Surgical Management of Multi-Organ Visceral Tumors In Patients With Von Hippel-Lindau Disease: A Single Stage Approach
Author:
Affiliation:
1. From the Urologic Oncology Branch and Surgery Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Urology
Reference21 articles.
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2. Identification of the von Hippel-Lindau disease tumor suppressor gene;Latif;Science,1993
3. von Hippel-Lindau disease affecting 43 members of a single kindred;Lamiell;Medicine,1989
4. Clinical and genetic characterization of pheochromocytoma in von Hippel-Lindau families. Comparison with sporadic pheochromocytoma gives insight into natural history of pheochromocytoma;Walther;J Urol,1999
5. Endolymphatic sac tumors. A source of morbid hearing loss in von Hippel-Lindau disease;Manski;JAMA,1997
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