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Treatable Inherited Movement Disorders in Children: Spotlight on Clinical and Biochemical Features
BACKGROUND: About 80% of monogenic metabolic diseases causing movement disorders (MDs) emerges during the first 2 decades of life, and a number of these conditions offers the opportunity of a disease‐modifying treatment. The implementation of enlarged neonatal screening programs and the impressive r...
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| Publicado no: | Mov Disord Clin Pract |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley & Sons, Inc.
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7011670/ https://ncbi.nlm.nih.gov/pubmed/32071932 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mdc3.12897 |
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