Cargando…
Pheochromocytoma associated with von Hippel-lindau disease in a Pakistani family
OBJECTIVES: The aim was to study the presentation, disease characteristics, operative outcome, and prognosis in patients with familial Pheochromocytoma associated with von Hippel-Lindau (VHL) disease. MATERIALS AND METHODS: There were six patients belonging to two generations of a single family who...
Autores principales: | Jalbani, Imran K., Nazim, Syed Muhammad, Abbas, Farhat |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4310102/ https://www.ncbi.nlm.nih.gov/pubmed/25657563 http://dx.doi.org/10.4103/0974-7796.148660 |
Ejemplares similares
-
Von Hippel-Lindau Syndrome: Diagnosis and Management of Hemangioblastoma and Pheochromocytoma
por: Vaganovs, P., et al.
Publicado: (2013) -
A malignant pheochromocytoma in a child with von Hippel-Lindau mutation
por: POPA, GHEORGHE, et al.
Publicado: (2017) -
Bilateral papillopathy as a presenting sign of pheochromocytoma associated with von Hippel–Lindau disease
por: Shah, Veeral, et al.
Publicado: (2014) -
A pediatric case of pheochromocytoma without apparent hypertension associated
with von Hippel-Lindau disease
por: Igaki, Junko, et al.
Publicado: (2018) -
Von Hippel-Lindau Disease
por: Hes, Frederik J, et al.
Publicado: (2005)