-Infiltrating Macrophages Are Associated with Metastasis Suppression in High-Grade Osteosarcoma: A Rationale for Treatment with Macrophage Activating Agents
  200. Survival after recurrent osteosarcoma: Data from 3 European Osteosarcoma Intergroup (EOI) randomized controlled trials
  201. Abstract 4295: High-throughput screening of osteosarcoma progression: A zebrafish model
  202. Concise Review: Mesenchymal Tumors: When Stem Cells Go Mad
  203. Chemotherapy-resistant osteosarcoma is highly susceptible to IL-15-activated allogeneic and autologous NK cells
  204. Genome-wide analysis of Ollier disease: Is it all in the genes?
  205. Cartilage ultrastructure in proteoglycan‐deficient zebrafish mutants brings to light new candidate genes for human skeletal disorders
  206. 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
  207. Distinct histological features characterize primary angiosarcoma of bone
  208. 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
  209. Late sarcoma development after curettage and bone grafting of benign bone tumors
  210. Pro-inflammatory chemokine-chemokine receptor interactions within the Ewing sarcoma microenvironment determine CD8+ T-lymphocyte infiltration and affect tumour progression
  211. The role of epidermal growth factor receptor in chordoma pathogenesis: a potential therapeutic target
  212. Tiling resolution array-CGH shows that somatic mosaic deletion of the EXT gene is causative in EXT gene mutation negative multiple osteochondromas patients
  213. Role of the transcription factor T (brachyury) in the pathogenesis of sporadic chordoma: a genetic and functional‐based study
  214. Cancer biology and genomics: translating discoveries, transforming pathology
  215. A nation‐wide study comparing sporadic and familial adenomatous polyposis‐related desmoid‐type fibromatoses
  216. Array-based comparative genomic hybridisation analysis reveals recurrent chromosomal alterations in primary diffuse large B cell lymphoma of bone
  217. No Haploinsufficiency but Loss of Heterozygosity for EXT in Multiple Osteochondromas
  218. Kinome profiling of myxoid liposarcoma reveals NF-kappaB-pathway kinase activity and Casein Kinase II inhibition as a potential treatment option
  219. Critical role of endoglin in tumor cell plasticity of Ewing sarcoma and melanoma
  220. Coactivated Platelet-Derived Growth Factor Receptor α and Epidermal Growth Factor Receptor Are Potential Therapeutic Targets in Intimal Sarcoma
  221. Imaging mass spectrometry of myxoid sarcomas identifies proteins and lipids specific to tumour type and grade, and reveals biochemical intratumour heterogeneity
  222. Heterogeneous and Complex Rearrangements of Chromosome Arm 6q in Chondromyxoid Fibroma
  223. Bisphosphonate treatment of aggressive primary, recurrent and metastatic Giant Cell Tumour of Bone
  224. Small deletions but not methylation underlie CDKN2A/p16 loss of expression in conventional osteosarcoma
  225. Hierarchical clustering of flow cytometry data for the study of conventional central chondrosarcoma
  226. DOG1 and CD117 are the antibodies of choice in the diagnosis of gastrointestinal stromal tumours
  227. Primary cilia organization reflects polarity in the growth plate and implies loss of polarity and mosaicism in osteochondroma
  228. Cartilage tumours and bone development: molecular pathology and possible therapeutic targets
  229. A Reappraisal of Hemangiopericytoma of Bone; Analysis of Cases Reclassified as Synovial Sarcoma and Solitary Fibrous Tumor of Bone
  230. Brostallicin versus doxorubicin as first-line chemotherapy in patients with advanced or metastatic soft tissue sarcoma: An EORTC Soft Tissue and Bone Sarcoma Group randomized phase II study.
  231. First-line chemotherapy for malignant peripheral nerve sheath tumor (MPNST) versus other histologic soft tissue sarcoma (STS) subtypes and as a prognostic factor for MPNST: An EORTC Soft Tissue and Bone Sarcoma Group (STBSG) study.
