Results 31 to 40 of about 5,631,965 (202)

The Paraganglioma of the Bladder in a Patient with Von Hippel-Lindau Syndrome

open access: yesAsian Pacific Journal of Cancer Care, 2023
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

Von Hippel-Lindau [PDF]

open access: yes, 2001
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]

open access: yes, 2023
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

open access: yesIJRETINA (International Journal of Retina), 2022
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

Von Hippel-Lindau [PDF]

open access: yes, 1998
Review on Von Hippel-Lindau, with data on clinics, and the genes ...
Capodano, AM
core   +1 more source

Clinical presentation, genotype-phenotype correlations, and outcome of pancreatic neuroendocrine tumors in Von Hippel-Lindau syndrome

open access: yes, 2021
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

open access: yesCurrent Oncology
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

open access: yes, 2021
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

Bone and Soft Tissue Neoplasms in Infants Versus Older Children: A Report From the Cancer in Young People in Canada Program

open access: yesPediatric Blood &Cancer, EarlyView.
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

open access: yesFEBS Letters, EarlyView.
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

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