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Pranesh Chakraborty

Showing results (81-90 of 154) with videos related to

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Personalized Medicine|May 16, 2018
Benefits and burdens of newborn screening: public understanding and decision-makingStuart G Nicholls, Brenda J Wilson, Holly Etchegary, et al.
Orphanet Journal of Rare Diseases|February 1, 2019
Incidental screen positive findings in a prospective cohort study in Matlab, Bangladesh: insights into expanded newborn screening for low-resource settingsMalia S Q Murphy, Pranesh Chakraborty, Jesmin Pervin, et al.
Orphanet Journal of Rare Diseases|January 10, 2019
Nutritional management of phenylalanine hydroxylase (PAH) deficiency in pediatric patients in Canada: a survey of dietitians' current practicesNataliya Yuskiv, Beth K Potter, Sylvia Stockler, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 27, 2026
Development and content validation of the Clinician-reported Genetic testing Utility InDEx for genomic newborn screening (C-GUIDE NBS)Salma Shickh, Stephanie Luca, Katharine Fooks, et al.
BMC Pediatrics|July 2, 2021
Health services use by children identified as heterozygous hemoglobinopathy mutation carriers via newborn screeningSara D Khangura, Beth K Potter, Christine Davies, et al.
Pediatrics|January 18, 2012
Citizens' values regarding research with stored samples from newborn screening in CanadaYvonne Bombard, Fiona A Miller, Robin Z Hayeems, et al.
Pediatrics|July 15, 2015
Public Perceptions of the Benefits and Risks of Newborn ScreeningFiona A Miller, Robin Z Hayeems, Yvonne Bombard, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|October 16, 2020
Newborn Screening for Spinal Muscular Atrophy: Ontario Testing and Follow-up RecommendationsHugh J McMillan, Kristin D Kernohan, Ed Yeh, et al.
Neurology|August 14, 2015
Natural history of succinic semialdehyde dehydrogenase deficiency through adulthoodSamuel Lapalme-Remis, Evan Cole Lewis, Christine De Meulemeester, et al.
European Journal of Human Genetics : EJHG|June 16, 2016
Consent for newborn screening: parents' and health-care professionals' experiences of consent in practiceHolly Etchegary, Stuart G Nicholls, Laure Tessier, et al.
Pageof 16

Showing results (81-90 of 154) with videos related to

Sort By:
Pageof 16
Personalized Medicine|May 16, 2018
Benefits and burdens of newborn screening: public understanding and decision-makingStuart G Nicholls, Brenda J Wilson, Holly Etchegary, et al.
Orphanet Journal of Rare Diseases|February 1, 2019
Incidental screen positive findings in a prospective cohort study in Matlab, Bangladesh: insights into expanded newborn screening for low-resource settingsMalia S Q Murphy, Pranesh Chakraborty, Jesmin Pervin, et al.
Orphanet Journal of Rare Diseases|January 10, 2019
Nutritional management of phenylalanine hydroxylase (PAH) deficiency in pediatric patients in Canada: a survey of dietitians' current practicesNataliya Yuskiv, Beth K Potter, Sylvia Stockler, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 27, 2026
Development and content validation of the Clinician-reported Genetic testing Utility InDEx for genomic newborn screening (C-GUIDE NBS)Salma Shickh, Stephanie Luca, Katharine Fooks, et al.
BMC Pediatrics|July 2, 2021
Health services use by children identified as heterozygous hemoglobinopathy mutation carriers via newborn screeningSara D Khangura, Beth K Potter, Christine Davies, et al.
Pediatrics|January 18, 2012
Citizens' values regarding research with stored samples from newborn screening in CanadaYvonne Bombard, Fiona A Miller, Robin Z Hayeems, et al.
Pediatrics|July 15, 2015
Public Perceptions of the Benefits and Risks of Newborn ScreeningFiona A Miller, Robin Z Hayeems, Yvonne Bombard, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|October 16, 2020
Newborn Screening for Spinal Muscular Atrophy: Ontario Testing and Follow-up RecommendationsHugh J McMillan, Kristin D Kernohan, Ed Yeh, et al.
Neurology|August 14, 2015
Natural history of succinic semialdehyde dehydrogenase deficiency through adulthoodSamuel Lapalme-Remis, Evan Cole Lewis, Christine De Meulemeester, et al.
European Journal of Human Genetics : EJHG|June 16, 2016
Consent for newborn screening: parents' and health-care professionals' experiences of consent in practiceHolly Etchegary, Stuart G Nicholls, Laure Tessier, et al.
Pageof 16