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Kate Gardner

Showing results (11-20 of 29) with videos related to

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Annals of Work Exposures and Health|December 13, 2022
Health and Safety Regulations for COVID-19: A Policy AnalysisLisa M Brosseau, Rachael M Jones, Kate Gardner, et al.
British Journal of Haematology|December 17, 2016
Interim assessment of liver damage in patients with sickle cell disease using new non-invasive techniquesEmma Drasar, Emer Fitzpatrick, Kate Gardner, et al.
Studies in Health Technology and Informatics|October 4, 2007
Sharing electronic laboratory results in a patient portal--a feasibility pilotJonathan S Wald, Karen Burk, Kate Gardner, et al.
British Journal of Haematology|June 22, 2010
Outcome of adults with sickle cell disease admitted to critical care - experience of a single institution in the UKKate Gardner, Cathy Bell, Jack L Bartram, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|April 10, 2014
Phase II study of cediranib in patients with advanced gastrointestinal stromal tumors or soft-tissue sarcomaIan Judson, Michelle Scurr, Kate Gardner, et al.
Stroke|June 16, 2016
Intracranial Aneurysms in Sickle-Cell Disease Are Associated With the Hemoglobin SS Genotype But Not With Moyamoya SyndromePeter Birkeland, Kate Gardner, Rachel Kesse-Adu, et al.
Journal of Adolescent and Young Adult Oncology|March 27, 2019
An Age Stratified Analysis of the Access to Care Continuum Across Three Tumor Groups: Are There Delays for AYA?Tristan Pettit, Louise Sue, Val Waugh, et al.
British Journal of Haematology|June 22, 2010
Outcome of children with sickle cell disease admitted to intensive care - a single institution experienceJack L Bartram, Swee L Thein, Kate Gardner, et al.
Haematologica|March 17, 2018
Proteomic analysis of plasma from children with sickle cell anemia and silent cerebral infarctionSanjay Tewari, George Renney, John Brewin, et al.
Haematologica|December 23, 2020
Genome wide association study of silent cerebral infarction in sickle cell disease (HbSS and HbSC)John N Brewin, Helen Rooks, Kate Gardner, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
Annals of Work Exposures and Health|December 13, 2022
Health and Safety Regulations for COVID-19: A Policy AnalysisLisa M Brosseau, Rachael M Jones, Kate Gardner, et al.
British Journal of Haematology|December 17, 2016
Interim assessment of liver damage in patients with sickle cell disease using new non-invasive techniquesEmma Drasar, Emer Fitzpatrick, Kate Gardner, et al.
Studies in Health Technology and Informatics|October 4, 2007
Sharing electronic laboratory results in a patient portal--a feasibility pilotJonathan S Wald, Karen Burk, Kate Gardner, et al.
British Journal of Haematology|June 22, 2010
Outcome of adults with sickle cell disease admitted to critical care - experience of a single institution in the UKKate Gardner, Cathy Bell, Jack L Bartram, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|April 10, 2014
Phase II study of cediranib in patients with advanced gastrointestinal stromal tumors or soft-tissue sarcomaIan Judson, Michelle Scurr, Kate Gardner, et al.
Stroke|June 16, 2016
Intracranial Aneurysms in Sickle-Cell Disease Are Associated With the Hemoglobin SS Genotype But Not With Moyamoya SyndromePeter Birkeland, Kate Gardner, Rachel Kesse-Adu, et al.
Journal of Adolescent and Young Adult Oncology|March 27, 2019
An Age Stratified Analysis of the Access to Care Continuum Across Three Tumor Groups: Are There Delays for AYA?Tristan Pettit, Louise Sue, Val Waugh, et al.
British Journal of Haematology|June 22, 2010
Outcome of children with sickle cell disease admitted to intensive care - a single institution experienceJack L Bartram, Swee L Thein, Kate Gardner, et al.
Haematologica|March 17, 2018
Proteomic analysis of plasma from children with sickle cell anemia and silent cerebral infarctionSanjay Tewari, George Renney, John Brewin, et al.
Haematologica|December 23, 2020
Genome wide association study of silent cerebral infarction in sickle cell disease (HbSS and HbSC)John N Brewin, Helen Rooks, Kate Gardner, et al.
Pageof 3