339 results on '"Dermawan, Josephine K."'
Search Results
2. ERBB2/ ERBB3-mutated S100/ SOX10-positive unclassified high-grade uterine sarcoma: first detailed description of a novel entity
3. The practical utility of AI-assisted molecular profiling in the diagnosis and management of cancer of unknown primary: an updated review
4. A Comprehensive Clinicopathologic and Molecular Reappraisal of GLI1-altered Mesenchymal Tumors with Pooled Outcome Analysis Showing Poor Survival in GLI1- amplified Versus GLI1-rearranged Tumors
5. Novel NONO::TFE3 fusion and ALK co-expression identified in a subset of cutaneous microcystic/reticular schwannoma
6. Modeling Extraordinary Response Through Targeting Secondary Alterations in Fusion-Associated Sarcoma
7. Novel CRTC1::MRTFB(MKL2) Gene Fusion Detected in Myxoid Mesenchymal Neoplasms With Myogenic Differentiation Involving Bone and Soft Tissues
8. Sequential genomic analysis using a multisample/multiplatform approach to better define rhabdomyosarcoma progression and relapse
9. Current updates in sarcoma biomarker discovery: emphasis on next-generation sequencing-based methods
10. Myxoid Pleomorphic Liposarcoma
11. Correction to: The practical utility of AI-assisted molecular profiling in the diagnosis and management of cancer of unknown primary: An updated review
12. NF1-Driven Rhabdomyosarcoma Phenotypes: A Comparative Clinical and Molecular Study of NF1-Mutant Rhabdomyosarcoma and NF1-Associated Malignant Triton Tumor
13. DNA Methylation Profiling Distinguishes Adamantinoma-Like Ewing Sarcoma From Conventional Ewing Sarcoma
14. The genetic landscape of SMARCB1 alterations in SMARCB1-deficient spectrum of mesenchymal neoplasms
15. Myxoid pleomorphic liposarcoma is distinguished from other liposarcomas by widespread loss of heterozygosity and significantly worse overall survival: a genomic and clinicopathologic study
16. Expanding the Molecular Diversity of CIC-Rearranged Sarcomas With Novel and Very Rare Partners
17. High-Grade Sarcomas with Myogenic Differentiation Harboring Hotspot PDGFRB Mutations
18. Comprehensive genomic profiling of EWSR1/FUS::CREB translocation-associated tumors uncovers prognostically significant recurrent genetic alterations and methylation-transcriptional correlates
19. Intraosseous glomus tumours with NOTCH2/3 fusions: two cases presenting in the long bones with review of the literature
20. Supplementary Figure S1 from Developing Novel Genomic Risk Stratification Models in Soft Tissue and Uterine Leiomyosarcoma
21. Supplementary Table S2 from Developing Novel Genomic Risk Stratification Models in Soft Tissue and Uterine Leiomyosarcoma
22. Primary sinonasal myxofibrosarcoma: a clinicopathological study of five cases and review of the literature
23. The Incidence and Significance of Calcium Pyrophosphate Dihydrate Deposits in Histologic Examinations of Total Hip, Knee, and Shoulder Joint Arthroplasties
24. YAP1-TFE3-fused hemangioendothelioma: a multi-institutional clinicopathologic study of 24 genetically-confirmed cases
25. FGFR1 fusions as a novel molecular driver in rhabdomyosarcoma
26. Developing Novel Genomic Risk Stratification Models in Soft Tissue and Uterine Leiomyosarcoma
27. Epithelioid hemangioendothelioma (EHE) with WWTR1::TFE3 gene fusion, a novel fusion variant
28. Superficial ALK-rearranged myxoid spindle cell neoplasm: a cutaneous soft tissue tumor with distinctive morphology and immunophenotypic profile
29. Update on Cutaneous Soft Tissue Tumors
30. Diagnostic Utility of a Custom 34-Gene Anchored Multiplex PCR-Based Next-Generation Sequencing Fusion Panel for the Diagnosis of Bone and Soft Tissue Neoplasms With Identification of Novel USP6 Fusion Partners in Aneurysmal Bone Cysts
31. Detection of GRM1 gene rearrangements in chondromyxoid fibroma: a comparison of fluorescence in‐situ hybridisation, RNA sequencing and immunohistochemical analysis.
32. Clinicopathologic and molecular correlates to neoadjuvant chemotherapy‐induced pathologic response in breast angiosarcoma.
33. Genomic profiling of pleomorphic rhabdomyosarcoma reveals a genomic signature distinct from that of embryonal rhabdomyosarcoma.
34. Comprehensive clinicopathological, molecular, and methylation analysis of mesenchymal tumors with NTRK and other kinase gene aberrations.
35. Evaluation of deeper levels in initially negative temporal artery biopsies and likelihood of a positive result
36. Vascular Neoplasms With NFATC1/C2 Gene Alterations
37. Correction to: The practical utility of AI-assisted molecular profiling in the diagnosis and management of cancer of unknown primary: An updated review
38. Translational Aspects of Epithelioid Sarcoma: Current Consensus
39. The practical utility of AI-assisted molecular profiling in the diagnosis and management of cancer of unknown primary: an updated review
40. Insulinoma-associated protein 1 (INSM1) is a sensitive and highly specific marker of neuroendocrine differentiation in primary lung neoplasms: an immunohistochemical study of 345 cases, including 292 whole-tissue sections
41. Spindle cell neoplasms with novel LTK fusion – Expanding the spectrum of kinase fusion‐positive soft tissue tumors.
42. When molecular outsmarts morphology: Malignant ossifying fibromyxoid tumors masquerading as osteosarcomas, including a novel CREBZF::PHF1 fusion
43. Supplementary Figure S5 from Novel Genomic Risk Stratification Model for Primary Gastrointestinal Stromal Tumors (GIST) in the Adjuvant Therapy Era
44. Data from Novel Genomic Risk Stratification Model for Primary Gastrointestinal Stromal Tumors (GIST) in the Adjuvant Therapy Era
45. Supplementary Tables S1-S5 from Novel Genomic Risk Stratification Model for Primary Gastrointestinal Stromal Tumors (GIST) in the Adjuvant Therapy Era
46. Novel NCOA2/3‐rearranged low‐grade fibroblastic spindle cell tumors: A report of five cases
47. Novel EWSR1::GFI1B gene fusion in angiofibroma of soft tissue
48. Untying the Gordian knot of composite hemangioendothelioma: Discovery of novel fusions
49. Myxoid Pleomorphic Liposarcoma
50. Novel Genomic Risk Stratification Model for Primary Gastrointestinal Stromal Tumors (GIST) in the Adjuvant Therapy Era
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