The health system impact of false positive newborn screening results for medium-chain acyl-CoA dehydrogenase deficiency: a cohort study
2016 · Orphanet Journal of Rare Diseases · 42 citations
https://doi.org/10.1186/s13023-016-0391-5
M
Maria D. Karaceper
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Maria D. Karaceper is an academic researcher from University of Ottawa. The author has contributed to research in topics: Metabolism and Genetic Disorders & Folate and B Vitamins Research & Genomics and Rare Diseases. The author has an h-index of 6, co-authored 13 publications.
ORCID: 0000-0002-1811-4116Papers by this author
worksScoping review of patient- and family-oriented outcomes and measures for chronic pediatric disease
2015 · BMC Pediatrics · 25 citations
https://doi.org/10.1186/s12887-015-0323-x
Health services use by children identified as heterozygous hemoglobinopathy mutation carriers via newborn screening
2021 · BMC Pediatrics · 3 citations
https://doi.org/10.1186/s12887-021-02751-8
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