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Anjali Sharathkumar

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Hematology Reports|September 22, 2022
Congenital Neutropenia with Specific Granulocyte Deficiency Caused by Novel Double Heterozygous <i>SMARCD2</i> MutationsAbukhiran Ibrahim, Anjali Sharathkumar, Heather McLaughlin, et al.
American Journal of Clinical Pathology|April 2, 2020
Discrepant Hemophilia A: An Underdiagnosed Disease EntityAhmad Al-Huniti, Anjali Sharathkumar, Michelle Krantz, et al.
Journal of Thrombosis and Thrombolysis|June 13, 2020
Implementation of automatic data extraction from an enterprise database warehouse (EDW) for validating pediatric VTE decision rule: a prospective observational study in a critical care populationRachael F Schultz, Anjali Sharathkumar, Soyang Kwon, et al.
International Journal of Medical Informatics|February 15, 2020
Pilot trial of semi-automated medical note writing using lexeme hypothesesDuane Gugel, Steven Lentz, Usha Perepu, et al.
Journal of Pediatric Hematology/Oncology|May 7, 2002
Allogeneic bone marrow transplantation in children with chronic myelogenous leukemiaAnjali Sharathkumar, Ian Thornley, E Fred Saunders, et al.
Medical and Pediatric Oncology|April 30, 2002
Misleading leads: don't assume an alpha-fetoprotein secreting tumour is of germ cell or hepatic originAnjali Sharathkumar, Peter J Shaw, Claire Cooke-Yarborough, et al.
Research and Practice in Thrombosis and Haemostasis|September 25, 2025
Characterization of the clinical and laboratory phenotype of hemophilia carriers and trends of utilization of hemostatic therapies: analysis of the American Thrombosis and Hemostasis Network datasetNeeraja Swaminathan, Alison Currie, Jianzhong Hu, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 17, 2023
Letter to the Editor: Experience with subcutaneous desmopressin in patients with von Willebrand disease (VWD) and qualitative platelet function disordersStephanie Saey, Anjali Sharathkumar, Karla Watkinson, et al.
American Journal of Medical Genetics. Part A|May 16, 2003
Malignant hematological disorders in children with Wolf-Hirschhorn syndromeAnjali Sharathkumar, Melanie Kirby, Melvin Freedman, et al.
Hospital Pediatrics|April 7, 2022
NT-proBNP Levels Following IVIG Treatment of Multisystem Inflammatory Syndrome in ChildrenAnna Schmitz, Kelly E Wood, Aditya Badheka, et al.
Pageof 5

Showing results (11-20 of 44) with videos related to

Sort By:
Pageof 5
Hematology Reports|September 22, 2022
Congenital Neutropenia with Specific Granulocyte Deficiency Caused by Novel Double Heterozygous <i>SMARCD2</i> MutationsAbukhiran Ibrahim, Anjali Sharathkumar, Heather McLaughlin, et al.
American Journal of Clinical Pathology|April 2, 2020
Discrepant Hemophilia A: An Underdiagnosed Disease EntityAhmad Al-Huniti, Anjali Sharathkumar, Michelle Krantz, et al.
Journal of Thrombosis and Thrombolysis|June 13, 2020
Implementation of automatic data extraction from an enterprise database warehouse (EDW) for validating pediatric VTE decision rule: a prospective observational study in a critical care populationRachael F Schultz, Anjali Sharathkumar, Soyang Kwon, et al.
International Journal of Medical Informatics|February 15, 2020
Pilot trial of semi-automated medical note writing using lexeme hypothesesDuane Gugel, Steven Lentz, Usha Perepu, et al.
Journal of Pediatric Hematology/Oncology|May 7, 2002
Allogeneic bone marrow transplantation in children with chronic myelogenous leukemiaAnjali Sharathkumar, Ian Thornley, E Fred Saunders, et al.
Medical and Pediatric Oncology|April 30, 2002
Misleading leads: don't assume an alpha-fetoprotein secreting tumour is of germ cell or hepatic originAnjali Sharathkumar, Peter J Shaw, Claire Cooke-Yarborough, et al.
Research and Practice in Thrombosis and Haemostasis|September 25, 2025
Characterization of the clinical and laboratory phenotype of hemophilia carriers and trends of utilization of hemostatic therapies: analysis of the American Thrombosis and Hemostasis Network datasetNeeraja Swaminathan, Alison Currie, Jianzhong Hu, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 17, 2023
Letter to the Editor: Experience with subcutaneous desmopressin in patients with von Willebrand disease (VWD) and qualitative platelet function disordersStephanie Saey, Anjali Sharathkumar, Karla Watkinson, et al.
American Journal of Medical Genetics. Part A|May 16, 2003
Malignant hematological disorders in children with Wolf-Hirschhorn syndromeAnjali Sharathkumar, Melanie Kirby, Melvin Freedman, et al.
Hospital Pediatrics|April 7, 2022
NT-proBNP Levels Following IVIG Treatment of Multisystem Inflammatory Syndrome in ChildrenAnna Schmitz, Kelly E Wood, Aditya Badheka, et al.
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