Showing results (1-10 of 210) with videos related to
Sort By:
Pageof 21
Blood Transfusion = Trasfusione Del Sangue|April 5, 2021
Algorithm development and diagnostic accuracy testing for non-invasive foetal RHD genotyping: an Indian experienceDisha Parchure, Manisha Madkaikar, Swati KulkarniTransfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|January 20, 2025
Weak or partial D: Importance of molecular characterization of D variantsAkshaya Tomar, Rati Devendra, Disha Parchure, et al.Transfusion|February 27, 2018
Molecular basis of weak D expression in the Indian population and report of a novel, predominant variant RHD alleleYann Fichou, Disha Parchure, Harita Gogri, et al.Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|April 26, 2018
Molecular genotyping of Indian blood group system antigens in Indian blood donorsHarita Gogri, Pranali Pitale, Manisha Madkaikar, et al.Journal of Clinical Laboratory Analysis|June 24, 2017
Screening for DEL phenotype in RhD negative IndiansSwati Kulkarni, Disha S Parchure, Vidya Gopalkrishnan, et al.Blood Transfusion = Trasfusione Del Sangue|December 2, 2020
Molecular characterization of rare D--/D-- variants in individuals of Indian originSwati Kulkarni, Garima Mishra, Harita Maru, et al.Transfusion|May 5, 2017
First report of Rh<sub>null</sub> individuals in the Indian population and characterization of the underlying molecular mechanismsSwati S Kulkarni, Kasiviswanathan Vasantha, Harita Gogri, et al.The Indian Journal of Medical Research|October 27, 2020
Red cell antigen phenotypes in blood donors & thalassaemia patients for creation of red cell antigen-matched inventorySwati Kulkarni, Bhavika Choudhary, Harita Gogri, et al.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.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.Pageof 21