Clinical and Biochemical Features of Pheochromocytoma Characteristic of Von Hippel–Lindau Syndrome
Clinical and Biochemical Features of Pheochromocytoma Characteristic of Von Hippel–Lindau Syndrome
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Cham: Springer International Publishing
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Language
English
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Cham: Springer International Publishing
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Background
Approximately 30% of patients with apparent sporadic pheochromocytoma (Pheo) may later prove to have an inherited predisposition syndrome, most commonly Von Hippel–Lindau (VHL) disease. Our aim was to compare the clinical and biochemical features of Pheo in VHL to those in sporadic disease to identify differences that may be used to g...
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Full title
Clinical and Biochemical Features of Pheochromocytoma Characteristic of Von Hippel–Lindau Syndrome
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TN_cdi_proquest_miscellaneous_2319199495
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2319199495
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ISSN
0364-2313
E-ISSN
1432-2323
DOI
10.1007/s00268-019-05299-y
