Cargando…
Investigation and Management of Apparently Sporadic Central Nervous System Haemangioblastoma for Evidence of Von Hippel–Lindau Disease
Haemangioblastomas are rare, highly vascularised tumours that typically occur in the cerebellum, brain stem and spinal cord. Up to a third of individuals with a haemangioblastoma will have von Hippel–Lindau (VHL) disease. Individuals with haemangioblastoma and underlying VHL disease present, on aver...
Autores principales: | Furness, Hugh, Salfity, Louay, Devereux, Johanna, Halliday, Dorothy, Hanson, Helen, Ruddy, Deborah M., Shah, Neha, Sultana, George, Woodward, Emma R., Sandford, Richard N., Snape, Katie M., Maher, Eamonn R. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8472407/ https://www.ncbi.nlm.nih.gov/pubmed/34573396 http://dx.doi.org/10.3390/genes12091414 |
Ejemplares similares
-
Repurposing propranolol as a drug for the treatment of retinal haemangioblastomas in von Hippel-Lindau disease
por: Albiñana, Virginia, et al.
Publicado: (2017) -
Retinal haemangioblastomas in von Hippel–Lindau germline mutation carriers: progression, complications and treatment outcome
por: Hajjaj, Anass, et al.
Publicado: (2020) -
Supratentorial dural-based haemangioblastoma in a Native American patient without Von Hippel Lindau Syndrome
por: Kaloostian, PE, et al.
Publicado: (2012) -
Supratentorial haemangioblastoma without von Hippel–Lindau syndrome in an adult: A rare tumor with review of literature
por: Pandey, Sharad, et al.
Publicado: (2016) -
Evaluation of tumour surveillance protocols and outcomes in von Hippel-Lindau disease in a national health service
por: Maher, Eamonn R., et al.
Publicado: (2022)