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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 serum
Sophia Krombholz, Andreas Thomas, Philippe Delahaut, et al.
Neurology
|
March 15, 2013
Pediatric neuroenhancement: ethical, legal, social, and neurodevelopmental implications
William D Graf, Saskia K Nagel, Leon G Epstein, et al.
Neurology
|
December 5, 2013
Author Response
William 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 mutation
Kinga 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 reports
Amanda 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 study
Philippe 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 Professors
Cory J Clark, Matias Fjeldmark, Louise Lu, et al.
Neurogenetics
|
August 25, 2007
Functional, histopathologic and natural history study of neuropathy associated with EGR2 mutations
Kinga Szigeti, Wojciech Wiszniewski, Gulam Mustafa Saifi, et al.
Plos One
|
September 26, 2024
Shared fate was associated with sustained cooperation during the COVID-19 pandemic
Diego Guevara Beltran, Jessica D Ayers, Scott Claessens, et al.
Annals of Neurology
|
September 22, 2007
Molecular consequences of dominant Bethlem myopathy collagen VI mutations
Naomi L Baker, Matthias Mörgelin, Rishika A Pace, et al.
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of 5
Search research articles
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Showing results (31-40 of 43) with videos related to
Sort By:
Page
of 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 serum
Sophia Krombholz, Andreas Thomas, Philippe Delahaut, et al.
Neurology
|
March 15, 2013
Pediatric neuroenhancement: ethical, legal, social, and neurodevelopmental implications
William D Graf, Saskia K Nagel, Leon G Epstein, et al.
Neurology
|
December 5, 2013
Author Response
William 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 mutation
Kinga 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 reports
Amanda 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 study
Philippe 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 Professors
Cory J Clark, Matias Fjeldmark, Louise Lu, et al.
Neurogenetics
|
August 25, 2007
Functional, histopathologic and natural history study of neuropathy associated with EGR2 mutations
Kinga Szigeti, Wojciech Wiszniewski, Gulam Mustafa Saifi, et al.
Plos One
|
September 26, 2024
Shared fate was associated with sustained cooperation during the COVID-19 pandemic
Diego Guevara Beltran, Jessica D Ayers, Scott Claessens, et al.
Annals of Neurology
|
September 22, 2007
Molecular consequences of dominant Bethlem myopathy collagen VI mutations
Naomi L Baker, Matthias Mörgelin, Rishika A Pace, et al.
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of 5