  232. Bone sarcomas: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up
  233. Gastrointestinal stromal tumours: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up
  234. 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
  235. Correlation of hypoxic signalling to histological grade and outcome in cartilage tumours
  236. Langerhans cell histiocytosis: fascinating dynamics of the dendritic cell–macrophage lineage
  237. Soft tissue sarcomas: introduction to the Virchows Archiv review issue
  238. Anti-inflammatory M2 type macrophages characterize metastasized and tyrosine kinase inhibitor-treated gastrointestinal stromal tumors
  239. Epidemiology of Primary Bone Tumors and Economical Aspects of Bone Metastases
  240. Prognostic and predictive factors for outcome to first-line ifosfamide-containing chemotherapy for adult patients with advanced soft tissue sarcomas
  241. Erratum: Profiling of high-grade central osteosarcoma and its putative progenitor cells identifies tumourigenic pathways
  242. Improved diagnosis and treatment of soft tissue sarcoma patients after implementation of national guidelines: A population-based study
  243. Sdhd and Sdhd/H19 Knockout Mice Do Not Develop Paraganglioma or Pheochromocytoma
  244. A balanced t(5;17) (p15;q22-23) in chondroblastoma: frequency of the re-arrangement and analysis of the candidate genes
  245. Genome‐wide transcriptome analyses reveal p53 inactivation mediated loss of miR‐34a expression in malignant peripheral nerve sheath tumours
  246. Prognostic factors in pulmonary metastasized high‐grade osteosarcoma
  247. Profiling of high-grade central osteosarcoma and its putative progenitor cells identifies tumourigenic pathways
  248. Dedifferentiated peripheral chondrosarcomas: regulation of EXT-downstream molecules and differentiation-related genes
  249. The Journal of Pathology 2008 Jeremy Jass Prize for Research Excellence in Pathology
  250. Imatinib Mesylate in Patients with WHO B3 Thymomas and Thymic Carcinomas
  251. Molecular characterization of commonly used cell lines for bone tumor research: A trans‐European EuroBoNet effort
  252. Molecular pathology of sarcomas: concepts and clinical implications
  253. Inactive Wnt/β-catenin pathway in conventional high-grade osteosarcoma
  254. Central chondrosarcoma progression is associated with pRb pathway alterations: CDK4 down-regulation and p16 overexpression inhibit cell growth in vitro
  255. Benign Cartilaginous Tumors of Bone
  256. Primary lymphoma of bone: extranodal lymphoma with favourable survival independent of germinal centre, post-germinal centre or indeterminate phenotype
  257. 275 Taxanes in angiosarcomas
  258. Osteosarcoma originates from mesenchymal stem cells in consequence of aneuploidization and genomic loss of Cdkn2
  259. Running GAGs: myxoid matrix in tumor pathology revisited
  260. 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
  261. Gastrointestinal Stromal Tumors I: Pathology, Pathobiology, Primary Therapy, and Surgical Issues
  262. Kinome Profiling of Chondrosarcoma Reveals Src-Pathway Activity and Dasatinib as Option for Treatment
  263. Cellular/intramuscular myxoma and grade I myxofibrosarcoma are characterized by distinct genetic alterations and specific composition of their extracellular matrix
  264. Lymphopenia as a Prognostic Factor for Overall Survival in Advanced Carcinomas, Sarcomas, and Lymphomas
  265. Cell Cycle/Apoptosis Molecule Expression Correlates with Imatinib Response in Patients with Advanced Gastrointestinal Stromal Tumors
  266. Reduced human leukocyte antigen expression in advanced-stage Ewing sarcoma: implications for immune recognition
  267. Sclerostin in Mineralized Matrices and van Buchem Disease
