Showing results (11-20 of 385) with videos related to

Sort By:
Pageof 39
The Journal of Molecular Diagnostics : JMD|February 24, 2018
Optimal Reference Gene Selection for Expression Studies in Human ReticulocytesAnu Aggarwal, Manu Jamwal, Ganesh K Viswanathan, et al.
World Journal of Methodology|March 29, 2016
Cation-exchange high-performance liquid chromatography for variant hemoglobins and HbF/A2: What must hematopathologists know about methodology?Prashant Sharma, Reena Das
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 31, 2026
Combining conventional and reticulocyte metrics enhances Iron deficiency detection in asymptomatic individualsMugdha Gautam, Prashant Sharma, Arnab Pal, et al.
Hemoglobin|February 11, 2022
Hb Mizuho (<i>HBB</i>: c.206T>C): Pitfalls of Screening Tests in an Unstable Hemoglobin Variant Diagnosed after Targeted Next-Generation SequencingDiksha D Yadav, Manu Jamwal, Namrata Singh, et al.
Nanotheranostics|April 17, 2023
Preclinical safety assessment of photoluminescent metal quantum clusters stabilized with autologous serum proteins for host specific theranosticsKritika Sood, Pranjali Yadav, Manu Jamwal, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|April 3, 2023
Genetic Spectrum in F13A1 Detected by Next-Generation Sequencing Among North Indian Patients with FXIII DeficiencyRitika Sharma, Manu Jamwal, Namrata Singh, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|June 12, 2023
Correction to: Genetic Spectrum in F13A1 Detected by Next-Generation Sequencing Among North Indian Patients with FXIII DeficiencyRitika Sharma, Manu Jamwal, Namrata Singh, et al.
Hematology (Amsterdam, Netherlands)|March 27, 2014
Anemia in malignancies: pathogenetic and diagnostic considerationsBalan Louis Gaspar, Prashant Sharma, Reena Das
Hematology (Amsterdam, Netherlands)|May 8, 2014
Congenital dyserythropoietic anemia, type II with SEC23B exon 12 c.1385 A → G mutation, and pseudo-Gaucher cells in two siblingsPrashant Sharma, Reena Das, Deepak Bansal, et al.
European Journal of Haematology|April 11, 2021
Congenital erythrocytosisNabhajit Mallik, Reena Das, Pankaj Malhotra, et al.
Pageof 39