Publications by authors named "David Sesser"

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Transient versus Permanent Congenital Hypothyroidism after the Age of 3 Years in Infants Detected on the First versus Second Newborn Screening Test in Oregon, USA.
George A Ford, Sara Denniston, David Sesser, Michael R Skeels, Stephen H LaFranchi

Horm Res Paediatr· April 2017

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Infants suspected to have very-long chain acyl-CoA dehydrogenase deficiency from newborn screening.
J Lawrence Merritt, Sverre Vedal, Jose E Abdenur, Sylvia M Au, Bruce A Barshop, David E Sesser

Mol Genet Metab· April 2014

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Congenital hypothyroidism caused by excess prenatal maternal iodine ingestion.
Kara J Connelly, Bruce A Boston, Elizabeth N Pearce, David Sesser, David Snyder

J Pediatr· October 2012

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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, David E Sesser

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, David E Sesser

Genet Med· March 2011

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Prevalence and distribution of the c.1436C→T sequence variant of carnitine palmitoyltransferase 1A among Alaska Native infants.
Bradford D Gessner, Melanie B Gillingham, Monique A Johnson, C Sue Richards, William E Lambert, David Sesser

J Pediatr· January 2011

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Follow-up of newborns with elevated screening T4 concentrations.
Stephen H Lafranchi, David B Snyder, David E Sesser, Michael R Skeels, Nalini Singh

J Pediatr· September 2003

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Initial treatment dose of L-thyroxine in congenital hypothyroidism.
Karin A Selva, Scott H Mandel, Leanne Rien, David Sesser, Richard Miyahira

J Pediatr· December 2002

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