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

Year Number of Results
1946 1
1947 3
1948 4
1949 1
1950 2
1951 6
1952 5
1953 4
1954 2
1956 4
1957 5
1958 4
1959 2
1960 4
1961 9
1962 2
1963 1
1964 7
1965 1
1966 2
1967 6
1968 7
1969 9
1970 4
1971 4
1972 3
1973 4
1974 5
1975 22
1976 17
1977 14
1978 20
1979 15
1980 16
1981 20
1982 21
1983 20
1984 34
1985 19
1986 28
1987 26
1988 33
1989 35
1990 39
1991 64
1992 38
1993 52
1994 67
1995 97
1996 84
1997 97
1998 94
1999 104
2000 129
2001 121
2002 129
2003 132
2004 143
2005 148
2006 165
2007 176
2008 162
2009 183
2010 175
2011 159
2012 170
2013 179
2014 166
2015 150
2016 180
2017 170
2018 170
2019 155
2020 187
2021 181
2022 200
2023 163
2024 194
2025 218
2026 77

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5,142 results

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Page 1
von Hippel-Lindau disease.
Lonser RR, Glenn GM, Walther M, Chew EY, Libutti SK, Linehan WM, Oldfield EH. Lonser RR, et al. Lancet. 2003 Jun 14;361(9374):2059-67. doi: 10.1016/S0140-6736(03)13643-4. Lancet. 2003. PMID: 12814730 Review.
von Hippel-Lindau disease is a heritable multisystem cancer syndrome that is associated with a germline mutation of the VHL tumour suppressor gene on the short arm of chromosome 3. ...Because of the complexities associated with management of the variou …
von Hippel-Lindau disease is a heritable multisystem cancer syndrome that is associated with a germline mutation …
Von Hippel-Lindau Disease.
Chan L, Tsang SH, Sharma T, Diaconita V. Chan L, et al. Adv Exp Med Biol. 2025;1467:225-227. doi: 10.1007/978-3-031-72230-1_44. Adv Exp Med Biol. 2025. PMID: 40736846 Review.
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: Update on Pathogenesis and Systemic Aspects.
Aronow ME, Wiley HE, Gaudric A, Krivosic V, Gorin MB, Shields CL, Shields JA, Jonasch EW, Singh AD, Chew EY. Aronow ME, et al. Retina. 2019 Dec;39(12):2243-2253. doi: 10.1097/IAE.0000000000002555. Retina. 2019. PMID: 31095066 Review.
METHODS: A PubMed search of the English language literature was reviewed using the following search terms: von Hippel-Lindau, von Hippel-Lindau disease, and VHL. Of 6,696 publications, the most current and pertinent information rel …
METHODS: A PubMed search of the English language literature was reviewed using the following search terms: von Hippel-Linda …
von Hippel-Lindau disease-related neoplasia with an emphasis on renal manifestations.
Tekin B, Erickson LA, Gupta S. Tekin B, et al. Semin Diagn Pathol. 2024 Jan;41(1):20-27. doi: 10.1053/j.semdp.2023.11.003. Epub 2023 Nov 8. Semin Diagn Pathol. 2024. PMID: 37980175 Review.
von Hippel-Lindau (VHL) disease is characterized by biallelic inactivation of the VHL gene leading to abnormal or absent VHL protein function, and constitutive activation of hypoxia-inducible factors (HIF) that leads to pro-tumorigenic signaling. ...Th …
von Hippel-Lindau (VHL) disease is characterized by biallelic inactivation of the VHL gene leading to abnormal o …
Von Hippel-Lindau disease-associated renal cell carcinoma: a call to action.
Larcher A, Rowe I, Belladelli F, Fallara G, Raggi D, Necchi A, Montorsi F, Capitanio U, Salonia A; OSR VHL Program. Larcher A, et al. Curr Opin Urol. 2022 Jan 1;32(1):31-39. doi: 10.1097/MOU.0000000000000950. Curr Opin Urol. 2022. PMID: 34783716 Review.
PURPOSE OF REVIEW: While the molecular and genetic bases of Von Hippel-Lindau (VHL) disease have been extensively investigated, limited evidence is available to guide diagnosis, local or systemic therapy, and follow-up. The aim of the current review is …
PURPOSE OF REVIEW: While the molecular and genetic bases of Von Hippel-Lindau (VHL) disease have been extensivel …
Von Hippel-Lindau disease.
Kaelin WG. Kaelin WG. Annu Rev Pathol. 2007;2:145-73. doi: 10.1146/annurev.pathol.2.010506.092049. Annu Rev Pathol. 2007. PMID: 18039096 Review.
von Hippel-Lindau disease, which is characterized by an increased risk of hemangioblastomas, clear cell renal carcinomas, and pheochromocytomas, is caused by inactivating mutations of the VHL tumor suppressor gene. The VHL gene product, pVHL, has multi …
von Hippel-Lindau disease, which is characterized by an increased risk of hemangioblastomas, clear cell renal ca …
Von Hippel-Lindau disease.
Maher ER. Maher ER. Eur J Cancer. 1994;30A(13):1987-90. doi: 10.1016/0959-8049(94)00391-h. Eur J Cancer. 1994. PMID: 7734212 Review. No abstract available.
Von Hippel-Lindau syndrome: clinical features, genetic foundations, and management strategies.
Harbi E, Aschner M. Harbi E, et al. Mol Biol Rep. 2025 Mar 5;52(1):281. doi: 10.1007/s11033-025-10403-8. Mol Biol Rep. 2025. PMID: 40042715 Review.
Von Hippel-Lindau Syndrome (VHL) is a rare, hereditary disorder characterized by the development of multiple tumors and cysts in various parts of the body due to mutations in the VHL gene on chromosome 3p25-26. ...
Von Hippel-Lindau Syndrome (VHL) is a rare, hereditary disorder characterized by the development of multiple tumors and …
[Gastroenterological manifestations of von Hippel-Lindau disease].
Koniusz J, Dąbkowski K, Buczek K, Gomółka A, Starzyńska T. Koniusz J, et al. Pol Merkur Lekarski. 2017 Aug 21;43(254):53-55. Pol Merkur Lekarski. 2017. PMID: 28875969 Review. Polish.
Von Hippel-Lindau disease is rare autosomal dominant disorder that results from mutation of VHL gene. ...The differential diagnosis of pancreatic lesions in patients with von Hippel Lindau syndrome plays an important role. The panc …
Von Hippel-Lindau disease is rare autosomal dominant disorder that results from mutation of VHL gene. ...The dif …
5,142 results