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Michael Bennett

Showing results (131-140 of 253) with videos related to

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European Journal of Haematology|November 1, 2015
Hb TAYBE: clinical and morphological findings IN 43 patientsAriel Koren, Carina Levin, Luci Zalman, et al.
Blood|September 28, 2002
Increased bone marrow allograft rejection by depletion of NK cells expressing inhibitory Ly49 NK receptors for donor class I antigensArati Raziuddin, Dan L Longo, Michael Bennett, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|June 3, 2015
Long-term Stability of Urinary Biomarkers of Acute Kidney Injury in ChildrenMeredith P Schuh, Edward Nehus, Qing Ma, et al.
Ophthalmology|April 3, 2012
Macular epiretinal brachytherapy in treated age-related macular degeneration: MERITAGE study: twelve-month safety and efficacy resultsPravin U Dugel, Robert Petrarca, Michael Bennett, et al.
Retina (Philadelphia, Pa.)|October 31, 2013
Macular epiretinal brachytherapy in treated age-related macular degeneration (MERITAGE): month 24 safety and efficacy resultsRobert Petrarca, Pravin U Dugel, Michael Bennett, et al.
BMJ Open Respiratory Research|May 14, 2026
Relationship between quantitative CT and cardiac function in patients with severe COPD exacerbations (ECOPD)Grace Talor Mussell, Joseph Kibbler, Michael Bennett, et al.
Molecular Genetics and Metabolism|August 8, 2013
Mitochondrial respiratory chain disease discrimination by retrospective cohort analysis of blood metabolitesColleen Clarke, Rui Xiao, Emily Place, et al.
Journal of Palliative Medicine|December 22, 2012
Global framework for noncommunicable diseases: how can we monitor palliative care?Liliana De Lima, Roberto Wenk, Eric Krakauer, et al.
Clinical Nephrology|March 25, 2014
Cardiac calcifications are more prevalent in children receiving hemodialysis than peritoneal dialysisPoyyapakkam Srivaths, Rajesh Krishnamurthy, Lori Brunner, et al.
Acta Haematologica|January 22, 2011
E109K is a SEC23B founder mutation among Israeli Moroccan Jewish patients with congenital dyserythropoietic anemia type IIAchiya Amir, Orly Dgany, Tanya Krasnov, et al.
Pageof 26

Showing results (131-140 of 253) with videos related to

Sort By:
Pageof 26
European Journal of Haematology|November 1, 2015
Hb TAYBE: clinical and morphological findings IN 43 patientsAriel Koren, Carina Levin, Luci Zalman, et al.
Blood|September 28, 2002
Increased bone marrow allograft rejection by depletion of NK cells expressing inhibitory Ly49 NK receptors for donor class I antigensArati Raziuddin, Dan L Longo, Michael Bennett, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|June 3, 2015
Long-term Stability of Urinary Biomarkers of Acute Kidney Injury in ChildrenMeredith P Schuh, Edward Nehus, Qing Ma, et al.
Ophthalmology|April 3, 2012
Macular epiretinal brachytherapy in treated age-related macular degeneration: MERITAGE study: twelve-month safety and efficacy resultsPravin U Dugel, Robert Petrarca, Michael Bennett, et al.
Retina (Philadelphia, Pa.)|October 31, 2013
Macular epiretinal brachytherapy in treated age-related macular degeneration (MERITAGE): month 24 safety and efficacy resultsRobert Petrarca, Pravin U Dugel, Michael Bennett, et al.
BMJ Open Respiratory Research|May 14, 2026
Relationship between quantitative CT and cardiac function in patients with severe COPD exacerbations (ECOPD)Grace Talor Mussell, Joseph Kibbler, Michael Bennett, et al.
Molecular Genetics and Metabolism|August 8, 2013
Mitochondrial respiratory chain disease discrimination by retrospective cohort analysis of blood metabolitesColleen Clarke, Rui Xiao, Emily Place, et al.
Journal of Palliative Medicine|December 22, 2012
Global framework for noncommunicable diseases: how can we monitor palliative care?Liliana De Lima, Roberto Wenk, Eric Krakauer, et al.
Clinical Nephrology|March 25, 2014
Cardiac calcifications are more prevalent in children receiving hemodialysis than peritoneal dialysisPoyyapakkam Srivaths, Rajesh Krishnamurthy, Lori Brunner, et al.
Acta Haematologica|January 22, 2011
E109K is a SEC23B founder mutation among Israeli Moroccan Jewish patients with congenital dyserythropoietic anemia type IIAchiya Amir, Orly Dgany, Tanya Krasnov, et al.
Pageof 26