Showing results (21-30 of 184) with videos related to
Sort By:
Pageof 19
Blood Cells, Molecules & Diseases|June 16, 2014
X-linked hyper IgM syndrome: clinical, immunological and molecular features in patients from IndiaManisha Madkaikar, Maya Gupta, Sushant Chavan, et al.Ocular Immunology and Inflammation|September 23, 2020
Chalazia, A Late Manifestation of Primary Immunodeficiency DisordersUmair Ahmed Bargir, Manisha MadkaikarGenes|February 3, 2021
A New Perspective on the Origin of DNA Double-Strand Breaks and Its Implications for AgeingBhabesh Kumar Tripathy, Kavita Pal, Snehal Shabrish, et al.Indian Journal of Pediatrics|February 28, 2016
Guidelines for Screening, Early Diagnosis and Management of Severe Combined Immunodeficiency (SCID) in IndiaManisha Madkaikar, Jahnavi Aluri, Sudhir GuptaBlood 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 KulkarniInternational Journal of Hematology|February 25, 2016
Antigen expression on a putative leukemic stem cell population and AML blastSwati Garg, Kanjaksha Ghosh, Manisha MadkaikarActa Haematologica|February 21, 2008
Spontaneous resolution of severe aplastic anemia following thymic hemorrhageKanjaksha Ghosh, Manisha Madkaikar, Farah JijinaInternational Journal of Stem Cells|January 4, 2014
Investigating cell surface markers on normal hematopoietic stem cells in three different niche conditionsSwati Garg, Manisha Madkaikar, Kanjaksha GhoshFrontiers in Immunology|March 13, 2018
Clinical, Immunological, and Molecular Findings in Five Patients with Major Histocompatibility Complex Class II Deficiency from IndiaJahnavi Aluri, Maya Gupta, Aparna Dalvi, et al.Journal of Clinical Immunology|October 5, 2016
Clinical, Immunological, and Molecular Findings of Patients with p47phox Defect Chronic Granulomatous Disease (CGD) in Indian FamiliesManasi Kulkarni, Mukesh Desai, Maya Gupta, et al.Pageof 19