Publications by authors named "Mary Seeterlin"

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Methionine adenosyltransferase I/III deficiency: Long-term follow-up and treatment of 3 adult siblings.
Allison Bannick, Sara Chase, Alyson Miner, Mary Seeterlin, Robert L Conway

Eur J Med Genet· December 2020

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Harmonizing Newborn Screening Laboratory Proficiency Test Results Using the CDC NSQAP Reference Materials.
Charles Austin Pickens, Maya Sternberg, Mary Seeterlin, Víctor R De Jesús, Mark Morrissey

Int J Neonatal Screen· September 2020

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Heptadecanoylcarnitine (C17) a novel candidate biomarker for newborn screening of propionic and methylmalonic acidemias.
Sabrina Malvagia, Christopher A Haynes, Laura Grisotto, Daniela Ombrone, Silvia Funghini, Mary Seeterlin

Clin Chim Acta· October 2015

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Newborn screening for dihydrolipoamide dehydrogenase deficiency: Citrulline as a useful analyte.
Shane C Quinonez, Andrea H Seeley, Mary Seeterlin, Eleanor Stanley, Ayesha Ahmad

Mol Genet Metab Rep· August 2014

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Case Report of Argininemia: The Utility of the Arginine/Ornithine Ratio for Newborn Screening (NBS).
Allison Jay, Mary Seeterlin, Eleanor Stanley, Robert Grier

JIMD Rep· February 2013

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Enhanced interpretation of newborn screening results without analyte cutoff values.
Gregg Marquardt, Robert Currier, David M S McHugh, Dimitar Gavrilov, Mark J Magera, Mary A Seeterlin

Genet Med· July 2012

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Clinical validation of cutoff target ranges in newborn screening of metabolic disorders by tandem mass spectrometry: a worldwide collaborative project.
David M S McHugh, Cynthia A Cameron, Jose E Abdenur, Mahera Abdulrahman, Ona Adair, Mary A Seeterlin

Genet Med· March 2011

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