Patricia L. Hall

Affiliations: 
Botany and Plant Pathology Michigan State University, East Lansing, MI 
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Rowe AD, Stoway SD, Åhlman H, et al. (2021) A Novel Approach to Improve Newborn Screening for Congenital Hypothyroidism by Integrating Covariate-Adjusted Results of Different Tests into CLIR Customized Interpretive Tools. International Journal of Neonatal Screening. 7
Hall PL, Wittenauer A, Hagar A. (2020) Post-Analytical Tools for the Triage of Newborn Screening Results in Follow-up Can Reduce Confirmatory Testing and Guide Performance Improvement. International Journal of Neonatal Screening. 6
Hall PL, Li H, Hagar AF, et al. (2020) Newborn Screening for X-Linked Adrenoleukodystrophy in Georgia: Experiences from a Pilot Study Screening of 51,081 Newborns. International Journal of Neonatal Screening. 6
Hall PL, Wittenauer A, Hagar A. (2020) Post-Analytical Tools for the Triage of Newborn Screening Results in Follow-up Can Reduce Confirmatory Testing and Guide Performance Improvement. International Journal of Neonatal Screening. 6: 20
Hall PL, Sanchez R, Hagar AF, et al. (2020) Two-Tiered Newborn Screening with Post-Analytical Tools for Pompe Disease and Mucopolysaccharidosis Type I Results in Performance Improvement and Future Direction. International Journal of Neonatal Screening. 6
Sadat R, Hall PL, Wittenauer AL, et al. (2019) Increased parental anxiety and a benign clinical course: Infants identified with short-chain acyl-CoA dehydrogenase deficiency and isobutyryl-CoA dehydrogenase deficiency through newborn screening in Georgia. Molecular Genetics and Metabolism
Hall PL, Lam C, Alexander JJ, et al. (2018) Urine oligosaccharide screening by MALDI-TOF for the identification of NGLY1 deficiency. Molecular Genetics and Metabolism
Li H, Byers HM, Diaz-Kuan A, et al. (2018) Acute liver failure in neonates with undiagnosed hereditary fructose intolerance due to exposure from widely available infant formulas. Molecular Genetics and Metabolism
Tortorelli S, Eckerman JS, Orsini JJ, et al. (2017) Moonlighting newborn screening markers: the incidental discovery of a second-tier test for Pompe disease. Genetics in Medicine : Official Journal of the American College of Medical Genetics
Hall PL, Laine R, Alexander JJ, et al. (2017) GM2 Activator Deficiency Caused by a Homozygous Exon 2 Deletion in GM2A. Jimd Reports
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