Publications by authors named "Kea Crivelly"

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Expanded Newborn Screening for Inborn Errors of Metabolism at a Single Center in Louisiana (2005-2024): Outcomes.
Jariya Upadia, Grace Noh, Kea Crivelly, Elise Aziz, Amy Cunningham

Int J Neonatal Screen· December 2025

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Thiamine-responsive maple syrup urine disease missed by newborn screen: A case report.
Jariya Upadia, Grace Noh, Kea Crivelly, Jennifer Smith, Hans C Andersson

Mol Genet Metab Rep· September 2025

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Maximal dietary responsiveness after tetrahydrobiopterin (BH4) in 19 phenylalanine hydroxylase deficiency patients: What super-responders can expect.
Jariya Upadia, Kea Crivelly, Grace Noh, Amy Cunningham, Caroline Cerminaro

Mol Genet Metab Rep· March 2024

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Use of pegvaliase in the management of phenylketonuria: Case series of early experience in US clinics.
Darius Adams, Hans C Andersson, Heather Bausell, Kea Crivelly, Caroline Eggerding

Mol Genet Metab Rep· September 2021

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Oral D-galactose supplementation in PGM1-CDG.
Sunnie Yan-Wai Wong, Therese Gadomski, Monique van Scherpenzeel, Tomas Honzik, Hana Hansikova, Kea Crivelly

Genet Med· November 2017

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False-Positive Newborn Screen Using the Beutler Spot Assay for Galactosemia in Glucose-6-Phosphate Dehydrogenase Deficiency.
Grace Stuhrman, Stefanie J Perez Juanazo, Kea Crivelly, Jennifer Smith, Hans Andersson

JIMD Rep· January 2017

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Autism in patients with propionic acidemia.
Peter Witters, Eric Debbold, Kea Crivelly, Kristel Vande Kerckhove, Karen Corthouts

Mol Genet Metab· December 2016

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