ALLMedicine™ Von Hippel-Lindau Disease Center
Research & Reviews 743 results
https://doi.org/10.1016/j.eprac.2021.03.005
Endocrine Practice : Official Journal of the American Col... Arnon L, Halperin R et. al.
Mar 19th, 2021 - The main causes for morbidity and mortality in von Hippel-Lindau (VHL) disease are central nervous system hemangioblastoma and clear cell renal cell carcinoma, whereas the effect of VHL-related pancreatic neuroendocrine tumors (PNET) on patient ou...
https://doi.org/10.1053/j.gastro.2021.02.033
Gastroenterology Kolokotronis T, Reis H
Feb 21st, 2021 - Multiple Hepatic and Pulmonary Tumours Combined with Bilateral Adrenal Masses in a Young Female with von Hippel-Lindau Disease.|2021|Kolokotronis T,Reis H,|
https://doi.org/10.1093/neuros/nyaa565
Neurosurgery Alvarez R, Mastorakos P et. al.
Jan 14th, 2021 - Retrobulbar hemangioblastomas involving the optic apparatus in patients with von Hippel-Lindau disease (VHL) are rare, with only 25 reported cases in the literature. To analyze the natural history of retrobulbar hemangioblastomas in a large cohort...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7644048
PloS One; Fields FR, Suresh N et. al.
Nov 5th, 2020 - Von Hippel-Lindau disease (VHL) is an autosomal dominant rare disease that causes the formation of angiogenic tumors. When functional, pVHL acts as an E3 ubiquitin ligase that negatively regulates hypoxia inducible factor (HIF). Genetic mutations ...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7528461
BMC Medical Genetics; Liu Z, Zhou J et. al.
Oct 2nd, 2020 - Central nervous system (CNS) hemangioblastomas are the most frequent cause of mortality in patients with Von Hippel-Lindau (VHL) disease, an autosomal dominant genetic disease resulting from germline mutations in the VHL tumor suppressor gene, wit...
Guidelines 1 results
https://www.cancer.gov/types/kidney/hp/renal-cell-carcinoma-genetics/vhl-syndrome?cid=eb_govdel
National Cancer Institute
Von Hippel-Lindau disease (VHL) is an autosomal dominant disease with a predisposition to multiple neoplasms. Germline pathogenic variants in the VHL gene predispose individuals to specific types of both benign and malignant tumors and cysts in ma...
Clinicaltrials.gov 753 results
https://doi.org/10.1016/j.eprac.2021.03.005
Endocrine Practice : Official Journal of the American Col... Arnon L, Halperin R et. al.
Mar 19th, 2021 - The main causes for morbidity and mortality in von Hippel-Lindau (VHL) disease are central nervous system hemangioblastoma and clear cell renal cell carcinoma, whereas the effect of VHL-related pancreatic neuroendocrine tumors (PNET) on patient ou...
https://doi.org/10.1053/j.gastro.2021.02.033
Gastroenterology Kolokotronis T, Reis H
Feb 21st, 2021 - Multiple Hepatic and Pulmonary Tumours Combined with Bilateral Adrenal Masses in a Young Female with von Hippel-Lindau Disease.|2021|Kolokotronis T,Reis H,|
https://doi.org/10.1093/neuros/nyaa565
Neurosurgery Alvarez R, Mastorakos P et. al.
Jan 14th, 2021 - Retrobulbar hemangioblastomas involving the optic apparatus in patients with von Hippel-Lindau disease (VHL) are rare, with only 25 reported cases in the literature. To analyze the natural history of retrobulbar hemangioblastomas in a large cohort...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7644048
PloS One; Fields FR, Suresh N et. al.
Nov 5th, 2020 - Von Hippel-Lindau disease (VHL) is an autosomal dominant rare disease that causes the formation of angiogenic tumors. When functional, pVHL acts as an E3 ubiquitin ligase that negatively regulates hypoxia inducible factor (HIF). Genetic mutations ...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7528461
BMC Medical Genetics; Liu Z, Zhou J et. al.
Oct 2nd, 2020 - Central nervous system (CNS) hemangioblastomas are the most frequent cause of mortality in patients with Von Hippel-Lindau (VHL) disease, an autosomal dominant genetic disease resulting from germline mutations in the VHL tumor suppressor gene, wit...
News 9 results
https://reference.medscape.com/viewarticle/826053_2
Aug 5th, 2019 - Von Hippel-Lindau disease is an autosomal dominant syndrome that confers predisposition to various neoplasms. Renal cell carcinoma develops in nearly 40% of patients with von Hippel-Lindau disease and is a major cause of death among these patients...
https://www.mdedge.com/gihepnews/article/203798/what-your-diagnosis-july-2019?channel=27662
Wai See Ma, MD, Hadi Moattar, MD, MBChB, PhD
Jun 28th, 2019 - The diagnosis von Hippel-Lindau disease The diagnosis is von Hippel-Lindau disease (VHL). Subsequent brain and renal magnetic resonance imaging showed features suggestive of a 5-mm right cerebellar hemangioblastoma and right renal cell carcinoma (.
https://www.mdedge.com/hematology-oncology/article/176202/renal-cell-carcinoma/pazopanib-active-against-renal-other
Susan London
Oct 2nd, 2018 - The oral, multitargeted tyrosine kinase inhibitor pazopanib (Votrient) is active and safe in patients with renal cell carcinoma and other neoplasms caused by von Hippel-Lindau disease, a phase 2 trial has found. Eric Jonasch, MD, and his coinvesti.
https://www.mdedge.com/neurology/article/118235/rare-diseases/vhl-alliance-publishes-suggested-vhl-surveillance-guidelines
Nov 7th, 2016 - The VHL Alliance has published suggested surveillance guidelines approved by the VHLA Clinical Advisory Council regarding testing for individuals at risk for von Hippel-Lindau disease (VHL) who do not yet have symptoms or those who are known to ha.
https://www.onclive.com/publications/oncology-business-news/2014/february-2014/integrating-genetic-counseling-into-an-oncology-practice-can-benefit-high-risk-families
Feb 25th, 2014 - Ellen T. Matloff, MS, CGC Genetic counseling—including testing and risk assessment—is one of the most rapidly growing areas of oncology and has become the standard of care for patients with a personal and family history of breast, ovary, or colon ...