Showing results (51-60 of 184) with videos related to
Sort By:
Pageof 19
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|October 12, 2025
Molecular characterization of rare S-s-U- phenotype in antenatal woman producing anti-U and anti-D and presenting HDFN during twin pregnancy: First report from IndiaHarita Maru, Pooja Kshirsagar, Seema Jadhav, et al.Biomedicines|January 21, 2023
Chronic Hepatitis B and Related Liver Diseases Are Associated with Reduced 25-Hydroxy-Vitamin D Levels: A Systematic Review and Meta-AnalysisAnindita Banerjee, Shreyasi Athalye, Naveen Khargekar, et al.Indian Journal of Pediatrics|July 23, 2013
X linked agammaglobulinemia: a single centre experience from IndiaRashid H Merchant, Deep Parekh, Noor Ahmad, et al.Oncology|March 5, 2024
Comprehensive Study of Chromosomal Copy Number Variations and Genomic Variations Predicting Overall Survival in Myelodysplastic SyndromesNehakumari Maurya, Chandrakala Shanmukhaiah, Somprakash Dhangar, et al.Pathogens (Basel, Switzerland)|March 27, 2024
Diagnosis and Management of Infections in Patients with Mendelian Susceptibility to Mycobacterial DiseaseAparna Dalvi, Umair Ahmed Bargir, Gita Natraj, et al.Journal of Clinical Immunology|January 24, 2020
X-Linked Hyper IgM Syndrome Presenting with Recurrent Tuberculosis-a Case ReportV P Krishnan, Prasad Taur, Ambreen Pandrowala, et al.Hematology (Amsterdam, Netherlands)|February 28, 2018
Novel mutation (R192C) in CYB5R3 gene causing NADH-cytochrome b5 reductase deficiency in eight Indian patients associated with autosomal recessive congenital methemoglobinemia type-IPrabhakar S Kedar, Vinod Gupta, Prashant Warang, et al.Hematology (Amsterdam, Netherlands)|April 12, 2022
Targeted next-generation sequencing revealed a novel homozygous mutation in the LRBA gene causes severe haemolysis associated with Inborn Errors of Immunity in an Indian familyPrabhakar Kedar, Rashmi Dongerdiye, Shanmukhaiah Chandrakala, et al.Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie|February 23, 2023
Phenotyping and Genotyping of HNA: Prevalence, Risk of Alloimmunization, and HNA Incompatibilities in IndiansHarita Gogri, Meghana Parihar, Swati Kulkarni, et al.Dental Research Journal|June 12, 2023
Response of stem cells derived from human exfoliated deciduous teeth to Bio-C Repair and Mineral Trioxide Aggregate Repair HP: Cytotoxicity and gene expression assessmentViral Maru, Manisha Madkaikar, Ashita Gada, et al.Pageof 19