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Geoffrey Miller

Showing results (31-40 of 43) with videos related to

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Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society|November 23, 2023
A combined top-down and bottom-up LC-HRMS/MS method for the quantification of human growth hormone in plasma and serumSophia Krombholz, Andreas Thomas, Philippe Delahaut, et al.
Neurology|March 15, 2013
Pediatric neuroenhancement: ethical, legal, social, and neurodevelopmental implicationsWilliam D Graf, Saskia K Nagel, Leon G Epstein, et al.
Neurology|December 5, 2013
Author ResponseWilliam D Graf, Saskia K Nagel, Nagel Osnabruck, et al.
Annals of Neurology|September 4, 2003
Disturbance of muscle fiber differentiation in congenital hypomyelinating neuropathy caused by a novel myelin protein zero mutationKinga Szigeti, Gulam Mustafa Saifi, Dawna Armstrong, et al.
The Yale Journal of Biology and Medicine|March 14, 2013
Novel mutations in the CLCN1 gene of myotonia congenita: 2 case reportsAmanda Amrita Lakraj, Geoffrey Miller, Alexander O Vortmeyer, et al.
Molecular Genetics and Metabolism|March 13, 2010
Early orthotopic liver transplantation in urea cycle defects: follow up of a developmental outcome studyPhilippe M Campeau, Penelope J Pivalizza, Geoffrey Miller, et al.
Perspectives on Psychological Science : a Journal of the Association for Psychological Science|May 16, 2024
Taboos and Self-Censorship Among U.S. Psychology ProfessorsCory J Clark, Matias Fjeldmark, Louise Lu, et al.
Neurogenetics|August 25, 2007
Functional, histopathologic and natural history study of neuropathy associated with EGR2 mutationsKinga Szigeti, Wojciech Wiszniewski, Gulam Mustafa Saifi, et al.
Plos One|September 26, 2024
Shared fate was associated with sustained cooperation during the COVID-19 pandemicDiego Guevara Beltran, Jessica D Ayers, Scott Claessens, et al.
Annals of Neurology|September 22, 2007
Molecular consequences of dominant Bethlem myopathy collagen VI mutationsNaomi L Baker, Matthias Mörgelin, Rishika A Pace, et al.
Pageof 5

Showing results (31-40 of 43) with videos related to

Sort By:
Pageof 5
Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society|November 23, 2023
A combined top-down and bottom-up LC-HRMS/MS method for the quantification of human growth hormone in plasma and serumSophia Krombholz, Andreas Thomas, Philippe Delahaut, et al.
Neurology|March 15, 2013
Pediatric neuroenhancement: ethical, legal, social, and neurodevelopmental implicationsWilliam D Graf, Saskia K Nagel, Leon G Epstein, et al.
Neurology|December 5, 2013
Author ResponseWilliam D Graf, Saskia K Nagel, Nagel Osnabruck, et al.
Annals of Neurology|September 4, 2003
Disturbance of muscle fiber differentiation in congenital hypomyelinating neuropathy caused by a novel myelin protein zero mutationKinga Szigeti, Gulam Mustafa Saifi, Dawna Armstrong, et al.
The Yale Journal of Biology and Medicine|March 14, 2013
Novel mutations in the CLCN1 gene of myotonia congenita: 2 case reportsAmanda Amrita Lakraj, Geoffrey Miller, Alexander O Vortmeyer, et al.
Molecular Genetics and Metabolism|March 13, 2010
Early orthotopic liver transplantation in urea cycle defects: follow up of a developmental outcome studyPhilippe M Campeau, Penelope J Pivalizza, Geoffrey Miller, et al.
Perspectives on Psychological Science : a Journal of the Association for Psychological Science|May 16, 2024
Taboos and Self-Censorship Among U.S. Psychology ProfessorsCory J Clark, Matias Fjeldmark, Louise Lu, et al.
Neurogenetics|August 25, 2007
Functional, histopathologic and natural history study of neuropathy associated with EGR2 mutationsKinga Szigeti, Wojciech Wiszniewski, Gulam Mustafa Saifi, et al.
Plos One|September 26, 2024
Shared fate was associated with sustained cooperation during the COVID-19 pandemicDiego Guevara Beltran, Jessica D Ayers, Scott Claessens, et al.
Annals of Neurology|September 22, 2007
Molecular consequences of dominant Bethlem myopathy collagen VI mutationsNaomi L Baker, Matthias Mörgelin, Rishika A Pace, et al.
Pageof 5