Meizhu Luo
Shenzhen, China
Last Updated: 09/26/2026
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Found 11 publications
A Rare Case of Infant B-ALL With SIN3A::NUTM1 Fusion: Durable Molecular Remission Achieved With Standard Acute Lymphoblastic Leukemia Chemotherapy.
Journal: Pediatric blood & cancer
Published: January 30, 2026
Successful Treatment and Prognostic Analysis of a Pediatric B-Cell Acute Lymphoblastic Leukemia With a Rare CREBBP::ZNF362 Fusion Gene.
Journal: Pediatric blood & cancer
Published: August 26, 2025
Case Report: Pediatric AML with TBC1D15::RAB21 fusion and FLT3-ITD/NPM1 co-mutation: diagnostic pitfalls in morphologic mimicry of acute promyelocytic leukemia.
Journal: Frontiers in oncology
Published: August 13, 2025
Novel and known fibrinogen gene mutations in Chinese pediatric patients with congenital dysfibrinogenemia: genetic and functional characterization.
Journal: Clinical biochemistry
Published: June 28, 2025
Pediatric B-Cell Acute Lymphoblastic Leukemia With FUS::FLI1 Fusion in an Infant With Measurable Residual Disease: Sustained Molecular Remission Achieved With Blinatumomab.
Journal: Pediatric blood & cancer
Published: April 04, 2025
A Novel TAL2::TCRB Fusion With PI3K/AKT Pathway Mutations in Pediatric T-Cell Acute Lymphoblastic Leukemia: Diagnostic and Therapeutic Implications.
Journal: Pediatric blood & cancer
Published: March 09, 2025
A Rare Case of Acute Leukemia With CBFA2T3::GLIS2 Fusion Exhibiting a T/Megakaryocyte Mixed Phenotype.
Journal: Pediatric blood & cancer
Published: December 30, 2024
The Diagnosis of Talaromyces marneffei Central Nervous System Infection in an HIV-Negative Child by Cytological Assay of a Cerebrospinal Fluid Smear.
Journal: Mycopathologia
Published: October 05, 2024
''Cannibalistic'' phagocytosis in acute megakaryoblastic leukemia with NUP98::KDM5A fusion.
Journal: Pediatric blood & cancer
Published: January 07, 2024
Vacuolization of large myeloid lineage and absence of erythroblast and megakaryocyte: Clues to the diagnosis of hereditary transcobalamin II deficiency.
Journal: Pediatric blood & cancer
Published: March 31, 2023
Severe erythroid hypoplasia and erythroblast vacuolization in a male with Brown-Vialetto-Van Laere syndrome 2 misdiagnosed as Diamond Blackfan anemia.
Journal: Pediatric blood & cancer
Published: February 13, 2023
Showing 1-11 of 11
Last Updated: 09/26/2026