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Germline mutations in the Von Hippel-Lindau disease ( VHL ) gene in families from North America, Europe, and Japan.
Von Hippel-Lindau disease is progressive, which means new tumours could develop at any time, but she refuses to let that hold her back.
Evidence of underlying conditions, such as von Hippel-Lindau disease, polycystic kidney disease, and cystic fibrosis, are often apparent on imaging (Figure 20).
Renal cysts, renal cancer and von Hippel-Lindau disease.
Clinical and genetic analysis of patients with pancreatic neuroendocrine tumors associated with von Hippel-Lindau disease.
von Hippel-Lindau disease gene alterations associated with endolymphatic sac tumor.
Differential grading of endolymphatic sac tumor by virtue of von Hippel-Lindau disease status.
VHL-gene deletion in single renal tubular epithelial cells and renal tubular cysts: further evidence for a cyst-dependent progression pathway of clear cell renal carcinoma in von Hippel-Lindau disease.
A 37-year-old woman with von Hippel-Lindau disease presented with a diagnosis of Meniere's disease that manifested as hearing loss and tinnitus on the left over several years and a recent increase in the frequency of vertigo attacks to one a day.
In particular, he had no manifestation of neurofibromatosis or von Hippel-Lindau disease.