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Cerebral Vasculopathy in Children with Neurofibromatosis Type 1
SIMPLE SUMMARY: Neurofibromatosis type 1 is a common autosomal dominant inherited condition, with variable phenotype among affected individuals. Abnormalities of the cerebral vasculature are an acknowledged but poorly understood complication, leading to high morbidity and mortality for individuals w...
Autores principales: | Lehman, Laura L., Ullrich, Nicole J. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10605225/ https://www.ncbi.nlm.nih.gov/pubmed/37894478 http://dx.doi.org/10.3390/cancers15205111 |
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