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N Hartley

Showing results (31-40 of 65) with videos related to

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The British Journal of General Practice : the Journal of the Royal College of General Practitioners|April 1, 1996
Pilot study of the acceptability of cystic fibrosis carrier testing during routine antenatal consultations in general practiceH Harris, D Scotcher, N Hartley, et al.
Veterinary Research|January 25, 2014
Frequency of IFNγ-producing T cells correlates with seroreactivity and activated T cells during canine Trypanosoma cruzi infectionAshley N Hartley, Gretchen Cooley, Sarah Gwyn, et al.
Case Reports in Pediatrics|August 29, 2012
Novel Autosomal Recessive c10orf2 Mutations Causing Infantile-Onset Spinocerebellar AtaxiaJessica N Hartley, Frances A Booth, Marc R Del Bigio, et al.
Clinical Orthopaedics and Related Research|May 1, 1978
Efficacy of graded-compression antiembolism stockings in patients undergoing total hip arthroplastyR W Barnes, R A Brand, W Clarke, et al.
Plant, Cell & Environment|April 25, 2017
Genome-wide association studies to identify rice salt-tolerance markersJuan Patishtan, Tom N Hartley, Raquel Fonseca de Carvalho, et al.
Journal of Telemedicine and Telecare|September 23, 2015
Exploring the predictors of home telehealth uptake by elderly Australian healthcare consumersT G Russell, N Gillespie, N Hartley, et al.
Journal of Genetic Counseling|April 28, 2023
Insights into genetic assistant practice and the workforce in North AmericaAngela Krutish, Xiao-Qing Liu, Christine Kelly, et al.
The Journal of Small Animal Practice|April 23, 2024
The epidemiology of tick infestation in dog breeds in the UKD G O'Neill, R Komutrattananon, D B Church, et al.
Diseases of the Colon and Rectum|June 1, 1996
Comparison of individual surgeon's performance. Risk-adjusted analysis with POSSUM scoring systemP M Sagar, M N Hartley, J MacFie, et al.
American Journal of Medical Genetics. Part A|December 18, 2018
A homozygous canonical splice acceptor site mutation in PRUNE1 is responsible for a rare childhood neurodegenerative disease in Manitoba Cree familiesJessica N Hartley, Louise R Simard, Valentina Ly, et al.
Pageof 7

Showing results (31-40 of 65) with videos related to

Sort By:
Pageof 7
The British Journal of General Practice : the Journal of the Royal College of General Practitioners|April 1, 1996
Pilot study of the acceptability of cystic fibrosis carrier testing during routine antenatal consultations in general practiceH Harris, D Scotcher, N Hartley, et al.
Veterinary Research|January 25, 2014
Frequency of IFNγ-producing T cells correlates with seroreactivity and activated T cells during canine Trypanosoma cruzi infectionAshley N Hartley, Gretchen Cooley, Sarah Gwyn, et al.
Case Reports in Pediatrics|August 29, 2012
Novel Autosomal Recessive c10orf2 Mutations Causing Infantile-Onset Spinocerebellar AtaxiaJessica N Hartley, Frances A Booth, Marc R Del Bigio, et al.
Clinical Orthopaedics and Related Research|May 1, 1978
Efficacy of graded-compression antiembolism stockings in patients undergoing total hip arthroplastyR W Barnes, R A Brand, W Clarke, et al.
Plant, Cell & Environment|April 25, 2017
Genome-wide association studies to identify rice salt-tolerance markersJuan Patishtan, Tom N Hartley, Raquel Fonseca de Carvalho, et al.
Journal of Telemedicine and Telecare|September 23, 2015
Exploring the predictors of home telehealth uptake by elderly Australian healthcare consumersT G Russell, N Gillespie, N Hartley, et al.
Journal of Genetic Counseling|April 28, 2023
Insights into genetic assistant practice and the workforce in North AmericaAngela Krutish, Xiao-Qing Liu, Christine Kelly, et al.
The Journal of Small Animal Practice|April 23, 2024
The epidemiology of tick infestation in dog breeds in the UKD G O'Neill, R Komutrattananon, D B Church, et al.
Diseases of the Colon and Rectum|June 1, 1996
Comparison of individual surgeon's performance. Risk-adjusted analysis with POSSUM scoring systemP M Sagar, M N Hartley, J MacFie, et al.
American Journal of Medical Genetics. Part A|December 18, 2018
A homozygous canonical splice acceptor site mutation in PRUNE1 is responsible for a rare childhood neurodegenerative disease in Manitoba Cree familiesJessica N Hartley, Louise R Simard, Valentina Ly, et al.
Pageof 7