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Development of newborn screening connect (NBS connect): a self-reported patient registry and its role in improvement of care for patients with inherited metabolic disorders.
Orphanet J Rare Dis. 2017 Jul 19;12(1):132. doi: 10.1186/s13023-017-0684-3.
Orphanet J Rare Dis. 2017.
PMID: 28724394
Free PMC article.
The role of evidence analysts in creating nutrition management guidelines for inherited metabolic disorders.
Osara Y, Coakley K, Aisthorpe A, Stembridge A, Quirk M, Splett PL, Rohr F, Singh RH.
Osara Y, et al.
J Eval Clin Pract. 2015 Dec;21(6):1235-43. doi: 10.1111/jep.12428. Epub 2015 Aug 12.
J Eval Clin Pract. 2015.
PMID: 26268585
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Natural history of children and adults with maple syrup urine disease in the NBS-MSUD Connect registry.
Kenneson A, Osara Y, Pringle T, Youngborg L, Singh RH.
Kenneson A, et al. Among authors: osara y.
Mol Genet Metab Rep. 2018 Jan 28;15:22-27. doi: 10.1016/j.ymgmr.2018.01.001. eCollection 2018 Jun.
Mol Genet Metab Rep. 2018.
PMID: 30023285
Free PMC article.
No abstract available.
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Nutrition management guideline for propionic acidemia: An evidence- and consensus-based approach.
Jurecki E, Ueda K, Frazier D, Rohr F, Thompson A, Hussa C, Obernolte L, Reineking B, Roberts AM, Yannicelli S, Osara Y, Stembridge A, Splett P, Singh RH.
Jurecki E, et al. Among authors: osara y.
Mol Genet Metab. 2019 Apr;126(4):341-354. doi: 10.1016/j.ymgme.2019.02.007. Epub 2019 Mar 4.
Mol Genet Metab. 2019.
PMID: 30879957
Free article.
Review.
No abstract available.
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