Diagnosing newborns with suspected mitochondrial disorders: an economic evaluation comparing early exome sequencing to current typical care
- 1 October 2021
- journal article
- research article
- Published by Elsevier BV in Genetics in Medicine
- Vol. 23 (10), 1854-1863
- https://doi.org/10.1038/s41436-021-01210-0
Abstract
No abstract availableThis publication has 32 references indexed in Scilit:
- Lifetime costs of cerebral palsyDevelopmental Medicine and Child Neurology, 2009
- Estimating Preference-Based Health Utilities Index Mark 3 Utility Scores for Childhood Conditions in England and ScotlandMedical Decision Making, 2009
- Diagnosis of mitochondrial DNA depletion syndromesArchives of Disease in Childhood, 2009
- Universal Newborn Hearing Screening: Systematic Review to Update the 2001 US Preventive Services Task Force RecommendationPEDIATRICS, 2008
- Long-term Outcome and Clinical Spectrum of 73 Pediatric Patients With Mitochondrial DiseasesPEDIATRICS, 2007
- Good Research Practices for Cost-Effectiveness Analysis Alongside Clinical Trials: The ISPOR RCT-CEA Task Force ReportValue in Health, 2005
- ECONOMIC COSTS OF MENTAL RETARDATION, CEREBRAL PALSY, HEARING LOSS, AND VISION IMPAIRMENTPublished by Emerald ,2005
- The epidemiology of mitochondrial disorders—past, present and futureBiochimica et Biophysica Acta (BBA) - Bioenergetics, 2004
- Clinical Spectrum, Morbidity, and Mortality in 113 Pediatric Patients With Mitochondrial DiseasePEDIATRICS, 2004
- Clinical spectrum and diagnosis of mitochondrial disordersAmerican Journal of Medical Genetics, 2001