  268. Similar gene expression profiles of sporadic, PGL2-, and SDHD-linked paragangliomas suggest a common pathway to tumorigenesis
  269. Genomic Profiling of Chondrosarcoma: Chromosomal Patterns in Central and Peripheral Tumors
  270. Extra‐abdominal subcutaneous metastasis of a gastrointestinal stromal tumor: report of a case and a review of the literature
  271. The molecular and cellular basis of exostosis formation in hereditary multiple exostoses
  272. The NFATc2 Gene Is Involved in a Novel Cloned Translocation in a Ewing Sarcoma Variant That Couples Its Function in Immunology to Oncology
  273. Aberrant Heparan Sulfate Proteoglycan Localization, Despite Normal Exostosin, in Central Chondrosarcoma
  274. Superior performance of liquid-based versus conventional cytology in a population-based cervical cancer screening program
  275. Genomic instability in giant cell tumor of bone. A study of 52 cases using DNA ploidy, relocalization FISH, and array‐CGH analysis
  276. Telomere‐associated proteins: cross‐talk between telomere maintenance and telomere‐lengthening mechanisms
  277. Assessment of Interobserver Variability and Histologic Parameters to Improve Reliability in Classification and Grading of Central Cartilaginous Tumors
  278. CD33+ CD14− Phenotype Is Characteristic of Multinuclear Osteoclast‐Like Cells in Giant Cell Tumor of Bone
  279. Imaging Multidrug Resistance in Osteosarcoma: A Pre-clinical Approach Using an Orthotopic Animal Model
  280. No genomic aberrations in Langerhans cell histiocytosis as assessed by diverse molecular technologies
  281. Reduced leucocyte cholesteryl ester transfer protein expression in acute coronary syndromes
  282. The cytotoxic effect of phenol and ethanol on the chondrosarcoma-derived cell line OUMS-27: AN IN VITRO EXPERIMENT
  283. Paclitaxel in patients with advanced angiosarcomas of soft tissue: A retrospective study of the EORTC soft tissue and bone sarcoma group
  284. NK cells recognize and lyse Ewing sarcoma cells through NKG2D and DNAM-1 receptor dependent pathways
  285. 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
  286. A chondrogenic gene expression signature in mesenchymal stem cells is a classifier of conventional central chondrosarcoma
  287. Results of Diagnostic Review in Pediatric Bone Tumors and Tumorlike Lesions
  288. Critical illness VR rehabilitation device (X-VR-D): Evaluation of the potential use for early clinical rehabilitation
  289. Aromatase inhibition in patients with recurrent and/or metastatic chondrosarcoma (CS)
  290. Prognostic and predictive factors for outcome to first-line ifosfamide-containing therapy (IFM) in patients (pts) with advanced soft tissue sarcomas (STS) treated in EORTC-STBSG studies
  291. Survival after recurrent osteosarcoma: Data from three European Osteosarcoma Intergroup (EOI) randomized controlled
  292. The diagnostic utility of DOG1 expression in KIT-negative GIST
  293. The end of adjuvant chemotherapy (adCT) era with doxorubicin-based regimen in resected high-grade soft tissue sarcoma (STS): Pooled analysis of the two STBSG-EORTC phase III clinical trials
  294. The Clinical Approach Towards Chondrosarcoma
  295. Gastrointestinal stromal tumors: ESMO Clinical Recommendations for diagnosis, treatment and follow-up
  296. Soft tissue sarcomas: ESMO Clinical Recommendations for diagnosis, treatment and follow-up
  297. A Phase II Study of Gefitinib for Patients with Advanced HER-1 Expressing Synovial Sarcoma Refractory to Doxorubicin-Containing Regimens
  298. The Clinical Approach Towards Chondrosarcoma
  299. Myxoid tumours of soft tissue: the so‐called myxoid extracellular matrix is heterogeneous in composition
  300. Telomere biology in giant cell tumour of bone
