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M Connor

Showing results (321-330 of 758) with videos related to

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Teaching and Learning in Medicine|October 27, 2023
Academic Leadership Academy Summer Program: Clerkship Transition Preparation for Underrepresented in Medicine Medical StudentsDenise M Connor, Alicia Fernandez, Sarah Alba-Nguyen, et al.
Cells|July 14, 2023
Retinal Injury Activates Complement Expression in Müller Cells Leading to Neuroinflammation and Photoreceptor Cell DeathSteven J Tabor, Kentaro Yuda, Jonathan Deck, et al.
The Journal of Hospital Infection|February 19, 2022
Cupriavidus spp. and other waterborne organisms in healthcare water systems across the UKT Inkster, G Wilson, J Black, et al.
Progress in AIDS Pathology|January 1, 1990
Neoplastic diseases in children with acquired immunodeficiency syndromeF J DiCarlo, V V Joshi, J M Oleske, et al.
The American Journal of Sports Medicine|July 9, 2010
Evolving management of middle-third clavicle fractures in the National Football LeagueRobert J Morgan, Larry S Bankston, Michael P Hoenig, et al.
Journal of Advanced Nursing|June 10, 2000
The Roper, Logan and Tierney (1996) model: perceptions and operationalization of the model in psychiatric nursing within a health board in IrelandK Murphy, A Cooney, D Casey, et al.
American Journal of Medical Genetics|July 12, 1996
Genetic localisation of MRX27 to Xq24-26 defines another discrete gene for non-specific X-linked mental retardationA K Gedeon, I A Glass, J M Connor, et al.
The American Journal of Sports Medicine|February 3, 2004
Prospective evaluation of thermal capsulorrhaphy for shoulder instability: indications and results, two- to five-year follow-upDonald F D'Alessandro, James P Bradley, James E Fleischli, et al.
The Journal of Bone and Joint Surgery. British Volume|January 1, 1988
Spondylothoracic and spondylocostal dysostosis. Hereditary forms of spinal deformityA P Roberts, A N Conner, J L Tolmie, et al.
Human Genetics|September 1, 1992
Detection of seven point mutations in the porphobilinogen deaminase gene in patients with acute intermittent porphyria, by direct sequencing of in vitro amplified cDNAC S Mgone, W G Lanyon, M R Moore, et al.
Pageof 76

Showing results (321-330 of 758) with videos related to

Sort By:
Pageof 76
Teaching and Learning in Medicine|October 27, 2023
Academic Leadership Academy Summer Program: Clerkship Transition Preparation for Underrepresented in Medicine Medical StudentsDenise M Connor, Alicia Fernandez, Sarah Alba-Nguyen, et al.
Cells|July 14, 2023
Retinal Injury Activates Complement Expression in Müller Cells Leading to Neuroinflammation and Photoreceptor Cell DeathSteven J Tabor, Kentaro Yuda, Jonathan Deck, et al.
The Journal of Hospital Infection|February 19, 2022
Cupriavidus spp. and other waterborne organisms in healthcare water systems across the UKT Inkster, G Wilson, J Black, et al.
Progress in AIDS Pathology|January 1, 1990
Neoplastic diseases in children with acquired immunodeficiency syndromeF J DiCarlo, V V Joshi, J M Oleske, et al.
The American Journal of Sports Medicine|July 9, 2010
Evolving management of middle-third clavicle fractures in the National Football LeagueRobert J Morgan, Larry S Bankston, Michael P Hoenig, et al.
Journal of Advanced Nursing|June 10, 2000
The Roper, Logan and Tierney (1996) model: perceptions and operationalization of the model in psychiatric nursing within a health board in IrelandK Murphy, A Cooney, D Casey, et al.
American Journal of Medical Genetics|July 12, 1996
Genetic localisation of MRX27 to Xq24-26 defines another discrete gene for non-specific X-linked mental retardationA K Gedeon, I A Glass, J M Connor, et al.
The American Journal of Sports Medicine|February 3, 2004
Prospective evaluation of thermal capsulorrhaphy for shoulder instability: indications and results, two- to five-year follow-upDonald F D'Alessandro, James P Bradley, James E Fleischli, et al.
The Journal of Bone and Joint Surgery. British Volume|January 1, 1988
Spondylothoracic and spondylocostal dysostosis. Hereditary forms of spinal deformityA P Roberts, A N Conner, J L Tolmie, et al.
Human Genetics|September 1, 1992
Detection of seven point mutations in the porphobilinogen deaminase gene in patients with acute intermittent porphyria, by direct sequencing of in vitro amplified cDNAC S Mgone, W G Lanyon, M R Moore, et al.
Pageof 76