Quantitative urine amino acid analysis using liquid chromatography tandem mass spectrometry and aTRAQ ® reagents von Held, Patrice K., White, Laura, Pasquali, Marzia

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Improving Reproducibility to Enhance Scientific Rigor through Consideration of Mouse Diet von Westmark, Cara J, Brower, James, Held, Patrice K

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21-Deoxycortisol is a Key Screening Marker for 21-Hydroxylase Deficiency von Held, Patrice K., Bialk, Eric R., Lasarev, Michael R., Allen, David B.

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Application of Principal Component Analysis to Newborn Screening for Congenital Adrenal Hyperplasia von Lasarev, Michael R, Bialk, Eric R, Allen, David B, Held, Patrice K

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Familial Hypercholesterolemia Biomarker Distribution in Dried Blood Spots von Held, Patrice K., Lasarev, Michael, Zhang, Xiao, Wiberley-Bradford, Amy E., Campbell, Kristin, Horner, Vanessa, Shao, Xiangqiang, Benoy, Megan, Dodge, Ann M., Peterson, Amy L.

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Screening for Methylmalonic and Propionic Acidemia: Clinical Outcomes and Follow-Up Recommendations von Held, Patrice K, Singh, Emily, Scott Schwoerer, Jessica

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Effects of Soy Protein Isolate on Fragile X Phenotypes in Mice von Westmark, Pamela R, Lyon, Greg, Gutierrez, Alejandra, Boeck, Brynne, Van Hammond, Olivia, Ripp, Nathan, Pagan-Torres, Nicole Arianne, Brower, James, Held, Patrice K, Scarlett, Cameron, Westmark, Cara J

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Newborn Screening for Congenital Adrenal Hyperplasia: Review of Factors Affecting Screening Accuracy von Held, Patrice K, Bird, Ian M, Heather, Natasha L

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Multiple 17-OHP Cutoff Co-Variates Fail to Improve 21-Hydroxylase Deficiency Screening Accuracy von Matharu, Preet K, Held, Patrice K, Allen, David B

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Analytical Validation of Familial Hypercholesterolemia Biomarkers in Dried Blood Spots von Held, Patrice K, Campbell, Kristin, Wiberley-Bradford, Amy E, Lasarev, Michael, Horner, Vanessa, Peterson, Amy

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Wisconsin’s Screening Algorithm for the Identification of Newborns with Congenital Adrenal Hyperplasia von Bialk, Eric R., Lasarev, Michael R., Held, Patrice K.

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Congenital adrenal hyperplasia cases identified by newborn screening in one- and two-screen states von Held, Patrice K., Shapira, Stuart K., Hinton, Cynthia F., Jones, Elizabeth, Hannon, W. Harry, Ojodu, Jelili

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Long-term outcomes in Amish patients diagnosed with propionic acidemia von Scott Schwoerer, Jessica, Clowes Candadai, Sarah, Held, Patrice K.

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Newborn Screening for Inherited Metabolic Disorders: Early Identification and Long-Term Care for Patients in the Plain Community, Wisconsin, 2011-2017 von Held, Patrice K., Rice, Gregory M., Kuhl, Ashley, Drilias, Nicoletta, Baker, Mei, Deline, James, Spicer, Gretchen, Sandrock, Claire, Seroogy, Christine M., Schwoerer, Jessica Scott

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Harmonizing Newborn Screening Laboratory Proficiency Test Results Using the CDC NSQAP Reference Materials von Pickens, Charles Austin, Sternberg, Maya, Seeterlin, Mary, De Jesús, Víctor R, Morrissey, Mark, Manning, Adrienne, Bhakta, Sonal, Held, Patrice K, Mei, Joanne, Cuthbert, Carla, Petritis, Konstantinos

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Single newborn screen or routine second screening for primary congenital hypothyroidism von Shapira, Stuart K., Hinton, Cynthia F., Held, Patrice K., Jones, Elizabeth, Harry Hannon, W., Ojodu, Jelili

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Clinical relevance of the discrepancy in phenylalanine concentrations analyzed using tandem mass spectrometry compared with ion-exchange chromatography in phenylketonuria von Stroup, Bridget M., Held, Patrice K., Williams, Phillip, Clayton, Murray K., Murali, Sangita G., Rice, Gregory M., Ney, Denise M.

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Development of an assay to simultaneously measure orotic acid, amino acids, and acylcarnitines in dried blood spots von Held, Patrice K., Haynes, Christopher A., De Jesús, Víctor R., Baker, Mei W.

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In Vivo Correction of Murine Tyrosinemia Type I by DNA-Mediated Transposition von Montini, Eugenio, Held, Patrice K., Noll, Meenakshi, Morcinek, Nicolas, Al-Dhalimy, Muhsen, Finegold, Milton, Yant, Stephen R., Kay, Mark A., Grompe, Markus

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Disorders of tyrosine catabolism von Held, Patrice K

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