  301. Incidence of Biopsy-Proven Bone Tumors in Children
  302. Lymphatics and bone
  303. Neurocutaneous Disorders Phakomatoses and Hamartoneoplastic Syndromes
  304. EWSR1-CREB1 and EWSR1-ATF1 Fusion Genes in Angiomatoid Fibrous Histiocytoma
  305. Frequent deletion of the CDKN2A locus in chordoma: analysis of chromosomal imbalances using array comparative genomic hybridisation
  306. CT‐guided, COBRA‐FISH‐assisted diagnosis of well‐differentiated liposarcoma (inflammatory subtype) of the retroperitoneum
  307. Increased HIF1α in SDH and FH deficient tumors does not cause microsatellite instability
  308. 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
  309. 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
  310. The role of noncartilage‐specific molecules in differentiation of cartilaginous tumors
  311. MR imaging characteristics in primary lymphoma of bone with emphasis on non-aggressive appearance
  312. Functional imaging of multidrug resistance in an orthotopic model of osteosarcoma using 99mTc-sestamibi
  313. Differences in telomerase expression by the CD1a+ cells in Langerhans cell histiocytosis reflect the diverse clinical presentation of the disease
  314. The Role of EXT1 in Nonhereditary Osteochondroma: Identification of Homozygous Deletions
  315. Identification of markers to characterize and sort human articular chondrocytes with enhanced in vitro chondrogenic capacity
  316. Improvement in Histologic Response But Not Survival in Osteosarcoma Patients Treated With Intensified Chemotherapy: A Randomized Phase III Trial of the European Osteosarcoma Intergroup
  317. Decreased EXT expression and intracellular accumulation of heparan sulphate proteoglycan in osteochondromas and peripheral chondrosarcomas
  318. Detection and molecular cytogenetic characterization of a novel ring chromosome in a histological variant of Ewing sarcoma
  319. Expression of Cellular FLICE Inhibitory Protein, Caspase-8, and Protease Inhibitor-9 in Ewing Sarcoma and Implications for Susceptibility to Cytotoxic Pathways
  320. Basic fibroblast growth factor and fibroblastic growth factor receptor–1 may contribute to head and neck paraganglioma development by an autocrine or paracrine mechanism
  321. 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
  322. Differences in Telomerase Expression by the CD1a+ Cells in Langerhans Cell Histiocytosis Reflects the Diverse Clinical Presentation of the Disease
  323. SOST expression is restricted to the great arteries during embryonic and neonatal cardiovascular development
  324. Osteosarcoma Derived from Cultured Mesenchymal Stem Cells.
  325. Sarcoma Derived from Cultured Mesenchymal Stem Cells
  326. Multidrug resistance mediated by ABC transporters in osteosarcoma cell lines: mRNA analysis and functional radiotracer studies
  327. Pathology of primary malignant bone and cartilage tumours
  328. Chondroid lipoma: findings on radiography and MRI (2006:7b)
  329. Array‐comparative genomic hybridization of central chondrosarcoma
  330. Giant cell tumors of the tendon sheath may present radiologically as intrinsic osseous lesions
  331. Peripheral chondrosarcoma progression is accompanied by decreased Indian Hedgehog signalling
  332. EXT‐related pathways are not involved in the pathogenesis of dysplasia epiphysealis hemimelica and metachondromatosis
  333. Nora’s lesion, a distinct radiological entity?
  334. Molecular cytogenetic characterization of four previously established and two newly established Ewing sarcoma cell lines
  335. Clinico-histologic parameters of osteosarcoma patients with late relapse
  336. 23 Assessment of molecular determinants of development and treatment efficacy in radiation induced sarcoma (RIS) — eortc translational research project 01/01
