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Pranesh Chakraborty

Showing results (111-120 of 154) with videos related to

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Molecular Genetics and Metabolism|December 23, 2017
Disturbed phospholipid metabolism in serine biosynthesis defects revealed by metabolomic profilingKevin E Glinton, Paul J Benke, Matthew A Lines, et al.
JIMD Reports|June 17, 2016
Severe Neonatal Presentation of Mitochondrial Citrate Carrier (SLC25A1) DeficiencyAmanda Smith, Skye McBride, Julien L Marcadier, et al.
Canadian Family Physician Medecin De Famille Canadien|June 15, 2021
Primary care providers' role in newborn screening result notification for cystic fibrosisRobin Z Hayeems, Fiona A Miller, Carolyn J Barg, et al.
JAMA Pediatrics|January 21, 2025
Outcomes of a Population-Based Congenital Cytomegalovirus Screening ProgramJessica K E Dunn, Pranesh Chakraborty, Emily Reuvers, et al.
European Journal of Human Genetics : EJHG|November 26, 2015
DNM1L-related mitochondrial fission defect presenting as refractory epilepsyJason R Vanstone, Amanda M Smith, Skye McBride, et al.
Genetics|October 25, 2017
Pyridoxine-Dependent Epilepsy in Zebrafish Caused by Aldh7a1 DeficiencyIzabella A Pena, Yann Roussel, Kate Daniel, et al.
BMJ (Clinical Research Ed.)|July 12, 2019
Health outcomes of young children born to mothers who received 2009 pandemic H1N1 influenza vaccination during pregnancy: retrospective cohort studyLaura K Walsh, Jessy Donelle, Linda Dodds, et al.
The Journal of Pediatrics|March 11, 2017
Psychosocial Response to Uncertain Newborn Screening Results for Cystic FibrosisRobin Z Hayeems, Fiona A Miller, Carolyn J Barg, et al.
Pediatrics|August 4, 2016
Parent Experience With False-Positive Newborn Screening Results for Cystic FibrosisRobin Z Hayeems, Fiona A Miller, Carolyn J Barg, et al.
Gates Open Research|July 13, 2021
External validation of machine learning models including newborn metabolomic markers for postnatal gestational age estimation in East and South-East Asian infantsSteven Hawken, Malia S Q Murphy, Robin Ducharme, et al.
Pageof 16

Showing results (111-120 of 154) with videos related to

Sort By:
Pageof 16
Molecular Genetics and Metabolism|December 23, 2017
Disturbed phospholipid metabolism in serine biosynthesis defects revealed by metabolomic profilingKevin E Glinton, Paul J Benke, Matthew A Lines, et al.
JIMD Reports|June 17, 2016
Severe Neonatal Presentation of Mitochondrial Citrate Carrier (SLC25A1) DeficiencyAmanda Smith, Skye McBride, Julien L Marcadier, et al.
Canadian Family Physician Medecin De Famille Canadien|June 15, 2021
Primary care providers' role in newborn screening result notification for cystic fibrosisRobin Z Hayeems, Fiona A Miller, Carolyn J Barg, et al.
JAMA Pediatrics|January 21, 2025
Outcomes of a Population-Based Congenital Cytomegalovirus Screening ProgramJessica K E Dunn, Pranesh Chakraborty, Emily Reuvers, et al.
European Journal of Human Genetics : EJHG|November 26, 2015
DNM1L-related mitochondrial fission defect presenting as refractory epilepsyJason R Vanstone, Amanda M Smith, Skye McBride, et al.
Genetics|October 25, 2017
Pyridoxine-Dependent Epilepsy in Zebrafish Caused by Aldh7a1 DeficiencyIzabella A Pena, Yann Roussel, Kate Daniel, et al.
BMJ (Clinical Research Ed.)|July 12, 2019
Health outcomes of young children born to mothers who received 2009 pandemic H1N1 influenza vaccination during pregnancy: retrospective cohort studyLaura K Walsh, Jessy Donelle, Linda Dodds, et al.
The Journal of Pediatrics|March 11, 2017
Psychosocial Response to Uncertain Newborn Screening Results for Cystic FibrosisRobin Z Hayeems, Fiona A Miller, Carolyn J Barg, et al.
Pediatrics|August 4, 2016
Parent Experience With False-Positive Newborn Screening Results for Cystic FibrosisRobin Z Hayeems, Fiona A Miller, Carolyn J Barg, et al.
Gates Open Research|July 13, 2021
External validation of machine learning models including newborn metabolomic markers for postnatal gestational age estimation in East and South-East Asian infantsSteven Hawken, Malia S Q Murphy, Robin Ducharme, et al.
Pageof 16