Acute care utilization for inherited metabolic diseases among children identified through newborn screening in New York state
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical)
Link
http://www.nature.com/articles/gim201421.pdf
Reference25 articles.
Cited by 8 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Family Experiences with Care for Children with Inherited Metabolic Diseases in Canada: A Cross-Sectional Survey;The Patient - Patient-Centered Outcomes Research;2021-07-20
2. A generic emergency protocol for patients with inborn errors of metabolism causing fasting intolerance: A retrospective, single‐center study and the generation of www.emergencyprotocol.net;Journal of Inherited Metabolic Disease;2021-05-04
3. Health services use among children diagnosed with medium-chain acyl-CoA dehydrogenase deficiency through newborn screening: a cohort study in Ontario, Canada;Orphanet Journal of Rare Diseases;2019-03-22
4. Biochemical screening of intellectually disabled and healthy children in Punjab, Pakistan: differences in liver function test and lipid profiles;International Journal of Developmental Disabilities;2019-01-15
5. Triheptanoin versus trioctanoin for long-chain fatty acid oxidation disorders: a double blinded, randomized controlled trial;Journal of Inherited Metabolic Disease;2017-09-04
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