  337. Soft tissue pathology
  338. Brachyury and chordoma: the chondroid–chordoid dilemma resolved?
  339. Local recurrence of myxofibrosarcoma is associated with increase in tumour grade and cytogenetic aberrations, suggesting a multistep tumour progression model
  340. F.139. Expression and Functional Relevance of cFLIP, PI-9 and Caspase 8 in Ewing's Sarcoma: Implications for Immunotherapy
  341. Tumor Cell Plasticity in Ewing Sarcoma, an Alternative Circulatory System Stimulated by Hypoxia
  342. Central high-grade osteosarcoma of bone: Diagnostic and genetic considerations
  343. Incidence of gastrointestinal stromal tumours is underestimated: Results of a nation-wide study
  344. Limited Rescue of Osteoclast‐Poor Osteopetrosis After Successful Engraftment by Cord Blood From an Unrelated Donor
  345. The histopathological differential diagnosis of mesenchymal tumours of the skin
  346. Estrogen Signaling Is Active in Cartilaginous Tumors: Implications for Antiestrogen Therapy as Treatment Option of Metastasized or Irresectable Chondrosarcoma
  347. TGF‐β1 drives partial myofibroblastic differentiation in chondromyxoid fibroma of bone
  348. Accuracy of radiography in grading and tissue-specific diagnosis—a study of 200 consecutive bone tumors of the hand
  349. Desmoplastic fibroma of bone: an immunohistochemical study including -catenin expression and mutational analysis for -catenin
  350. 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...
  351. Emerging pathways in the development of chondrosarcoma of bone and implications for targeted treatment
  352. cDNA expression profiling of chondrosarcomas: Ollier disease resembles solitary tumours and alteration in genes coding for components of energy metabolism occurs with increasing grade
  353. 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”
  354. 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
  355. Presence of osteoclast-like multinucleated giant cells in the bone and nonostotic lesions of Langerhans cell histiocytosis
  356. The use of Bcl-2 and PTHLH immunohistochemistry in the diagnosis of peripheral chondrosarcoma in a clinicopathological setting
  357. Prenatal Detection of Orbital Rhabdomyosarcoma
  358. Absence of IHH and retention of PTHrP signalling in enchondromas and central chondrosarcomas
  359. Chondromyxoid fibroma resemblesin vitro chondrogenesis, but differs in expression of signalling molecules
  360. Bifurcation of the femur with tibial agenesis and additional anomalies
  361. 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
  362. 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
  363. MRI of Adamantinoma of Long Bones in Correlation with Histopathology
  364. Multiple Osteochondromas: Clinicopathological and Genetic Spectrum and Suggestions for Clinical Management
  365. Aggressive angiomyxoma: a clinicopathological and immunohistochemical study of 11 cases with long-term follow-up
  366. Enchondromatosis (Ollier disease, Maffucci syndrome) is not caused by the PTHR1 mutation p.R150C
  367. 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
  368. Soft-Tissue Tumors: Value of Static and Dynamic Gadopentetate Dimeglumine–enhanced MR Imaging in Prediction of Malignancy
  369. Magnetic resonance imaging of knee cartilage using a water selective balanced steady‐state free precession sequence
  370. Progression-free survival in gastrointestinal stromal tumours with high-dose imatinib: randomised trial
  371. 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
  372. Cathepsin K Is the Principal Protease in Giant Cell Tumor of Bone
  373. Changing concepts in the pathological basis of soft tissue and bone sarcoma treatment
  374. A phase II study of ET-743/trabectedin (`Yondelis') for patients with advanced gastrointestinal stromal tumours
  375. Solitary fibrous tumour: the emerging clinicopathologic spectrum of an entity and its differential diagnosis
  376. 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
  377. Overexpression of the HER-2 oncogene does not play a role in high-grade osteosarcomas
  378. Somatic loss of maternal chromosome 11 causes parent-of-origin-dependent inheritance in SDHD-linked paraganglioma and phaeochromocytoma families
  379. Chondroma and chondrosarcoma of the larynx
  380. Multiparameter DNA flow‐sorting demonstrates diploidy and SDHD wild‐type gene retention in the sustentacular cell compartment of head and neck paragangliomas: chief cells are the only neoplastic component
  381. Molecular analysis of the INK4A/INK4A‐ARF gene locus in conventional (central) chondrosarcomas and enchondromas: indication of an important gene for tumour progression
  382. Langerhans cell histiocytosis: A pathologic combination of oncogenesis and immune dysregulation
  383. A distinct phenotype characterizes tumors from a putative genetic trait involving chondrosarcoma and breast cancer occurring in the same patient
