Increased baroreceptor sensitivity in a patient with hereditary spastic paraplegia – type SPG11
An 18 years old male patient was diagnosed with genetically confirmed hereditary spastic paraplegia of type SPG11 - a rare disease of neurodegeneration. During normal clinical routine investigation, he presented with a moderate sinus bradycardia. The function of the cardiovascular system was investi...
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| Autors principals: | , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
De Gruyter
2018-09-01
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| Col·lecció: | Current Directions in Biomedical Engineering |
| Matèries: | |
| Accés en línia: | https://doi.org/10.1515/cdbme-2018-0119 |
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