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Chart validation of an algorithm for identifying hereditary progressive muscular dystrophy in healthcare claims
BACKGROUND: Muscular dystrophies (MDs) are a group of inherited conditions characterized by progressive muscle degeneration and weakness. The rarity and heterogeneity of the population with MD have hindered therapeutic developments as well as epidemiological and health outcomes research. The objecti...
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| Publicado no: | BMC Med Res Methodol |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6688201/ https://ncbi.nlm.nih.gov/pubmed/31399066 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12874-019-0816-7 |
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