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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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| 發表在: | Neurol Genet |
|---|---|
| Main Authors: | , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Wolters Kluwer
2020
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| 主題: | |
| 在線閱讀: | 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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