Showing results (101-110 of 123) with videos related to
Sort By:
Pageof 13
BMC Gastroenterology|August 24, 2021
TPMT and NUDT15 polymorphisms in thiopurine induced leucopenia in inflammatory bowel disease: a prospective study from IndiaNarinder Grover, Prateek Bhatia, Antriksh Kumar, et al.Clinical Lymphoma, Myeloma & Leukemia|April 28, 2022
Clinico-hematological and Outcome Profile of Pediatric B-other-ALL and BCR::ABL1-like pre-B-ALL: An Integrated Genomic Study From North IndiaSrinivasan Peyam, Prateek Bhatia, Minu Singh, et al.The Journal of Molecular Diagnostics : JMD|February 15, 2024
Comprehensive Genomic Analysis Identifies a Diverse Landscape of Sideroblastic and Nonsideroblastic Iron-Related Anemias with Novel and Pathogenic Variants in an Iron-Deficient Endemic SettingPankaj Sharma, Prateek Bhatia, Minu Singh, et al.European Journal of Pediatrics|December 22, 2025
Change in composition of blood after passing through circuit of automated device versus manual clinical method for neonatal exchange transfusionsSourabh Dutta, Neha Sharma, Suchet Sachdev, et al.Expert Review of Clinical Pharmacology|March 8, 2021
Prevalence of polymorphisms in thiopurine metabolism and association with adverse outcomes: a South Asian region-specific systematic review and meta-analysisAnuraag Jena, Daya Krishna Jha, Praveen Kumar-M, et al.Pediatric Neurology|February 7, 2026
Neurological Consequences of Infantile Vitamin B12 Deficiency - A Prospective Cohort StudyPawan Kumar, Naveen Sankhyan, Sameer Vyas, et al.Brain & Development|November 29, 2025
Neurological manifestations and clinical outcomes in pediatric Alexander disease: single-center cohort and identification of novel GFAP variantsRenu Suthar, Yashu Sharma, Arushi Gahlot Saini, et al.Expert Review of Clinical Pharmacology|February 8, 2025
Effectiveness and safety of thiopurines in inflammatory bowel disease patients with NUDT15 polymorphism: a real-world retrospective studyAbhirup Chatterjee, Prateek Bhatia, Saroj K Sinha, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 6, 2022
Identification of novel pathogenic variants in the GCDH gene and assessment of neurodevelopmental outcomes in 24 children with glutaric aciduria type 1Pradip Paria, Arushi Gahlot Saini, Savita Attri, et al.Pediatric Blood & Cancer|May 21, 2025
A Comparative Analysis of Clinical Utility of Cytogenetics and Copy-Number-Integrated Risk Stratification Scores in a Prospective Cohort of Pediatric B-Cell Acute Lymphoblastic LeukemiaAjmeera A Azeez, Prateek Bhatia, Sangeetha Kirubanandhan, et al.Pageof 13