Last Updated: 09/26/2026
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Found 10 publications
Mutation-specific NPM1 immunohistochemistry is a sensitive method for detecting residual disease in mid- and postinduction bone marrows: comparison of NPM1 immunohistochemistry, NPM1 real-time polymerase chain reaction, and flow cytometric studies.
Journal: American journal of clinical pathology
Published: January 16, 2026
The Utility of TRBC1 Immunohistochemistry in the Evaluation of T-Cell Lymphomas.
Journal: The American journal of surgical pathology
Published: July 22, 2025
A Rare Case of Concurrent Neuroblastoma and Acute Myeloid Leukemia With CBFA2T3::GLIS2 Fusion: A Diagnostic and Therapeutic Dilemma.
Journal: Pediatric blood & cancer
Published: April 02, 2025
DNMT3A R882 Mutations Confer Unique Clinicopathologic Features in MDS Including a High Risk of AML Transformation.
Journal: Frontiers in oncology
Published: January 06, 2022
The significance of genetic mutations and their prognostic impact on patients with incidental finding of isolated del(20q) in bone marrow without morphologic evidence of a myeloid neoplasm.
Journal: Blood cancer journal
Published: October 26, 2019
A Rare Case of Extramedullary Relapse of Multiple Myeloma Causing Bowel Obstruction.
Journal: Case reports in hematology
Published: January 08, 2019
Pseudo-monoclonal gammopathy: a report of four cases.
Journal: Haematologica
Published: August 05, 2017
Increased Multinucleated Megakaryocytes as an Isolated Finding in Bone Marrow: A Rare Finding and Its Clinical Significance.
Journal: American journal of clinical pathology
Published: April 22, 2017
Clinical course of patients with incidental finding of 20q- in the bone marrow without a morphologic evidence of myeloid neoplasm.
Journal: American journal of hematology
Published: February 03, 2016
Transient monosomy 7 in a chronic myelogenous leukemia patient during nilotinib therapy: a case report.
Journal: Clinical case reports
Published: October 01, 2015
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Last Updated: 09/26/2026