354 results on '"Al-Ibraheemi, Alyaa"'
Search Results
2. Molecular profiling of 888 pediatric tumors informs future precision trials and data-sharing initiatives in pediatric cancer
3. Lipoblastoma Arising in the Head and Neck: A Clinicopathologic Analysis of 20 Cases
4. Papillary Hemangioma Harbors Somatic GNA11 and GNAQ Mutations
5. ALK-Rearranged Epithelioid Mesenchymal Neoplasm: Expanding the Spectrum of Tyrosine Kinase–Altered Mesenchymal Tumors
6. CTNNB1 and APC Mutations in Sinonasal Myxoma: Expanding the Spectrum of Tumors Driven By WNT/β-catenin Pathway
7. Papillary Hemangioma Harbors Somatic GNA11 and GNAQ mutations
8. Molecular profiling identifies targeted therapy opportunities in pediatric solid cancer
9. Spectrum of Liver Pathology in Dyskeratosis Congenita
10. Addressing the diagnostic and therapeutic dilemmas of ovarian immature teratoma: Report from a clinicopathologic consensus conference
11. Primary Clear Cell Sarcoma of Bone: Clinicopathologic Study of a Rare Presentation
12. Ewing Sarcoma of the Female Genital Tract: Clinicopathologic Analysis of 21 Cases With an Emphasis on the Differential Diagnosis of Gynecologic Round Cell, Spindle, and Epithelioid Neoplasms.
13. Early Graft Loss With Suspected Seventh‐Day Syndrome Following Pediatric Liver Transplantation.
14. Perivascular Epithelioid Cell–Family Tumors in Children, Adolescents and Young Adults:Clinicopathologic Features in 70 Cases
15. Novel BRAF gene fusions and activating point mutations in spindle cell sarcomas with histologic overlap with infantile fibrosarcoma
16. Novel variants in the stem cell niche factor WNT2B define the disease phenotype as a congenital enteropathy with ocular dysgenesis
17. Newcomers in Vascular Anomalies
18. Vascular Anomalies of the Head and Neck: A Pediatric Overview
19. Primary Adrenal Epithelioid Angiosarcoma: A Case Report.
20. Immunohistochemical Expression of Lymphatic Endothelial Markers in Blue Rubber Bleb Nevus Syndrome.
21. Recurrent and novel USP6 fusions in cranial fasciitis identified by targeted RNA sequencing
22. Imaging findings in epithelioid hemangioendothelioma
23. Rare FGFR Oncogenic Alterations in Sequenced Pediatric Solid and Brain Tumors Suggest FGFR Is a Relevant Molecular Target in Childhood Cancer
24. Intramuscular fast-flow vascular anomaly contains somatic MAP2K1 and KRAS mutations
25. Aberrant receptor tyrosine kinase signaling in lipofibromatosis: a clinicopathological and molecular genetic study of 20 cases
26. Malignant Tenosynovial Giant Cell Tumor: The True “Synovial Sarcoma?” A Clinicopathologic, Immunohistochemical, and Molecular Cytogenetic Study of 10 Cases, Supporting Origin from Synoviocytes
27. Verrucous Venous Malformation—Subcutaneous Variant
28. The Pathologic Diagnosis of Pediatric Soft Tissue Tumors in the Era of Molecular Medicine: The Sarcoma Pediatric Pathology Research Interest Group Perspective.
29. Primary Adrenal Epithelioid Angiosarcoma: A Case Report
30. Arteriovenous malformation associated with a HRAS mutation
31. A somatic activating NRAS variant associated with kaposiform lymphangiomatosis
32. Pathogenic variants in PIK3CA are associated with clinical phenotypes of kaposiform lymphangiomatosis, generalized lymphatic anomaly, and central conducting lymphatic anomaly
33. The Pathologic Diagnosis of Pediatric Soft Tissue Tumors in the Era of Molecular Medicine: The Sarcoma Pediatric Pathology Research Interest Group Perspective
34. Data from Genomic Patterns of Malignant Peripheral Nerve Sheath Tumor (MPNST) Evolution Correlate with Clinical Outcome and Are Detectable in Cell-Free DNA
35. Supplementary Figures 1-15 from Genomic Patterns of Malignant Peripheral Nerve Sheath Tumor (MPNST) Evolution Correlate with Clinical Outcome and Are Detectable in Cell-Free DNA
36. Supplementary Tables S1 and S2 from Genomic Patterns of Malignant Peripheral Nerve Sheath Tumor (MPNST) Evolution Correlate with Clinical Outcome and Are Detectable in Cell-Free DNA
37. Plexiform Myofibroblastoma: Clinicopathologic Analysis of 36 Cases of a Distinctive Benign Tumor of Soft Tissue Affecting Mainly Children and Young Adults
38. Fibrous hamartoma of infancy: a clinicopathologic study of 145 cases, including 2 with sarcomatous features
39. Arteriovenous Malformation MAP2K1 Mutation Causes Local Cartilage Overgrowth by a Cell-Non Autonomous Mechanism
40. FGFR1 gene fusions in a subset of pediatric mesenchymal tumors: Expanding the genetic spectrum of tumors sharing histologic overlap with infantile fibrosarcoma and "NTRK‐rearranged" spindle cell neoplasms.
41. Surgical Management of Fibroadipose Vascular Anomaly of the Lower Extremities
42. Paraspinal mesenchymal tumors: the overlap between neuropathology and soft tissue pathology
43. Figure S1 from Genomic and Immunologic Characterization of INI1-Deficient Pediatric Cancers
44. Supplementary Table 1 and Supplementary Figure Legends from Genomic and Immunologic Characterization of INI1-Deficient Pediatric Cancers
45. Genomic analysis reveals germline and somatic PDGFRB variants with clinical implications in familial infantile myofibromatosis
46. PTEN hamartoma of the soft tissue: the initial manifestation of an underlying PTEN hamartoma tumor syndrome in a 4-year-old female
47. Genomic patterns of malignant peripheral nerve sheath tumor (MPNST) evolution correlate with clinical outcome and are detectable in cell-free DNA
48. Comparison of Controlled Attenuation Parameter and Liver Biopsy to Assess Hepatic Steatosis in Pediatric Patients
49. Fibroadipose Vascular Anomaly in the Upper Extremity: A Distinct Entity With Characteristic Clinical, Radiological, and Histopathological Findings
50. Selected Diagnostically Challenging Pediatric Soft Tissue Tumors
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.