  384. Dedifferentiated Adamantinoma With Revertant Mesenchymal Phenotype
  385. Expression of cartilage growth plate signalling molecules in chondroblastoma
  386. 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
  387. 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
  388. Pathology of soft tissue sarcomas with emphasis on molecular diagnostic techniques
  389. Langerhans-cell histiocytosis: neoplasia or unbridled inflammation?
  390. Response to Fadeel and Henter: Langerhans cell histiocytosis: a combination of carcinogenesis and inflammation
  391. Multiple primary malignancies in osteosarcoma patients. Incidence and predictive value of osteosarcoma subtype for cancer syndromes related with osteosarcoma
  392. G2M arrest, blocked apoptosis, and low growth fraction may explain indolent behavior of head and neck paragangliomas
  393. Aberrant Chemokine Receptor Expression and Chemokine Production by Langerhans Cells Underlies the Pathogenesis of Langerhans Cell Histiocytosis
  394. Langerhans-cell histiocytosis 'insight into DC biology'
  395. Dynamic contrast-enhanced MR imaging in monitoring response to isolated limb perfusion in high-grade soft tissue sarcoma: initial results
  396. Amplification of 17p11.2∼p12, including PMP22, TOP3A, and MAPK7, in high-grade osteosarcoma
  397. Clear cell sarcoma of the stomach
  398. Expression of Cell Cycle–Related Gene Products in Langerhans Cell Histiocytosis
  399. Technical Considerations in CT-Guided Radiofrequency Thermal Ablation of Osteoid Osteoma: Tricks of the Trade
  400. Hemicortical allograft reconstruction after resection of low-grade malignant bone tumours
  401. Diagnosis and prognosis of chondrosarcoma of bone
  402. 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
  403. Gemcitabine in advanced adult soft-tissue sarcomas. A phase II study of the EORTC Soft Tissue and Bone Sarcoma Group
  404. Intermediate grade osteosarcoma and chondrosarcoma arising in an osteochondroma. A case report of a patient with hereditary multiple exostoses
  405. Diffusion‐weighted MRI in the characterization of soft‐tissue tumors
  406. Scale‐invariant segmentation of dynamic contrast‐enhanced perfusion MR images with inherent scale selection
  407. Cartilage-forming tumours of bone and soft tissue and their differential diagnosis
  408. Chromosome 9 Alterations and Trisomy 22 in Central Chondrosarcoma: A Cytogenetic and DNA Flow Cytometric Analysis of Chondrosarcoma Subtypes
  409. High quality RNA isolation from tumours with low cellularity and high extracellular matrix component for cDNA microarrays: application to chondrosarcoma
  410. Retain or sacrifice the posterior cruciate ligament in total knee arthroplasty? A histopathological study of the cruciate ligament in osteoarthritic and rheumatoid disease
  411. Synovial sarcoma: dynamic contrast-enhanced MR imaging features
  412. The histopathological differential diagnosis of gastrointestinal stromal tumours
  413. Adamantinoma-like Ewing's sarcoma and Ewing's-like adamantinoma. The t(11; 22), t(21; 22) status
  414. Malignant melanoma is genetically distinct from clear cell sarcoma of tendons and aponeurosis (malignant melanoma of soft parts)
  415. An association between cartilaginous tumours and breast cancer in the national pathology registration in The Netherlands points towards a possible genetic trait
  416. Chondrosarcoma is not characterized by detectable telomerase activity
  417. Human granzyme B mediates cartilage proteoglycan degradation and is expressed at the invasive front of the synovium in rheumatoid arthritis
  418. Retroperitoneal extraskeletal osteosarcoma
  419. Assessment of the influence of preoperative chemotherapy in patients with osteosarcoma by dynamic contrast-enhanced MRI using pharmacokinetic modeling
  420. Up-Regulation of PTHrP and Bcl-2 Expression Characterizes the Progression of Osteochondroma towards Peripheral Chondrosarcoma and Is a Late Event in Central Chondrosarcoma
  421. Infantile‐type digital fibromatosis tumour in an adult
  422. Near-Haploidy and Subsequent Polyploidization Characterize the Progression of Peripheral Chondrosarcoma
  423. Malignant progression in multiple enchondromatosis (Ollier's disease): An autopsy-based molecular genetic study
  424. Detection of areas with viable remnant tumor in postchemotherapy patients with Ewing’s sarcoma by dynamic contrast-enhanced MRI using pharmacokinetic modeling
  425. MR imaging of clear cell sarcoma (malignant melanoma of the soft parts): a multicenter correlative MRI-pathology study of 21 cases and literature review
