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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1977 1
1978 1
1980 1
1982 2
1983 2
1984 4
1985 1
1987 5
1988 7
1989 10
1990 6
1991 10
1992 9
1993 9
1994 15
1995 27
1996 20
1997 34
1998 30
1999 16
2000 33
2001 32
2002 26
2003 39
2004 42
2005 52
2006 55
2007 47
2008 44
2009 49
2010 39
2011 30
2012 42
2013 44
2014 29
2015 35
2016 43
2017 35
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2019 31
2020 32
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2022 37
2023 26
2024 9

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1,050 results

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Page 1
Von Hippel-Lindau disease.
Chittiboina P, Lonser RR. Chittiboina P, et al. Handb Clin Neurol. 2015;132:139-56. doi: 10.1016/B978-0-444-62702-5.00010-X. Handb Clin Neurol. 2015. PMID: 26564077 Free PMC article. Review.
von Hippel-Lindau (VHL) disease is an inheritable condition with an incidence of 1 in 36000 live births. ...In this chapter, we summarize the current state of knowledge in VHL disease....
von Hippel-Lindau (VHL) disease is an inheritable condition with an incidence of 1 in 36000 live births. ...In t …
Von Hippel-Lindau disease: insights into oxygen sensing, protein degradation, and cancer.
Kaelin WG Jr. Kaelin WG Jr. J Clin Invest. 2022 Sep 15;132(18):e162480. doi: 10.1172/JCI162480. J Clin Invest. 2022. PMID: 36106637 Free PMC article. Review.
Germline loss-of-function mutations of the VHL tumor suppressor gene cause von Hippel-Lindau disease, which is associated with an increased risk of hemangioblastomas, clear cell renal cell carcinomas (ccRCCs), and paragangliomas. ...Five of these agent …
Germline loss-of-function mutations of the VHL tumor suppressor gene cause von Hippel-Lindau disease, which is a …
VHL, the story of a tumour suppressor gene.
Gossage L, Eisen T, Maher ER. Gossage L, et al. Nat Rev Cancer. 2015 Jan;15(1):55-64. doi: 10.1038/nrc3844. Nat Rev Cancer. 2015. PMID: 25533676 Review.
Since the Von Hippel-Lindau (VHL) disease tumour suppressor gene VHL was identified in 1993 as the genetic basis for a rare disorder, it has proved to be of wide medical and scientific interest. ...As our understanding of the importance of VHL matures, …
Since the Von Hippel-Lindau (VHL) disease tumour suppressor gene VHL was identified in 1993 as the genetic basis …
Von Hippel-Lindau disease and Sturge-Weber syndrome.
Perlman S. Perlman S. Handb Clin Neurol. 2018;148:823-826. doi: 10.1016/B978-0-444-64076-5.00053-3. Handb Clin Neurol. 2018. PMID: 29478617 Review.
The primary neurologic involvement in both von Hippel-Lindau (VHL) disease and Sturge-Weber syndrome (SWS) is vascular tumor/vascular malformation, but molecular pathogenesis, long-term symptom evolution, and treatment are quite different. ...
The primary neurologic involvement in both von Hippel-Lindau (VHL) disease and Sturge-Weber syndrome (SWS …
Von Hippel-Lindau Syndrome.
Ben-Skowronek I, Kozaczuk S. Ben-Skowronek I, et al. Horm Res Paediatr. 2015;84(3):145-52. doi: 10.1159/000431323. Epub 2015 Aug 5. Horm Res Paediatr. 2015. PMID: 26279462 Free article. Review.
Von Hippel-Lindau (VHL) disease is a hereditary cancer syndrome characterized by the development of multiple vascular tumours. ...The course of VHL syndrome is associated with the development of multiple vascular tumours. ...
Von Hippel-Lindau (VHL) disease is a hereditary cancer syndrome characterized by the development of multi …
Von Hippel-Lindau Disease.
Tsang SH, Sharma T. Tsang SH, et al. Adv Exp Med Biol. 2018;1085:201-203. doi: 10.1007/978-3-319-95046-4_42. Adv Exp Med Biol. 2018. PMID: 30578515 Review.
von Hippel-Lindau Disease: Review of Genetics and Imaging.
Shanbhogue KP, Hoch M, Fatterpaker G, Chandarana H. Shanbhogue KP, et al. Radiol Clin North Am. 2016 May;54(3):409-22. doi: 10.1016/j.rcl.2015.12.004. Epub 2016 Mar 21. Radiol Clin North Am. 2016. PMID: 27153780 Review.
von Hippel-Lindau (VHL) disease is an autosomal-dominant, hereditary, multisystem neoplasia syndrome with increased susceptibility to several benign and malignant tumors. ...Imaging and management of this entity are therefore multidisciplinary. …
von Hippel-Lindau (VHL) disease is an autosomal-dominant, hereditary, multisystem neoplasia syndrome with …
von Hippel-Lindau syndrome.
Chou A, Toon C, Pickett J, Gill AJ. Chou A, et al. Front Horm Res. 2013;41:30-49. doi: 10.1159/000345668. Epub 2013 Mar 19. Front Horm Res. 2013. PMID: 23652669 Review.
von Hippel-Lindau (VHL) disease is an autosomal-dominant familial cancer syndrome associated with mutations of the VHL tumor suppressor gene (3p25-26). ...Visceral cysts in the kidney, pancreas and epididymis, nonfunctioning pancreatic neuroendo …
von Hippel-Lindau (VHL) disease is an autosomal-dominant familial cancer syndrome associated with mutatio …
Familial Neoplastic Syndromes.
Eaton RG, Lonser RR. Eaton RG, et al. Neurol Clin. 2022 May;40(2):405-420. doi: 10.1016/j.ncl.2021.11.012. Epub 2022 Mar 31. Neurol Clin. 2022. PMID: 35465883 Review.
The most common neoplastic syndromes clinically relevant to neurology and neurologic surgery, include neurofibromatosis type 1, neurofibromatosis type 2, and Von Hippel-Lindau disease. We define the epidemiology, genetics, clinical presentation, and ma …
The most common neoplastic syndromes clinically relevant to neurology and neurologic surgery, include neurofibromatosis type 1, neurofibroma …
Tumors in von Hippel-Lindau Syndrome: From Head to Toe-Comprehensive State-of-the-Art Review.
Ganeshan D, Menias CO, Pickhardt PJ, Sandrasegaran K, Lubner MG, Ramalingam P, Bhalla S. Ganeshan D, et al. Radiographics. 2018 May-Jun;38(3):849-866. doi: 10.1148/rg.2018170156. Epub 2018 Mar 30. Radiographics. 2018. PMID: 29601266 Free article. Review.
Von Hippel-Lindau syndrome (VHL) is an autosomal-dominant hereditary tumor disease that arises owing to germline mutations in the VHL gene, located on the short arm of chromosome 3. ...
Von Hippel-Lindau syndrome (VHL) is an autosomal-dominant hereditary tumor disease that arises owing to g …
1,050 results