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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...

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Pubblicato in:Urol Ann
Autori principali: Jalbani, Imran K., Nazim, Syed Muhammad, Abbas, Farhat
Natura: Artigo
Lingua:Inglês
Pubblicazione: Medknow Publications & Media Pvt Ltd 2015
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4310102/
https://ncbi.nlm.nih.gov/pubmed/25657563
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0974-7796.148660
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