𝔖 Bobbio Scriptorium
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MANAGEMENT OF HEREDITARY PHEOCHROMOCYTOMA IN VON HIPPEL-LINDAU KINDREDS WITH PARTIAL ADRENALECTOMY

✍ Scribed by WALTHER, McCLELLAN M.; KEISER, HARRY R.; CHOYKE, PETER L.; RAYFORD, WALTER; LYNE, J. CHRIS; LINEHAN, W. MARSTON


Book ID
123372482
Publisher
Lippincott Williams and Wilkins
Year
1999
Tongue
English
Weight
400 KB
Volume
161
Category
Article
ISSN
0022-5347

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## Abstract Von Hippel–Lindau (VHL) disease type 2A is an inherited tumor syndrome characterized by predisposition to pheochromocytoma (pheo), retinal hemangioma (RA), and central nervous system hemangioblastoma (HB). Specific VHL subtypes display genotype–phenotype correlations but, unlike other f