  426. Re. Review Article entitled ?The neoplastic pathogenesis of solitary and multiple osteochondromas?
  427. Cartilaginous Tumors: Fast Contrast-enhanced MR Imaging
  428. Bone tumors
  429. An update of diagnostic strategies using molecular genetic and magnetic resonance imaging techniques for musculoskeletal tumors
  430. Soft Tissue Tumours of the Retroperitoneum
  431. Molecular genetic characterization of both components of a dedifferentiated chondrosarcoma, with implications for its histogenesis
  432. Primary non-Hodgkin’s lymphoma of bone: a clinicopathological investigation of 60 cases
  433. Chondrosarcoma of the phalanx
  434. Loss of heterozygosity and DNA ploidy point to a diverging genetic mechanism in the origin of peripheral and central chondrosarcoma
  435. A phase II study of cisplatin, ifosfamide and doxorubicin in operable primary, axial skeletal and metastatic osteosarcoma
  436. Myxoid tumours of soft tissue
  437. Neoadjuvant Chemotherapy With Doxorubicin and Cisplatin in Malignant Fibrous Histiocytoma of Bone: A European Osteosarcoma Intergroup Study
  438. EXT-Mutation Analysis and Loss of Heterozygosity in Sporadic and Hereditary Osteochondromas and Secondary Chondrosarcomas
  439. Diagnostic and prognostic implications of the unfolding molecular biology of bone and soft tissue tumours.
  440. Adenocarcinoma arising within a tailgut cyst: clinicopathological description and follow up of an unusual case.
  441. Translocation (11;22)(q24;q12) in a small cell tumor of the thigh in a 2-year-old boy: Immunohistology, cytogenetics, molecular genetics, and review of the literature*1
  442. Segmentation of Dynamic Contrast-Enhanced MR-Images of Post Chemotherapy Ewing’s Sarcoma with a Pharmacokinetic Model and a Neural Network
  443. Ring Chromosome 4 as the Sole Cytogenetic Anomaly in a Chondroblastoma
  444. Musculoskeletal tumors: does fast dynamic contrast-enhanced subtraction MR imaging contribute to the characterization?
  445. Clear cell sarcoma of tendons and aponeuroses (malignant melanoma of soft parts) and cutaneous melanoma: exploring the histogenetic relationship between these two clinicopathological entities
  446. Local recurrence of a phyllodes tumour of the breast presenting with widespread differentiation to a telangiectatic osteosarcoma
  447. Maligne Knorpeltumoren
  448. Chondroblastic osteosarcoma: characterisation by gadolinium-enhanced MR imaging correlated with histopathology
  449. Preoperative evaluation and monitoring chemotherapy in patients with high-grade osteogenic and Ewing's sarcoma: review of current imaging modalities
  450. How is the mutational status for tumor suppressors p53 and p16INK4A in MFH of the bone?
  451. Expression of growth factors and their receptors in adamantinoma of long bones and the implication for its histogenesis
