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Human Vaccines & Immunotherapeutics|February 9, 2018
T-cell receptor excision circle levels and safety of paediatric immunization: A population-based self-controlled case series analysisKumanan 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 aciduriaJulien 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 KenyaSteven Hawken, Victoria Ward, A Brianne Bota, et al.
Public Health Ethics|August 7, 2019
What is in a Name? Parent, Professional and Policy-Maker Conceptions of Consent-Related Language in the Context of Newborn ScreeningStuart G Nicholls, Holly Etchegary, Laure Tessier, et al.
International Braz J Urol : Official Journal of the Brazilian Society of Urology|January 28, 2017
Robotic Assisted Radical Cystoprostatectomy and Intracorporeal Ileal Conduit Urinary Diversion for a Kidney Transplant RecipientPeter A Caputo, Daniel Ramirez, Matthew Maurice, et al.
Clinical Toxicology (Philadelphia, Pa.)|September 17, 2025
Transdermal buprenorphine patch-facilitated induction of sublingual buprenorphine in hospitalized patients receiving full agonist opioids: a retrospective cohort studySimon J Ostrowski, Alek Adkins, David Goldfarb, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 17, 2012
Preemptive renal transplant candidate survival, access to care, and renal function at listingRachel B Fissell, Titte Srinivas, Rich Fatica, et al.
Journal of Inherited Metabolic Disease|October 28, 2010
Diagnosis of glutaric aciduria type 1 by measuring 3-hydroxyglutaric acid in dried urine spots by liquid chromatography tandem mass spectrometryOsama Y Al-Dirbashi, Stefan Kölker, Dione Ng, et al.
Molecular Genetics and Metabolism|September 13, 2015
Biotinidase deficiency: Spectrum of molecular, enzymatic and clinical information from newborn screening Ontario, Canada (2007-2014)Srinitya Gannavarapu, Chitra Prasad, Jennifer DiRaimo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 11, 2012
Achieving the "triple aim" for inborn errors of metabolism: a review of challenges to outcomes research and presentation of a new practice-based evidence frameworkBeth K Potter, Pranesh Chakraborty, Jonathan B Kronick, et al.
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