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JGH Open : an Open Access Journal of Gastroenterology and Hepatology|April 14, 2020
An unusual case of hereditary transthyretin-related amyloidosis and ulcerative colitis in a young Indian girlVishal Sharma, Pankaj Sharma, Minu Singh, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|February 7, 2022
Impact of HFE-2 and HAMP Gene Variations on Iron Overload in Pediatric Patients with Non-Transfusion Dependent Thalassemia: A Pilot StudyNiteesh Bharadwaj, Srinivasan Peyam, Prateek Bhatia, et al.
Blood Cells, Molecules & Diseases|April 10, 2025
Clinical and genetic spectrum of SBDS and DNAJC21 gene variants in bone marrow failure cases: Atypical and cryptic presentationsSwetha Palla, Prateek Bhatia, Sudhanshi Raina, et al.
Virchows Archiv : an International Journal of Pathology|July 17, 2023
MYCN amplification, TERT rearrangements and ATRX mutations in neuroblastoma: clinicopathological correlates- an Indian perspectiveAadya N Kerkar, Dheeraj Chinnam, Aanchal Verma, et al.
Leukemia & Lymphoma|July 4, 2018
Deletion of CDKN2A/B is associated with inferior relapse free survival in pediatric B cell acute lymphoblastic leukemiaM Kathiravan, Minu Singh, Prateek Bhatia, et al.
Molecular Biology Reports|June 23, 2026
TP53 isoform dysregulation in pediatric B-ALL: identifying markers of favorable prognosis and relapse-associated dynamicParminder Kaur, T K Hasib, Sargeet Kaur, et al.
Blood Cells, Molecules & Diseases|March 18, 2020
PEST domain NOTCH mutations confer a poor relapse free survival in pediatric T-ALL: Data from a tertiary care centre in IndiaPrateek Bhatia, Sidharth Totadri, Minu Singh, et al.
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