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Research Involvement and Engagement|September 15, 2021
Patient and family engagement in the development of core outcome sets for two rare chronic diseases in childrenShelley M Vanderhout, Maureen Smith, Nicole Pallone, et al.
Plos One|December 17, 2011
Adverse events following 12 and 18 month vaccinations: a population-based, self-controlled case series analysisKumanan Wilson, Steven Hawken, Jeffrey C Kwong, et al.
Acta Obstetricia Et Gynecologica Scandinavica|September 29, 2024
Outcomes of pregnancies with varying levels of nuchal translucency measurements: A population-based retrospective study in Ontario, CanadaKara Bellai-Dussault, Shelley D Dougan, Deshayne B Fell, et al.
Kidney International Reports|June 2, 2018
Association Between Newborn Metabolic Profiles and Pediatric Kidney DiseaseManish M Sood, Malia S Q Murphy, Steven Hawken, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|March 31, 2023
Ethical and practical considerations related to data sharing when collecting patient-reported outcomes in care-based child health researchShelley Vanderhout, Beth K Potter, Maureen Smith, et al.
Plos One|March 12, 2019
A quality assessment of Health Management Information System (HMIS) data for maternal and child health in Jimma Zone, EthiopiaMariame Ouedraogo, Jaameeta Kurji, Lakew Abebe, et al.
BMC Public Health|November 6, 2019
Utilization of key preventive measures for pregnancy complications and malaria among women in Jimma Zone, EthiopiaMariame Ouedraogo, Jaameeta Kurji, Lakew Abebe, et al.
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.
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