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Leukemia Research|August 22, 2022
Pneumocystis jirovecii pneumonia [PJP]: An unrecognized concern in AML patients on VenetoclaxSujay Rainchwar, Rohan Halder, Reema Singh, et al.European Journal of Haematology|July 5, 2022
Busulfan and cyclophosphamide-based conditioning regimen still holds the promise of being a safe and efficacious regimen for allogeneic transplantation in patients with transfusion-dependent thalassemia, even in high riskPallavi Mehta, Jyotsna Kapoor, Aakanksha Singh, et al.Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|November 20, 2019
Primary Plasma Cell Leukemia: A Retrospective Study of a Rare Disease From Tertiary Cancer Centre From IndiaNeha Yadav, Mukul Aggarwal, Pallavi Mehta, et al.Journal of Hematopathology|May 16, 2026
VEXAS syndrome: a comprehensive clinicopathologic and genetic analysis of a predominantly Indian cohortDheeraj Chinnam, Aadya Kerkar, Rohit Gulati, et al.Stem Cell Research & Therapy|December 21, 2025
CRISPR editing of HPFH3 genotype induces γ-globin expression and reverses sickle cell disease and β-thalassemia phenotypesSangam Giri Goswami, Pragya Gupta, V R Arvinden, et al.Bone Marrow Transplantation|September 7, 2020
Setting up and sustaining blood and marrow transplant services for children in middle-income economies: an experience-driven position paper on behalf of the EBMT PDWPLawrence Faulkner, Marta Verna, Attilio Rovelli, et al.Pageof 4