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Pediatrics
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June 1, 2016
Using Newborn Screening Bloodspots for Research: Public Preferences for Policy Options
Robin Z Hayeems, Fiona A Miller, Carolyn J Barg, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 23, 2025
Newborn screening for common genetic variants associated with permanent hearing loss: Implementation in Ontario and review of the first 3 years
Kristin D Kernohan, Lauren Gallagher, Marie Pigeon, et al.
Molecular Genetics and Metabolism
|
January 23, 2009
A Delphi clinical practice protocol for the management of very long chain acyl-CoA dehydrogenase deficiency
Georgianne L Arnold, Johan Van Hove, Debra Freedenberg, et al.
Scientific Reports
|
November 2, 2019
Association between newborn screening analytes and hypoxic ischemic encephalopathy
Lindsay A Wilson, Deshayne B Fell, Steven Hawken, et al.
International Journal of Technology Assessment in Health Care
|
October 3, 2008
Guidance for considering ethical, legal, and social issues in health technology assessment: application to genetic screening
Beth K Potter, Denise Avard, Ian D Graham, et al.
European Journal of Human Genetics : EJHG
|
February 20, 2014
Public views on participating in newborn screening using genome sequencing
Yvonne Bombard, Fiona A Miller, Robin Z Hayeems, et al.
JIMD Reports
|
September 26, 2015
Detailed Biochemical and Bioenergetic Characterization of FBXL4-Related Encephalomyopathic Mitochondrial DNA Depletion
Ghadi Antoun, Skye McBride, Jason R Vanstone, et al.
Human Vaccines & Immunotherapeutics
|
February 9, 2018
T-cell receptor excision circle levels and safety of paediatric immunization: A population-based self-controlled case series analysis
Kumanan Wilson, Daniel Rodriguez Duque, Malia S Q Murphy, et al.
Orphanet Journal of Rare Diseases
|
July 10, 2013
Mutations in ALDH6A1 encoding methylmalonate semialdehyde dehydrogenase are associated with dysmyelination and transient methylmalonic aciduria
Julien L Marcadier, Amanda M Smith, Daniela Pohl, et al.
PLOS Global Public Health
|
March 24, 2023
Real world external validation of metabolic gestational age assessment in Kenya
Steven Hawken, Victoria Ward, A Brianne Bota, et al.
Page
of 16
Search research articles
Search
Showing results (91-100 of 154) with videos related to
Sort By:
Page
of 16
Pediatrics
|
June 1, 2016
Using Newborn Screening Bloodspots for Research: Public Preferences for Policy Options
Robin Z Hayeems, Fiona A Miller, Carolyn J Barg, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 23, 2025
Newborn screening for common genetic variants associated with permanent hearing loss: Implementation in Ontario and review of the first 3 years
Kristin D Kernohan, Lauren Gallagher, Marie Pigeon, et al.
Molecular Genetics and Metabolism
|
January 23, 2009
A Delphi clinical practice protocol for the management of very long chain acyl-CoA dehydrogenase deficiency
Georgianne L Arnold, Johan Van Hove, Debra Freedenberg, et al.
Scientific Reports
|
November 2, 2019
Association between newborn screening analytes and hypoxic ischemic encephalopathy
Lindsay A Wilson, Deshayne B Fell, Steven Hawken, et al.
International Journal of Technology Assessment in Health Care
|
October 3, 2008
Guidance for considering ethical, legal, and social issues in health technology assessment: application to genetic screening
Beth K Potter, Denise Avard, Ian D Graham, et al.
European Journal of Human Genetics : EJHG
|
February 20, 2014
Public views on participating in newborn screening using genome sequencing
Yvonne Bombard, Fiona A Miller, Robin Z Hayeems, et al.
JIMD Reports
|
September 26, 2015
Detailed Biochemical and Bioenergetic Characterization of FBXL4-Related Encephalomyopathic Mitochondrial DNA Depletion
Ghadi Antoun, Skye McBride, Jason R Vanstone, et al.
Human Vaccines & Immunotherapeutics
|
February 9, 2018
T-cell receptor excision circle levels and safety of paediatric immunization: A population-based self-controlled case series analysis
Kumanan Wilson, Daniel Rodriguez Duque, Malia S Q Murphy, et al.
Orphanet Journal of Rare Diseases
|
July 10, 2013
Mutations in ALDH6A1 encoding methylmalonate semialdehyde dehydrogenase are associated with dysmyelination and transient methylmalonic aciduria
Julien L Marcadier, Amanda M Smith, Daniela Pohl, et al.
PLOS Global Public Health
|
March 24, 2023
Real world external validation of metabolic gestational age assessment in Kenya
Steven Hawken, Victoria Ward, A Brianne Bota, et al.
Page
of 16