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Frontiers in Pediatrics|August 5, 2021
The Use of Whole Genome and Exome Sequencing for Newborn Screening: Challenges and Opportunities for Population HealthAudrey C Woerner, Renata C Gallagher, Jerry Vockley, et al.Molecular Genetics and Metabolism|November 9, 2007
Glutaric aciduria type 2 and newborn screening: commentaryJerry VockleyJournal of Inherited Metabolic Disease|October 7, 2008
Metabolism as a complex genetic trait, a systems biology approach: implications for inborn errors of metabolism and clinical diseasesJerry VockleyMolecular Genetics and Metabolism|July 3, 2007
Newborn screening: After the thrill is goneJerry VockleyThe American Journal of Managed Care|August 26, 2020
Long-chain fatty acid oxidation disorders and current management strategiesJerry VockleyAmerican Journal of Medical Genetics. Part C, Seminars in Medical Genetics|April 8, 2006
Isovaleric acidemia: new aspects of genetic and phenotypic heterogeneityJerry Vockley, Regina EnsenauerCurrent Genetic Medicine Reports|March 26, 2013
Neuropsychiatric Symptoms in Inborn Errors of Metabolism: Incorporation of Genomic and Metabolomic Analysis into Therapeutics and PreventionLisa Pan, Jerry VockleyExpert Review of Clinical Pharmacology|July 9, 2025
A pharmacological profile of triheptanoin for the treatment of long-chain fatty acid oxidation disordersRaelynn Forsyth, Jerry VockleyScience Translational Medicine|May 25, 2022
Lysine acylation causes collateral damage in inborn errors of metabolismEric S Goetzman, Jerry VockleyMolecular Genetics and Metabolism|August 3, 2011
Thoroughly modern medicineGeorgianne L Arnold, Jerry VockleyPageof 28