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James MacKenzie

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Clinics in Dermatology|June 21, 2025
Current applications of artificial intelligence in dermatology offices and potential ethical landminesJames MacKenzie, Christina Coric, Yee Won Kim, et al.
Fertility and Sterility|September 13, 2003
High frequency of cesarean section, antepartum hemorrhage, placenta previa, and preterm delivery in in-vitro fertilization twin pregnanciesPenny R Smithers, Jane Halliday, Lyndon Hale, et al.
Plastic and Reconstructive Surgery. Global Open|May 8, 2026
Radiographic Indications for Orbital Blowout Fracture Reconstruction: A Critical Review of 2 Decades of LiteratureAhmed M Hashem, James MacKenzie, Alexander Flores, et al.
Clinical Dysmorphology|December 1, 2007
Sudden death in a patient with mosaic ring X Turner syndrome and a neuronal migration disorderCheryl Longman, James MacKenzie, Rosslyn Rankin, et al.
The American Journal of Medicine|November 4, 2019
Two Birds, One Stone-An Odd Case of OligoarthritisOluseye Oduyale, Allison Bailey, James MacKenzie, et al.
Journal of Biomedical Informatics|August 14, 2012
Avatar-based simulation in the evaluation of diagnosis and management of mental health disorders in primary careRachel M Satter, Trevor Cohen, Pierina Ortiz, et al.
Annals of Vascular Surgery|October 21, 2019
Early Cannulation ePTFE Arteriovenous Access Grafts are Associated with a Low Incidence of Pseudoaneurysm FormationDouglas James MacKenzie, Andrej Isaak, Jennifer Nash, et al.
Acta Neuropathologica|March 23, 2006
An immunohistochemical study of cases of sporadic and inherited frontotemporal lobar degeneration using 3R- and 4R-specific tau monoclonal antibodiesRohan de Silva, Tammaryn Lashley, Catherine Strand, et al.
Nature Genetics|March 2, 2011
Mutations in the pre-replication complex cause Meier-Gorlin syndromeLouise S Bicknell, Ernie M H F Bongers, Andrea Leitch, et al.
Nature Genetics|December 27, 2011
Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroidsRosa Rademakers, Matt Baker, Alexandra M Nicholson, et al.
Pageof 3

Showing results (21-30 of 30) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
Clinics in Dermatology|June 21, 2025
Current applications of artificial intelligence in dermatology offices and potential ethical landminesJames MacKenzie, Christina Coric, Yee Won Kim, et al.
Fertility and Sterility|September 13, 2003
High frequency of cesarean section, antepartum hemorrhage, placenta previa, and preterm delivery in in-vitro fertilization twin pregnanciesPenny R Smithers, Jane Halliday, Lyndon Hale, et al.
Plastic and Reconstructive Surgery. Global Open|May 8, 2026
Radiographic Indications for Orbital Blowout Fracture Reconstruction: A Critical Review of 2 Decades of LiteratureAhmed M Hashem, James MacKenzie, Alexander Flores, et al.
Clinical Dysmorphology|December 1, 2007
Sudden death in a patient with mosaic ring X Turner syndrome and a neuronal migration disorderCheryl Longman, James MacKenzie, Rosslyn Rankin, et al.
The American Journal of Medicine|November 4, 2019
Two Birds, One Stone-An Odd Case of OligoarthritisOluseye Oduyale, Allison Bailey, James MacKenzie, et al.
Journal of Biomedical Informatics|August 14, 2012
Avatar-based simulation in the evaluation of diagnosis and management of mental health disorders in primary careRachel M Satter, Trevor Cohen, Pierina Ortiz, et al.
Annals of Vascular Surgery|October 21, 2019
Early Cannulation ePTFE Arteriovenous Access Grafts are Associated with a Low Incidence of Pseudoaneurysm FormationDouglas James MacKenzie, Andrej Isaak, Jennifer Nash, et al.
Acta Neuropathologica|March 23, 2006
An immunohistochemical study of cases of sporadic and inherited frontotemporal lobar degeneration using 3R- and 4R-specific tau monoclonal antibodiesRohan de Silva, Tammaryn Lashley, Catherine Strand, et al.
Nature Genetics|March 2, 2011
Mutations in the pre-replication complex cause Meier-Gorlin syndromeLouise S Bicknell, Ernie M H F Bongers, Andrea Leitch, et al.
Nature Genetics|December 27, 2011
Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroidsRosa Rademakers, Matt Baker, Alexandra M Nicholson, et al.
Pageof 3