Results 31 to 40 of about 5,631,965 (202)
The Paraganglioma of the Bladder in a Patient with Von Hippel-Lindau Syndrome
Paragangliomas are neuroendocrine neoplasms. They can be functional or non-functional. Although they can be seen in different localizations, they are rarely seen in the bladder. They may accompany hereditary syndromes.
Sevda Dalar
doaj +1 more source
Review on Von Hippel-Lindau, with data on clinics, and the genes ...
Richard, S
core +1 more source
First, do no harm: surgical management of von Hippel Lindau syndrome [PDF]
Von Hippel Lindau (VHL) syndrome is an inherited condition that is associated with retinal and central nervous system haemangioblastomas, as well as renal and pancreatic cysts (Varshney et al., 2017).
Hannah Farley, Farley, Hannah
core +1 more source
DIAGNOSING VON HIPPEL LINDAU DISEASE BY RETINAL CAPILLARY HAEMANGIOBLASTOMAS
Introduction: Von Hippel-Lindau (VHL) syndrome is a disease characterized by the formation of tumors or cysts in many different parts of the body caused by germline. The prevalence of this autosomal dominant condition is very rare.
Yurike Mandrasari +3 more
doaj +1 more source
Review on Von Hippel-Lindau, with data on clinics, and the genes ...
Capodano, AM
core +1 more source
Data regarding the clinical management and follow-up of pancreatic neuroendocrine tumors (PanNETs) associated with Von Hippel-Lindau (VHL) syndrome are limited.
D'Onofrio, M +17 more
core +1 more source
First Single-Centre Experience with the Novel HIF-α Inhibitor Belzutifan in Switzerland
Belzutifan is a new HIF-α inhibitor mainly used in two different indications: von Hippel–Lindau syndrome-associated renal cell carcinoma, haemangioblastomas and pancreatic neuroendocrine tumours, as well as sporadic advanced pre-treated renal cell ...
Tobias Peres +4 more
doaj +1 more source
Von Hippel–Lindau syndrome (VHL-syndrome) is a rare hereditary tumor syndrome predisposing affected patients to hemangioblastomas in the central nervous system (CNS) and retina, kidney cancer and also to neuroendocrine tumors including pheochromocytoma and pancreatic neuroendocrine tumors.
openaire +2 more sources
ABSTRACT Background and Aims Infant bone and soft tissue neoplasms present distinct clinical challenges and lack large‐scale data to inform treatment decisions. This study aims to characterize bone and soft tissue neoplasms in infants in Canada and to compare their outcomes with those of older pediatric patients.
Samuel Sassine +21 more
wiley +1 more source
Going viral − Virus‐targeting nanobodies for research, diagnostics and therapy
The increasing prevalence of viral diseases represents a major threat for global human health. Nanobodies, small binding fragments derived from camelid heavy‐chain antibodies, offer versatile tools for viral research, diagnostics, and antiviral therapy.
Domenic Ebert, Ulrich Rothbauer
wiley +1 more source

