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Phillip Cox

Showing results (21-30 of 34) with videos related to

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Brain : a Journal of Neurology|October 15, 2019
A novel lethal recognizable polymicrogyric syndrome caused by ATP1A2 homozygous truncating variantsNicolas Chatron, Sara Cabet, Eudeline Alix, et al.
Journal of Sport Rehabilitation|May 25, 2021
Severity of Overuse Injury Impacts Self-Efficacy and Quality of Life in Runners: A 2-Year Prospective Cohort StudyShannon L Mihalko, Phillip Cox, Edward Ip, et al.
Human Molecular Genetics|April 10, 2015
Germline recessive mutations in PI4KA are associated with perisylvian polymicrogyria, cerebellar hypoplasia and arthrogryposisAlistair T Pagnamenta, Malcolm F Howard, Eva Wisniewski, et al.
Translational Behavioral Medicine|April 11, 2018
Effect of intensive diet and exercise on self-efficacy in overweight and obese adults with knee osteoarthritis: The IDEA randomized clinical trialShannon L Mihalko, Phillip Cox, Daniel P Beavers, et al.
Journal of Medical Genetics|April 3, 2007
The Shwachman-Bodian-Diamond syndrome gene mutations cause a neonatal form of spondylometaphysial dysplasia (SMD) resembling SMD Sedaghatian typeGen Nishimura, Eiji Nakashima, Yuichiro Hirose, et al.
CMI Communications|May 6, 2026
Clinical and Genomic Characterization of Serratia Bloodstream InfectionsRoberta Monardo, Lawrence P Park, Felicia Ruffin, et al.
The Journal of Infectious Diseases|May 22, 2025
Escherichia coli Type III Secretion System 2 (ETT2) is Associated with Patient Mortality in Bloodstream InfectionsJoshua T Thaden, Phillip Cox, Paa Kwesi Ankrah, et al.
Journal of Medical Genetics|April 19, 2012
Mutations in GRIP1 cause Fraser syndromeMaartje J Vogel, Patrick van Zon, Louise Brueton, et al.
Human Molecular Genetics|December 23, 2006
The Meckel-Gruber Syndrome proteins MKS1 and meckelin interact and are required for primary cilium formationHelen R Dawe, Ursula M Smith, Andrew R Cullinane, et al.
American Journal of Human Genetics|July 11, 2006
Mutations in the embryonal subunit of the acetylcholine receptor (CHRNG) cause lethal and Escobar variants of multiple pterygium syndromeNeil V Morgan, Louise A Brueton, Phillip Cox, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
Brain : a Journal of Neurology|October 15, 2019
A novel lethal recognizable polymicrogyric syndrome caused by ATP1A2 homozygous truncating variantsNicolas Chatron, Sara Cabet, Eudeline Alix, et al.
Journal of Sport Rehabilitation|May 25, 2021
Severity of Overuse Injury Impacts Self-Efficacy and Quality of Life in Runners: A 2-Year Prospective Cohort StudyShannon L Mihalko, Phillip Cox, Edward Ip, et al.
Human Molecular Genetics|April 10, 2015
Germline recessive mutations in PI4KA are associated with perisylvian polymicrogyria, cerebellar hypoplasia and arthrogryposisAlistair T Pagnamenta, Malcolm F Howard, Eva Wisniewski, et al.
Translational Behavioral Medicine|April 11, 2018
Effect of intensive diet and exercise on self-efficacy in overweight and obese adults with knee osteoarthritis: The IDEA randomized clinical trialShannon L Mihalko, Phillip Cox, Daniel P Beavers, et al.
Journal of Medical Genetics|April 3, 2007
The Shwachman-Bodian-Diamond syndrome gene mutations cause a neonatal form of spondylometaphysial dysplasia (SMD) resembling SMD Sedaghatian typeGen Nishimura, Eiji Nakashima, Yuichiro Hirose, et al.
CMI Communications|May 6, 2026
Clinical and Genomic Characterization of Serratia Bloodstream InfectionsRoberta Monardo, Lawrence P Park, Felicia Ruffin, et al.
The Journal of Infectious Diseases|May 22, 2025
Escherichia coli Type III Secretion System 2 (ETT2) is Associated with Patient Mortality in Bloodstream InfectionsJoshua T Thaden, Phillip Cox, Paa Kwesi Ankrah, et al.
Journal of Medical Genetics|April 19, 2012
Mutations in GRIP1 cause Fraser syndromeMaartje J Vogel, Patrick van Zon, Louise Brueton, et al.
Human Molecular Genetics|December 23, 2006
The Meckel-Gruber Syndrome proteins MKS1 and meckelin interact and are required for primary cilium formationHelen R Dawe, Ursula M Smith, Andrew R Cullinane, et al.
American Journal of Human Genetics|July 11, 2006
Mutations in the embryonal subunit of the acetylcholine receptor (CHRNG) cause lethal and Escobar variants of multiple pterygium syndromeNeil V Morgan, Louise A Brueton, Phillip Cox, et al.
Pageof 4