Latest papers

Isolate vertigo crisis revealing an endolymphatic sac tumor.

Von Hippel Lindau syndrome.

Verteporfin photodynamic therapy of retinal capillary hemangioblastoma in von Hippel-Lindau disease.

Endolymphatic sac tumor and von Hippel-Lindau disease in a single family.

Double-trouble in mitosis caused by von Hippel-Lindau tumor-suppressor protein inactivation.

Preretinal neovascularization after bevacizumab injections in a patient with von Hippel-Lindau syndrome

Familial and genetic researches on three Chinese families with von Hippel-Lindau disease.

Hereditary and familial kidney cancer.

Novel human pathological mutations. Gene symbol: VHL. Disease: Von Hippel-Lindau syndrome.

Disseminated hemangioblastomatosis of the central nervous system without von Hippel-Lindau disease: a case report.

Genetics of pheochromocytoma and paraganglioma in Spanish patients.

Pancreatic endocrine microadenomatosis in patients with von Hippel-Lindau disease: characterization by VHL/HIF pathway proteins expression.

VHL Awareness Month.

[18F]FDG PET/CT in pancreatic neuroendocrine tumours associated with von Hippel Lindau Syndrome.

LDH-A inhibition, a therapeutic strategy for treatment of hereditary leiomyomatosis and renal cell cancer

Hypogonadotrophic hypogonadism due to intrasellar hemangioblastoma in von Hippel-Lindau syndrome.

Outcome of twin babies free of Von Hippel–Lindau disease after a double-factor preimplantation genetic diagnosis: monogenetic mutation analysis and comprehensive aneuploidy screening

[Adrenalectomy for preservation of adrenocortical function. Indication and results]

[Hereditary renal cancer]

Pituitary stalk hemangioblastomas in von Hippel-Lindau disease.