Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Manasi MUNDADA"'
Publikováno v:
Türk Patoloji Dergisi, Vol 40, Iss 2, Pp 128-133 (2024)
Objective: SMARCA4-deficient undifferentiated tumor (SMARCA4-UT) is a highly malignant neoplasm with an undifferentiated or rhabdoid phenotype, posing a diagnostic challenge. This case report aims to create awareness about this rare neoplasm while de
Externí odkaz:
https://doaj.org/article/4462016a8f3a4270bf0257aac494ba76
Autor:
Rachna KHERA, Faiq AHMED, Manasi MUNDADA, Sudha S MURTHY, Sandhya DEVİG, Senthil J RAJAPPA, Krishna Mohan MALLAVARAPU, A SANTA, Pavan KUMAR
Publikováno v:
Türk Patoloji Dergisi, Vol 34, Iss 2, Pp 171-174 (2018)
Objective: Molecular genetic analysis of FLT3, NPM1, and CEBPA is already the standard of care in patients with acute myeloid leukaemia (AML) and represents the most frequent genetic alterations and important diagnostic and prognostic indicators. Thi
Externí odkaz:
https://doaj.org/article/bc3fabc837824264b9a72d9672262069
Publikováno v:
Asian Journal of Oncology, Vol 03, Iss 02, Pp 155-157 (2017)
Anaplastic large-cell lymphoma (ALCL) is a distinct type of T-cell lymphoma showing varied clinicopathological features. The clinical entities identified are systemic and primary cutaneous types. ALK+ ALCL are more common in childhood with predominan
Externí odkaz:
https://doaj.org/article/e3f36603e9a14313b9be801ab84bafbd
Autor:
Manogna Das Oravakandy, Faiq Ahmed, Rachna Khera, Manasi Mundada, Sudha S. Murthy, Senthil J. Rajappa, M. V. T. Krishna Mohan, B. Pavan Kumar, A. Santa
Publikováno v:
Indian journal of hematologyblood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion. 38(4)
Nucleophosmin (NPM1) mutation is one of the most common recurring genetic abnormalities seen in acute myeloid leukemia (AML). Immunohistochemistry serves as a cost effective and simple surrogate testing method for detection of NPM1 mutation. This stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::acf9002dbd862ecb2cafea59dbda6e50
https://pubmed.ncbi.nlm.nih.gov/36258732
https://pubmed.ncbi.nlm.nih.gov/36258732