Increasing support for the prevention of adverse childhood experiences and substance use: Implementation of narrative change strategies in local health departments. mwilliam2024-02-26T09:13:37-05:00February 26th, 2024| Read More
An Exploration of Genetic Test Utilization, Genetic Counseling, and Consanguinity within the Inborn Errors of Metabolism Collaborative (IBEMC) mwilliam2024-10-03T07:13:52-04:00January 9th, 2023| Read More
Comparison of Methods of Initial Ascertainment in 58 Cases of Propionic Acidemia Enrolled in the Inborn Errors of Metabolism Information System Reveals Significant Differences in Time to Evaluation and Symptoms at Presentation mwilliam2024-10-03T07:14:13-04:00January 9th, 2023| Read More
Insurance coverage of medical foods for treatment of inherited metabolic disorders mwilliam2024-10-03T07:14:50-04:00December 2nd, 2022| Read More
Clinical validation of cutoff target ranges in newborn screening of metabolic disorders by tandem mass spectrometry: a worldwide collaborative project mwilliam2024-10-03T07:15:03-04:00December 2nd, 2022| Read More
Inborn Errors of Metabolism Collaborative: large-scale collection of data on long-term follow-up for newborn-screened conditions mwilliam2024-10-03T07:15:21-04:00December 2nd, 2022| Read More
Outcomes of cases with 3-methylcrotonyl-CoA carboxylase (3-MCC) deficiency – Report from the Inborn Errors of Metabolism Information System mwilliam2024-10-03T07:15:34-04:00December 2nd, 2022| Read More
Outcomes and genotype-phenotype correlations in 52 individuals with VLCAD deficiency diagnosed by NBS and enrolled in the IBEM-IS database mwilliam2024-10-03T07:15:46-04:00December 2nd, 2022| Read More
Comparison of Methods of Initial Ascertainment in 58 Cases of Propionic Acidemia Enrolled in the Inborn Errors of Metabolism Information System Reveals Significant Differences in Time to Evaluation and Symptoms at Presentation mwilliam2024-10-03T07:15:58-04:00December 2nd, 2022| Read More
Connect with MPHI