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Hereditary cerebral amyloid angiopathy, Piedmont-type mutation
OBJECTIVE: We present here a case report of a patient with a family history of intracerebral hemorrhages (ICHs) who presented with multiple large lobar hemorrhages in rapid succession, with cognitive sparing, who was found to have a mutation in the β-amyloid coding sequence of amyloid precursor prot...
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| Vydáno v: | Neurol Genet |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Wolters Kluwer
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7164975/ https://ncbi.nlm.nih.gov/pubmed/32337337 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/NXG.0000000000000411 |
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