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Severe Hypocalcemia in a Patient with Tuberous Sclerosis Complex
Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disorder affecting multiple organs, including the brain, skin, lung, and kidney. Among the multiple comorbidities in TSC, bone mineral disturbances remain relatively unrecognized, and only a few studies have reported alteration in cal...
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| Publicat a: | Electrolyte Blood Press |
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| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
The Korean Society of Electrolyte Metabolism
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6629601/ https://ncbi.nlm.nih.gov/pubmed/31338111 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5049/EBP.2019.17.1.21 |
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