  452. MR imaging based strategies in limb salvage surgery for osteosarcoma of the distal femur
  453. Usefulness of radiography in differentiating enchondroma from central grade 1 chondrosarcoma.
  454. Cytogenetic analysis of adamantinoma of long bones: Further indications for a common histogenesis with osteofibrous dysplasia
  455. Absence of Epstein-Barr virus (EBV) in a gastrointestinal stromal cell tumour (GIST) in an adult human immunodeficiency virus-seropositive patient with past EBV infection
  456. Skin Metastases of Osteogenic Sarcoma
  457. Does magnetic resonance imaging make a difference for patients with musculoskeletal sarcoma?
  458. Malignant astrocytoma-derived region of common amplification in chromosomal band 17p12 is frequently amplified in high-grade osteosarcomas
  459. Distribution of extracellular matrix components in adamantinoma of long bones suggests fibrous-to-epithelial transformation
  460. Molecular Identification of a Partial Hydatidiform Mole
  461. Late Malignant Transformation of a Benign Giant-Cell Tumor of Bone. A Case Report*
  462. Accuracy of the Jamshidi Trocar Biopsy in the Diagnosis of Bone Tumors
  463. Tumor-associated eosinophilic infiltrate of cervical cancer is indicative for a less effective immune response
  464. Dynamic contrast-enhanced MR imaging of musculoskeletal tumors: Basic principles and clinical applications
  465. Can conventional radiographs be used to monitor the effect of neoadjuvant chemotherapy in patients with osteogenic sarcoma?
  466. Calcified meningioma of the skull base simulating chondrosarcoma
  467. Lymph node staging standards in gastric cancer.
  468. Osteosarcoma and Ewing's sarcoma after neoadjuvant chemotherapy: value of dynamic MR imaging in detecting viable tumor before surgery.
  469. Translocation Identification of an Ews-Pseudogene Using Detection by RT-PCR in Ewings-Sarcoma
  470. Keratin immunoreactivity in melanoma of soft parts (clear cell sarcoma)
  471. Treatment of high-grade bone sarcomas with neoadjuvant chemotherapy: the utility of sequential color Doppler sonography in predicting histopathologic response.
  472. Can MRI predict the histopathological response in patients with osteosarcoma after the first cycle of chemotherapy?
  473. Glomerulopathy induced by a single monoclonal autoantibody against GP330
  474. Immunostaining of chain-specific keratins on formalin-fixed, paraffin-embedded tissues: a comparison of various antigen retrieval systems using microwave heating and proteolytic pre-treatments.
  475. Classification of histopathologic changes following chemotherapy in Ewing's sarcoma of bone
  476. Monitoring the effect of chemotherapy in Ewing's sarcoma of bone with MR imaging
  477. Adamantinoma of the long bones. A clinicopathological study of thirty-two patients with emphasis on histological subtype, precursor lesion, and biological behavior.
  478. Changes in tumor perfusion induced by chemotherapy in bone sarcomas: color Doppler flow imaging compared with contrast-enhanced MR imaging and three-phase bone scintigraphy.
  479. Metastasis of Breast Carcinoma to a Primary Mucinous Cystadenocarcinoma of the Ovary
  480. Adamantinoma of the Long Bones: Keratin Subclass Immunoreactivity Pattern with Reference to Its Histogenesis
  481. Reply
  482. Diagnosis of low-grade chondrosarcoma.
  483. Cartilaginous tumors: correlation of gadolinium-enhanced MR imaging and histopathologic findings.
  484. Antigen size influences the type of glomerular pathology in chronic serum sickness
  485. Endothelial Activation Antigens in Pulmonary Leukostasis in Leukemia
  486. Unusual Manifestations of Yersinia enterocolitica Infections Diagnosed Using Novel Methods
  487. Differential renal uptake of 201T1
  488. Renal Uptake of TI-201 in Hypertensive Patients Undergoing Myocardial Perfusion Imaging
  489. Development of Progressive Glomerulosclerosis in Experimental Chronic Serum Sickness
  490. Pathogenesis of experimental lupus nephritis: a role foranti-basement membrane and anti-tubular brush border antibodiesin murine chronic graft-versus-hostdisease
  491. Myxoid tumours of soft tissue
  492. Segmentation of bone tumor in MR perfusion images using neural networks and multiscale pharmacokinetic features
  493. Pitfalls in pathology of soft tissue sarcomas