199 results on '"Sharma, Mehar Chand"'
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2. Deciphering pancreatic neuroendocrine tumors: Unveiling through circulating small extracellular vesicles
3. Evaluation of KIAA1549::BRAF fusions and clinicopathological insights of pilocytic astrocytomas
4. Malignancy arising in adamantinomatous craniopharyngioma: Report of a rare case with unusual morphologic features
5. MYCN immunohistochemistry as surrogate marker for MYCN-amplified spinal ependymomas
6. Spinal astroblastoma, MN1 altered in 3‐year‐old child: An uncommon tumor at an unusual site
7. Pathology and Molecular Pathology of Ependymoma
8. Management protocol and surgical techniques for MRI–Negative Cushing’s disease: a series of 6 cases
9. RNA Sequencing of Intraoperative Peritumoral Tissues Reveals Potential Pathways Involved in Glioma-Related Seizures
10. Spinal atypical teratoid rhabdoid tumor-narrative review and report of a rare case managed with multimodality approach
11. Pediatric Adrenocortical Neoplasms: A Study Comparing Three Histopathological Scoring Systems
12. Ubiquitin specific peptidase 37 and PCNA interaction promotes osteosarcoma pathogenesis by modulating replication fork progression
13. Formulation and validation of a baseline prognostic score for osteosarcoma treated uniformly with a non-high dose methotrexate-based protocol from a low middle income healthcare setting: a single centre analysis of 594 patients
14. Invasive Fungal Infection of the Duramater as the Presenting Manifestation of Disseminated Sarcoidosis (P10-10.005)
15. Abstract 335: Ubiquitin Specific Peptidase 37promotes Osteosarcoma oncogenesis by interacting with PCNA and impacting constitutive replication fork movement.
16. Giant Cells Lesions of Oral and Maxillofacial Region – A Proposed Diagnostic Algorithm
17. A Rare Case of Primary Intracranial Ewing's Sarcoma
18. Splenic Lymphomas: A Tertiary Care Center Experience and Review of Literature
19. Non-invasive intravoxel incoherent motion MRI in prediction of histopathological response to neoadjuvant chemotherapy and survival outcome in osteosarcoma at the time of diagnosis
20. Electromagnetic field stimulation facilitates motor neuron excitability, myogenesis and muscle contractility in spinal cord transected rats
21. Extensive Cystic Changes in a Mediastinal Solitary Fibrous Tumour Causing a Diagnostic Dilemma
22. TCL-306 Application of the Proposed Immunohistochemistry Algorithm for the Prognostication of GATA3 and TBX21 Subtypes of Peripheral T-Cell Lymphoma, Not Otherwise Specified
23. Poster: TCL-306 Application of the Proposed Immunohistochemistry Algorithm for the Prognostication of GATA3 and TBX21 Subtypes of Peripheral T-Cell Lymphoma, Not Otherwise Specified
24. A Mediastinal Mass in a Middle-Aged Woman From a Rare Cause
25. Chemotherapy response evaluation using diffusion weighted MRI in Ewing Sarcoma: A single center experience
26. Multiple Paragangliomas with Novel Mutation: A Rare Entity
27. Altered expression of activating transcription factor 3 in the hippocampus of patients with mesial temporal lobe epilepsy-hippocampal sclerosis (MTLE-HS)
28. Amphicrine Medullary Thyroid Carcinoma — a Case-Based Review Expanding on Its MUC Expression Profile
29. EPEN-20. PDL1 expression and tumor-infiltrating immune cell subpopulations: The role of immune-checkpoint molecules in the prognosis of patients with supratentorial ependymoma and its correlation to survival
30. Transcriptomic profiling of nonneoplastic cortical tissues reveals epileptogenic mechanisms in dysembryoplastic neuroepithelial tumors
31. To compare the performance of various classification criteria in patients of idiopathic inflammatory myopathies in South Asian population. (P16-13.001)
32. Overexpression of prothymosin-α in glioma is associated with tumor aggressiveness and poor prognosis
33. ALK-Negative Primary Cutaneous Anaplastic Large Cell Lymphoma With Systemic Involvement or Systemic ALCL With Cutaneous Lesion. A Diagnostic Dilemma
34. Atrophic Kidney Like Lesion: A Provisional Entity With Brief Review of Literature
35. Comprehensive molecular subgrouping of pleomorphic xanthoastrocytomas (PXA)
36. TTF-1: a well-favoured addition to the immunohistochemistry armamentarium as a diagnostic marker of SEGA
37. Poster: ABCL-321: Clinicopathological Profile of Gastrointestinal Lymphoma Diagnosed Over a Period of 6-Years: A Tertiary Care Center Experience
38. ABCL-321: Clinicopathological Profile of Gastrointestinal Lymphoma Diagnosed Over a Period of 6-Years: A Tertiary Care Center Experience
39. TCL-239: Clinical, Pathological, and Prognostic Implications of RHOAG17V Mutation in Peripheral T-Cell Lymphomas
40. Poster: TCL-239: Clinical, Pathological, and Prognostic Implications of RHOAG17V Mutation in Peripheral T-Cell Lymphomas
41. Diagnostic added value of interictal magnetic source imaging in presurgical evaluation of persons with epilepsy: A prospective blinded study
42. Dedifferentiated vallecular liposarcoma in supraglottic larynx: A case report with review of literature
43. Altered hippocampal kynurenine pathway metabolism contributes to hyperexcitability in human mesial temporal lobe epilepsy–hippocampal sclerosis
44. Focal amplification of FAL1, an oncogenic enhancer lncRNA mapping to chromosome 1q is associated with dysregulated BMI1/p21 axis and an adverse event in intracranial ependymomas
45. Analysis of Histomorphological/molecular Association and Immune Checkpoint Regulators in Epithelioid Glioblastoma and Pleomorphic Xanthoastrocytoma: Are These Tumors Potential Candidate for Immune Checkpoint Blockade
46. Prognostic impact of Notch1 receptor and clinicopathological High‐Risk Predictors in lacrimal gland adenoid cystic carcinoma
47. Comparative contribution of magnetoencephalography (MEG) and single-photon emission computed tomography (SPECT) in pre-operative localization for epilepsy surgery: A prospective blinded study
48. Lymphoma subtypes in India: a tertiary care center review
49. Correction to: EZH2 inhibitory protein (EZHIP/Cxorf67) expression correlates strongly with H3K27me3 loss in posterior fossa ependymomas and is mutually exclusive with H3K27M mutations
50. Mutational Spectrum of CAPN3 with Genotype-Phenotype Correlations in Limb Girdle Muscular Dystrophy Type 2A/R1 (LGMD2A/LGMDR1) Patients in India
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