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John J Mitchell

Showing results (21-30 of 73) with videos related to

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Molecular Genetics and Metabolism|August 11, 2005
Tetrahydrobiopterin-responsive phenylketonuria: the New South Wales experienceJohn J Mitchell, Bridget Wilcken, Ian Alexander, et al.
Nutrients|September 28, 2021
Impact of COVID-19 Pandemic on Weight and BMI among UK Adults: A Longitudinal Analysis of Data from the HEBECO StudySamuel J Dicken, John J Mitchell, Jessica Newberry Le Vay, et al.
American Journal of Epidemiology|July 3, 2025
Bidirectional associations of Physical Activity and Cognitive Function in Midlife Adults: A Longitudinal Analysis across 26 years follow-upJohn J Mitchell, Mark Hamer, Sarah N James, et al.
Diabetes Research and Clinical Practice|October 24, 2025
Changes in 24-hour daily movement associated with reduced 5-year diabetes risk in the 1970 British Cohort StudyJohn J Mitchell, Joanna M Blodgett, Nicholas A Koemel, et al.
Analytica Chimica Acta|August 28, 2016
UPLC-MS/MS detection of disaccharides derived from glycosaminoglycans as biomarkers of mucopolysaccharidosesChristiane Auray-Blais, Pamela Lavoie, Shunji Tomatsu, et al.
Orphanet Journal of Rare Diseases|June 30, 2018
Using a meta-narrative literature review and focus groups with key stakeholders to identify perceived challenges and solutions for generating robust evidence on the effectiveness of treatments for rare diseasesKylie Tingley, Doug Coyle, Ian D Graham, et al.
The Lancet Regional Health. Europe|November 5, 2024
Prevalence, predictors, and patterns of patient reported non-motor outcomes six months after stroke: a prospective cohort studyHatice Ozkan, Gareth Ambler, Gargi Banerjee, et al.
Paediatrics & Child Health|June 27, 2019
Muscle problems in juvenile-onset acid maltase deficiency (Pompe disease)Eugenio Zapata-Aldana, Hugh J McMillan, Tony Rupar, et al.
The Journal of Molecular Diagnostics : JMD|March 6, 2016
Detection and Quantification of Mosaic Mutations in Disease Genes by Next-Generation SequencingLan Qin, Jing Wang, Xia Tian, et al.
Human Mutation|November 20, 2010
Maternal riboflavin deficiency, resulting in transient neonatal-onset glutaric aciduria Type 2, is caused by a microdeletion in the riboflavin transporter gene GPR172BGladys Ho, Atsushi Yonezawa, Satohiro Masuda, et al.
Pageof 8

Showing results (21-30 of 73) with videos related to

Sort By:
Pageof 8
Molecular Genetics and Metabolism|August 11, 2005
Tetrahydrobiopterin-responsive phenylketonuria: the New South Wales experienceJohn J Mitchell, Bridget Wilcken, Ian Alexander, et al.
Nutrients|September 28, 2021
Impact of COVID-19 Pandemic on Weight and BMI among UK Adults: A Longitudinal Analysis of Data from the HEBECO StudySamuel J Dicken, John J Mitchell, Jessica Newberry Le Vay, et al.
American Journal of Epidemiology|July 3, 2025
Bidirectional associations of Physical Activity and Cognitive Function in Midlife Adults: A Longitudinal Analysis across 26 years follow-upJohn J Mitchell, Mark Hamer, Sarah N James, et al.
Diabetes Research and Clinical Practice|October 24, 2025
Changes in 24-hour daily movement associated with reduced 5-year diabetes risk in the 1970 British Cohort StudyJohn J Mitchell, Joanna M Blodgett, Nicholas A Koemel, et al.
Analytica Chimica Acta|August 28, 2016
UPLC-MS/MS detection of disaccharides derived from glycosaminoglycans as biomarkers of mucopolysaccharidosesChristiane Auray-Blais, Pamela Lavoie, Shunji Tomatsu, et al.
Orphanet Journal of Rare Diseases|June 30, 2018
Using a meta-narrative literature review and focus groups with key stakeholders to identify perceived challenges and solutions for generating robust evidence on the effectiveness of treatments for rare diseasesKylie Tingley, Doug Coyle, Ian D Graham, et al.
The Lancet Regional Health. Europe|November 5, 2024
Prevalence, predictors, and patterns of patient reported non-motor outcomes six months after stroke: a prospective cohort studyHatice Ozkan, Gareth Ambler, Gargi Banerjee, et al.
Paediatrics & Child Health|June 27, 2019
Muscle problems in juvenile-onset acid maltase deficiency (Pompe disease)Eugenio Zapata-Aldana, Hugh J McMillan, Tony Rupar, et al.
The Journal of Molecular Diagnostics : JMD|March 6, 2016
Detection and Quantification of Mosaic Mutations in Disease Genes by Next-Generation SequencingLan Qin, Jing Wang, Xia Tian, et al.
Human Mutation|November 20, 2010
Maternal riboflavin deficiency, resulting in transient neonatal-onset glutaric aciduria Type 2, is caused by a microdeletion in the riboflavin transporter gene GPR172BGladys Ho, Atsushi Yonezawa, Satohiro Masuda, et al.
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